NOP56 ribonucleoprotein

Preferred Label : NOP56 ribonucleoprotein;

Approved symbol HGNC : NOP56;

Name synonyms HGNC : spinocerebellar ataxia 36;

Alias symbols HGNC : SCA36;

Chromosome HGNC : 20p13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000101361;

Details

Origin ID

HGNC:15911;

UMLS CUI

C2678521;

Automatic exact mappings (from CISMeF team)
- NOP56 ribonucleoprotein [ORDO Gene]
- Nop56 ribonuclear protein [OMIM gene]
- Spinocerebellar ataxia type 36 (disorder) [SNOMED CT concept]
NCIt concept
- NOP56 Gene [NCIt concept]
OMIM gene
- Nop56 ribonuclear protein [OMIM gene]
Orphanet gene
- NOP56 ribonucleoprotein [ORDO Gene]
See also inter- (CISMeF)
- Spinocerebellar ataxia 36 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NOP56 Gene [NCIt concept]
- NOP56 gene [LOINC component]
- Nop56 ribonuclear protein [OMIM gene]

Keyword's position in hierarchy(ies) :

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