View SLC25A12 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC25A12
Gene name solute carrier family 25 (aspartate/glutamate carrier), member 12
Chromosome 2
Chromosomal band q24
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_003705.4, NR_047549.1
Associated with diseases 612949
Citation reference(s) -
Curators (0) -
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 0
Hidden variants 0
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 10982
Entrez Gene 8604
PubMed articles SLC25A12
OMIM - Gene 603667
OMIM - Diseases 612949 (Hypomyelination, global cerebral, 612949 (3))
HGMD SLC25A12
GeneCards SLC25A12
GeneTests SLC25A12


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001147 2 transcript variant 2 NR_047549.1 - 2
00001148 2 transcript variant 1 NM_003705.4 NP_003696.2 2


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

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium