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Protein Coding Gene : Slc22a19 solute carrier family 22 (organic anion transporter), member 19

Primary Identifier  MGI:2442751 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  207151
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables organic anion transmembrane transporter activity and toxin transmembrane transporter activity. Acts upstream of or within organic anion transport. Predicted to be located in basolateral plasma membrane. Is expressed in metanephros. Human ortholog(s) of this gene implicated in Lynch syndrome and mismatch repair cancer syndrome. Orthologous to several human genes including SLC22A25 (solute carrier family 22 member 25).
  • synonyms:
  • MGC:29260,
  • Oat5,
  • solute carrier family 22 (organic anion transporter), member 9,
  • solute carrier family 22 (organic anion transporter), member 19,
  • D630043A20Rik,
  • RIKEN cDNA D630043A20 gene,
  • Slc22a19,
  • Slc22a9

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Exons

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0 Involved In Mutations

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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

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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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