The SLC25A42 gene homepage

General information
Gene symbol SLC25A42
Gene name solute carrier family 25, member 42
Chromosome 19
Chromosomal band p13.11
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_178526.4
Exon/intron information NM_178526.4 exon/intron table
Associated with diseases MECREN
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 19
Unique public DNA variants reported 5
Individuals with public variants 16
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated May 05, 2025
Version SLC25A42:250505

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_178526.4.
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 https://www.LOVD.nl/SLC25A42
HGNC HGNC:28380
Entrez Gene 284439
PubMed articles SLC25A42
OMIM - Gene 610823
OMIM - Diseases MECREN (Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression)
HGMD SLC25A42
GeneCards SLC25A42
NIH Genetic Testing Registry SLC25A42
Orphanet SLC25A42


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019224 19 solute carrier family 25, member 42 NM_178526.4 NP_848621.2 19


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