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Protein Coding Gene : Slc35a2 solute carrier family 35 (UDP-galactose transporter), member A2
Primary Identifier  MGI:1345297 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  22232
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables UDP-galactose transmembrane transporter activity. Acts upstream of or within UDP-galactose transmembrane transport. Is active in Golgi membrane. Is expressed in several structures, including genitourinary system; heart; liver; lung; and spleen. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIm. Orthologous to human SLC35A2 (solute carrier family 35 member A2).
  • synonyms:
  • Slc35a2,
  • hemadsorption decreased 1,
  • MGI:2147880,
  • Ugalt,
  • MGD-MRK-10607,
  • expressed sequence AI327289,
  • Had1,
  • MGD-MRK-10608,
  • MGI:101928,
  • Had-1,
  • UGT,
  • UDP-galactose translocator,
  • Sfc8,
  • AI327289,
  • solute carrier family 35 (UDP-galactose transporter), member A2,
  • MGD-MRK-18759
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 CDSs

0 Exons

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0 Involved In Mutations

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0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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