Kell blood group protein, mcleod syndrome-associated

Preferred Label : Kell blood group protein, mcleod syndrome-associated;

Symbol : XK;

CISMeF acronym : XK;

Type : Gene;

Alternative titles and symbols : Kell blood group precursor; Xk locus; Precursor substance, kell blood group; Kell complex, 37-kd component; KX;

Ensembl ID : ENSG00000047597;

Prefixed ID : *314850;

Details

Origin ID

314850;

UMLS CUI

C1421537;

Automatic exact mappings (from CISMeF team)
- Membrane Transport Protein XK [NCIt concept]
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [ORDO Gene]
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [HGNC gene]
- XK Gene [NCIt concept]
- XK wt Allele [NCIt concept]
False automatic mappings
- Kosovo [NCIt concept]
HGNC gene
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [HGNC gene]
NCIt concept(s)
- Membrane Transport Protein XK [NCIt concept]
- XK Gene [NCIt concept]
- XK wt Allele [NCIt concept]
ORDO concept(s)
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [ORDO Gene]
Phenotypes related
- Mcleod syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [HGNC gene]
- XK Gene [NCIt concept]

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