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OPA2 optic atrophy 2 (obscure) [ Homo sapiens (human) ]

Gene ID: 4977, updated on 6-Nov-2023

Summary

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Gene symbol
OPA2
Gene description
optic atrophy 2 (obscure)
Primary source
MIM:311050
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
Xp11.4-p11.2

Bibliography

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Related articles in PubMed

  1. A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome. Assink JJ, et al. Am J Hum Genet, 1997 Oct. PMID 9382106, Free PMC Article

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.
    Title: Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.
Submit: New GeneRIF Correction

Phenotypes

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optic atrophy 2 (obscure)

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases