HXA11 Polyclonal Antibody, 100ul Gene Editing subcellular location:Associated with the endoplasmic

subcellular location:Associated with the endoplasmic reticulum and nuclear

The encoded protein belongs to the D (or Zizimin) subfamily of DOCK proteins| which also contain an N-terminal pleckstrin homology domain

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

supplied by OMIM

a region associated with Cornelia de Lange syndrome

HXA11 Polyclonal Antibody, 100ul Gene Editing subcellular location:Associated with the endoplasmicIn vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved