(4)!00666 00140.37500 00000.12500
00140.37500 00000.12500
00140.75000 00000.37500 !


U37352 Cluster Incl. U37352:Human protein phosphatase 2A Balpha1 regulatory subunit mRNA, complete cds /cds=(88,1632) /gb=U37352 /gi=1203811 /ug=Hs.171734 /len=4064 40786_at 140.7 

Aliases

 

Descriptions

 

External Ids

B56G 1, 2

B' alpha regulatory subunit 2

HGNC: 93111

KIAA0044 3

PP2A, B subunit, B' gamma isoform 2, 3

Entrez Gene: 55272

MGC23064 2

PP2A, B subunit, B56 gamma isoform 2, 3

UniProtKB: Q133623

PR61G 1, 2

PP2A, B subunit, PR61 gamma isoform 2, 3

Ensembl: ENSG000000783047


PP2A, B subunit, R5 gamma isoform 2, 3


Renal carcinoma antigen NY-REN-29 3

Serine/threonine protein phosphatase 2A, 56 kDa regulatory
subunit, gamma isoform 2

gamma isoform of regulatory subunit B56, protein
phosphatase 2A 2

protein phosphatase 2, regulatory subunit B (B56), gamma
isoform 1, 2

protein phosphatase 2, regulatory subunit B', gamma isoform 2

serine/threonine-protein phosphatase 2A 56 kDa regulatory
subunit gamma isoform 2


Search outside databases for aliases for PPP2R5C gene

Previous GC identifers: GC14P099667 GC14P096091 GC14P100219 GC14P100266 GC14P101345

Summaries
for PPP2R5C

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EntrezGene summary for PPP2R5C:

The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein

phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative

control of cell growth and division. It consists of a common heteromeric core enzyme, which is

composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety

of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and

catalytic activity. This gene encodes a gamma isoform of the regulatory subunit B56 subfamily.

Alternatively spliced transcript variants encoding different isoforms have been identified.

[provided by RefSeq]


UniProtKB/Swiss-Prot: 2A5G_HUMAN, Q13362

Function: The B regulatory subunit might modulate substrate selectivity and catalytic activity, and

also might direct the localization of the catalytic enzyme to a particular subcellular compartment

Gene Wiki entry for PPP2R5C


AI953789 Cluster Incl. AI953789:wx69d10.x1 Homo sapiens cDNA, 3 end /clone=IMAGE-2548915 /clone_end=3 /gb=AI953789 /gi=5746099 /ug=Hs.75742 /len=813 36683_at 140.7


00140.87500 00000.12500
00141.12500 00000.25000 !
X99142 Cluster Incl. X99142:H.sapiens mRNA for hair keratin, hHb6 /cds=(0,1451) /gb=X99142 /gi=1903219 /ug=Hs.182508 /len=2028 32329_at 141.1



Aliases

 

Descriptions

 

External Ids

FLJ25176 2

Type II hair keratin Hb6 3

HGNC: 64631

HB6 2, 5

hard keratin, type II, 6 2

Entrez Gene: 38922

Hb1 2

keratin 86 2

UniProtKB: O437903

Hb6 1

keratin protein HB6 2

Ensembl: ENSG000001704427

K2.11 3

keratin, hair, basic, 6 (monilethrix) 1, 2


K86 3


KRTHB1 2

KRTHB6 2, 3, 5

Keratin-86 3

MNX 1, 2

hHb6 2


Search outside databases for aliases for KRT86 gene

Summaries
for KRT86

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EntrezGene summary for KRT86:

The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin,

it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type

II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct

subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and

KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5.

All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB1 and

KRTHB3, is found primarily in the hair cortex. Mutations in this gene and KRTHB1 have been

observed in patients with a rare dominant hair disease, monilethrix. [provided by RefSeq]


Gene Wiki entry for KRT86


AF091085 Cluster Incl. AF091085:Homo sapiens clone 638 unknown mRNA, complete sequence /cds=(91,687) /gb=AF091085 /gi=3860007 /ug=Hs.169992 /len=836 40514_at 141.1
00141.25000 00000.12500
00141.50000 00000.25000 !
AF015128 Cluster Incl. AF015128:Homo sapiens IgG heavy chain variable region (Vh26) mRNA, partial cds /cds=(0,176) /gb=AF015128 /gi=2367522 /ug=Hs.135635 /len=374 35566_f_at 141.5



Aliases

 

Descriptions

 

External Ids

2-5-3p 2

Exocyst complex component Exo70 3

HGNC: 232141

DKFZp686J04253 2

exocyst complex component 7 2

Entrez Gene: 232652

EX070 2


UniProtKB: Q9UPT53

EXO70 1, 2, 3

Ensembl: ENSG000001824737

EXOC1 2


Exo70p 1, 2

FLJ40965 2

FLJ46415 2

KIAA1067 1, 3

YJL085W 1, 2


Search outside databases for aliases for EXOC7 gene

Previous GC identifer: GC17M074674

Summaries
for EXOC7

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EntrezGene summary for EXOC7:

EXOC7 is a component of the exocyst, which is an evolutionarily conserved octameric protein complex

essential for exocytosis. The exocyst targets secretory vesicles at specific domains of the plasma

membrane for cell surface expansion and protein secretion (Zuo et al., 2006 [PubMed

17086175]).[supplied by OMIM]


UniProtKB/Swiss-Prot: EXOC7_HUMAN, Q9UPT5

Function: Component of the exocyst complex involved in the docking of exocystic vesicles with

fusion sites on the plasma membrane. In adipocytes, plays a crucial role in targeting SLC2A4

vesicle to the plasma membrane in response to insulin, perhaps directing the vesicle to the

precise site of fusion (By similarity)

Gene Wiki entry for EXOC7


00141.75000 00000.25000 !
U79291 Cluster Incl. U79291:Human clone 23721 mRNA sequence /cds=UNKNOWN /gb=U79291 /gi=1710271 /ug=Hs.83572 /len=1342 38443_at 141.6



Aliases

 

Descriptions

 

External Ids

BPTP3 1, 2

Noonan syndrome 1 1

HGNC: 96441

CFC 2

Protein-tyrosine phosphatase 2C 2, 3

Entrez Gene: 57812

EC 3.1.3.48 3

protein tyrosine phosphatase, non-receptor type 11 2

UniProtKB: Q061243

MGC14433 2

protein tyrosine phosphatase-2 2

Ensembl: ENSG000001792957

NS1 2, 5



PTP-1D 2, 3

PTP-2C 3

PTP2C 1, 2, 3, 5

SH-PTP2 1, 2, 3

SH-PTP3 2, 3

SHP-2 1, 3

SHP2 1, 2, 5

SHPTP2 3

Shp2 3


Search outside databases for aliases for PTPN11 gene

Previous GC identifers: GC12P111712 GC12P112333 GC12P112639 GC12P111268

Summaries
for PTPN11

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EntrezGene summary for PTPN11:

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs

are known to be signaling molecules that regulate a variety of cellular processes including cell

growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem

Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the

interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and

plays a regulatory role in various cell signaling events that are important for a diversity of

cell functions, such as mitogenic activation, metabolic control, transcription regulation, and

cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid

leukemia. [provided by RefSeq]


UniProtKB/Swiss-Prot: PTN11_HUMAN, Q06124

Function: Acts downstream of various receptor and cytoplasmic protein tyrosine kinases to

participate in the signal transduction from the cell surface to the nucleus

Gene Wiki entry for PTPN11


00141.87500 00000.12500
00142.12500 00000.25000 !
AF013512 Cluster Incl. AF013512:untitled /cds=(106,1551) /gb=AF013512 /gi=2653816 /ug=Hs.154078 /len=1887 35013_at 142.1



Aliases

 

Descriptions

 

External Ids

MGC22233 2

LPS-binding protein 2

HGNC: 65171

OTTHUMP00000030965 2

lipopolysaccharide binding protein 2

Entrez Gene: 39292


lipopolysaccharide-binding protein 1, 2

UniProtKB: P184283


Ensembl: ENSG000001299887


Search outside databases for aliases for LBP gene

Previous GC identifers: GC20P036703 GC20P037613 GC20P037660

Summaries
for LBP

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EntrezGene summary for LBP:

The protein encoded by this gene is involved in the acute-phase immunologic response to

gram-negative bacterial infections. Gram-negative bacteria contain a glycolipid,

lipopolysaccharide (LPS), on their outer cell wall. Together with bactericidal

permeability-increasing protein (BPI), the encoded protein binds LPS and interacts with the CD14

receptor, probably playing a role in regulating LPS-dependent monocyte responses. Studies in mice

suggest that the encoded protein is necessary for the rapid acute-phase response to LPS but not

for the clearance of LPS from circulation. This protein is part of a family of structurally and

functionally related proteins, including BPI, plasma cholesteryl ester transfer protein (CETP),

and phospholipid transfer protein (PLTP). Finally, this gene is found on chromosome 20,

immediately downstream of the BPI gene. [provided by RefSeq]


UniProtKB/Swiss-Prot: LBP_HUMAN, P18428

Function: Binds to the lipid A moiety of bacterial lipopolysaccharides (LPS), a glycolipid present

in the outer membrane of all Gram-negative bacteria. The LBP/LPS complex seems to interact with

the CD14 receptor

Gene Wiki entry for LBP (Lipopolysaccharide-binding_protein)


D87673 D87673 /FEATURE= /DEFINITION=D87673 Homo sapiens mRNA for heat shock transcription factor 4, complete cds 720_at 142.1



Aliases

 

Descriptions

 

