Gene Gene information from NCBI Gene database.
Entrez ID 388662
Gene name Solute carrier family 6 member 17
Gene symbol SLC6A17
Synonyms (NCBI Gene)
MRT48NTT4
Chromosome 1
Chromosome location 1p13.3
Summary The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs375380880 C>G,T Pathogenic Coding sequence variant, missense variant
rs775085213 G>A Pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
199
miRTarBase ID miRNA Experiments Reference
MIRT572975 hsa-miR-1273d HITS-CLIP 23824327
MIRT572973 hsa-miR-6793-3p HITS-CLIP 23824327
MIRT572972 hsa-miR-4286 HITS-CLIP 23824327
MIRT653462 hsa-miR-4433a-5p HITS-CLIP 23824327
MIRT653461 hsa-miR-128-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IEA
GO:0006811 Process Monoatomic ion transport IEA
GO:0006814 Process Sodium ion transport IEA
GO:0006836 Process Neurotransmitter transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610299 31399 ENSG00000197106
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H1V8
Protein name Sodium-dependent neutral amino acid transporter SLC6A17 (Sodium-dependent neurotransmitter transporter NTT4) (Solute carrier family 6 member 17)
Protein function Synaptic vesicle transporter with apparent selectivity for neutral amino acids. The transport is sodium-coupled but chloride-independent, likely driven by the proton electrochemical gradient generated by vacuolar H(+)-ATPase in an overall electr
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00209 SNF 60 643 Sodium:neurotransmitter symporter family Family
Sequence
Sequence length 727
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Pathogenic rs775085213, rs375380880 RCV000167526
RCV000167527
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Benign; Likely benign rs41313405 RCV005900770
Familial cancer of breast Benign; Likely benign rs41313405 RCV005900767
Long QT syndrome Likely benign rs796052160 RCV000190153
Lung cancer Benign; Likely benign rs41313405 RCV005900774
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 36553681