Entity Details

Primary name OTOG
Entity type gene
Source Source Link

Details

PrimaryID340990
RefseqGeneNG_033191
SymbolOTOG
Nameotogelin
Chromosome11
Location11p15.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2003-03-28
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsOTOG_HUMAN

GO terms

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GOName
GO:0005198 structural molecule activity
GO:0005615 extracellular space
GO:0005829 cytosol
GO:0007605 sensory perception of sound
GO:0008344 adult locomotory behavior
GO:0016324 apical plasma membrane
GO:0031012 extracellular matrix
GO:0046373 L-arabinose metabolic process
GO:0046556 alpha-L-arabinofuranosidase activity

Diseases

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Disease IDSourceNameDescription
614945 OMIMDeafness, autosomal recessive, 18B (DFNB18B)A form of non-syndromic deafness characterized by a moderate hearing impairment, which can be associated with vestibular dysfunction, and a flat to shallow 'U' or slightly downsloping shaped audiograms. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
OTOGUBCBioGRID23314748 details
OTOGOTOGHPRD9405633 details