OTOGL - Gene browser | 3billion

OTOGL

OTOGL

otogelin like

HCNC Approved Symbol: OTOGL (HGNC:26901)
Genomic Coordinates: 12:80,099,537 - 80,380,880 (12q21.31)
Synonyms: FLJ90579, C12orf64
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

10Patients

In total, 10 patients were diagnosed with a variant in the OTOGL gene.

Frequently observed phenotypes(Top 5 only)

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

010
Patient count

Hearing loss: 5 (50.0%)
Patient Count: 5 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (50.0%)
Hearing impairment: 4 (40.0%)
Patient Count: 4 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (40.0%)
Precocious puberty in females: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)

Last updated: 2024-06-30

OTOGL - Gene browser | 3billion