External Ids

CTM 2, 5

HSF 4 3

HGNC: 52271

hHSF4 3

HSTF 4 3

Entrez Gene: 32992


cataract, Marner 1

UniProtKB: Q9ULV53

heat shock transcription factor 4 2, 3

Ensembl: ENSG000001028787



Search outside databases for aliases for HSF4 gene

Previous GC identifers: GC16P057891 GC16P067576 GC16P066932 GC16P066974

Summaries
for HSF4

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EntrezGene summary for HSF4:

Heat-shock transcription factors (HSFs) activate heat-shock response genes under conditions of heat

or other stresses. HSF4 lacks the carboxyl-terminal hydrophobic repeat which is shared among all

vertebrate HSFs and has been suggested to be involved in the negative regulation of DNA binding

activity. Two alternatively spliced transcripts encoding distinct isoforms and possessing

different transcriptional activity have been described. [provided by RefSeq]


UniProtKB/Swiss-Prot: HSF4_HUMAN, Q9ULV5

Function: DNA-binding protein that specifically binds heat shock promoter elements (HSE). Isoform

HSF4A represses transcription while the isoform HSF4B activates transcription

Gene Wiki entry for HSF4


00142.37500 00000.25000 !
AA461365 Cluster Incl. AA461365:zx70e07.r1 Homo sapiens cDNA, 5 end /clone=IMAGE-796836 /clone_end=5 /gb=AA461365 /gi=2186485 /ug=Hs.237742 /len=591 39271_at 142.3



Aliases

 

Descriptions

 

External Ids

CD-RAP 1, 2

melanoma inhibitory activity 2, 3

HGNC: 70761



Entrez Gene: 81902

UniProtKB: Q166743

Ensembl: ENSG000002130547


Search outside databases for aliases for MIA gene

Previous GC identifers: GC19P041920 GC19P041673 GC19P045958 GC19P045975 GC19P045976

Summaries
for MIA

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UniProtKB/Swiss-Prot: MIA_HUMAN, Q16674

Function: Elicits growth inhibition on melanoma cells in vitro as well as some other

neuroectodermal tumors, including gliomas

Gene Wiki entry for MIA (Melanoma_inhibitory_activity)


00142.50000 00000.12500
00142.75000 00000.25000 !
AF001461 Cluster Incl. AF001461:Homo sapiens Kruppel-like zinc finger protein Zf9 mRNA, complete cds /cds=(30,881) /gb=AF001461 /gi=3378030 /ug=Hs.76526 /len=1354 37026_at 142.7



Aliases

 

Descriptions

 

External Ids

BCD1 2, 3, 5

B-cell-derived protein 1 3

HGNC: 22351

CBA1 2

Core promoter element-binding protein 3

Entrez Gene: 13162

COPEB 2, 3, 5

GC-rich sites-binding factor GBF 3

UniProtKB: Q996123

CPBP 1, 2, 3

Kruppel-like factor 6 2

Ensembl: ENSG000000670827

DKFZp686N0199 2

Kruppel-like zinc finger protein Zf9 2


GBF 1, 2

Proto-oncogene BCD1 3

PAC1 1, 2

Transcription factor Zf9 3

ST12 2, 3

core promoter element binding protein 1, 2

ZF9 2, 5

prostate adenocarcinoma-1 2

Zf9 1

protooncogene B-cell derived 1 2


suppression of tumorigenicity 12 (prostate) 2


Search outside databases for aliases for KLF6 gene

Summaries
for KLF6

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EntrezGene summary for KLF6:

This gene encodes a member of the Kruppel-like family of transcription factors. The zinc finger

protein is a transcriptional activator, and functions as a tumor suppressor. Multiple transcript

variants encoding different isoforms have been found for this gene, some of which are implicated

in carcinogenesis. [provided by RefSeq]


UniProtKB/Swiss-Prot: KLF6_HUMAN, Q99612

Function: Transcriptional activator (By similarity). Binds a GC box motif. Could play a role in

B-cell growth and development

Gene Wiki entry for KLF6


00143.12500 00000.37500 !
U67156 U67156 /FEATURE= /DEFINITION=HSU67156 Human mitogen-activated kinase kinase kinase 5 (MAPKKK5) mRNA, complete cds 1327_s_at 143.1



Aliases

 

Descriptions

 

External Ids

ASK-1 3

Apoptosis signal-regulating kinase 1 3

HGNC: 68571

ASK1 1, 2, 3, 5

MAP/ERK kinase kinase 5 2

Entrez Gene: 42172

EC 2.7.11.25 3

MAPK/ERK kinase kinase 5 2, 3

UniProtKB: Q996833

MAPKKK5 1, 2, 3, 5

MEK kinase 5 3

Ensembl: ENSG000001974427

MEKK5 2, 3, 5

MEKK 5 3


OTTHUMP00000017275 2

apoptosis signal regulating kinase 1 2


mitogen-activated protein kinase kinase kinase 5 2


Search outside databases for aliases for MAP3K5 gene

Previous GC identifers: GC06M136500 GC06M136725 GC06M136858

Summaries
for MAP3K5

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EntrezGene summary for MAP3K5:

Mitogen-activated protein kinase (MAPK) signaling cascades include MAPK or extracellular

signal-regulated kinase (ERK), MAPK kinase (MKK or MEK), and MAPK kinase kinase (MAPKKK or MEKK).

MAPKK kinase/MEKK phosphorylates and activates its downstream protein kinase, MAPK kinase/MEK,

which in turn activates MAPK. The kinases of these signaling cascades are highly conserved, and

homologs exist in yeast, Drosophila, and mammalian cells. MAPKKK5 contains 1,374 amino acids with

all 11 kinase subdomains. Northern blot analysis shows that MAPKKK5 transcript is abundantly

expressed in human heart and pancreas. The MAPKKK5 protein phosphorylates and activates MKK4

(aliases SERK1, MAPKK4) in vitro, and activates c-Jun N-terminal kinase (JNK)/stress-activated

protein kinase (SAPK) during transient expression in COS and 293 cells; MAPKKK5 does not activate

MAPK/ERK. [provided by RefSeq]


UniProtKB/Swiss-Prot: M3K5_HUMAN, Q99683

Function: Component of a protein kinase signal transduction cascade. Phosphorylates and activates

MAP2K4 and MAP2K6, which in turn activate the JNK and p38 MAP kinases, respectively.

Overexpression induces apoptotic cell death

Gene Wiki entry for MAP3K5 (ASK1)


AB014609 Cluster Incl. AB014609:Homo sapiens mRNA for KIAA0709 protein, complete cds /cds=(116,4555) /gb=AB014609 /gi=3327231 /ug=Hs.7835 /len=5641 37408_at 143.1



Aliases

 

Descriptions

 

External Ids

CD280 1, 2, 5

CD280 antigen 3

HGNC: 168751

CLEC13E 1, 2

Endocytic receptor 180 3

Entrez Gene: 99022

ENDO180 1, 2, 3, 5

Macrophage mannose receptor 2 3

UniProtKB: Q9UBG03

FLJ35911 2

UPAR-associated protein 3

Ensembl: ENSG000000110287

KIAA0709 1, 2, 3

Urokinase receptor-associated protein 3


UPARAP 2, 3, 5

Urokinase-type plasminogen activator receptor-associated
protein 3


endocytic receptor (macrophage mannose receptor family) 2

mannose receptor, C type 2 2

urokinase plasminogen activator receptor-associated protein 2


Search outside databases for aliases for MRC2 gene

Previous GC identifers: GC17P060392 GC17P063131 GC17P061045 GC17P061178

Summaries
for MRC2

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EntrezGene summary for MRC2:

MRC2 is a recycling endocytic receptor that functions in cell motility and remodeling of the

extracellular matrix by promoting cell migration and uptake of collagens for intracellular

degradation (Wienke et al., 2007 [PubMed 17974964]).[supplied by OMIM]


UniProtKB/Swiss-Prot: MRC2_HUMAN, Q9UBG0

Function: May play a role as endocytotic lectin receptor displaying calcium-dependent lectin

activity. Internalizes glycosylated ligands from the extracellular space for release in an

endosomal compartment via clathrin-mediated endocytosis. May be involved in plasminogen activation

system controlling the extracellular level of PLAUR/PLAU, and thus may regulate protease activity

at the cell surface. May contribute to cellular uptake, remodeling and degradation of

extracellular collagen matrices. May play a role during cancer progression as well as in other

chronic tissue destructive diseases acting on collagen turnover. May participate in remodeling of

extracellular matrix co-operating with the matrix metalloproteinases (MMPs)


AF012108 Cluster Incl. AF012108:Homo sapiens Amplified in Breast Cancer (AIB1) mRNA, complete cds /cds=(200,4462) /gb=AF012108 /gi=2331249 /ug=Hs.225977 /len=6818 33381_at 143.1



 

 

Descriptions

 

External Ids

ACTR 1, 2, 3

Amplified in breast cancer-1 protein 3

HGNC: 76701

AIB-1 2, 3

CBP-interacting protein 2, 3

Entrez Gene: 82022

AIB1 1, 2, 3, 5

Receptor-associated coactivator 3 2, 3

UniProtKB: Q9Y6Q93

CAGH16 1, 2

Steroid receptor coactivator protein 3 2, 3

Ensembl: ENSG000001241517

CTG26 2

Thyroid hormone receptor activator molecule 1 2, 3


EC 2.3.1.48 3

amplified in breast cancer-1 2

KAT13B 1, 2

nuclear receptor coactivator 3 2

MGC141848 2


NCoA-3 3

OTTHUMP00000031716 2

OTTHUMP00000031718 2

RAC-3 3

RAC3 1, 2, 3

SRC-3 1, 2, 3

SRC3 1, 2

TNRC14 2, 5

TNRC16 1, 2

TRAM-1 1, 2, 3

TRAM1 3

bHLHe42 1, 2

p/CIP 1

pCIP 2, 3


Search outside databases for aliases for NCOA3 gene

Previous GC identifers: GC20P045859 GC20P046769 GC20P046816

Summaries
for NCOA3

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EntrezGene summary for NCOA3:

