SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1

Preferred Label : SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1;

Approved symbol HGNC : SAMHD1;

Name synonyms HGNC : HD domain containing 1; Aicardi-Goutieres syndrome 5; monocyte protein 5;

Alias symbols HGNC : HDDC1; MOP-5; SBBI88; AGS5; Mg11;

Chromosome HGNC : 20q11.23;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000101347;

Details

Origin ID

HGNC:15925;

UMLS CUI

C1423837;

Automatic exact mappings (from CISMeF team)
- Aicardi-Goutieres syndrome 5 [MeSH Supplementary Concept]
- Aicardi-Goutieres syndrome 5 [MeSH concept]
- Aicardi-goutieres syndrome 5 [OMIM Phenotype]
- SAM Domain and HD Domain-Containing Protein 1 [NCIt concept]
- SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 [ORDO Gene]
- Sam domain- and hd domain-containing protein 1 [OMIM gene]
NCIt concept
- SAMHD1 Gene [NCIt concept]
OMIM gene
- Sam domain- and hd domain-containing protein 1 [OMIM gene]
Orphanet gene
- SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 [ORDO Gene]
See also inter- (CISMeF)
- Aicardi-Goutieres Syndrome 5 [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SAMHD1 Gene [NCIt concept]
- Sam domain- and hd domain-containing protein 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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