Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
inorganic pyrophosphatase 2
Summary
- Gene Symbol
-
- PPA2
- Aliases
-
- FLJ20459
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Hydrolase
- Magnesium
- Metal-binding
- Mitochondrion
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9H2U2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphate-containing compound metabolic process | ||
| regulation of mitochondrial membrane potential | ||
| diphosphate metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial matrix | ||
| synapse |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| magnesium ion binding | ||
| inorganic diphosphate phosphatase activity | ||
| inorganic diphosphate phosphatase activity | ||
| protein serine/threonine phosphatase activity | ||
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Inorganic pyrophosphatase
- Functional Category
-
- C: Energy production and conversion
- E: Amino acid transport and metabolism
- P: Inorganic ion transport and metabolism
| Gene Ontology |
|---|
| hydrolase activity |
| inorganic diphosphate phosphatase activity |
| magnesium ion binding |
| metal ion binding |
| phosphate-containing compound metabolic process |
| InterPro |
|---|
| Inorganic pyrophosphatase superfamily |
| Inorganic pyrophosphatase |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001635 | Congestive heart failure |
| HP:0001639 | Hypertrophic cardiomyopathy |
| HP:0001645 | Sudden cardiac death |
| HP:0001662 | Bradycardia |
| HP:0001685 | Myocardial fibrosis |
| HP:0001942 | Metabolic acidosis |
| HP:0003593 | Infantile onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:617222 |
|
| OMIM:617223 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
