Molecular cloning and characterization of human GIPC3, a novel gene homologous to human GIPC1 and GIPC2.

The DNA sequence and biology of human chromosome 19.

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human.

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.

A reference map of the human binary protein interactome.

GIPC3 couples to MYO6 and PDZ domain proteins, and shapes the hair cell apical region.

PDZ domain-containing protein GIPC3

PDZ domain-containing protein GIPC3

Beta-galactoside alpha-2,6-sialyltransferase 2

Pleckstrin homology domain-containing family A member 2

GIPC3 manual evidence and species boundaries