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OPEM ophthalmoplegia, external, with myopia [ Homo sapiens (human) ]

Gene ID: 4981, updated on 25-Jun-2020

Summary

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Gene symbol
OPEM
Gene description
ophthalmoplegia, external, with myopia
Primary source
MIM:311000
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:
chromosome: X

Bibliography

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Related articles in PubMed

  1. Recessive sex-linked inheritance of external ophthalmoplegia and myopia coincident with other dysplasias. SALLERAS A, et al. Br J Ophthalmol, 1950 Nov. PMID 14791930, Free PMC Article
  2. Recessive sex-linked inheritance of congenital external ophthalmoplegia and myopia coincident with other dysplasias. A reappraisal after 15 years. Ortiz de Zarate JC. Br J Ophthalmol, 1966 Oct. PMID 5928925, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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ophthalmoplegia, external, with myopia

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases