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Harmonin / USH1C

Usher syndrome 1C (autosomal recessive, severe)

Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

Gene Name: Usher syndrome 1C (autosomal recessive, severe)
Synonyms: USH1C, AIE-75, Antigen NY-CO-38/NY-CO-37, AIE75, DFNB18, DFNB18A, Harmonin, PDZ-45, NY-CO-38, Usher syndrome type-1C protein, Ush1cpst, NY-CO-37, PDZ-73, PDZ73, Protein PDZ-73
Target Sequences: NM_005709 NP_005700.2 Q9Y6N9

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If you do not find the reagent or information you require, please contact Customer.Support@LSBio.com to inquire about additional products in development.

PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).