Nop10 ribonucleoprotein

Preferred Label : Nop10 ribonucleoprotein;

Symbol : NOP10;

CISMeF acronym : NOLA3;

Type : Gene;

Alternative titles and symbols : Nop10, s. cerevisiae, homolog of; NOLA3; Nucleolar protein family a, member 3;

Ensembl ID : ENSG00000182117;

Prefixed ID : *606471;

Détails

Origin ID

606471;

UMLS CUI

C1422602;

Automatic exact mappings (from CISMeF team)
- H/ACA Ribonucleoprotein Complex Subunit 3 [NCIt concept]
- NOP10 Gene [NCIt concept]
- NOP10 ribonucleoprotein [HGNC gene]
- NOP10 ribonucleoprotein [ORDO Gene]
- NOP10 wt Allele [NCIt concept]
HGNC gene
- NOP10 ribonucleoprotein [HGNC gene]
NCIt concept(s)
- H/ACA Ribonucleoprotein Complex Subunit 3 [NCIt concept]
- NOP10 Gene [NCIt concept]
- NOP10 wt Allele [NCIt concept]
ORDO concept(s)
- NOP10 ribonucleoprotein [ORDO Gene]
Phenotypes related
- Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2 [OMIM Phenotype]
- Dyskeratosis congenita, autosomal recessive 1 [OMIM Phenotype]
- Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NOP10 Gene [NCIt concept]
- NOP10 ribonucleoprotein [HGNC gene]

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