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MYP1 myopia 1 (X-linked) [ Homo sapiens (human) ]

Gene ID: 4657, updated on 2-Oct-2019

Summary

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Gene symbol
MYP1
Gene description
myopia 1 (X-linked)
Primary source
MIM:310460
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
BED

Genomic context

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Location:
Xq28

Bibliography

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Related articles in PubMed

  1. Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterization. Guo X, et al. Arch Ophthalmol, 2010 Nov. PMID 21060050
  2. X-linked high myopia associated with cone dysfunction. Young TL, et al. Arch Ophthalmol, 2004 Jun. PMID 15197065

GeneRIFs: Gene References Into Functions

Phenotypes

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myopia 1 (X-linked)

General gene information

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Other Names

  • Myopia, X-linked (Bornholm eye disease)
  • Myopia-1 (Bornholm eye disease)
  • myopia 1 (X-linked, Bornholm eye disease included)

Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases