INF2 - Gene browser

INF2

inverted formin 2

HCNC Approved Symbol: INF2 (HGNC:23791)
Genomic Coordinates: 14:104,689,618 - 104,722,535 (14q32.33)
Synonyms: MGC13251, C14orf151, C14orf173
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

16Patients

In total, 16 patients were diagnosed with a variant in the INF2 gene.

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

016
Patient count

Focal segmental glomerulosclerosis: 6 (37.5%)
Patient Count: 6 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
6 (37.5%)
Proteinuria: 3 (18.8%)
Patient Count: 3 (18.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (18.8%)
Chronic kidney disease: 3 (18.8%)
Patient Count: 3 (18.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (18.8%)
Glomerulonephritis: 2 (12.5%)
Patient Count: 2 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (12.5%)
Stage 5 chronic kidney disease: 2 (12.5%)
Patient Count: 2 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (12.5%)