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USH1A Usher syndrome 1A (autosomal recessive, severe) [ Homo sapiens (human) ]

Gene ID: 7393, discontinued on 1-Aug-2014
  • This record has been withdrawn by HGNC.
Official Symbol
USH1Aprovided by HGNC
Official Full Name
Usher syndrome 1A (autosomal recessive, severe)provided by HGNC
Primary source
HGNC:HGNC:12595
See related
MIM:276900
Gene type
unknown
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
USH1
Summary
DISCONTINUED: This record has been withdrawn by HGNC.

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Associated conditions

Description Tests
Usher syndrome 1A (autosomal recessive, severe)
GeneReviews: Not available

Markers

Property

  • phenotype only
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