HCCS Polyclonal Antibody, 20ul Cell Proliferation Familial dysautonomia is also associated

Familial dysautonomia is also associated with chromosome 9 though through the gene IKAP

under certain conditions

ADAMTS17 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family

The crystallin alpha B has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions

HCCS Polyclonal Antibody, 20ul Cell Proliferation Familial dysautonomia is also associatedCytochrome c type heme lyase encoded by HCCS is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in HCCS are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for HCCS.