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
cell division control protein 42
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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