3billion
back to listBack to List

MTR

5-methyltetrahydrofolate-homocysteine methyltransferase

HCNC Approved Symbol
MTR (HGNC:7468)
Genomic Coordinates
1:236,795,281 - 236,903,981 (1q43)
Synonyms
cblG
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Neural tube defects, folate-sensitive, susceptibility to}
601634AR
Homocystinuria-megaloblastic anemia, cblG complementation type
250940AR

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results