OTOG - Gene browser

OTOG

otogelin

HCNC Approved Symbol: OTOG (HGNC:8516)
Genomic Coordinates: 11:17,547,259 - 17,646,044 (11p15.1)
Synonyms: mlemp, OTGN, FLJ46346
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

22Patients

In total, 22 patients were diagnosed with a variant in the OTOG gene.

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

022
Patient count

Hearing loss: 13 (59.1%)
Patient Count: 13 (59.1%)
% of total patients presenting each phenotype is shown in parentheses.
13 (59.1%)
Intellectual disability: 4 (18.2%)
Patient Count: 4 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
4 (18.2%)
Abnormal facial shape: 2 (9.1%)
Patient Count: 2 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.1%)
Agenesis of corpus callosum: 2 (9.1%)
Patient Count: 2 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.1%)
Agenesis of the corpus callosum: 2 (9.1%)
Patient Count: 2 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.1%)