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Protein Coding Gene : Slc35b2 solute carrier family 35, member B2

Primary Identifier  MGI:1921086 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  73836
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables 3'-phosphoadenosine 5'-phosphosulfate transmembrane transporter activity. Predicted to be involved in 3'-phosphoadenosine 5'-phosphosulfate transport; chondroitin sulfate biosynthetic process; and transmembrane transport. Is active in Golgi membrane. Is expressed in several structures, including craniocervical region bone; otic capsule; retina nuclear layer; shoulder bone; and submandibular gland primordium. Human ortholog(s) of this gene implicated in hypomyelinating leukodystrophy 26. Orthologous to human SLC35B2 (solute carrier family 35 member B2).
  • synonyms:
  • solute carrier family 35, member B1,
  • AA407792,
  • solute carrier family 35, member B2,
  • MGI:2146743,
  • AI842275,
  • Slc35b1,
  • PAPST1,
  • expressed sequence AI842275,
  • expressed sequence AA407792,
  • RIKEN cDNA 1110003M08 gene,
  • Slc35b2,
  • 1110003M08Rik,
  • MGI:2146929

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

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

11 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

 

Other

0 Driver For