Entity Details

Primary name GIPC3
Entity type gene
Source Source Link

Details

PrimaryID126326
RefseqGeneNG_031943
SymbolGIPC3
NameGIPC PDZ domain containing family member 3
Chromosome19
Location19p13.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-29
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsGIPC3_HUMAN

GO terms

Show/Hide Table

Diseases

Show/Hide Table
Disease IDSourceNameDescription
601869 OMIMDeafness, autosomal recessive, 15 (DFNB15)A form of non-syndromic sensorineural hearing loss with prelingual onset. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.

Interactions

6 interactions

InteractorPartnerSourcesPublicationsLink
GIPC3ST6GAL2BioGRID, IntAct32296183 details
GIPC3PLEKHA2BioGRID, IntAct32296183 details
GIPC3FZD3HPRD12011974 details
GIPC3ENO1BioGRID22658674 details
GIPC3SHMT2BioGRID22658674 details
GIPC3MOV10BioGRID22658674 details