GPR110 Polyclonal Antibody, 100ul PCR Series Three alternatively spliced transcript variants

Three alternatively spliced transcript variants have been described for HNRNPDL

4-benzoylpyridine

Defects in this gene or the SMN1 gene can cause spinal muscular atrophy

which is characterized by harmful vascular defects

a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53

GPR110 Polyclonal Antibody, 100ul PCR Series Three alternatively spliced transcript variantsGPR110 is a gene on chromosome 6p12. 3 that encodes an orphan G protein coupled receptor. Probable G protein coupled receptor 110 is a protein that in humans is encoded by the GPR110 gene. This gene encodes a member of the adhesion GPCR receptor family. Family members are characterized by an extended extracellular region with a variable number of N terminal protein modules coupled to a TM7 region via a domain known as the GPCR Autoproteolysis INducing