Na***nal Institutes of Health (.gov) : Gene ResultTBX1 T-box transcription factor 1 [ (human)]
This gene is a member of a phylogenetically conserved family of genes that share a DNA-binding domain, the T-box. T-box genes encode ...
Na***nal Institutes of Health (.gov) : 6899 - HomoloGene Result
1: HomoloGene: 6899 conserved in Eukaryota ASS1 argininosuccinate synthase 1 Homo sapiens ASS1 argininosuccinate synthase 1 Pan troglodytes LOC716168 ...
Pe***e also ask : Is DiGeorge syndrome hereditary?
DiGeorge syndrome is caused by a problem with a person's genes, called 22q11 deletion. It is not usually passed on to a child by their parents, but it is in a few cases. It's often diagnosed soon after birth with a blood test to check for the genetic fault.
Pe***e also ask : What is the disease TBX1?
In humans, TBX1 haploinsufficiency is the etiology responsible for 22q11DS, a clinical syndrome with a varied phenotypic spectrum, including thymic hypoplasia, congenital cardiac defects, facial dysmorphisms, velopharyngeal insufficiency with or without cleft palate and immune deficiency (20).
Pe***e also ask : What kind of protein is tbx5?
On the basis of this action, the T-box 5 protein is called a transcription factor. During embryonic development, the T-box 5 protein turns on (activates) genes involved in the normal development of the hands and arms (upper limbs).