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| Term | USH2 complex | ID (Ontology) | GO:1990696 (Gene Ontology) |
| 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.[ PubMed:25406310 ] | ||
| Also Known As | "USH2 quaternary protein complex" | ||
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cellular_component |__protein-containing complex |__USH2 complex |
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| Is a | protein-containing complex | ||
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