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PRD primary retinal dysplasia [ Homo sapiens (human) ]

Gene ID: 5548, updated on 2-Oct-2019

Summary

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Gene symbol
PRD
Gene description
primary retinal dysplasia
Primary source
MIM:312550
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:
Xp11.3

Bibliography

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Related articles in PubMed

  1. X-linked recessive primary retinal dysplasia is linked to the Norrie disease locus. Ravia Y, et al. Hum Mol Genet, 1993 Aug. PMID 8401512
  2. Phosphorylation of amphiphysin I by minibrain kinase/dual-specificity tyrosine phosphorylation-regulated kinase, a kinase implicated in Down syndrome. Murakami N, et al. J Biol Chem, 2006 Aug 18. PMID 16733250

GeneRIFs: Gene References Into Functions

Phenotypes

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primary retinal dysplasia

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases