NOS1AP - Gene browser | 3billion

NOS1AP

NOS1AP

nitric oxide synthase 1 adaptor protein

HCNC Approved Symbol: NOS1AP (HGNC:16859)
Genomic Coordinates: 1:162,069,691 - 162,370,475 (1q23.3)
Synonyms: KIAA0464, CAPON
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 NOS1AP 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 nephrotic syndrome: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
End stage renal disease: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Stage 5 chronic kidney disease: 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

NOS1AP - Gene browser | 3billion