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Gene : SLC35A2 Homo sapiens

Name  ? solute carrier family 35 member A2 Cytological Location  Xp11.23
Brief Description  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]
  • synonyms:
  • UGT1,
  • UGT2,
  • solute carrier family 35 (UDP-galactose transporter), member 2,
  • uc004dlo.4,
  • UGAT,
  • CDG2M,
  • solute carrier family 35 (UDP-galactose transporter), member A2,
  • UGALT,
  • D88146,
  • UGT2,
  • UGT,
  • UGTL,
  • HGNC:11022,
  • UGALT,
  • UGTL,
  • SLC35A2,
  • UDP-Gal-Tr,
  • OTTHUMG00000024129,
  • NM_005660,
  • UGT,
  • CDGX,
  • UGAT,
  • UGT1
  • identifiers:
  • 7355,
  • ENSG00000102100,
  • SLC35A2

Genome feature

Region: gene ? Length: 8779  
Location: X:48903180-48911958 reverse strand Cyto location: Xp11.23

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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16 SN Ps

5 Cross References

18 Data Sets

15 Homologues

0 Located Features

90 Rna Seq Results