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Protein Coding Gene : Slc6a17 solute carrier family 6 (neurotransmitter transporter), member 17
Primary Identifier  MGI:2442535 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  229706
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable symporter activity. Involved in brain development. Predicted to be located in cell projection; cytoplasmic vesicle; and membrane. Predicted to be active in several cellular components, including GABA-ergic synapse; glutamatergic synapse; and synaptic vesicle membrane. Is expressed in several structures, including nervous system. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 48. Orthologous to human SLC6A17 (solute carrier family 6 member 17).
  • synonyms:
  • expressed sequence AW490886,
  • NTT4,
  • AW490886,
  • MGI:2139986,
  • Slc6a17,
  • RIKEN cDNA D130012J15 gene,
  • D130012J15Rik,
  • solute carrier family 6 (neurotransmitter transporter), member 17
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

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

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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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0 Driver For





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