O10H5 Polyclonal Antibody, 100ul Diagnostic Probes & Oligos This protein was subsequently designated

This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa

The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators

Mutations in this gene cause a multiple congenital anomaly syndrome in human patients

Alternatively spliced transcript variants have been found for CHST8

O10H5 Polyclonal Antibody, 100ul Diagnostic Probes & Oligos This protein was subsequently designatedOlfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G protein coupled receptors (GPCR) arising from single coding exon genes. Olfactory receptors share a 7 transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein mediated