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ATPase H+ transporting accessory protein 2
Summary
- Gene Symbol
-
- ATP6AP2
- Aliases
-
- APT6M8-9
- ATP6M8-9
- M8-9
- PRR
- RENR
- V-ATPase M8.9 subunit
- prorenin receptor
- renin receptor
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Cleavage on pair of basic residues
- Congenital disorder of glycosylation
- Cytoplasmic vesicle
- Disease variant
- Endoplasmic reticulum
- Endosome
- Epilepsy
- Intellectual disability
- Lysosome
- Neurodegeneration
- Parkinsonism
- Phosphoprotein
- Postsynaptic cell membrane
- Receptor
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| O75787 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular pH reduction |
|
|
| regulation of MAPK cascade | ||
| eye pigmentation | ||
| lysosomal lumen acidification | ||
| positive regulation of transforming growth factor beta1 production |
GO Hierarchy
biological process
metabolic process [inference]
homeostatic process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of macromolecule metabolic process [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| autophagosome membrane | ||
| clathrin-coated vesicle membrane | ||
| vacuolar proton-transporting V-type ATPase, V0 domain | ||
| external side of plasma membrane | ||
| axon |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| signaling receptor activity | ||
| protein binding |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050678 | Blau syndrome | |
| DOID:0050848 | obstructive sleep apnea | |
| DOID:0060135 | apraxia | |
| DOID:0060224 | atrial fibrillation | |
| DOID:0060249 | scoliosis | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060309 | syndromic X-linked intellectual disability | |
| DOID:0060318 | acute promyelocytic leukemia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001250 | Seizure |
| HP:0001257 | Spasticity |
| HP:0001263 | Global developmental delay |
| HP:0001265 | Hyporeflexia |
| HP:0001270 | Motor delay |
| HP:0001272 | Cerebellar atrophy |
| HP:0001288 | Gait disturbance |
| HP:0001300 | Parkinsonism |
| HP:0001310 | Dysmetria |
| HP:0001347 | Hyperreflexia |
| Disease ID | Disease Name |
|---|---|
| ORPHA:363654 |
|
| OMIM:300911 |
|
| OMIM:301045 |
|
| OMIM:300423 |
|
| ORPHA:93952 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115161222 | SALTR15149 | ||
| 101164352 | ORYLA09522 | ||
| 100696552 | ORENI21475 | ||
| 115588545 | SPAAU27754 | ||
| 380574 | Xenbase:XB-GENE-6078197 | ||
| 734500 | Xenbase:XB-GENE-17342836 | ||
| 496778 | Xenbase:XB-GENE-964301 | ||
| 101950998 | CHRPI15060 | ||
| 109305918 | CROPO02562 | ||
| 113444744 | PSETE17543 |
