WT1 - Gene browser

WT1

WT1 transcription factor

HCNC Approved Symbol: WT1 (HGNC:12796)
Genomic Coordinates: 11:32,387,775 - 32,435,539 (11p13)
Synonyms: WAGR, WIT-2, AWT1, NPHS4, WT-1, GUD
Disease Associations: This gene is associated with the following 6 diseases in OMIM.

31Patients

In total, 31 patients were diagnosed with a variant in the WT1 gene.

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

031
Patient count

Proteinuria: 14 (45.2%)
Patient Count: 14 (45.2%)
% of total patients presenting each phenotype is shown in parentheses.
14 (45.2%)
Nephrotic syndrome: 7 (22.6%)
Patient Count: 7 (22.6%)
% of total patients presenting each phenotype is shown in parentheses.
7 (22.6%)
Focal segmental glomerulosclerosis: 3 (9.7%)
Patient Count: 3 (9.7%)
% of total patients presenting each phenotype is shown in parentheses.
3 (9.7%)
Genital ambiguity: 3 (9.7%)
Patient Count: 3 (9.7%)
% of total patients presenting each phenotype is shown in parentheses.
3 (9.7%)
Glomerulonephritis: 3 (9.7%)
Patient Count: 3 (9.7%)
% of total patients presenting each phenotype is shown in parentheses.
3 (9.7%)