SLC6A9 - Gene browser | 3billion

SLC6A9

SLC6A9

solute carrier family 6 member 9

HCNC Approved Symbol: SLC6A9 (HGNC:11056)
Genomic Coordinates: 1:43,996,483 - 44,031,462 (1p34.1)
Synonyms: GLYT1, GlyT-1
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 SLC6A9 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

Axial hypotonia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Developmental delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Focal seizures: 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

SLC6A9 - Gene browser | 3billion