AVIL - Gene browser | 3billion

AVIL

AVIL

advillin

HCNC Approved Symbol: AVIL (HGNC:14188)
Genomic Coordinates: 12:57,797,380 - 57,818,734 (12q14.1)
Synonyms: p92, FLJ12386, ADVIL, DOC6
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the AVIL gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Nephrotic syndrome: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Nephrotic syndrome, steroid-resistant: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Steroid-resistant nephrotic syndrome: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

AVIL - Gene browser | 3billion