Atp13a2 - ATPase cation transporting 13A2 Gene
Also Known as RGD1307977
Species: Rattus norvegicus
Summary
Predicted to enable ABC-type polyamine transporter activity; phosphatidic acid binding activity; and phosphatidylinositol-3,5-bisphosphate binding activity. Involved in regulation of autophagosome size and regulation of mitochondrion organization. Predicted to be located in several cellular components, including cytoplasmic vesicle; neuronal cell body; and vacuole. Predicted to be integral component of lysosomal membrane. Human ortholog(s) of this gene implicated in Kufor-Rakeb syndrome; Parkinson's disease; and hereditary spastic paraplegia. Orthologous to human ATP13A2 (ATPase cation transporting 13A2). [provided by Alliance of Genome Resources, Apr 2022]
Atp13a2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001173432.1 | NP_001166903.1 | polyamine-transporting ATPase 13A2 |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in regulation of autophagosome size |
IMP
IMP: Inferred from mutant phenotype
|
22186024 | RGD |
| involved in regulation of mitochondrion organization |
IMP
IMP: Inferred from mutant phenotype
|
22186024 | RGD |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
polyamine-transporting ATPase 13A2 |
|
|