X-linked Kx blood group antigen, Kell and VPS13A binding protein

Preferred Label : X-linked Kx blood group antigen, Kell and VPS13A binding protein;

Approved symbol HGNC : XK;

Name synonyms HGNC : McLeod syndrome; Kx antigen;

Alias symbols HGNC : X1k; XKR1; Kx;

Chromosome HGNC : Xp21.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000047597;

Details

Origin ID

HGNC:12811;

UMLS CUI

C1421537;

Automatic exact mappings (from CISMeF team)
- Blood group deletion syndrome (disorder) [SNOMED CT concept]
- K antigens [MeSH Supplementary Concept]
- Kell blood group protein, mcleod syndrome-associated [OMIM gene]
- McLeod syndrome [PASCAL descriptor]
- McLeod syndrome [ICD-11 More detail]
- Mcleod syndrome [OMIM Phenotype]
- Membrane Transport Protein XK [NCIt concept]
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [ORDO Gene]
- kx antigen [MeSH concept]
- neuroacanthocytosis, mcleod type [MeSH Supplementary Concept]
NCIt concept
- XK Gene [NCIt concept]
OMIM gene
- Kell blood group protein, mcleod syndrome-associated [OMIM gene]
Orphanet gene
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Kell blood group protein, mcleod syndrome-associated [OMIM gene]
- XK Gene [NCIt concept]

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