The SLC25A26 gene homepage

General information
Gene symbol SLC25A26
Gene name solute carrier family 25 member 26
Chromosome 3
Chromosomal band p14.2
Imprinted Unknown
Genomic reference NC_000003.11
Transcript reference NM_001164796.1
Associated with diseases COXPD28
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 15
Individuals with public variants 3
Hidden variants 5
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 26, 2016
Date last updated February 26, 2024
Version SLC25A26:240226

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
Homepage URL http://www.LOVD.nl/SLC25A26
HGNC 20661
Entrez Gene 115286
PubMed articles SLC25A26
OMIM - Gene 611037
OMIM - Diseases COXPD28 (Combined oxidative phosphorylation deficiency 28)
HGMD SLC25A26
GeneCards SLC25A26
GeneTests SLC25A26
Orphanet SLC25A26


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024192 3 solute carrier family 25 (S-adenosylmethionine carrier), member 26, transcript variant 2 NM_001164796.1 NP_001158268.1 15


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