Opa1 mitochondrial dynamin-like gtpase

Preferred Label : Opa1 mitochondrial dynamin-like gtpase;

Symbol : OPA1;

CISMeF acronym : OPA1;

Type : Gene;

Alternative titles and symbols : Dynamin-like 120-kd protein, mitochondrial; KIAA0567; Opa1 gene;

Ensembl ID : ENSG00000198836;

Prefixed ID : *605290;

Details

Origin ID

605290;

UMLS CUI

C1417953;

Automatic exact mappings (from CISMeF team)
- Dynamin-Like 120 kDa Protein, Mitochondrial [NCIt concept]
- MED12 wt Allele [NCIt concept]
- OPA1 Gene [NCIt concept]
- OPA1 gene [LOINC component]
- OPA1 mitochondrial dynamin like GTPase [ORDO Gene]
- OPA1 mitochondrial dynamin like GTPase [HGNC gene]
- OPA1 wt Allele [NCIt concept]
- Optic Atrophy 1 [NCIt concept]
- mediator complex subunit 12 [ORDO Gene]
- mediator complex subunit 12 [HGNC gene]
HGNC gene
- OPA1 mitochondrial dynamin like GTPase [HGNC gene]
NCIt concept(s)
- Dynamin-Like 120 kDa Protein, Mitochondrial [NCIt concept]
- OPA1 Gene [NCIt concept]
- OPA1 wt Allele [NCIt concept]
ORDO concept(s)
- OPA1 mitochondrial dynamin like GTPase [ORDO Gene]
Phenotypes related
- Behr syndrome [OMIM Phenotype]
- Glaucoma, normal tension, susceptibility to [OMIM Phenotype]
- Mitochondrial dna depletion syndrome 14 (cardioencephalomyopathic type) [OMIM Phenotype]
- Optic atrophy 1 [OMIM Phenotype]
- Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OPA1 Gene [NCIt concept]
- OPA1 gene [LOINC component]
- OPA1 mitochondrial dynamin like GTPase [HGNC gene]

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