HLX1 Polyclonal Antibody, 100ul Centrifuge Tube (Bottle) Mutations in this gene cause

Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II

This gene encodes the human homolog of the proto-oncogene c-kit

transparent and visible

The encoded protein interacts with the mitochondrial calcium uniporter

The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status

HLX1 Polyclonal Antibody, 100ul Centrifuge Tube (Bottle) Mutations in this gene causeHLX is a Protein Coding gene. H2. 0 Like Homeobox is a transcription factor required for TBX21 T bet dependent maturation of Th1 cells as well as maintenance of Th1 specific gene expression. Involved in embryogenesis and hematopoiesis Diseases associated with HLX include ovarian endodermal sinus tumor and ovarian primitive germ cell tumor. Among its related pathways are IL12 mediated signaling events. Gene Ontology (GO) annotations related to HLX