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
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying entries 1 - 10 of 16 in total
DO ID Disease Name Source
DOID:0050665 fetal alcohol syndrome
DOID:0080377 peroxisomal biogenesis disorder
DOID:10763 hypertension
DOID:10976 membranous glomerulonephritis
DOID:11054 urinary bladder cancer
DOID:1289 neurodegenerative disease
DOID:1612 breast cancer
DOID:2377 multiple sclerosis
DOID:2841 asthma
DOID:3459 breast carcinoma
The Human Phenotype Ontology
Displaying entries 1 - 10 of 31 in total
HPO ID HPO Term
HP:0000272 Malar flattening
HP:0000324 Facial asymmetry
HP:0000431 Wide nasal bridge
HP:0000483 Astigmatism
HP:0000486 Strabismus
HP:0000501 Glaucoma
HP:0000518 Cataract
HP:0000545 Myopia
HP:0000568 Microphthalmia
HP:0000639 Nystagmus
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: February 17, 2025