Amnion-associated transmembrane protein

Preferred Label : Amnion-associated transmembrane protein;

Symbol : AMN;

CISMeF acronym : AMN;

Type : Gene;

Alternative titles and symbols : Amnionless, mouse, homolog of;

Ensembl ID : ENSG00000166126;

Prefixed ID : *605799;

Détails

Origin ID

605799;

UMLS CUI

C1422785;

Automatic exact mappings (from CISMeF team)
- ABCD1 wt Allele [NCIt concept]
- ATP binding cassette subfamily D member 1 [ORDO Gene]
- ATP binding cassette subfamily D member 1 [HGNC gene]
- N-Amyl-N-Methylnitrosoamine [NCIt concept]
- adrenoleukodystrophy [MeSH Descriptor]
- amnion associated transmembrane protein [ORDO Gene]
- amnion associated transmembrane protein [HGNC gene]
HGNC gene
- amnion associated transmembrane protein [HGNC gene]
NCIt concept(s)
- AMN Gene [NCIt concept]
- AMN wt Allele [NCIt concept]
- Protein Amnionless [NCIt concept]
ORDO concept(s)
- amnion associated transmembrane protein [ORDO Gene]
Phenotypes related
- Imerslund-grasbeck syndrome 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- AMN Gene [NCIt concept]
- amnion associated transmembrane protein [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients