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OPA6 optic atrophy 6 (autosomal recessive) [ Homo sapiens (human) ]

Gene ID: 777778, updated on 5-Aug-2018

Summary

Official Symbol
OPA6provided by HGNC
Official Full Name
optic atrophy 6 (autosomal recessive)provided by HGNC
Primary source
HGNC:HGNC:33170
See related
MIM:258500
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ROA1

Bibliography

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Phenotypes

Associated conditions

Description Tests
optic atrophy 6 (autosomal recessive)
GeneReviews: Not available

Interactions

Products Interactant Other Gene Complex Source Pubs Description
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