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Protein Coding Gene : Slc6a15 solute carrier family 6 (neurotransmitter transporter), member 15

Primary Identifier  MGI:2143484 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  103098
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables branched-chain amino acid:sodium symporter activity; neutral L-amino acid:sodium symporter activity; and proline:sodium symporter activity. Involved in L-leucine transport and proline transport. Located in membrane. Is expressed in alimentary system; central nervous system; dorsal root ganglion; metanephros; and sensory organ. Orthologous to human SLC6A15 (solute carrier family 6 member 15).
PHENOTYPE: Mice homozygous for a null allele exhibit decreased synaptosome transport activities but exhibit no behavioral abnormalities. [provided by MGI curators]
  • synonyms:
  • MGI:2143583,
  • solute carrier family 6 (neurotransmitter transporter), member 15,
  • AI326451,
  • expressed sequence AI326450,
  • MGI:2143584,
  • v7-3,
  • AA536730,
  • expressed sequence AA536730,
  • AI326450,
  • Slc6a15,
  • expressed sequence AI326451

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 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

6 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