LRTOMT - Gene browser

LRTOMT

leucine rich transmembrane and O-methyltransferase domain containing

HCNC Approved Symbol: LRTOMT (HGNC:25033)
Genomic Coordinates: 11:72,080,850 - 72,110,782 (11q13.4)
Synonyms: COMT2, CFAP111, LRTOMT1, LRTOMT2, LRRC51, DFNB63
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

9Patients

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

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

09
Patient count

Hearing loss: 7 (77.8%)
Patient Count: 7 (77.8%)
% of total patients presenting each phenotype is shown in parentheses.
7 (77.8%)
Congenital hearing loss: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Blue sclera: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)
Digital webbing: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)
High-arched palate: 1 (11.1%)
Patient Count: 1 (11.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (11.1%)