RTCD1 Polyclonal Antibody, 100ul Nucleic Acid Amplification Mutations in this gene cause

Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6)

causes vasodilation

It acts as serine protease that converts hepatocyte growth factor to the active form

which is characterized by skeletal dysplasia with generalized limb bone shortening

RTCD1 Polyclonal Antibody, 100ul Nucleic Acid Amplification Mutations in this gene causeRTCA (RNA 3' terminal phosphate cyclase) encodes a member of the RNA 3' phosphate cyclase family. The encoded protein plays a role in RNA metabolism by catalyzing the ATP dependent conversion of the 3' phosphate of RNA substrates to a 2',3' cyclic phosphodiester. Alternatively spliced transcript variants encoding multiple isoforms have been observed for RTCA.