NPHS2 - Gene browser

NPHS2

NPHS2 stomatin family member, podocin

HCNC Approved Symbol: NPHS2 (HGNC:13394)
Genomic Coordinates: 1:179,550,539 - 179,575,948 (1q25.2)
Synonyms: SRN1, PDCN
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

12Patients

In total, 12 patients were diagnosed with a variant in the NPHS2 gene.

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

012
Patient count

Steroid-resistant nephrotic syndrome: 7 (58.3%)
Patient Count: 7 (58.3%)
% of total patients presenting each phenotype is shown in parentheses.
7 (58.3%)
Hypertension: 4 (33.3%)
Patient Count: 4 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
4 (33.3%)
Microscopic hematuria: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Chronic cough: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Clubbing of fingers: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)