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HGNC UniGene Nucleotide OMIM UCSC
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FLASH GENE
Symbol COCH contributors: mct - updated : 29-03-2023
HGNC name coagulation factor C homolog, cochlin (Limulus polyphemus)
HGNC id 2180
ASSOCIATED DISORDERS
corresponding disease(s) DFNA9 , DFNB110
related resource Hereditary Hearing Loss Homepage
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional       loss of function
results in conductive hearing loss that protects against physiologic and molecular effects of noise trauma
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS