HESX1 Polyclonal Antibody, 100ul Monoclonal Antibodies KAT7 is a gene on

KAT7 is a gene on chromosome 17q21

neuronal growth cone collapse and cell migration

The human protein is able to interact with other molecules of the same protein

Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3

CERKL encodes a protein (ceramide kinase like) with ceramide kinase-like domains

HESX1 Polyclonal Antibody, 100ul Monoclonal Antibodies KAT7 is a gene onThis gene encodes a conserved homeobox protein that is a transcriptional repressor in the developing forebrain and pituitary gland. Mutations in this gene are associated with septooptic dysplasia, HESX1 related growth hormone deficiency, and combined pituitary hormone deficiency.