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USH1E Usher syndrome 1E (autosomal recessive, severe) [ Homo sapiens (human) ]

Gene ID: 7396, updated on 2-Oct-2019

Summary

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Gene symbol
USH1E
Gene description
Usher syndrome 1E (autosomal recessive, severe)
Primary source
MIM:602097
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:
21q21

Bibliography

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Related articles in PubMed

  1. A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21. Chaïb H, et al. Hum Mol Genet, 1997 Jan. PMID 9002666
  2. The DNA sequence of human chromosome 21. Hattori M, et al. Nature, 2000 May 18. PMID 10830953

GeneRIFs: Gene References Into Functions

Phenotypes

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Usher syndrome 1E (autosomal recessive, severe)

General gene information

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Markers

Other Names

  • Usher syndrome-2A, autosomal recessive, severe

Property

  • phenotype only

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