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MYP12 myopia 12 (high grade, autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 664780, updated on 31-Aug-2024

Summary

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Official Symbol
MYP12provided by HGNC
Official Full Name
myopia 12 (high grade, autosomal dominant)provided by HGNC
Primary source
MIM:609995
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:
2q37.1

Bibliography

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Related articles in PubMed

  1. Linkage replication of the MYP12 locus in common myopia. Chen CY, et al. Invest Ophthalmol Vis Sci, 2007 Oct. PMID 17898262
  2. Identification of a novel locus on 2q for autosomal dominant high-grade myopia. Paluru PC, et al. Invest Ophthalmol Vis Sci, 2005 Jul. PMID 15980214

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
myopia 12 (high grade, autosomal dominant)
OMIM: 609995GeneReviews: Not available

General gene information

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Property

  • phenotype only

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