SLC25A20 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC25A20
Gene name solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
Chromosome 3
Chromosomal band p21.31
Imprinted Unknown
Genomic reference NC_000003.11
Transcript reference NM_000387.5
Associated with diseases CACTD
Citation reference(s) -
Curators (0) -
Total number of public variants reported 8
Unique public DNA variants reported 8
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Notes MSeqDR-LSDB
Date created November 12, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 1421
Entrez Gene 788
PubMed articles SLC25A20
OMIM - Gene 613698
OMIM - Diseases CACTD (CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY)
HGMD SLC25A20
GeneCards SLC25A20
GeneTests SLC25A20


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001158 3 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 NM_000387.5 NP_000378.1 8


Copyright & disclaimer
; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium