DisGeNET - a database of gene-disease associations

Gene: OTOA ×

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	146183
Gene Symbol:	OTOA

OTOA

CUI:	C0452138
Disease:	Sensorineural hearing loss, bilateral

Sensorineural hearing loss, bilateral

0.200

Biomarker

MGD

A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation.

2012