| USH1C |
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| Identifiers |
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| Aliases | USH1C, AIE-75, DFNB18, DFNB18A, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1cpst, USH1 protein network component harmonin |
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| External IDs | OMIM: 605242; MGI: 1919338; HomoloGene: 77476; GeneCards: USH1C; OMA:USH1C - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 7 (mouse) |
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| | Band | 7 B3|7 29.66 cM | Start | 45,844,774 bp |
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| End | 45,887,927 bp |
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| Wikidata |
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Harmonin is a protein that in humans is encoded by the USH1C gene. It is expressed in sensory cells of the inner ear and retina, where it plays a role in hearing, balance, and vision. Mutations at the USH1C locus cause Usher syndrome type 1c and nonsyndromic sensorineural deafness.