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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
multiple inositol-polyphosphate phosphatase 1
Summary
- Gene Symbol
-
- MINPP1
- Aliases
-
- MIPP
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cell membrane
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Hydrolase
- Reference proteome
- Secreted
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9UNW1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular monoatomic cation homeostasis | ||
| bone mineralization | ||
| ossification | ||
| inositol phosphate metabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen | ||
| plasma membrane | ||
| extracellular space | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| 3-phytase activity | ||
| inositol pentakisphosphate phosphatase activity | ||
| inositol-1,4,5,6-tetrakisphosphate 6-phosphatase activity | ||
| 4-phytase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Phosphatase
- Functional Category
-
- E: Amino acid transport and metabolism
- I: Lipid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
| Gene Ontology |
|---|
| acid phosphatase activity |
| hydrolase activity |
| InterPro |
|---|
| Histidine acid phosphatase, eukaryotic |
| Histidine phosphatase superfamily, clade-2 |
| Histidine phosphatase superfamily |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112333 | pontocerebellar hypoplasia type 16 | |
| DOID:3969 | thyroid gland papillary carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001336 | Myoclonus |
| HP:0001344 | Absent speech |
| HP:0001347 | Hyperreflexia |
| HP:0001442 | Typified by somatic mosaicism |
| HP:0002015 | Dysphagia |
| HP:0002060 | Abnormal cerebral morphology |
| HP:0002071 | Abnormality of extrapyramidal motor function |
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002104 | Apnea |
| HP:0002119 | Ventriculomegaly |
| Disease ID | Disease Name |
|---|---|
| OMIM:188470 |
|
| ORPHA:319487 |
|
| OMIM:619527 |
|
| ORPHA:284339 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000594
- Gene Name
- multiple inositol-polyphosphate phosphatase 1
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 17330 | MGI:1336159 | MOUSE25357 | ||
| 29688 | RGD:3089 | RATNO20394 | ||
| 31544 | FB:FBgn0026060 | |||
| 39841 | FB:FBgn0026061 | |||
| 394075 | ZFIN:ZDB-GENE-040426-888 | DANRE03931 | ||
| 450579 | 9598_0:002b97 | PANTR01077 | ||
| 499084 | RGD:1564801 | |||
| 541067 | BOVIN21119 | |||
| 561891 | ZFIN:ZDB-GENE-060929-1194 | DANRE13086 | ||
| 704362 | MACMU46164 |
