View SLC25A19 gene homepage

General information
Gene symbol SLC25A19
Gene name solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
Chromosome 17
Chromosomal band q25.1
Imprinted Unknown
Genomic reference NG_008274.1
Transcript reference NM_021734.4
Associated with diseases MCPHA, THMD-4
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Links to other resources
HGNC 14409
Entrez Gene 60386
PubMed articles SLC25A19
OMIM - Gene 606521
OMIM - Diseases MCPHA (microcephaly, Amish type (MCPHA))
THMD-4 (Thiamine metabolism dysfunction syndrome, type 4 (THMD-4))

Active transcripts




NCBI ID     

NCBI Protein ID     

00019201 17 transcript variant 2 NM_021734.4 NP_068380.3 0