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Details of AMT gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| AMT | GCST | P48728 | GCST_HUMAN | 275
| ENSG00000145020
| Aminomethyltransferase, mitochondrial | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Non-ketotic hyperglycinemia (NKH) [MIM:605899]: Autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms. Note=The disease is caused by mutations affecting the gene represented in this entry. |
605899 |
