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MYP13 myopia 13 [ Homo sapiens (human) ]

Gene ID: 677764, updated on 2-Oct-2019

Summary

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Gene symbol
MYP13
Gene description
myopia 13
Primary source
MIM:300613
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:
Xq23-q25

Bibliography

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Related articles in PubMed

  1. Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1. Zhang Q, et al. J Hum Genet, 2007. PMID 17351708
  2. Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. Zhang Q, et al. J Med Genet, 2006 May. PMID 16648373, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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myopia 13

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases