NIPA2 wt Allele

Preferred Label : NIPA2 wt Allele;

NCIt synonyms : MGC5466; NIPA Magnesium Transporter 2 wt Allele; Nonimprinted Gene In Prader-Willi Syndrome/Angelman Syndrome Chromosome Region 2 Gene; Non Imprinted In Prader-Willi/Angelman Syndrome 2 Gene; SLC57A2;

NCIt definition : Human NIPA2 wild-type allele is located in the vicinity of 15q11.2 and is approximately 29 kb in length. This allele, which encodes magnesium transporter NIPA2 protein, may be involved in prostate cancer.;

NCIt note : The NIPA2 gene lies in between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region on chromosome 15. (OMIM);

GenBank Accession Number : AY732242;

Details

Origin ID

C75739;

UMLS CUI

C2698411;

OMIM relation
- Nipa magnesium transporter 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 15q11.2 [NCIt concept]
gene_plays_role_in_process
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients