SLC35A2 gene homepage

General information
Gene symbol SLC35A2
Gene name solute carrier family 35 (UDP-galactose transporter), member A2
Chromosome X
Chromosomal band p11.23-p11.22
Imprinted Unknown
Genomic reference NC_000023.10
Transcript reference NM_005660.1
Exon/intron information NM_005660.1 exon/intron table
Associated with diseases CDG-2M
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 73
Unique public DNA variants reported 69
Individuals with public variants 37
Hidden variants 1
Date created September 13, 2012
Date last updated July 12, 2019
Version SLC35A2:190712

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_005660.1.
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 11022
Entrez Gene 7355
PubMed articles SLC35A2
OMIM - Gene 314375
OMIM - Diseases CDG-2M (glycosylation, congenital disorder of, type IIm (CDG-2M))
HGMD SLC35A2
GeneCards SLC35A2
GeneTests SLC35A2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000575 X transcript variant 1 NM_005660.1 NP_005651.1 73


Copyright & disclaimer
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