The protein encoded by this gene is a nuclear receptor coactivator that interacts with nuclear

hormone receptors to enhance their transcriptional activator functions. The encoded protein has

histone acetyltransferase activity and recruits p300/CBP-associated factor and CREB binding

protein as part of a multisubunit coactivation complex. This protein is initially found in the

cytoplasm but is translocated into the nucleus upon phosphorylation. Two transcript variants

encoding different isoforms have been found for this gene. In addition, a polymorphic repeat

region is found in the C-terminus of the encoded protein. [provided by RefSeq]


UniProtKB/Swiss-Prot: NCOA3_HUMAN, Q9Y6Q9

Function: Nuclear receptor coactivator that directly binds nuclear receptors and stimulates the

transcriptional activities in a hormone-dependent fashion. Plays a central role in creating a

multisubunit coactivator complex, which probably acts via remodeling of chromatin. Involved in the

coactivation of different nuclear receptors, such as for steroids (GR and ER), retinoids (RARs and

RXRs), thyroid hormone (TRs), vitamin D3 (VDR) and prostanoids (PPARs). Displays histone

acetyltransferase activity. Also involved in the coactivation of the NF-kappa-B pathway via its

interaction with the NFKB1 subunit

Gene Wiki entry for NCOA3 (Nuclear_receptor_coactivator_3)


00143.25000 00000.12500
00143.50000 00000.25000 !
L32832 Cluster Incl. L32832:Homo sapiens zinc finger homeodomain protein (ATBF1-A) mRNA, complete cds /cds=(673,11784) /gb=L32832 /gi=976346 /ug=Hs.101842 /len=11893 37114_at 143.6



Aliases

 

Descriptions

 

External Ids

ATBF1 2, 3, 5

AT motif-binding factor 3

HGNC: 7771

ATBT 2

AT motif-binding factor 1 2

Entrez Gene: 4632

OTTHUMP00000174934 2

AT-binding transcription factor 1 1, 2, 3

UniProtKB: Q159113

ZFH-3 3

Alpha-fetoprotein enhancer-binding protein 3

Ensembl: ENSG000001408367


Zinc finger homeodomain protein 3 3


zinc finger homeobox 3 2


Search outside databases for aliases for ZFHX3 gene

Summaries
for ZFHX3

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UniProtKB/Swiss-Prot: ZFHX3_HUMAN, Q15911

Function: Transcriptional activator that binds to the AT-rich core sequence of the enhancer element

of the AFP gene

Gene Wiki entry for ZFHX3 (ATBF1)


00143.75000 00000.25000 !
Y08200 Y08200 /FEATURE= /DEFINITION=HSRABGTRA Homo sapiens mRNA for rab geranylgeranyl transferase, alpha-subunit 100_g_at 143.7



Aliases

 

Descriptions

 

External Ids

EC 2.5.1.60 3

Geranylgeranyl transferase type II subunit alpha 2, 3

HGNC: 97951

PTAR3 1, 2

Rab GG transferase alpha 2, 3

Entrez Gene: 58752


Rab GGTase alpha 2, 3

UniProtKB: Q926963

Rab geranyl-geranyltransferase subunit alpha 3

Ensembl: ENSG000001009497

Rab geranylgeranyltransferase alpha 2


Rab geranylgeranyltransferase subunit alpha 3

Rab geranylgeranyltransferase, alpha subunit 2

protein prenyltransferase alpha subunit repeat containing 3 2


Search outside databases for aliases for RABGGTA gene

Previous GC identifers: GC14M022107 GC14M018522 GC14M022724

Summaries
for RABGGTA

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UniProtKB/Swiss-Prot: PGTA_HUMAN, Q92696

Function: Catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to

both cysteines in Rab proteins with an -XXCC, -XCXC and -CCXX C-terminal, such as RAB1A, RAB3A and

RAB5A respectively


U85611 U85611 /FEATURE= /DEFINITION=HSU85611 Human DNA-PK interaction protein (KIP) mRNA, complete cds 1020_s_at 143.7



Aliases

 

Descriptions

 

External Ids

CALMYRIN 1

DNA-PKcs-interacting protein 3

HGNC: 169201

CIB 1, 2, 3

DNA-dependent protein kinase interacting protein 2

Entrez Gene: 105192

Calmyrin 3

Kinase-interacting protein 3

UniProtKB: Q998283

KIP 1, 2, 3

SNK-interacting protein 2-28 3

Ensembl: ENSG000001850437

KIP1 2

Snk interacting protein 2-28 2


PRKDCIP 3

calcium and integrin binding 1 2

SIP2-28 1, 2, 3

calcium and integrin binding 1 (calmyrin) 2

calmyrin 2

calcium and integrin binding protein 2


calcium and integrin binding, protein kinase interacting
protein 2


Search outside databases for aliases for CIB1 gene

Previous GC identifers: GC15P087395 GC15M084280 GC15M088360 GC15M088503

Summaries
for CIB1

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EntrezGene summary for CIB1:

The protein encoded by this gene is a member of the calcium-binding protein family. The specific

function of this protein has not yet been determined; however this protein is known to interact

with DNA-dependent protein kinase and may play a role in kinase-phosphatase regulation of DNA end

joining. This protein also interacts with integrin alpha(IIb)beta(3), which may implicate this

protein as a regulatory molecule for alpha(IIb)beta(3). [provided by RefSeq]


UniProtKB/Swiss-Prot: CIB1_HUMAN, Q99828

Function: May convert the inactive conformation of integrin alpha-IIb/beta3 to an active form

through the binding to the integrin cytoplasmic domain

Gene Wiki entry for CIB1


00143.87500 00000.12500
00144.12500 00000.25000 !
X80907 Cluster Incl. X80907:H.sapiens mRNA for p85 beta subunit of phosphatidyl-inositol-3-kinase /cds=(241,2427) /gb=X80907 /gi=2160047 /ug=Hs.211586 /len=3201 34197_at 144.2



Aliases

 

Descriptions

 

External Ids

P85B 1, 2

PI3-kinase p85 subunit beta 3

HGNC: 89801

p85 1, 2

PtdIns-3-kinase p85-beta 3

Entrez Gene: 52962

p85-BETA 2

phosphatidylinositol 3-kinase, regulatory subunit,
polypeptide 2 (p85 beta) 2

UniProtKB: O004593


Ensembl: ENSG000001056477

phosphoinositide-3-kinase, regulatory subunit 2 (beta) 2


phosphoinositide-3-kinase, regulatory subunit 2 (p85 beta) 2

phosphoinositide-3-kinase, regulatory subunit, polypeptide
2 (p85 beta) 2


Search outside databases for aliases for PIK3R2 gene

Previous GC identifers: GC19P018760 GC19P018658 GC19P018108 GC19P018127

Summaries
for PIK3R2

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UniProtKB/Swiss-Prot: P85B_HUMAN, O00459

Function: Binds to activated (phosphorylated) protein-tyrosine kinases, through its SH2 domain, and

acts as an adapter, mediating the association of the p110 catalytic unit to the plasma membrane

Gene Wiki entry for PIK3R2


00144.37500 00000.25000 !
00144.50000 00000.12500
00144.62500 00000.12500
00144.87500 00000.25000 !
J02939 Cluster Incl. J02939:Human membrane glycoprotein 4F2 antigen heavy chain mRNA /cds=(109,1698) /gb=J02939 /gi=182864 /ug=Hs.79748 /len=1863 38029_at 144.9



Aliases

 

Descriptions

 

External Ids

4F2 1, 2

4F2 cell-surface antigen heavy chain 2

HGNC: 110261

4F2HC 1, 2

4F2 heavy chain 2

Entrez Gene: 65202

4F2hc 3

4F2 heavy chain antigen 3

UniProtKB: P081953

4T2HC 1, 2

CD98 antigen 3

Ensembl: ENSG000001680037

CD98 1, 2

CD98 heavy chain 2


CD98HC 1, 2

Lymphocyte activation antigen 4F2 large subunit 2, 3

MDU1 2, 3, 5

antigen defined by monoclonal antibody 4F2, heavy chain 2

NACAE 1, 2, 5

antigen identified by monoclonal antibodies 4F2, TRA1.10,
TROP4, and T43 2


heavy chain 2

monoclonal antibody 44D7 2

solute carrier family 3 (activators of dibasic and neutral
amino acid transport), member 2 2


Search outside databases for aliases for SLC3A2 gene

Previous GC identifers: GC11P065136 GC11P064199 GC11P062874 GC11P062398

Summaries
for SLC3A2

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EntrezGene summary for SLC3A2:

This gene is a member of the solute carrier family and encodes a cell surface, transmembrane

protein with an alpha amylase domain. The protein exists as the heavy chain of a heterodimer,

covalently bound through di-sulfide bonds to one of several possible light chains. It associates

with integrins and mediates integrin-dependent signaling related to normal cell growth and

tumorigenesis. Alternate transcriptional splice variants, encoding different isoforms, have been

characterized. [provided by RefSeq]


UniProtKB/Swiss-Prot: 4F2_HUMAN, P08195

Function: Required for the function of light chain amino-acid transporters. Involved in

sodium-independent, high-affinity transport of large neutral amino acids such as phenylalanine,

tyrosine, leucine, arginine and tryptophan. Involved in guiding and targeting of LAT1 and LAT2 to

the plasma membrane. When associated with SLC7A6 or SLC7A7 acts as an arginine/glutamine

exchanger, following an antiport mechanism for amino acid transport, influencing arginine release

in exchange for extracellular amino acids. Plays a role in nitric oxide synthesis in human

umbilical vein endothelial cells (HUVECs) via transport of L-arginine. Required for normal and

neoplastic cell growth. When associated with SLC7A5/LAT1, is also involved in the transport of

