ARHGAP8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Rho GTPase-activating protein 8 is a protein that in humans is encoded by the ARHGAP8 gene.[5][6]

AliasesARHGAP8, BPGAP1, PP610, Rho GTPase activating protein 8
End44,862,788 bp[1]
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ARHGAP8
Identifiers
AliasesARHGAP8, BPGAP1, PP610, Rho GTPase activating protein 8
External IDsOMIM: 609405; MGI: 1920417; HomoloGene: 23645; GeneCards: ARHGAP8; OMA:ARHGAP8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_181335
NM_001017526
NM_001198726

NM_001164627
NM_001164628
NM_001205334
NM_028455

RefSeq (protein)

NP_001017526
NP_001185655
NP_851852

NP_001158099
NP_001158100
NP_001192263
NP_082731

Location (UCSC)Chr 22: 44.75 – 44.86 MbChr 15: 84.6 – 84.66 Mb
PubMed search[3][4]
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Function

This gene encodes a member of the RHOGAP family. GAP (GTPase-activating) family proteins participate in signaling pathways that regulate cell processes involved in cytoskeletal changes. GAP proteins alternate between an active (GTP-bound) and inactive (GDP-bound) state based on the GTP:GDP ratio in the cell. Rare read-through transcripts, containing exons from the PRR5 gene which is located immediately upstream, led to the original description of this gene as encoding a RHOGAP protein containing the proline-rich domains characteristic of PRR5 proteins. Alternatively spliced variants encoding different isoforms have been described.[6]

References

Further reading

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