SLC6A5 - Gene browser | 3billion

SLC6A5

SLC6A5

solute carrier family 6 member 5

HCNC Approved Symbol: SLC6A5 (HGNC:11051)
Genomic Coordinates: 11:20,599,608 - 20,659,285 (11p15.1)
Synonyms: GLYT2, GlyT-2, NET1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SLC6A5 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Epilepsy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hyperekplexia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Poor sucking: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

SLC6A5 - Gene browser | 3billion