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)

miscellaneous:Enzyme activity requires the presence of both kinase domains

GO annotations related to this gene include damaged DNA binding and DNA-directed DNA polymerase activity

and may also have a role in controlling cell growth and/or differentiation

The synergy of this protein and the APP is required to mediate neuromuscular transmission

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.