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USH1C, USH1 protein network component harmonin

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USH1C, USH1 protein network component harmonin

  • This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

  • Gene Synonyms (harmonin, Usher syndrome 1C (autosomal recessive, severe), antigen NY-CO-38/NY-CO-37, autoimmune enteropathy-related antigen AIE-75, renal carcinoma antigen NY-REN-3, usher syndrome type-1C protein, AIE-75, DFNB18, DFNB18A, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1cpst,)
  • NCBI Gene ID: 10083
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A0S2Z4V1
    UNIPROT ID#>>A0A0S2Z4U9
    UNIPROT ID#>>Q9Y6N9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

USH1 protein network component harmonin interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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