Gene
gatm
- ID
- ZDB-GENE-021015-1
- Name
- glycine amidinotransferase (L-arginine:glycine amidinotransferase)
- Symbol
- gatm Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to have glycine amidinotransferase activity. Predicted to be involved in creatine biosynthetic process. Predicted to localize to mitochondrion. Is expressed in several structures, including digestive system; mesoderm; musculature system; ovary; and yolk syncytial layer. Human ortholog(s) of this gene implicated in AGAT deficiency and Fanconi syndrome. Orthologous to human GATM (glycine amidinotransferase).
- Genome Resources
- Note
-
Added for the Thisse expression data.
- Comparative Information
-
- All Expression Data
- 11 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb409 (14 images)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
AGAT deficiency | Alliance | Cerebral creatine deficiency syndrome 3 | 612718 |
Fanconi renotubular syndrome 1 | Alliance | Fanconi renotubular syndrome 1 | 134600 |
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Family | IPR033195 | Glycine/inosamine-phosphate amidinotransferase |
Domain Details Per Protein
Protein | Length | Glycine/inosamine-phosphate amidinotransferase |
---|---|---|
UniProtKB:F8W4N8
|
272 | |
UniProtKB:F8W3L4
|
258 | |
UniProtKB:Q6PH19
|
422 | |
UniProtKB:F1QX52
|
422 | |
UniProtKB:F8W4S0
|
113 |
Interactions and Pathways
No data available
Plasmids
No data available