GO curators for mouse genes have assigned the following annotations to the gene product of Tbx19. (This text reflects annotations as of Wednesday, January 23, 2013.) Summary from NCBI RefSeq
[Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq, Jul 2008]Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Tbx19
participates in the following biological processes:
Budry L et al. (2012) The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling. Genes Dev, 26:2299-310. (PubMed:23070814)
Liu J et al. (2001) Tbx19, a tissue-selective regulator of POMC gene expression. Proc Natl Acad Sci U S A, 98:8674-9. (PubMed:11447259)
Pulichino AM et al. (2003) Tpit determines alternate fates during pituitary cell differentiation. Genes Dev, 17:738-47. (PubMed:12651892)