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Protein Coding Gene : Slc7a3 solute carrier family 7 (cationic amino acid transporter, y+ system), member 3

Primary Identifier  MGI:1100521 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  11989
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables L-arginine transmembrane transporter activity and L-lysine transmembrane transporter activity. Involved in L-lysine transmembrane transport. Acts upstream of or within L-arginine transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including 4-cell stage embryo; brain; gut; hindlimb phalanx; and urinary system. Orthologous to human SLC7A3 (solute carrier family 7 member 3).
PHENOTYPE: Mice homozygous for a null allele exhibit normal and malignant hematopoiesis. [provided by MGI curators]
  • synonyms:
  • amino acid transporter, cationic 3,
  • Atrc3,
  • Cat3,
  • solute carrier family 7 (cationic amino acid transporter, y+ system), member 3,
  • SLC7A2,
  • SLC7A1,
  • Slc7a3

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

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

 

Other

0 Driver For