zgc:111878 antibody, 2900089E13Rik antibody, DNC antibody, MUP1 antibody, TPC antibody, MCPHA antibody, THMD3 antibody, THMD4 antibody, solute carrier family 25 member 19 antibody, solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 antibody, Slc25a19 antibody, slc25a19 antibody, SLC25A19 antibody
Background
This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene.,SLC25A19,DNC,MCPHA,MUP1,THMD3,THMD4,TPC,SLC25A19