Gene

slc6a17

ID
ZDB-GENE-030131-8187
Name
solute carrier family 6 member 17
Symbol
slc6a17 Nomenclature History
Previous Names
  • fj59a05
  • si:dkey-71l10.2
  • wu:fj59a05
Type
protein_coding_gene
Location
Chr: 8 Mapping Details/Browsers
Description
Predicted to have symporter activity. Predicted to be involved in neutral amino acid transport and sodium ion transmembrane transport. Predicted to localize to intrinsic component of membrane and synaptic vesicle. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human SLC6A17 (solute carrier family 6 member 17).
Genome Resources
Note
None
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc6a17 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Mental retardation, autosomal recessive 48 616269
Associated With slc6a17 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR000175 Sodium:neurotransmitter symporter
Family IPR002438 Neutral amino acid SLC6 transporter
Homologous_superfamily IPR037272 Sodium:neurotransmitter symporter superfamily
Domain Details Per Protein
Protein Length Neutral amino acid SLC6 transporter Sodium:neurotransmitter symporter Sodium:neurotransmitter symporter superfamily
UniProtKB:X1WEE1 730
UniProtKB:A5WUQ3 732
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Gene Tree
Ensembl
Citations