L-DOPA across the blood-brain barrier, and that of thyroid hormones triiodothyronine (T3) and

thyroxine (T4) across the cell membrane in tissues such as placenta. Involved in the uptake of

methylmercury (MeHg) when administered as the L-cysteine or D,L-homocysteine complexes, and hence

plays a role in metal ion homeostasis and toxicity. When associated with SLC7A5 or SLC7A8,

involved in the cellular activity of small molecular weight nitrosothiols, via the stereoselective

transport of L-nitrosocysteine (L-CNSO) across the transmembrane. Together with ICAM1, regulates

the transport activity LAT2 in polarized intestinal cells, by generating and delivering

intracellular signals. When associated with SLC7A5, plays an important role in transporting

L-leucine from the circulating blood to the retina across the inner blood-retinal barrier

Gene Wiki entry for SLC3A2


00145.00000 00000.12500
00145.12500 00000.12500
00145.50000 00000.37500 !
AA780049 Cluster Incl. AA780049:zj24f06.s1 Homo sapiens cDNA, 3 end /clone=451235 /clone_end=3 /gb=AA780049 /gi=2839380 /ug=Hs.173987 /len=587 40615_at 145.5
AF057297 Cluster Incl. AF057297:Homo sapiens ornithine decarboxylase antizyme 2 (OAZ2) mRNA, complete cds /cds=UNKNOWN /gb=AF057297 /gi=3766169 /ug=Hs.74563 /len=1850 36146_at 145.5



Aliases

 

Descriptions

 

External Ids

AZ2 2, 3

ODC-Az 2 3

HGNC: 80961


ornithine decarboxylase antizyme 2 2

Entrez Gene: 49472


UniProtKB: O951903

Ensembl: ENSG000001803047


Search outside databases for aliases for OAZ2 gene

Previous GC identifers: GC15P060699 GC15M9D0083 GC15M062558

Summaries
for OAZ2

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EntrezGene summary for OAZ2:

Ornithine decarboxylase catalyzes the conversion of ornithine to putrescine in the first and

apparently rate-limiting step in polyamine biosynthesis. The ornithine decarboxylase antizymes

play a role in the regulation of polyamine synthesis by binding to and inhibiting ornithine

decarboxylase. Antizyme expression is auto-regulated by polyamine-enhanced translational

frameshifting. The antizyme encoded by this gene inhibits ornithine decarboxylase but does not

accelerate its degradation. [provided by RefSeq]


UniProtKB/Swiss-Prot: OAZ2_HUMAN, O95190

Function: Binds to, and destabilizes, ornithine decarboxylase. Does not accelerate ornithine

decarboxylase degeneration (By similarity)

Gene Wiki entry for OAZ2


00145.75000 00000.25000 !
X57398 Cluster Incl. X57398:Human mRNA for pM5 protein /cds=(0,3572) /gb=X57398 /gi=35526 /ug=Hs.227823 /len=4086 33414_at 145.7



Aliases

 

Descriptions

 

External Ids

Nomo 2

NODAL modulator 1 2

HGNC: 300601

PM5 1, 2, 3

pM5 protein, telomeric copy 2

Entrez Gene: 234202

pM5 3


UniProtKB: Q151553


Ensembl: ENSG000001035127


Search outside databases for aliases for NOMO1 gene

Summaries
for NOMO1

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EntrezGene summary for NOMO1:

This gene encodes a protein originally thought to be related to the collagenase gene family. This

gene is one of three highly similar genes in a region of duplication located on the p arm of

chromosome 16. These three genes encode closely related proteins that may have the same function.

The protein encoded by one of these genes has been identified as part of a protein complex that

participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6,

which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma

elasticum (PXE). [provided by RefSeq]


UniProtKB/Swiss-Prot: NOMO1_HUMAN, Q15155

Function: May antagonize Nodal signaling (By similarity)

Gene Wiki entry for NOMO1


AL021396 Cluster Incl. AL021396:Human DNA sequence from clone 971N18 on chromosome 20p12 Contains processed pseudogene PHKBP1, novel gene, ESTs, CA repeat (D20S907), STSs and GSSs /cds=(0,790) /gb=AL021396 /gi=4490930 /ug=Hs.169358 /len=2059 40478_at 145.7AJ010346 Cluster Incl. AJ010346:Homo sapiens mRNA for RING-H2 protein RNF6, alternative exon 1a /cds=(360,2417) /gb=AJ010346 /gi=4583651 /ug=Hs.32597 /len=3503 35656_at 145.7

Refernce - ncbi.nih.gov



AJ010346 Cluster Incl. AJ010346:Homo sapiens mRNA for RING-H2 protein RNF6, alternative exon 1a /cds=(360,2417) /gb=AJ010346 /gi=4583651 /ug=Hs.32597 /len=3503 35656_at 145.7



Aliases

 

Descriptions

 

External Ids

DKFZp686P0776 1, 2

RING-H2 protein 3

HGNC: 100691

OTTHUMP00000018154 2

RING-H2 protein RNF-6 2

Entrez Gene: 60492

OTTHUMP00000018155 2

ring finger protein (C3H2C3 type) 6 2

UniProtKB: Q9Y2523

OTTHUMP00000018156 2

ring finger protein 6 2

Ensembl: ENSG000001278707




Search outside databases for aliases for RNF6 gene

Previous GC identifers: GC13M024766 GC13M020766 GC13M025636 GC13M024584 GC13M024504

Summaries
for RNF6

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EntrezGene summary for RNF6:

The protein encoded by this gene contains a RING-H2 finger motif. Deletions and mutations in this

gene were detected in esophageal squamous cell carcinoma (ESCC), suggesting that this protein may

be a potential tumor suppressor. Studies of the mouse counterpart suggested a role of this protein

in the transcription regulation that controls germinal differentiation. Multiple alternatively

spliced transcript variants encoding the same protein are observed. [provided by RefSeq]


00145.87500 00000.12500
00146.12500 00000.25000 !
X13839 Cluster Incl. X13839:Human mRNA for vascular smooth muscle alpha-actin /cds=(47,1180) /gb=X13839 /gi=28329 /ug=Hs.195851 /len=1330 32755_at 146.1



Aliases

 

Descriptions

 

External Ids

AAT6 2, 5

Cell growth-inhibiting gene 46 protein 3

HGNC: 1301

ACTSA 1, 2, 3, 5

actin, alpha 2, smooth muscle, aorta 2

Entrez Gene: 592

ACTVS 3

alpha 2 actin 2

UniProtKB: P627363

Alpha-actin-2 3

alpha-cardiac actin 2

Ensembl: ENSG000001077967

OTTHUMP00000020042 2

growth-inhibiting gene 46 2




Search outside databases for aliases for ACTA2 gene

Previous GC identifers: GC10M089576 GC10M089916 GC10M090826 GC10M090359

Summaries
for ACTA2

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EntrezGene summary for ACTA2:

The protein encoded by this gene belongs to the actin family of proteins, which are highly

conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and

gamma actin isoforms have been identified, with alpha actins being a major constituent of the

contractile apparatus, while beta and gamma actins are involved in the regulation of cell

motility. This actin is an alpha actin that is found in skeletal muscle. Defects in this gene

cause aortic aneurysm familial thoracic type 6. Multiple alternatively spliced variants, encoding

the same protein, have been identified. [provided by RefSeq]


UniProtKB/Swiss-Prot: ACTA_HUMAN, P62736

Function: Actins are highly conserved proteins that are involved in various types of cell motility

and are ubiquitously expressed in all eukaryotic cells

Gene Wiki entry for ACTA2


00146.25000 00000.12500
00146.62500 00000.37500 !
AB014595 Cluster Incl. AB014595:Homo sapiens mRNA for KIAA0695 protein, complete cds /cds=(78,2231) /gb=AB014595 /gi=3327203 /ug=Hs.155976 /len=4376 40141_at 146.5



Aliases

 

Descriptions

 

External Ids

CUL-4B 3

cullin 4B 2

HGNC: 25551

DKFZp686F1470 2


Entrez Gene: 84502

KIAA0695 2, 3

UniProtKB: Q136203

MRXHF2 2, 5

Ensembl: ENSG000001582907

MRXSC 2, 5


OTTHUMP00000023946 2

OTTHUMP00000023947 2

SFM2 2, 5

cullin-4B 2


Search outside databases for aliases for CUL4B gene

Previous GC identifers: GC0XM114476 GC0XM116644 GC0XM117633 GC0XM118412 GC0XM119440

Summaries
for CUL4B

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EntrezGene summary for CUL4B:

This gene is a member of the cullin family. The encoded protein forms a complex that functions as

an E3 ubiquitin ligase and catalyzes the polyubiquitination of specific protein substrates in the

cell. The protein interacts with a ring finger protein, and is required for the proteolysis of

several regulators of DNA replication including chromatin licensing and DNA replication factor 1

and cyclin E. Multiple transcript variants encoding different isoforms have been found for this

gene. [provided by RefSeq]


UniProtKB/Swiss-Prot: CUL4B_HUMAN, Q13620

Function: Core component of multiple cullin-RING-based E3 ubiquitin-protein ligase complexes which

mediate the ubiquitination and subsequent proteasomal degradation of target proteins. As a

scaffold protein may contribute to catalysis through positioning of the substrate and the

ubiquitin-conjugating enzyme. The functional specificity of the E3 ubiquitin-protein ligase

complex depends on the variable substrate recognition subunit. DC4BX(DTL) plays a role in

PCNA-dependent polyubiquitination of CDT1 in response to radiation-induced DNA damage and during

DNA replication. Required for histone H3 and histone H4 ubiquitination in response to ultraviolet

and may be important for subsequent DNA repair

Gene Wiki entry for CUL4B


00146.87500 00000.25000 !
U04953 Cluster Incl. U04953:Human isoleucyl-tRNA synthetase mRNA, complete cds /cds=(255,4043) /gb=U04953 /gi=450850 /ug=Hs.172801 /len=4508 40827_at 146.8



Aliases

 

Descriptions

 

External Ids

EC 6.1.1.5 3

Isoleucine--tRNA ligase 3

HGNC: 53301

FLJ20736 2

isoleucine tRNA ligase 1, cytoplasmic 2

Entrez Gene: 33762

IARS1 1, 2

isoleucine tRNA synthetase 2

UniProtKB: P412523

ILERS 2

isoleucyl-tRNA synthetase 2

Ensembl: ENSG000001963057

ILRS 1, 2



IRS 2, 3

IleRS 3

PRO0785 2


Search outside databases for aliases for IARS gene

Previous GC identifers: GC09M085799 GC09M086700 GC09M088271 GC09M090314 GC09M092052

Summaries
for IARS

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EntrezGene summary for IARS:

Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because

of their central role in linking amino acids with nucleotide triplets contained in tRNAS,

aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution.

