Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol PBX1 contributors: Shn - updated : 20-01-2020
HGNC name pre-B-cell leukemia homeobox 1
HGNC id 8632
ANIMAL & CELL MODELS
  • Pbx1-deficient mice die at embryonic day 15/16 with severe hypoplasia or aplasia of multiple organs and widespread patterning defects of the axial and appendicular skeleton
  • Pbx-dependent EMT programs mediate murine upper lip/primary palate morphogenesis and fusion via regulation of Snail1
  • Pbx1-/- mouse embryos have pancreatic hypoplasia and marked defects in exocrine and endocrine cell differentiation prior to death at embryonic day (E) 15 or E16
  • Pbx1+/- adult mice have pancreatic islet malformations, impaired glucose tolerance and hypoinsulinemia
  • Silencing of PBX1 by RNAi in MC3T3-E1 cells decreased the expression of Runx2 and Osterix, the critical transcription factors for osteogenesis, but accelerated cell proliferation and bone nodule formation
  • tissue-specific deletion of Pbx1 in mice corneal epithelium results in corneal dystrophy