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

Messages of several sizes can be detected in northern blots but sequence information cannot confirm the identity of the shorter messages

The encoded protein interacts with the mitochondrial calcium uniporter

where these barriers are required for normal hearing

SIGLEC (sialic acid binding Ig-like lectin) family

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