|  Help  |  About  |  Contact Us

Protein Coding Gene : Slc22a3 solute carrier family 22 (organic cation transporter), member 3

Primary Identifier  MGI:1333817 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  20519
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables monoamine transmembrane transporter activity; neurotransmitter transmembrane transporter activity; and quaternary ammonium group transmembrane transporter activity. Involved in histamine transport and monoamine transport. Acts upstream of or within several processes, including histamine uptake; quaternary ammonium group transport; and regulation of appetite. Located in several cellular components, including apical plasma membrane; mitochondrial membrane; and neuronal cell body. Is expressed in several structures, including brain; dermis; extraembryonic component; genitourinary system; and thymus primordium. Orthologous to human SLC22A3 (solute carrier family 22 member 3).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to paraquat-induced dopamine neuron neurotoxicity. [provided by MGI curators]
  • synonyms:
  • Slc22a3,
  • Oct3,
  • solute carrier family 22 (organic cation transporter), member 3,
  • Orct3,
  • EMT

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

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

8 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