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SLC6A17

solute carrier family 6 member 17

HCNC Approved Symbol
SLC6A17 (HGNC:31399)
Genomic Coordinates
1:110,150,494 - 110,202,202 (1p13.3)
Synonyms
NTT4
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC6A17 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
SLC6A17 - Gene browser | 3billion