OPA1
optic atrophy 1 (autosomal dominant)
同義詞:
MGM1, NPG, NTG, largeG
物種:
Human OPA1 (4976), Mouse Opa1 (74143), Rat Opa1 (171116), cow OPA1 (524142), chicken OPA1 (424900), sheep OPA1 (101106813), dog OPA1 (477129), Zebrafish opa1 (492332), domestic cat OPA1 (101086671), Domestic Rabbit OPA1 (100344494) ...更多
UniProtKB ID:
基因 ID:
- Human(4976) Summary: This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
- Mouse(74143) optic atrophy 1
- Rat(171116) optic atrophy 1
- cow(524142) optic atrophy 1 (autosomal dominant)
- chicken(424900) optic atrophy 1 (autosomal dominant)
- sheep(101106813) optic atrophy 1 (autosomal dominant)
- dog(477129) optic atrophy 1 (autosomal dominant)
- Zebrafish(492332) optic atrophy 1 (human)
- domestic cat(101086671) optic atrophy 1 (autosomal dominant)
- Domestic Rabbit(100344494) optic atrophy 1 (autosomal dominant)
- Horse(100059993) optic atrophy 1 (autosomal dominant)
- domestic guinea pig(100717402) optic atrophy 1 (autosomal dominant)
- naked mole-rat(101698766) optic atrophy 1 (autosomal dominant)
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