NP_766422.2
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
235,757 Da
NCBI Official Full Name
lipoxygenase homology domain-containing protein 1
NCBI Official Synonym Full Names
lipoxygenase homology domains 1
NCBI Protein Information
lipoxygenase homology domain-containing protein 1
UniProt Protein Name
Lipoxygenase homology domain-containing protein 1
UniProt Entry Name
LOXH1_MOUSE
UniProt Comments for LOXHD1
LOXHD1: Involved in hearing. Required for normal function of hair cells in the inner ear. Defects in LOXHD1 are the cause of deafness autosomal recessive type 77 (DFNB77). A form of non-syndromic deafness characterized by preserved low-frequency hearing, and a trend toward mild to moderate mid-frequency and high-frequency hearing loss during childhood and adolescence. Hearing loss progresses to become moderate to severe at mid and high frequencies during adulthood. 4 isoforms of the human protein are produced by alternative splicing.
Protein type: Unknown function
Cellular Component: stereocilium; cell projection; membrane
Molecular Function: calcium channel activity
Biological Process: sensory perception of sound; detection of mechanical stimulus
Research Articles on LOXHD1
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