SLC5A5 - Gene browser | 3billion

SLC5A5

SLC5A5

solute carrier family 5 member 5

HCNC Approved Symbol: SLC5A5 (HGNC:11040)
Genomic Coordinates: 19:17,871,945 - 17,895,174 (19p13.11)
Synonyms: NIS
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 SLC5A5 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

Congenital hypothyroidism: 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

SLC5A5 - Gene browser | 3billion