AMN wt Allele - CISMeF

Preferred Label : AMN wt Allele;

NCIt synonyms : Amnionless Homolog (Mouse) Gene; PRO1028; Amnionless, Mouse, Homolog of Gene; Amnionless Gene; Amnionless Homolog Gene; IGS2; Amnion Associated Transmembrane Protein wt Allele; UNQ513/PRO1028;

NCIt definition : Human AMN wild-type allele is located in the vicinity of 14q32.32 and is approximately 11 kb in length. This allele, which encodes protein amnionless, is involved in cobalamin absorption. Mutation of the gene is associated with autosomal recessive megaloblastic anemia 2 (Imerslund-Grasbeck syndrome 2).;

NCI Metathesaurus CUI : CL1912931;

GenBank Accession Number : AF328788;

Details

Origin ID

C192684;

UMLS CUI

C5780762;

OMIM relation
- Amnion-associated transmembrane protein [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Endocytotic Process [NCIt concept]
- Intracellular Transport [NCIt concept]
- Ligand Binding [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Subcellular Protein Targeting [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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