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SLC6A15

Synonyms
NTT73, SBAT1, V7-3, hv7-3
External resources
Summary
This gene encodes a member of the solute carrier family 6 protein family which transports neutral amino acids. The encoded protein is thought to play a role in neuronal amino acid transport (PMID: 16185194) and may be associated with major depression (PMID: 21521612). Multiple transcript variants encoding different isoforms have been found for this gene.

Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
2,139
Likely benign
542
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on SLC6A15 gene.

Phenotype class
Patients in 3billion (%)

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