Isoleucine-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family and has been

identified as a target of autoantibodies in the autoimmune disease polymyositis/dermatomyositis.

Two alternatively spliced variants have been isolated that represent alternate 5' UTRs.

[provided by RefSeq]


Gene Wiki entry for IARS


00147.00000 00000.12500
00147.12500 00000.12500
00147.37500 00000.25000 !
U94888 Cluster Incl. U94888:Homo sapiens CC-chemokine receptor 10 (CCR10) mRNA, complete cds /cds=(15,1169) /gb=U94888 /gi=2213808 /ug=Hs.117572 /len=1238 32484_at 147.3



Aliases

 

Descriptions

 

External Ids

CCR10 1, 2, 3, 5

C-C chemokine receptor D6 3

HGNC: 15651

CCR9 1, 2, 5

CC-chemokine-binding receptor JAB61 2

Entrez Gene: 12382

CMKBR9 2, 3, 5

Chemokine receptor CCR-10 3

UniProtKB: O005903

D6 1, 2, 5

Chemokine receptor CCR-9 3

Ensembl: ENSG000001446487

MGC126678 2

Chemokine-binding protein D6 3


MGC138250 2

chemokine (C-C motif) receptor 9 2

hD6 2

chemokine (C-C) receptor 9 2


chemokine binding protein 2 2

chemokine receptor D6 2


Search outside databases for aliases for CCBP2 gene

Previous GC identifers: GC03P042155 GC03P042030 GC03P042665 GC03P042811

Summaries
for CCBP2

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EntrezGene summary for CCBP2:

This gene encodes a beta chemokine receptor, which is predicted to be a seven transmembrane protein

similar to G protein-coupled receptors. Chemokines and their receptor-mediated signal transduction

are critical for the recruitment of effector immune cells to the inflammation site. This gene is

expressed in a range of tissues and hemopoietic cells. The expression of this receptor in

lymphatic endothelial cells and overexpression in vascular tumors suggested its function in

chemokine-driven recirculation of leukocytes and possible chemokine effects on the development and

growth of vascular tumors. This receptor appears to bind the majority of beta-chemokine family

members; however, its specific function remains unknown. This gene is mapped to chromosome 3p21.3,

a region that includes a cluster of chemokine receptor genes. [provided by RefSeq]


UniProtKB/Swiss-Prot: CCBP2_HUMAN, O00590

Function: Receptor for C-C type chemokines including SCYA2/MCP-1, SCY3/MIP-1-alpha, SCYA5/RANTES

and SCYA7/MCP-3

Gene Wiki entry for CCBP2


00147.87500 00000.50000 !
D43642 Cluster Incl. D43642:Human YL-1 mRNA for YL-1 protein (nuclear protein with DNA-binding ability), complete cds /cds=(43,1137) /gb=D43642 /gi=806519 /ug=Hs.2430 /len=1324 33873_at 147.8



Aliases

 

Descriptions

 

External Ids

MGC39481 2

Neuronal tropomodulin 2, 3

HGNC: 118721

N-TMOD 2

tropomodulin 2 (neuronal) 2

Entrez Gene: 297672

N-Tmod 3


UniProtKB: Q9NZR13

NTMOD 1, 2, 3

Ensembl: ENSG000001288727



Search outside databases for aliases for TMOD2 gene

Previous GC identifers: GC15P047601 GC15P045089 GC15P049622 GC15P049759

Summaries
for TMOD2

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EntrezGene summary for TMOD2:

This gene encodes a neuronal-specific member of the tropomodulin family of actin-regulatory

proteins. The encoded protein caps the pointed end of actin filaments preventing both elongation

and depolymerization. The capping activity of this protein is dependent on its association with

tropomyosin. Alternatively spliced transcript variants encoding different isoforms have been

described. [provided by RefSeq]


UniProtKB/Swiss-Prot: TMOD2_HUMAN, Q9NZR1

Function: Blocks the elongation and depolymerization of the actin filaments at the pointed end. The

Tmod/TM complex contributes to the formation of the short actin protofilament, which in turn

defines the geometry of the membrane skeleton (By similarity)


U66616 U66616 /FEATURE= /DEFINITION=HSU66616 Human SWI/SNF complex 170 KDa subunit (BAF170) mRNA, complete cds 453_at 147.8



Aliases

 

Descriptions

 

External Ids

BAF170 1, 2, 3, 5

BRG1-associated factor 170 3

HGNC: 111051

CRACC2 1, 2

SWI/SNF complex 170 kDa subunit 2, 3

Entrez Gene: 66012

Rsc8 1, 2

SWI/SNF related, matrix associated, actin dependent
regulator of chromatin, subfamily c, member 2 2

UniProtKB: Q8TAQ23


Ensembl: ENSG000001396137

SWI/SNF-related matrix-associated actin-dependent regulator
of chromatin c2 2


SWI/SNF-related matrix-associated actin-dependent regulator
of chromatin subfamily C member 2 3

SWI3-like protein 2

chromatin remodeling complex BAF170 subunit 2

mammalian chromatin remodeling complex BRG1-associated
factor 170 2


Search outside databases for aliases for SMARCC2 gene

Previous GC identifers: GC12M056496 GC12P056713 GC12M056272

Summaries
for SMARCC2

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EntrezGene summary for SMARCC2:

The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members

display helicase and ATPase activities and which are thought to regulate transcription of certain

genes by altering the chromatin structure around those genes. The encoded protein is part of the

large ATP-dependent chromatin remodeling complex SNF/SWI and contains a predicted leucine zipper

motif typical of many transcription factors. Alternatively spliced transcript variants encoding

different isoforms have been found for this gene. [provided by RefSeq]


UniProtKB/Swiss-Prot: SMRC2_HUMAN, Q8TAQ2

Function: Involved in transcriptional activation and repression of select genes by chromatin

remodeling (alteration of DNA-nucleosome topology). Can stimulate the ATPase activity of the

catalytic subunit of these complexes. May be required for CoREST dependent repression of neuronal

specific gene promoters in non-neuronal cells. Also involved in vitamin D-coupled transcription

regulation via its association with the WINAC complex, a chromatin-remodeling complex recruited by

vitamin D receptor (VDR), which is required for the ligand-bound VDR-mediated transrepression of

the CYP27B1 gene

Gene Wiki entry for SMARCC2


AF017656 Cluster Incl. AF017656:Homo sapiens G protein beta 5 subunit mRNA, complete cds /cds=(99,1160) /gb=AF017656 /gi=2570403 /ug=Hs.155090 /len=1471 38176_at 147.9



Aliases

 

Descriptions

 

External Ids

FLJ37457 2

G protein, beta subunit 5L 2

HGNC: 44011

FLJ43714 2

G protein, beta-5 subunit 2

Entrez Gene: 106812

GB5 1, 2

Transducin beta chain 5 2, 3

UniProtKB: O147753

Gbeta5 3

guanine nucleotide binding protein (G protein), beta 5 2

Ensembl: ENSG000000699667


guanine nucleotide-binding protein, beta subunit 5L 2


guanine nucleotide-binding protein, beta-5 subunit 2


Search outside databases for aliases for GNB5 gene

Previous GC identifers: GC15M047972 GC15M045460 GC15M049992 GC15M050129

Summaries
for GNB5

(According to Entrez Gene, Wikipedia's Gene Wiki,
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EntrezGene summary for GNB5:

Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between

receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These

subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits

are important regulators of alpha subunits, as well as of certain signal transduction receptors

and effectors. Alternatively spliced transcript variants encoding different isoforms exist.

[provided by RefSeq]


UniProtKB/Swiss-Prot: GBB5_HUMAN, O14775

Function: Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or

transducer in various transmembrane signaling systems. The beta and gamma chains are required for

the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction

Gene Wiki entry for GNB5


AI147237 Cluster Incl. AI147237:qb36f02.x1 Homo sapiens cDNA, 3 end /clone=IMAGE-1698363 /clone_end=3 /gb=AI147237 /gi=3674919 /ug=Hs.210732 /len=474 34105_f_at 147.9
00148.12500 00000.25000 !
S69272 Cluster Incl. S69272:cytoplasmic antiproteinase=38 kda intracellular serine proteinase inhibitor [human, placenta, mRNA, 1465 nt] /cds=(188,1318) /gb=S69272 /gi=546087 /ug=Hs.41072 /len=1465 34789_at 148.1



Aliases

 

Descriptions

 

External Ids

CAP 1, 2, 3

Cytoplasmic antiproteinase 3

HGNC: 89501

DKFZp686I04222 2

Placental thrombin inhibitor 3

Entrez Gene: 52692

MGC111370 2

Proteinase inhibitor 6 3

UniProtKB: P352373

MSTP057 2

protease inhibitor 6 (placental thrombin inhibitor) 2

Ensembl: ENSG000001245707

OTTHUMP00000017778 2

serine (or cysteine) proteinase inhibitor, clade B
(ovalbumin), member 6 1, 2


OTTHUMP00000017779 2

serpin peptidase inhibitor, clade B (ovalbumin), member 6 2

OTTHUMP00000017780 2


OTTHUMP00000017781 2

OTTHUMP00000017782 2

OTTHUMP00000017783 2

PI-6 3

PI6 2, 3, 5

PTI 1, 2, 3

SPI3 2


Search outside databases for aliases for SERPINB6 gene

Previous GC identifer: GC06M002933

Summaries
for SERPINB6

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UniProtKB/Swiss-Prot: SPB6_HUMAN, P35237

Function: Inhibits thrombin

Gene Wiki entry for SERPINB6


L22005 L22005 /FEATURE= /DEFINITION=HUMCDC34H Human ubiquitin conjugating enzyme mRNA, partial cds 1273_r_at 148.1



Aliases

 

Descriptions

 

External Ids

E2-CDC34 1, 2, 3

Ubiquitin-conjugating enzyme E2-32 kDa complementing 2, 3

HGNC: 17341

EC 6.3.2.19 3

Ubiquitin-protein ligase R1 3

Entrez Gene: 9972

UBC3 1, 2

cell division cycle 34 1

UniProtKB: P494273

UBE2R1 1, 2, 3

cell division cycle 34 homolog (S. cerevisiae) 2

Ensembl: ENSG000000998047


ubiquitin carrier protein 2


ubiquitin-conjugating enzyme Cdc34 2

ubiquitin-protein ligase 2


Search outside databases for aliases for CDC34 gene

Previous GC identifers: GC19P000542 GC19P000566 GC19P000471

Summaries
for CDC34

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EntrezGene summary for CDC34:

The protein encoded by this gene is a member of the ubiquitin-conjugating enzyme family.

Ubiquitin-conjugating enzyme catalyzes the covalent attachment of ubiquitin to other proteins.

This protein is a part of the large multiprotein complex, which is required for ubiquitin-mediated

degradation of cell cycle G1 regulators, and for the initiation of DNA replication. [provided by

RefSeq]


UniProtKB/Swiss-Prot: UB2R1_HUMAN, P49427

Function: Catalyzes the covalent attachment of ubiquitin to other proteins. May be involved in

degradation of katenin

Gene Wiki entry for CDC34


00148.37500 00000.25000 !
L35594 Cluster Incl. L35594:Human autotaxin mRNA, complete cds /cds=(49,2796) /gb=L35594 /gi=537905 /ug=Hs.174185 /len=3231 41123_s_at 148.3



Aliases

 

Descriptions

 

External Ids

ATX 1, 2, 3

E-NPP 2 3

HGNC: 33571

ATX-X 2

Extracellular lysophospholipase D 3

Entrez Gene: 51682

AUTOTAXIN 2

ectonucleotide pyrophosphatase/phosphodiesterase 2 2

UniProtKB: Q138223

Autotaxin 3

phosphodiesterase I/nucleotide pyrophosphatase 2 2

Ensembl: ENSG000001369607

EC 3.1.4.39 3

plasma lysophospholipase D 2


FLJ26803 2


LysoPLD 2, 3

NPP2 2

PD-IALPHA 1, 2

PDNP2 2, 3, 5

autotaxin 2

autotaxin-t 2


Search outside databases for aliases for ENPP2 gene

Previous GC identifers: GC08M119556 GC08M120575 GC08M120238 GC08M120525

Summaries
for ENPP2

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EntrezGene summary for ENPP2:

The protein encoded by this gene functions as both a phosphodiesterase, which cleaves

phosphodiester bonds at the 5' end of oligonucleotides, and a phospholipase, which catalyzes

production of lysophosphatidic acid (LPA) in extracellular fluids. LPA evokes growth factor-like

responses including stimulation of cell proliferation and chemotaxis. This gene product stimulates

the motility of tumor cells and has angiogenic properties, and its expression is upregulated in

several kinds of carcinomas. The gene product is secreted and further processed to make the

biologically active form. Several alternatively spliced transcript variants encoding different

isoforms have been identified. [provided by RefSeq]


UniProtKB/Swiss-Prot: ENPP2_HUMAN, Q13822

Function: Hydrolyzes lysophospholipids to produce lysophosphatidic acid (LPA) in extracellular

fluids. Major substrate is lysophosphatidylcholine. Also can act on sphingosylphosphphorylcholine

producing sphingosine-1-phosphate, a modulator of cell motility. Can hydrolyze, in vitro,

bis-pNPP, to some extent pNP-TMP, and barely ATP. Involved in several motility-related processes

such as angiogenesis and neurite outgrowth. Acts as an angiogenic factor by stimulating migration

of smooth muscle cells and microtubule formation. Stimulates migration of melanoma cells, probably

via a pertussis toxin-sensitive G protein. May have a role in induction of parturition. Possible

involvement in cell proliferation and adipose tissue development. Tumor cell motility-stimulating

factor

Gene Wiki entry for ENPP2 (Autotaxin)


AB014533 Cluster Incl. AB014533:Homo sapiens mRNA for KIAA0633 protein, partial cds /cds=(0,3951) /gb=AB014533 /gi=3327079 /ug=Hs.33010 /len=5289 35669_at 148.4



Aliases

 

Descriptions

 

External Ids

DKFZp686G13227 2

cordon-bleu homolog 2

HGNC: 221991

KIAA0633 1, 2, 3

cordon-bleu homolog (mouse) 2

Entrez Gene: 232422

MGC131893 2


UniProtKB: O751283


Ensembl: ENSG000001060787


Search outside databases for aliases for COBL gene

Previous GC identifers: GC07M050548 GC07M050791 GC07M050825 GC07M050858


00148.50000 00000.12500
00148.62500 00000.12500
00148.87500 00000.25000 !
U09002 Cluster Incl. U09002:Human N-methyl-D-aspartate receptor modulatory subunit 2A (hNR2A) mRNA, complete cds /cds=(155,4549) /gb=U09002 /gi=558748 /ug=Hs.167464 /len=6137 38236_at 148.7



Aliases

 

Descriptions

 

External Ids

NMDAR2A 2, 3, 5

N-methyl D-aspartate receptor subtype 2A 3

HGNC: 45851

NR2A 2, 3

N-methyl-D-aspartate receptor channel, subunit epsilon-1 2

Entrez Gene: 29032

OTTHUMP00000160135 2

N-methyl-D-aspartate receptor subunit 2A 2

UniProtKB: Q128793

OTTHUMP00000174531 2

NMDA receptor subtype 2A 2

Ensembl: ENSG000001834547

hNR2A 3

glutamate receptor, ionotropic, N-methyl D-aspartate 2A 2




Search outside databases for aliases for GRIN2A gene

Previous GC identifers: GC16M009658 GC16M009991 GC16M009822

Summaries
for GRIN2A

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EntrezGene summary for GRIN2A:

N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate-gated ion channels. These

receptors have been shown to be involved in long-term potentiation, an activity-dependent increase

in the efficiency of synaptic transmission thought to underlie certain kinds of memory and

learning. NMDA receptor channels are heteromers composed of the key receptor subunit NMDAR1

(GRIN1) and 1 or more of the 4 NMDAR2 subunits: NMDAR2A (GRIN2A), NMDAR2B (GRIN2B), NMDAR2C

(GRIN2C) and NMDAR2D (GRIN2D). Alternatively spliced transcript variants encoding different

isoforms have been found for this gene. [provided by RefSeq]


UniProtKB/Swiss-Prot: NMDE1_HUMAN, Q12879

Function: NMDA receptor subtype of glutamate-gated ion channels possesses high calcium permeability

and voltage-dependent sensitivity to magnesium. Activation requires binding of agonist to both

types of subunits

Gene Wiki entry for GRIN2A


M12174 M12174 /FEATURE= /DEFINITION=HUMRHOA Human ras-related rho mRNA (clone 6), partial cds 1826_at 148.9



Aliases

 

Descriptions

 

External Ids

ARH6 2, 3

Aplysia RAS-related homolog 6 2

HGNC: 6681

ARHB 2, 3

oncogene RHO H6 2

Entrez Gene: 3882

H6 3

ras homolog gene family, member B 2

UniProtKB: P627453

MST081 1, 2


Ensembl: ENSG000001438787

MSTP081 2


RHOH6 1, 2

RhoB 1


Search outside databases for aliases for RHOB gene

Previous GC identifers: GC02P020632 GC02P020568

Summaries
for RHOB

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UniProtKB/Swiss-Prot: RHOB_HUMAN, P62745

Function: Mediates apoptosis in neoplastically transformed cells after DNA damage. Not essential

for development but affects cell adhesion and growth factor signaling in transformed cells. Plays

a negative role in tumorigenesis as deletion causes tumor formation. Involved in intracellular

protein trafficking of a number of proteins. Targets PKN1 to endosomes and is involved in

trafficking of the EGF receptor from late endosomes to lysosomes. Also required for stability and

nuclear trafficking of AKT1/AKT which promotes endothelial cell survival during vascular

development

Gene Wiki entry for RHOB


00149.00000 00000.12500
00149.25000 00000.25000 !
D88153 Cluster Incl. D88153:Homo sapiens mRNA for HYA22, complete cds /cds=(147,1169) /gb=D88153 /gi=2289785 /ug=Hs.147189 /len=4763 40196_at 149.2



