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Ontology explorer

Gene ontology
Version 2014-12-22
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Details for USH2 complex
Gene ontology ID
GO:1990696
Definition
A protein complex composed of four proteins, loss of which results in Usher Syndrome type 2 (USH2 syndrome), a leading genetic cause of combined hearing and vision loss. This complex is conserved in many species; in mice, it is composed of USH2A, GPR98 (aka ADGRV1), WHRN, and PDZD7
Synonyms
1. USH2 quaternary protein complex
References
1. GOC: krc
2. PMID 25406310
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