GIDRP88 Polyclonal Antibody, 100ul Gene Editing and these and other mutations

and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD)

and is found in either a latent form composed of a mature peptide homodimer

CSNK1A1L resides in the cytoplasm and participates in the Wnt signaling pathway

Induces thymocyte apoptosis when overexpressed

GIDRP88 Polyclonal Antibody, 100ul Gene Editing and these and other mutationsR3HCC1L (R3H Domain And Coiled Coil Containing 1 Like) is a Protein Coding gene. Diseases associated with R3HCC1L include cutaneous anthrax. GO annotations related to this gene include nucleotide binding. An important paralog of this gene is R3HCC1.