AMT

Aminomethyltransferase
Diseases associated with this gene: GCE
LOVD Gene: AMT
NCBI Gene: AMT
Gene Home Reference: AMT
Ensembl gene: ENSG00000145020
Ensembl location: ENSG00000145020

OMIM gene: 238310
Download all AMT variants in ATOM XML format.
Download all AMT variants in tab-separated format.

 Finnish Variants

Filtered from source LSDB
There are no Finnish mutations for this gene. See the GLDC gene for Finnish mutations causing GCE (NKH).

 All Variants

Source LSDB
  AMT - All Variants






FinDis has received funding from the Academy of Finland, Center of Excellence in Disease Genetics
and the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement number 200754 - the GEN2PHEN project.