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

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