GIPC3 Required for postnatal maturation of the hair bundle and long-term survival of hair cells and spiral ganglion. Defects in GIPC3 are the cause of deafness autosomal recessive type 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. Belongs to the GIPC family. Note: This description may include information from UniProtKB.
Chromosomal Location of Human Ortholog: 19p13.3
Cellular Component:  vesicle
Disease: Deafness, Autosomal Recessive 15
Reference #:  Q8TF64 (UniProtKB)
Alt. Names/Synonyms: C19orf64; DKFZp686J1198; FLJ40925; GIPC PDZ domain containing family, member 3; GIPC3; PDZ domain protein GIPC3; PDZ domain-containing protein GIPC3
Gene Symbols: GIPC3
Molecular weight: 33,982 Da
Basal Isoelectric point: 5.5  Predict pI for various phosphorylation states
Select Structure to View Below


Protein Structure Not Found.

Cross-references to other databases:  STRING  |  cBioPortal  |  Wikipedia  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Pfam  |  Phospho.ELM  |  GeneCards  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene  |  InnateDB