Nipa magnesium transporter 1

Preferred Label : Nipa magnesium transporter 1;

Symbol : NIPA1;

CISMeF acronym : NIPA1;

Type : Gene;

Alternative titles and symbols : Nonimprinted gene in prader-willi syndrome/angelman syndrome chromosome region 1;

Ensembl ID : ENSG00000170113;

Prefixed ID : *608145;

Details

Origin ID

608145;

UMLS CUI

C1424705;

Automatic exact mappings (from CISMeF team)
- NIPA magnesium transporter 1 [HGNC gene]
- NIPA magnesium transporter 1 [ORDO Gene]
- NIPA1 Gene [NCIt concept]
- NIPA1 gene [LOINC component]
HGNC gene
- NIPA magnesium transporter 1 [HGNC gene]
NCIt concept(s)
- Magnesium Transporter NIPA1 [NCIt concept]
- NIPA1 Gene [NCIt concept]
- NIPA1 wt Allele [NCIt concept]
ORDO concept(s)
- NIPA magnesium transporter 1 [ORDO Gene]
Phenotypes related
- Spastic paraplegia 6, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NIPA magnesium transporter 1 [HGNC gene]
- NIPA1 Gene [NCIt concept]
- NIPA1 gene [LOINC component]

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