Type | Description |
---|---|
Definition | Rho GTPase activating protein 5 |
Date | Results | Publications |
---|---|---|
2019-12-14 11:10:00 | These results indicate that SIRT1 suppresses migration and invasion of gastric cancer by downregulating ARHGAP5 through an interaction with c-JUN, and these phenomena represent a novel mechanism of the antitumor action of SIRT1. | 30250020 |
2017-08-12 11:59:00 | only collagen-IV elicits the formation of proteolytically active podosomes through a mechanism involving increased Src phosphorylation, p190RhoGAP-B (also known as ARHGAP5) relocalisation and MT1-MMP (also known as MMP14) cell surface exposure at podosome sites. | 27231093 |
2017-07-29 11:24:00 | Brazilian Amerindian ancestry compared to Asian, European, and African Genomes.SNPs within or proximal to CIITA (rs6498115), SMC6 (rs1834619), and KLHL29 (rs2288697) were most differentiated in the Amerindian-specific branch. SNPs in ADAMTS9 (rs7631391), DOCK2 (rs77594147), SLC28A1 (rs28649017), ARHGAP5 (rs7151991), and CIITA (rs45601437) in the Asian comparison. | 28100790 |
2016-04-09 10:03:00 | This newly identified miR-744/ARHGAP5 pathway provides further insight into the progression and metastasis of NPC and indicates potential novel therapeutic targets for NPC. | 25961434 |
2014-05-24 10:14:00 | Ectopic expression of p190B suppressed the miR-494-induced EGFR upregulation. | 24316134 |
Type | IDs |
---|---|
Synonymous | GFI2, RhoGAP5, p190-B, p190BRhoGAP |
Gene |
UniProtKB-ID:
RHG05_HUMAN
UniprotKB:
Q13017
UniParc:
UPI000057B85C,
UPI000057B85B,
UPI0000E01412,
UPI00001FD3A9
EMBL:
AB209751,
BC075799,
BC129929,
AK292966,
BC129928,
BC032723,
CH471078,
BC050059,
U17032
Ensembl:
ENSG00000100852
KO:
hsa:394
|
Nucleutide sequences |
EMBL-CDS:
BAD92988.1,
AAH32723.1,
AAH75799.1,
EAW65935.1,
AAI29930.1,
AAA95963.1,
BAF85655.1,
AAH50059.1,
EAW65936.1,
EAW65937.1,
AAI29929.1,
EAW65938.1
Ensembl_TRS:
ENST00000556611,
ENST00000433497,
ENST00000539826,
ENST00000396582,
ENST00000345122
|
Protein sequencees |
Ensembl_PRO:
ENSP00000371897,
ENSP00000452222,
ENSP00000441692,
ENSP00000379827,
ENSP00000407395
RefSeq:
NP_001025226.1,
XP_005267692.1,
XP_016876777.1,
NP_001164.2,
XP_005267693.1
|
Others |
UniRef100:
UniRef100_Q13017
UniRef90:
UniRef90_Q13017
UniRef50:
UniRef50_Q13017
UniGene:
Hs.592313
CCDS:
CCDS45095.1,
CCDS32062.1
|
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Refseq |
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