DUOX2 - Gene browser

DUOX2

dual oxidase 2

HCNC Approved Symbol: DUOX2 (HGNC:13273)
Genomic Coordinates: 15:45,092,650 - 45,114,172 (15q21.1)
Synonyms: P138-TOX, P138(TOX), THOX2, LNOX2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

35Patients

In total, 35 patients were diagnosed with a variant in the DUOX2 gene.

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

035
Patient count

Congenital hypothyroidism: 18 (51.4%)
Patient Count: 18 (51.4%)
% of total patients presenting each phenotype is shown in parentheses.
18 (51.4%)
Hypothyroidism, congenital: 12 (34.3%)
Patient Count: 12 (34.3%)
% of total patients presenting each phenotype is shown in parentheses.
12 (34.3%)
Developmental delay: 3 (8.6%)
Patient Count: 3 (8.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (8.6%)
Congenital goiter: 3 (8.6%)
Patient Count: 3 (8.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (8.6%)
Thyroid defect in oxidation and organification of iodide: 3 (8.6%)
Patient Count: 3 (8.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (8.6%)