Mitofusin 2 - CISMeF

Preferred Label : Mitofusin 2;

Symbol : MFN2;

CISMeF acronym : MFN2;

Type : Gene;

Alternative titles and symbols : KIAA0214;

Ensembl ID : ENSG00000116688;

Prefixed ID : *608507;

Details

Origin ID

608507;

UMLS CUI

C1424611;

Automatic exact mappings (from CISMeF team)
- MFN2 Gene [NCIt concept]
- MFN2 gene [LOINC component]
- MFN2 wt Allele [NCIt concept]
- Mitofusin-2 [NCIt concept]
- mitofusin 2 [ORDO Gene]
- mitofusin 2 [HGNC gene]
HGNC gene
- mitofusin 2 [HGNC gene]
NCIt concept(s)
- MFN2 Gene [NCIt concept]
- MFN2 wt Allele [NCIt concept]
- Mitofusin-2 [NCIt concept]
ORDO concept(s)
- mitofusin 2 [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth disease, axonal, autosomal dominant, type 2a2a [OMIM Phenotype]
- Charcot-marie-tooth disease, axonal, autosomal recessive, type 2a2b [OMIM Phenotype]
- Lipomatosis, multiple symmetric, with or without axonal peripheral neuropathy [OMIM Phenotype]
- Neuropathy, hereditary motor and sensory, type via, with optic atrophy [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MFN2 Gene [NCIt concept]
- MFN2 gene [LOINC component]
- mitofusin 2 [HGNC gene]

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