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	47
Unique public DNA variants reported	40
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

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00001158	3	solute carrier family 25 (carnitine/acylcarnitine translocase), member 20	NM_000387.5	NP_000378.1	47

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