F-box only protein 11

Preferred Label : F-box only protein 11;

Symbol : FBXO11;

CISMeF acronym : FBXO11;

Type : Gene;

Alternative titles and symbols : Vitiligo-associated protein 1; Protein arginine methyltransferase 9; FBX11; VIT1; PRMT9;

Ensembl ID : ENSG00000138081;

Prefixed ID : *607871;

Details

Origin ID

607871;

UMLS CUI

C1422085;

Automatic exact mappings (from CISMeF team)
- F-Box Only Protein 11 [NCIt concept]
- F-box protein 11 [ORDO Gene]
- F-box protein 11 [HGNC gene]
- FBXO11 Gene [NCIt concept]
- FBXO11 wt Allele [NCIt concept]
- protein arginine methyltransferase 9 [HGNC gene]
HGNC gene
- F-box protein 11 [HGNC gene]
NCIt concept(s)
- F-Box Only Protein 11 [NCIt concept]
- FBXO11 Gene [NCIt concept]
- FBXO11 wt Allele [NCIt concept]
Phenotypes related
- Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- F-box protein 11 [HGNC gene]
- FBXO11 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients