OR1F1 Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Mutations in this gene have

Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles

The members of this family share structural similarity

that is independently expressed in smooth muscle and functions to stabilize unphosphorylated myosin filaments

Naturally-occurring readthrough transcription between this gene and upstream GeneID: 147081 results in transcripts that encode isoforms that share similarity with the products of this gene

It is included in a cluster of homeobox D genes located on chromosome 2

OR1F1 Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Mutations in this gene haveOlfactory 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