Aliases

 

Descriptions

 

External Ids

C3orf8 2, 3

CTD (carboxy-terminal domain, RNA polymerase II,
polypeptide A) small phosphatase-like 2

HGNC: 168901

CTDSP-like 3

Entrez Gene: 102172

NIF-like protein 3

EC 3.1.3.- 3

UniProtKB: O151943

NLI-interacting factor 1 3

HYA22 1, 2

Ensembl: ENSG000001446777

Nuclear LIM interactor-interacting factor 1 3

NIF1 3


Protein YA22 3

NIFL 3

Small C-terminal domain phosphatase 3 3

PSR1 1, 2

Small CTD phosphatase 3 2, 3

RBSP3 2, 3

chromosome 3 open reading frame 8 1

SCP3 1, 2, 3


YA22 3

hYA22 3


Search outside databases for aliases for CTDSPL gene

Previous GC identifer: GC03P037863

Summaries
for CTDSPL

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UniProtKB/Swiss-Prot: CTDSL_HUMAN, O15194

Function: May function as a phosphatase involved in the regulation of cell growth and

differentiation

Gene Wiki entry for CTDSPL


00149.37500 00000.12500
00149.50000 00000.12500
00149.75000 00000.25000 !
AF082657 Cluster Incl. AF082657:Homo sapiens Era GTPase A protein (HERA-A) mRNA, partial cds /cds=(0,1332) /gb=AF082657 /gi=3415108 /ug=Hs.3426 /len=1839 34379_at 149.7



Aliases

 

Descriptions

 

External Ids

CEGA 3

Conserved ERA-like GTPase 3

HGNC: 34241

ERA 2

Era (E. coli G-protein homolog)-like 1 1, 2

Entrez Gene: 262842

ERA-W 3

Era G-protein-like 1 (E. coli) 2

UniProtKB: O756163

ERAL1A 2

Era-like 1 2

Ensembl: ENSG000001325917

HERA 3

GTPase, human homolog of E. coli essential cell cycle
protein Era 2


HERA-A 2


HERA-B 1, 2

hERA 3


Search outside databases for aliases for ERAL1 gene

Previous GC identifers: GC17P027027 GC17P029081 GC17P027327


00149.87500 00000.12500
00150.12500 00000.25000 !
U09510 Cluster Incl. U09510:Human glycyl-tRNA synthetase mRNA, complete cds /cds=(364,2421) /gb=U09510 /gi=595304 /ug=Hs.75280 /len=2462 36581_at 150.1



Aliases

 

Descriptions

 

External Ids

CMT2D 2, 5

Charcot-Marie-Tooth neuropathy 2D 1, 2

HGNC: 41621

DSMAV 1, 2

Charcot-Marie-Tooth neuropathy, neuronal type, D 2

Entrez Gene: 26172

EC 6.1.1.14 3

Glycine--tRNA ligase 3

UniProtKB: P412503

GlyRS 1, 2, 3

glycine tRNA ligase 2

Ensembl: ENSG000001061057

HMN5 2, 5

glycyl-tRNA synthetase 2


SMAD1 1, 2, 5



Search outside databases for aliases for GARS gene

Previous GC identifers: GC07P030276 GC07P030342 GC07P030376 GC07P030407

Summaries
for GARS

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EntrezGene summary for GARS:

This gene encodes glycyl-tRNA synthetase, one of the aminoacyl-tRNA synthetases that charge tRNAs

with their cognate amino acids. The encoded enzyme is an (alpha)2 dimer which belongs to the class

II family of tRNA synthetases. It has been shown to be a target of autoantibodies in the human

autoimmune diseases, polymyositis or dermatomyositis. [provided by RefSeq]


Gene Wiki entry for GARS (Glycyl-tRNA_synthetase)


00150.37500 00000.25000 !
U56998 U56998 /FEATURE= /DEFINITION=HSU56998 Human putative serine/threonine protein kinase PRK (prk) mRNA, complete cds 806_at 150.2



Aliases

 

Descriptions

 

External Ids

CNK 2, 3

Cytokine-inducible serine/threonine-protein kinase 3

HGNC: 21541

EC 2.7.11.21 3

FGF-inducible kinase 2, 3

Entrez Gene: 12632

FNK 1, 2, 3

Polo-like kinase 3 2, 3

UniProtKB: Q9H4B43

OTTHUMP00000010159 2

Proliferation-related kinase 2, 3

Ensembl: ENSG000001738467

PLK-3 3

cytokine-inducible kinase 1, 2


PRK 1, 2, 3

polo-like kinase 3 (Drosophila) 2



Search outside databases for aliases for PLK3 gene

Previous GC identifers: GC01P044679 GC01P044934

Summaries
for PLK3

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EntrezGene summary for PLK3:

Cytokine-inducible kinase is a putative serine/threonine kinase. CNK contains both a catalytic

domain and a putative regulatory domain. It may play a role in regulation of cell cycle

progression and tumorigenesis. [provided by RefSeq]


UniProtKB/Swiss-Prot: PLK3_HUMAN, Q9H4B4

Function: Serine/threonine protein kinase involved in regulating M phase functions during the cell

cycle. May also be part of the signaling network controlling cellular adhesion. In vitro, is able

to phosphorylate CDC25C and casein

Gene Wiki entry for PLK3


00150.50000 00000.12500
00150.62500 00000.12500
00150.87500 00000.25000 !
D87076 Cluster Incl. D87076:Human mRNA for KIAA0239 gene, partial cds /cds=(0,1716) /gb=D87076 /gi=1510152 /ug=Hs.9729 /len=5630 38342_at 150.8



Aliases

 

Descriptions

 

External Ids

JADE2 2, 3

PHD finger protein 15 2, 3

HGNC: 229841

KIAA0239 1, 2, 3


Entrez Gene: 233382

OTTHUMP00000159386 2

UniProtKB: Q9NQC13


Ensembl: ENSG000000431437


Search outside databases for aliases for PHF15 gene

Previous GC identifers: GC05P133892 GC05P133937

Summaries
for PHF15

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UniProtKB/Swiss-Prot: JADE2_HUMAN, Q9NQC1

Function: Component of the HBO1 complex which has a histone H4-specific acetyltransferase activity,

a reduced activity toward histone H3 and is responsible for the bulk of histone H4 acetylation in

vivo


00151.00000 00000.12500
00151.12500 00000.12500
00151.25000 00000.12500
00151.75000 00000.50000 !
AF018631 Cluster Incl. AF018631:untitled /cds=(35,1666) /gb=AF018631 /gi=2674074 /ug=Hs.78885 /len=1996 37274_at 151.7
00151.87500 00000.12500
00152.12500 00000.25000 !
U23946 U23946 /FEATURE= /DEFINITION=HSU23946 Human putative tumor suppressor (LUCA15) mRNA, complete cds 1556_at 152.1



Aliases

 

Descriptions

 

External Ids

FLJ39876 2

Protein G15 3

HGNC: 99021

G15 2

Putative tumor suppressor LUCA15 3

Entrez Gene: 101812

H37 1, 2

RNA binding motif protein 5 2

UniProtKB: P527563

LUCA15 1, 2

RNA-binding motif protein 5 3

Ensembl: ENSG000000037567

RMB5 2

Renal carcinoma antigen NY-REN-9 3




Search outside databases for aliases for RBM5 gene

Previous GC identifers: GC03M049830 GC03M050000 GC03P049980 GC03P050085

Summaries
for RBM5

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UniProtKB/Swiss-Prot: RBM5_HUMAN, P52756

Function: Component of the spliceosome A complex. Regulates alternative splicing of a number of

mRNAs. May modulate splice site pairing after recruitment of the U1 and U2 snRNPs to the 5' and 3'

splice sites of the intron. May both positively and negatively regulate aopotosis by regulating

the alternative splicing of several genes involved in this process, including FAS and

CASP2/caspase-2. In the case of FAS, promotes exclusion of exon 6 thereby producing a soluble form

of FAS that inhibits apoptosis. In the case of CASP2/caspase-2, promotes exclusion of exon 9

thereby producing a catalytically active form of CASP2/Caspase-2 that induces apoptosis

Gene Wiki entry for RBM5


00152.25000 00000.12500
00152.50000 00000.25000 !
U61397 U61397 /FEATURE= /DEFINITION=HSU61397 Human ubiquitin-homology domain protein PIC1 mRNA, complete cds 155_s_at 152.5



Aliases

 

Descriptions

 

External Ids

DAP-1 2

GAP modifying protein 1 2

HGNC: 125021

GMP1 1, 2, 3

GAP-modifying protein 1 3

Entrez Gene: 73412

OFC10 1, 2, 5

SMT3 homolog 3 3

UniProtKB: P631653

PIC1 1, 2

SMT3 suppressor of mif two 3 homolog 1 2

Ensembl: ENSG000001160307

SENP2 2

SMT3 suppressor of mif two 3 homolog 1 (S. cerevisiae) 2


SMT3 2, 5

SMT3 suppressor of mif two 3 homolog 1 (yeast) 1

SMT3C 1, 2, 3

Ubiquitin-homology domain protein PIC1 3

SMT3H3 1, 2, 3

Ubiquitin-like protein SMT3C 3

SUMO-1 1, 2, 3

Ubiquitin-like protein UBL1 3

Sentrin 3

ubiquitin-like 1 (sentrin) 1, 2

UBL1 2, 3, 5



Search outside databases for aliases for SUMO1 gene

Previous GC identifers: GC02M203274 GC02M202896

Summaries
for SUMO1

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EntrezGene summary for SUMO1:

This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein

family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as

part of a post-translational modification system. However, unlike ubiquitin which targets proteins

for degradation, this protein is involved in a variety of cellular processes, such as nuclear

transport, transcriptional regulation, apoptosis, and protein stability. It is not active until

the last four amino acids of the carboxy-terminus have been cleaved off. Several pseudogenes have

been reported for this gene. Alternate transcriptional splice variants encoding different isoforms

have been characterized. [provided by RefSeq]


UniProtKB/Swiss-Prot: SUMO1_HUMAN, P63165

Function: Ubiquitin-like protein which can be covalently attached to target lysines as a monomer.

