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Gene: SLC35A2 (solute carrier family 35 member A2) Homo sapiens
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Symbol: SLC35A2
Name: solute carrier family 35 member A2
Description: This gene encodes a member of the nucleotide-sugar transporter family. The encoded protein is a multi-pass membrane protein. It transports UDP-galactose from the cytosol into Golgi vesicles, where it serves as a glycosyl donor for the generation of glycans. Mutations in this gene cause congenital disorder of glycosylation type IIm (CDG2M). Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2014]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CDG2M; CDGX; solute carrier family 35 (UDP-galactose transporter), member 2; solute carrier family 35 (UDP-galactose transporter), member A2; UDP-Gal-Tr; UDP-galactose translocator; UDP-galactose transporter; UGALT; UGAT; UGT; UGT1; UGT2; UGTL
Orthologs:
Mus musculus (house mouse) : Slc35a2 (solute carrier family 35 (UDP-galactose transporter), member A2)  MGI  Alliance
Rattus norvegicus (Norway rat) : Slc35a2 (solute carrier family 35 member A2)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Slc35a2 (solute carrier family 35 member A2)
Pan paniscus (bonobo/pygmy chimpanzee) : SLC35A2 (solute carrier family 35 member A2)
Canis lupus familiaris (dog) : SLC35A2 (solute carrier family 35 member A2)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Slc35a2 (solute carrier family 35 member A2)
Sus scrofa (pig) : SLC35A2 (solute carrier family 35 member A2)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X48,903,183 - 48,911,958 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X48,760,459 - 48,769,235 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X48,645,403 - 48,654,179 (-)NCBINCBI36hg18NCBI36
Build 34X48,516,706 - 48,525,165NCBI
CeleraX52,894,294 - 52,903,071 (+)NCBI
Cytogenetic MapXp11.23NCBI
HuRefX46,416,492 - 46,425,389 (-)NCBIHuRef
CHM1_1X48,791,599 - 48,800,377 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SLC35A2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1353471
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.