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COMT

catechol-O-methyltransferase

HCNC Approved Symbol
COMT (HGNC:2228)
Genomic Coordinates
22:19,941,772 - 19,969,975 (22q11.21)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Panic disorder, susceptibility to}
167870?Autosomal dominant
{Schizophrenia, susceptibility to}
181500AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the COMT gene.

Frequently observed phenotypes

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

No Results