1. Gene
  2. RHOV - ras homolog family member V Gene

RHOV - ras homolog family member V Gene

Homo sapiens

Also known as CHP; ARHV; WRCH2

Gene ID: 171177 | Gene type: protein coding

About RHOV

Cytogenetic location: 15q15.1 Genomic coordinates (GRCh38): 15:40,872,214-40,874,234 (from NCBI)

This gene has 1 transcript (splice variant), 241 orthologues and 22 paralogues. Biased expression in esophagus (RPKM 34.6), skin (RPKM 27.2) and 5 other tissues.

Summary

Predicted to enable GTP binding activity and GTPase activity. Predicted to be involved in several processes, including Cdc42 protein signal transduction; cell projection assembly; and endocytosis. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

RHOV Products(1)

mRNA Protein Name
NM_133639.4 NP_598378.3 rho-related GTP-binding protein RhoV

RHOV Protein Structure

Ras

Ras: Ras family (33 - 203)

  • 0
  • 100
  • 200
  • 236 a.a.
Protein Preferred Names Protein Names

rho-related GTP-binding protein RhoV

CDC42-like GTPase 2

Related Diseases

Diseases Alias
Ascaridiasis

Ascariasis

Toxic Megacolon

Megacolon, Toxic

Toxic Dilatation Of Colon

Toxic Functional Megacolon

Deafness, Autosomal Recessive 104

DFNB104

Autosomal Recessive Nonsyndromic Deafness 104

Autosomal Recessive Deafness 104

Deafness, Autosomal Recessive, 104

Deafness, Autosomal Recessive, Type 104

Deafness, Autosomal Dominant 1, With Or Without Thrombocytopenia

Konigsmark Syndrome

DFNA1

Autosomal Dominant Nonsyndromic Deafness 1

Lfhl1

Deafness, Autosomal Dominant 1

Autosomal Dominant Deafness 1

Autosomal Dominant Deafness 1, With Or Without Thrombocytopenia

Hereditary Low Frequency Hearing Loss 1

Diaph1-Related Sensorineural Hearing Loss-Thrombocytopenia Syndrome

Diaph1-Related Sensorineural Deafness-Thrombocytopenia Syndrome

Hereditary Low-Frequency Hearing Loss

Hereditary Low-Frequency Sensorineural Hearing Loss

Lfsnhl1

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 1

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 1

Deafness, Autosomal Dominant, Type 1

Clostridium Difficile Colitis

Pseudomembranous Colitis

Colitis Pseudomembranous

Enterocolitis, Pseudomembranous

Pseudomembranous Enterocolitis

Clostridium Difficile Infection

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus RHOV VGNC VGNC:55140
Mus musculus RHOV MGD MGI:2444227
Rattus norvegicus RHOV RGD RGD:628824
Canis familiaris RHOV VGNC VGNC:45566
Felis catus RHOV VGNC VGNC:64619