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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 |
|---|---|---|
| Golgi lumen acidification |
|
|
| synaptic vesicle lumen acidification | ||
| central nervous system maturation | ||
| head morphogenesis | ||
| angiotensin maturation |
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 |
|---|---|---|
| extracellular exosome | ||
| Golgi membrane |
|
|
| endosome membrane | ||
| lysosome | ||
| tertiary granule membrane |
|
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:0000047 | Hypospadias |
| HP:0000298 | Mask-like facies |
| HP:0000338 | Hypomimic face |
| HP:0000341 | Narrow forehead |
| HP:0000347 | Micrognathia |
| HP:0000369 | Low-set ears |
| HP:0000750 | Delayed speech and language development |
| HP:0000952 | Jaundice |
| HP:0000973 | Cutis laxa |
| HP:0001249 | Intellectual disability |
| 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 |
|---|---|---|---|
| 118898556 | BALMU23340 | ||
| 100665148 | LOXAF06611 | ||
| 100514935 | PIGXX37169 | ||
| 513520 | BOVIN37224 | ||
| 102173826 | CAPHI30823 | ||
| 100344856 | RABIT13421 | ||
| 100768578 | CRIGR00616 | ||
| 70495 | MGI:1917745 | MOUSE66510 | |
| 302526 | RGD:1561269 | RATNO44552 | |
| 100732838 | CAVPO14397 |
