patatin like domain 8, phospholipase A2
| UniProt | Protein Name |
|---|---|
| Q9NP80 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| prostaglandin biosynthetic process |
|
|
| lipid metabolic process |
|
|
| fatty acid metabolic process |
|
|
| arachidonate metabolic process |
|
|
| arachidonate metabolic process |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| peroxisome |
|
|
| peroxisome |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycerophospholipase activity |
|
|
| phosphatidylcholine lysophospholipase A1 activity |
|
|
| phosphatidylcholine lysophospholipase A1 activity |
|
|
| A2-type glycerophospholipase activity |
|
|
| A2-type glycerophospholipase activity |
|
| Gene Ontology |
|---|
| arachidonic acid metabolic process |
| calcium-independent phospholipase A2 activity |
| hydrolase activity |
| lipid metabolic process |
| phospholipase activity |
| InterPro |
|---|
| Acyl transferase/acyl hydrolase/lysophospholipase |
| Patatin-like phospholipase domain containing protein 8-like |
| Patatin-like phospholipase domain |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001257 | Spasticity |
| HP:0001260 | Dysarthria |
| HP:0001310 | Dysmetria |
| HP:0001332 | Dystonia |
| HP:0002151 | Increased circulating lactate concentration |
| HP:0002384 | Focal impaired awareness seizure |
| HP:0003128 | Lactic acidosis |
| Disease ID | Disease Name |
|---|---|
| OMIM:251950 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026