The SLC25A46 gene homepage

General information
Gene symbol SLC25A46
Gene name solute carrier family 25 member 46
Chromosome 5
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NC_000005.9
Transcript reference NM_001303249.1, NM_138773.2
Associated with diseases OPA
Citation reference(s) -
Curators (1) XY Liu
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 2
Hidden variants -
Date created June 13, 2017
Date last updated June 13, 2017
Version SLC25A46:170613

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 25198
Entrez Gene 91137
PubMed articles SLC25A46
OMIM - Gene 610826
OMIM - Diseases OPA (Optic Atrophy)
HGMD SLC25A46
GeneCards SLC25A46
GeneTests SLC25A46


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000268 5 solute carrier family 25, member 46, transcript variant 1 NM_138773.2 NP_620128.1 1
00000270 5 solute carrier family 25, member 46, transcript variant 2 NM_001303249.1 NP_001290178.1 1


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