Does not seem to be involved in protein degradation and may function as an antagonist of ubiquitin

in the degradation process. Plays a role in a number of cellular processes such as nuclear

transport, DNA replication and repair, mitosis and signal transduction. Involved in targeting

RANGAP1 to the nuclear pore complex protein RANBP2. Covalent attachment to its substrates requires

prior activation by the E1 complex SAE1-SAE2 and linkage to the E2 enzyme UBE2I, and can be

promoted by an E3 ligase such as PIAS1-4, RANBP2 or CBX4

Gene Wiki entry for SUMO1 (Small_ubiquitin-related_modifier_1)


00152.62500 00000.12500
00153.12500 00000.50000 !
AJ007509 Cluster Incl. AJ007509:Homo sapiens mRNA for E1B-55kDa-associated protein /cds=(173,2743) /gb=AJ007509 /gi=3319955 /ug=Hs.155218 /len=3513 40106_at 153



Aliases

 

Descriptions

 

External Ids

E1B-AP5 1, 2, 3

Adenovirus early region 1B-associated protein 5 2, 3

HGNC: 170111

E1BAP5 1, 2, 3

E1B 55kDa associated protein 5 2

Entrez Gene: 111002

FLJ12944 1, 2

E1B-55 kDa-associated protein 5 3

UniProtKB: Q9BUJ23

HNRPUL1 2, 3

E1B-55kDa-associated protein 5 2

Ensembl: ENSG000001053237


heterogeneous nuclear ribonucleoprotein U-like 1 2



Search outside databases for aliases for HNRNPUL1 gene

Summaries
for HNRNPUL1

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EntrezGene summary for HNRNPUL1:

This gene encodes a nuclear RNA-binding protein of the heterogeneous nuclear ribonucleoprotein

(hnRNP) family. This protein binds specifically to adenovirus E1B-55kDa oncoprotein. It may play

an important role in nucleocytoplasmic RNA transport, and its function is modulated by E1B-55kDa

in adenovirus-infected cells. Two transcript variants encoding different isoforms have been found

for this gene. Additional variants have also been found, but their full-length natures have not

been determined. [provided by RefSeq]


UniProtKB/Swiss-Prot: HNRL1_HUMAN, Q9BUJ2

Function: Acts as a basic transcriptional regulator. Represses basic transcription driven by

several virus and cellular promoters. When associated with BRD7, activates transcription of

glucocorticoid-responsive promoter in the absence of ligand-stimulation. Plays also a role in mRNA

processing and transport. Binds avidly to poly(G) and poly(C) RNA homopolymers in vitro

Gene Wiki entry for HNRNPUL1 (HNRPUL1)


00153.87500 00000.75000 !
Z37986 Cluster Incl. Z37986:H.sapiens mRNA for phenylalkylamine binding protein /cds=(111,803) /gb=Z37986 /gi=780262 /ug=Hs.75105 /len=1061 32536_at 154



Aliases

 

Descriptions

 

External Ids

3-beta-hydroxysteroid-delta-8,delta-7-isomerase 2

Cholestenol Delta-isomerase 3

HGNC: 31331

CDPX2 2, 5

Chondrodysplasia punctata-2, X-linked dominant (Happle
syndrome) 2

Entrez Gene: 106822

CHO2 1, 2

UniProtKB: Q151253

D8-D7 sterol isomerase 3

CPX 1, 2, 5

Ensembl: ENSG000001471557

Delta(8)-Delta(7) sterol isomerase 3

CPXD 1, 2, 5


Emopamil-binding protein 3

EC 5.3.3.5 3

emopamil binding protein (sterol isomerase) 2


emopamil-binding protein (sterol isomerase) 1, 2

sterol 8-isomerase 2


Search outside databases for aliases for EBP gene

Previous GC identifers: GC0XP047183 GC0XP046640 GC0XP047427 GC0XP047428 GC0XP048136

Summaries
for EBP

(According to Entrez Gene, Wikipedia's Gene Wiki,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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EntrezGene summary for EBP:

The protein encoded by this gene is an integral membrane protein of the endoplasmic reticulum. It

is a high affinity binding protein for the antiischemic phenylalkylamine Ca2+ antagonist

[3H]emopamil and the photoaffinity label [3H]azidopamil. It is similar to sigma receptors and may

be a member of a superfamily of high affinity drug-binding proteins in the endoplasmic reticulum

of different tissues. This protein shares structural features with bacterial and eukaryontic drug

transporting proteins. It has four putative transmembrane segments and contains two conserved

glutamate residues which may be involved in the transport of cationic amphiphilics. Another

prominent feature of this protein is its high content of aromatic amino acid residues (>23%) in

its transmembrane segments. These aromatic amino acid residues have been suggested to be involved

in the drug transport by the P-glycoprotein. Mutations in this gene cause Chondrodysplasia

punctata 2 (CDPX2; also known as Conradi-Hunermann syndrome). [provided by RefSeq]


UniProtKB/Swiss-Prot: EBP_HUMAN, Q15125

Function: Catalyzes the conversion of Delta(8)-sterols to their corresponding Delta(7)-isomers


L10333 Cluster Incl. L10333:Homo sapiens neuroendocrine-specific protein A (NSP) mRNA, complete cds /cds=(122,2452) /gb=L10333 /gi=307306 /ug=Hs.99947 /len=3202 39178_at 154



Aliases

 

Descriptions

 

External Ids

MGC133250 2

Neuroendocrine-specific protein 1, 2, 3

HGNC: 104671

NSP 2, 3, 5

reticulon 1 2

Entrez Gene: 62522



UniProtKB: Q167993

Ensembl: ENSG000001399707


Search outside databases for aliases for RTN1 gene

Previous GC identifers: GC14M057386 GC14M053855 GC14M058052

Summaries
for RTN1

(According to Entrez Gene, Wikipedia's Gene Wiki,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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EntrezGene summary for RTN1:

This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the

endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in

neuroendocrine cells. Alternatively spliced transcript variants encoding different isoforms have

been identified. Multiple promoters rather than alternative splicing of internal exons seem to be

involved in this diversity. [provided by RefSeq]


UniProtKB/Swiss-Prot: RTN1_HUMAN, Q16799

Function: May be involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine

cells

Gene Wiki entry for RTN1


00154.12500 00000.25000 !
M92843 Cluster Incl. M92843:H.sapiens zinc finger transcriptional regulator mRNA, complete cds /cds=(59,1039) /gb=M92843 /gi=183442 /ug=Hs.1665 /len=1746 40448_at 154.1



Aliases

 

Descriptions

 

External Ids

G0S24 1, 2, 3

G0/G1 switch regulatory protein 24 3

HGNC: 128621

GOS24 2

Growth factor-inducible nuclear protein NUP475 3

Entrez Gene: 75382

NUP475 1, 2

Protein TIS11A 3

UniProtKB: P266513

RNF162A 1, 2, 3

Zinc finger protein 36 homolog 3

Ensembl: ENSG000001280167

TIS11 1, 2, 3

zinc finger protein 36, C3H type, homolog 2


TIS11A 3

zinc finger protein 36, C3H type, homolog (mouse) 2

TTP 1, 2, 3, 5

zinc finger protein, C3H type, 36 homolog 2

Zfp-36 3

zinc finger protein, C3H type, 36 homolog (mouse) 1

tristetraprolin 2



Search outside databases for aliases for ZFP36 gene

Previous GC identifers: GC19P040538 GC19P040288 GC19P044573

Summaries
for ZFP36

(According to Entrez Gene, Wikipedia's Gene Wiki,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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UniProtKB/Swiss-Prot: TTP_HUMAN, P26651

Function: Probable regulatory protein with a novel zinc finger structure involved in regulating the

response to growth factors. Has been experimentally shown to be able to bind zinc

Gene Wiki entry for ZFP36


00154.37500 00000.25000 !
AB000584 AB000584 /FEATURE= /DEFINITION=AB000584 Homo sapiens mRNA for TGF-beta superfamily protein, complete cds 1890_at 154.3



Aliases

 

Descriptions

 

External Ids

GDF-15 2, 3

Macrophage inhibitory cytokine 1 3

HGNC: 301421

MIC-1 1, 2, 3

NSAID (nonsteroidal anti-inflammatory drug)-activated
protein 1 2

Entrez Gene: 95182

MIC1 1, 2, 3, 5

UniProtKB: Q999883

NSAID-activated gene 1 protein 3

NAG-1 1, 2, 3

Ensembl: ENSG000001305137

NSAID-regulated gene 1 protein 3

NRG-1 3


Placental TGF-beta 3

PDF 1, 2, 3, 5

Placental bone morphogenetic protein 3

PLAB 1, 2, 3, 5

Prostate differentiation factor 2, 3

PTGF-beta 2

growth differentiation factor 15 2

PTGFB 1, 2, 3



Search outside databases for aliases for GDF15 gene

Previous GC identifers: GC00U914343 GC19P018318

Summaries
for GDF15

(According to Entrez Gene, Wikipedia's Gene Wiki,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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