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 11 - 20 of 31 in total
HPO ID HPO Term
HP:0000648 Optic atrophy
HP:0000677 Oligodontia
HP:0000689 Dental malocclusion
HP:0000691 Microdontia
HP:0000698 Conical tooth
HP:0001156 Brachydactyly
HP:0001249 Intellectual disability
HP:0001263 Global developmental delay
HP:0001442 Typified by somatic mosaicism
HP:0001852 Sandal gap
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: April 7, 2025