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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
aminomethyltransferase
Summary
- Gene Symbol
-
- AMT
- Aliases
-
- GCST
- NKH
- glycine cleavage system protein T
- nonketotic hyperglycinemia
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Aminotransferase
- Disease variant
- Mitochondrion
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| P48728 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycine decarboxylation via glycine cleavage system | ||
| glycine catabolic process |
|
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
catabolic process [inference]
cellular metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial matrix |
|
|
| mitochondrion | ||
| nucleoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| transaminase activity | ||
| aminomethyltransferase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050569 | Seckel syndrome | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050709 | early infantile epileptic encephalopathy | |
| DOID:0050841 | focal hand dystonia | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060058 | lymphoma | |
| DOID:0060192 | Crohn's colitis | |
| DOID:0060254 | Robinow syndrome | |
| DOID:0060357 | chylomicron retention disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001250 | Seizure |
| HP:0002878 | Respiratory failure |
| HP:0003623 | Neonatal onset |
| HP:0008288 | Nonketotic hyperglycinemia |
| HP:0010851 | EEG with burst suppression |
| HP:0010864 | Intellectual disability, severe |
| HP:0011342 | Mild global developmental delay |
| HP:0011463 | Childhood onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:620398 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 178960 | WB:WBGene00017765 | ||
| 34474 | FB:FBgn0032287 | ||
| 103176711 | CALMI11336 | ||
| 102365617 | LATCH19640 | ||
| 450000 | ZFIN:ZDB-GENE-041010-114 | DANRE43009 | |
| 103022813 | ASTMX17747 | ||
| 108265911 | ICTPU30125 | ||
| 113575842 | ELEEL16222 | ||
| 115168309 | SALTR75706 | ||
| 115545316 | GADMO27409 |
