ras homolog family member A

Summary
Gene Symbol
  • RHOA
Aliases
  • RHOH12
  • Rho12
Organism
Homo sapiens (human)
NCBI Gene
387
HGNC
667
PubChem
387
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ADP-ribosylation
  • Cell division
  • Cell membrane
  • Cell projection
  • Cytoskeleton
  • Direct protein sequencing
  • Disease variant
  • Ectodermal dysplasia
  • GTP-binding
  • Glycoprotein
  • Host-virus interaction
  • Hydrolase
  • Isopeptide bond
  • Lipoprotein
  • Magnesium
  • Membrane
  • Methylation
  • Nucleus
  • Phosphoprotein
  • Prenylation
  • Proteomics identification
  • Proto-oncogene
  • Reference proteome
  • Ubl conjugation
Proteins
Displaying all 7 entries
UniProt Protein Name
P61586
  • Rho cDNA clone 12
B4DKN9
A0A024R324
C9JX21
C9JRM1
A0A7I2YQV1
Q9BVT0
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 28 in total
GO Term Evidence Code PMID
nucleus
endosome
endoplasmic reticulum membrane
cytosol
cytosol
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
GTPase
Functional Category
  • T: Signal transduction mechanisms
  • U: Intracellular trafficking, secretion, and vesicular transport
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:3459 breast carcinoma
The Human Phenotype Ontology
Displaying entries 21 - 30 of 31 in total
HPO ID HPO Term
HP:0003577 Congenital onset
HP:0004552 Scarring alopecia of scalp
HP:0006297 Enamel hypoplasia
HP:0006335 Persistence of primary teeth
HP:0007663 Reduced visual acuity
HP:0007946 Unilateral narrow palpebral fissure
HP:0009779 3-4 toe syndactyly
HP:0009918 Ectopia pupillae
HP:0009928 Thick nasal alae
HP:0010055 Broad hallux
Displaying 1 entry
Disease ID Disease Name
OMIM:618727
  • ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 8, 2025