Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
3.1.3.62
Hydrolases;
Acting on ester bonds;
Phosphoric-monoester hydrolases;
multiple inositol-polyphosphate phosphatase
3.1.3.80
Hydrolases;
Acting on ester bonds;
Phosphoric-monoester hydrolases;
2,3-bisphosphoglycerate 3-phosphatase
PDB | Resolution (Å) | PDB name |
---|
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0030282 | bone mineralization |
Biological Process | GO:0043647 | inositol phosphate metabolic process |
Biological Process | GO:0001503 | ossification |
Biological Process | GO:0006797 | polyphosphate metabolic process |
Molecular Function | GO:0003993 | acid phosphatase activity |
Molecular Function | GO:0034417 | bisphosphoglycerate 3-phosphatase activity |
Molecular Function | GO:0052826 | inositol hexakisphosphate 2-phosphatase activity |
Molecular Function | GO:0052745 | inositol phosphate phosphatase activity |
Molecular Function | GO:0030351 | inositol-1,3,4,5,6-pentakisphosphate 3-phosphatase activity |
Molecular Function | GO:0051717 | inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity |
Molecular Function | GO:0101006 | protein histidine phosphatase activity |
Cellular Component | GO:0005783 | endoplasmic reticulum |
Cellular Component | GO:0005788 | endoplasmic reticulum lumen |
Cellular Component | GO:0070062 | extracellular exosome |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-1855231 | Synthesis of IPs in the ER lumen | Leaf | R-HSA-1430728 | Metabolism |
Location | ECO term | Pubmed |
---|---|---|
Endoplasmic reticulum lumen | ECO:0000250 |
HPO ID | HPO name |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000028 | Cryptorchidism |
HP:0000054 | Micropenis |
HP:0000062 | Ambiguous genitalia |
HP:0000133 | Gonadal dysgenesis |
HP:0000151 | Aplasia of the uterus |
HP:0000215 | Thick upper lip vermilion |
HP:0000218 | High palate |
HP:0000252 | Microcephaly |
HP:0000286 | Epicanthus |
HP:0000347 | Micrognathia |
HP:0000369 | Low-set ears |
HP:0000400 | Macrotia |
HP:0000431 | Wide nasal bridge |
HP:0000448 | Prominent nose |
HP:0000508 | Ptosis |
HP:0000518 | Cataract |
HP:0000582 | Upslanted palpebral fissure |
HP:0000639 | Nystagmus |
HP:0000648 | Optic atrophy |
HP:0000853 | Goiter |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001263 | Global developmental delay |
HP:0001276 | Hypertonia |
HP:0001321 | Cerebellar hypoplasia |
HP:0001336 | Myoclonus |
HP:0001344 | Absent speech |
HP:0001347 | Hyperreflexia |
HP:0001428 | Somatic mutation |
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 |
HP:0002120 | Cerebral cortical atrophy |
HP:0002176 | Spinal cord compression |
HP:0002194 | Delayed gross motor development |
HP:0002365 | Hypoplasia of the brainstem |
HP:0002380 | Fasciculations |
HP:0002500 | Abnormal cerebral white matter morphology |
HP:0002509 | Limb hypertonia |
HP:0002510 | Spastic tetraplegia |
HP:0002650 | Scoliosis |
HP:0002653 | Bone pain |
HP:0002730 | Chronic noninfectious lymphadenopathy |
HP:0002733 | Abnormal lymph node morphology |
HP:0002757 | Recurrent fractures |
HP:0002895 | Papillary thyroid carcinoma |
HP:0003003 | Colon cancer |
HP:0003202 | Skeletal muscle atrophy |
HP:0003623 | Neonatal onset |
HP:0004305 | Involuntary movements |
HP:0005280 | Depressed nasal bridge |
HP:0005994 | Nodular goiter |
HP:0006528 | Chronic lung disease |
HP:0006731 | Follicular thyroid carcinoma |
HP:0006766 | Papillary renal cell carcinoma |
HP:0006955 | Olivopontocerebellar hypoplasia |
HP:0008665 | Clitoral hypertrophy |
HP:0008936 | Axial hypotonia |
HP:0010862 | Delayed fine motor development |
HP:0012110 | Hypoplasia of the pons |
HP:0012288 | Neoplasm of head and neck |
HP:0012531 | Pain |
HP:0012856 | Abnormal scrotal rugation |
HP:0030197 | Fatigable weakness of skeletal muscles |
HP:0030260 | Microphallus |
HP:0030261 | Absent penis |
HP:0030674 | Antenatal onset |
HP:0033725 | Thin corpus callosum |
HP:0040198 | Non-medullary thyroid carcinoma |
HP:3000037 | Abnormal neck blood vessel morphology |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
thyroid cancer, nonmedullary, 2 | MONDO:0008566 | C73 | chapter2, Neoplasms | OMIM:188470 |