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Protein Coding Gene : Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14

Primary Identifier  MGI:1890216 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  56774
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables (R)-carnitine transmembrane transporter activity. Involved in (R)-carnitine transmembrane transport. Located in apical plasma membrane. Is expressed in large intestine and lung. Human ortholog(s) of this gene implicated in obesity. Orthologous to human SLC6A14 (solute carrier family 6 member 14).
PHENOTYPE: Mice hemizygous or homozygous for a null allele are viable, fertile and overtly normal. Homozygous females show normal plasma amino acid levels and mammary gland development but exhibit delayed development and reduced growth of mammary tumors in spontaneous mouse models of breast cancer. [provided by MGI curators]
  • synonyms:
  • Slc6a14,
  • RIKEN cDNA 1110007A17 gene,
  • solute carrier family 6 (neurotransmitter transporter), member 14,
  • MGI:1921782,
  • 1110007A17Rik,
  • 9030613J17Rik,
  • MGI:1921088,
  • ATB0plus,
  • CATB0plus,
  • RIKEN cDNA 9030613J17 gene

Features --> Cross References

Genome

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

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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

 

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