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USH2B Usher syndrome 2B (autosomal recessive, mild) [ Homo sapiens (human) ]

Gene ID: 7400, discontinued on 15-Jul-2010
Official Symbol
USH2Bprovided by HGNC
Official Full Name
Usher syndrome 2B (autosomal recessive, mild)provided by HGNC
Primary source
HGNC:HGNC:12602
See related
MIM:605472
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Associated conditions

Description Tests
Usher syndrome 2B (autosomal recessive, mild)
GeneReviews: Not available

Markers

Property

  • phenotype only
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