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Gene : RHOQ Homo sapiens

Name  ? ras homolog family member Q Cytological Location  2p21
Brief Description  ras homolog family member Q
description  This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. The encoded protein is an important signalling protein for sarcomere assembly and has been shown to play a significant role in the exocytosis of the solute carrier family 2, facilitated glucose transporter member 4 and other proteins, possibly acting as the signal that turns on the membrane fusion machinery. Three related pseudogene have been identified on chromosomes 2 and 14. [provided by RefSeq, Aug 2011]
  • synonyms:
  • HEL-S-42,
  • HGNC:17736,
  • RASL7A,
  • TC10,
  • ARHQ,
  • TC10,
  • ARHQ,
  • RASL7A,
  • OTTHUMG00000150653,
  • TC10A,
  • M31470,
  • ras homolog gene family, member Q,
  • RHOQ,
  • NM_012249,
  • uc002rva.4,
  • RAS-like, family 7, member A
  • identifiers:
  • 23433,
  • ENSG00000119729,
  • RHOQ

Genome feature

Region: gene ? Length: 42280  
Location: 2:46542409-46584688 Cyto location: 2p21


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Disease

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Other

230 SN Ps

5 Cross References

15 Data Sets

28 Homologues

0 Located Features

90 Rna Seq Results