TRIOBP - Gene browser | 3billion

TRIOBP

TRIOBP

TRIO and F-actin binding protein

HCNC Approved Symbol: TRIOBP (HGNC:17009)
Genomic Coordinates: 22:37,697,048 - 37,776,556 (22q13.1)
Synonyms: HRIHFB2122, KIAA1662, Tara, TAP68, DFNB28
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

9Patients

In total, 9 patients were diagnosed with a variant in the TRIOBP gene.

Frequently observed phenotypes(Top 5 only)

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

09
Patient count

Hearing loss: 5 (55.6%)
Patient Count: 5 (55.6%)
% of total patients presenting each phenotype is shown in parentheses.
5 (55.6%)
Hearing impairment: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Congenital hearing loss: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)
Sensorineural hearing impairment: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)

Last updated: 2024-06-30

TRIOBP - Gene browser | 3billion