The SLC25A22 gene homepage

General information
Gene symbol SLC25A22
Gene name solute carrier family 25 (mitochondrial carrier: glutamate), member 22
Chromosome 11
Chromosomal band p15.5
Imprinted Unknown
Genomic reference NG_023407.1
Transcript reference NM_001191060.1
Associated with diseases EIEE3
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 39
Unique public DNA variants reported 32
Individuals with public variants 38
Hidden variants 4
Date created May 03, 2013
Date last updated July 07, 2023
Version SLC25A22:230707

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 19954
Entrez Gene 79751
PubMed articles SLC25A22
OMIM - Gene 609302
OMIM - Diseases EIEE3 (encephalopathy, epileptic, early infantile, type 3 (EIEE-3))
Orphanet SLC25A22

Active transcripts




NCBI ID     

NCBI Protein ID     

00019204 11 transcript variant 1 NM_001191060.1 NP_001177989.1 39

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