Gene Gene information from NCBI Gene database.
Entrez ID 28968
Gene name Solute carrier family 6 member 16
Gene symbol SLC6A16
Synonyms (NCBI Gene)
NT5NTT5
Chromosome 19
Chromosome location 19q13.33
Summary SLC6A16 shows structural characteristics of an Na(+)- and Cl(-)-dependent neurotransmitter transporter, including 12 transmembrane (TM) domains, intracellular N and C termini, and large extracellular loops containing multiple N-glycosylation sites.[suppli
miRNA miRNA information provided by mirtarbase database.
26
miRTarBase ID miRNA Experiments Reference
MIRT018187 hsa-miR-335-5p Microarray 18185580
MIRT025508 hsa-miR-34a-5p Proteomics 21566225
MIRT029566 hsa-miR-26b-5p Microarray 19088304
MIRT1366118 hsa-miR-421 CLIP-seq
MIRT1366119 hsa-miR-4270 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005326 Function Neurotransmitter transmembrane transporter activity NAS 11112352
GO:0005886 Component Plasma membrane IBA
GO:0006836 Process Neurotransmitter transport IEA
GO:0006836 Process Neurotransmitter transport NAS 11112352
GO:0006865 Process Amino acid transport IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607972 13622 ENSG00000063127
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9GZN6
Protein name Orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 (Solute carrier family 6 member 16)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00209 SNF 103 685 Sodium:neurotransmitter symporter family Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in peripheral tissues, particularly in testis, pancreas, and prostate.
Sequence
Sequence length 736
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Cervical cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MULTIPLE SCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SYSTEMIC LUPUS ERYTHEMATOSUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations