The SLC25A13 gene homepage

General information
Gene symbol SLC25A13
Gene name solute carrier family 25 member 13
Chromosome 7
Chromosomal band q21.3
Imprinted Unknown
Genomic reference NG_012247.2
Transcript reference NM_001160210.1, NM_014251.2, NR_027662.1
Associated with diseases CTLN2, NICCD
Citation reference(s) -
Curators (1) MyHVP
Total number of public variants reported 15
Unique public DNA variants reported 5
Individuals with public variants 12
Hidden variants 6
Download all this gene's data Download all data
Date created March 31, 2021
Date last updated August 01, 2021
Version SLC25A13:210801

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 10983
Entrez Gene 10165
PubMed articles SLC25A13
OMIM - Gene 603859
OMIM - Diseases CTLN2 (Citrullinemia, Type II, Adult-Onset)
NICCD (Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency)
HGMD SLC25A13
GeneCards SLC25A13
GeneTests SLC25A13


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000437 7 transcript variant 2 NM_014251.2 NP_055066.1 10
00000436 7 transcript variant 1 NM_001160210.1 NP_001153682.1 5
00000438 7 transcript variant 3 NR_027662.1 - -


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