UniProt | Protein Name |
---|---|
Q96N66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
layer formation in cerebral cortex | ||
lipid modification | ||
phosphatidylcholine acyl-chain remodeling | ||
ventricular system development | ||
phosphatidylinositol biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
mitochondria-associated endoplasmic reticulum membrane | ||
endoplasmic reticulum membrane |
|
|
membrane |
GO Term | Evidence Code | PMID |
---|---|---|
1-acylglycerol-3-phosphate O-acyltransferase activity |
|
|
O-acyltransferase activity | ||
protein binding | ||
2-acylglycerol-3-phosphate O-acyltransferase activity |
|
|
lysophospholipid acyltransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:4964 | neurotic disorder | |
DOID:5082 | liver cirrhosis | |
DOID:543 | dystonia | |
DOID:5517 | stomach carcinoma | |
DOID:684 | hepatocellular carcinoma | |
DOID:784 | chronic kidney disease | |
DOID:8927 | learning disability | |
DOID:9351 | diabetes mellitus | |
DOID:9352 | type 2 diabetes mellitus | |
DOID:9452 | steatotic liver disease |
HPO ID | HPO Term |
---|---|
HP:0002123 | Generalized myoclonic seizure |
HP:0002126 | Polymicrogyria |
HP:0002197 | Generalized-onset seizure |
HP:0002373 | Febrile seizure (within the age range of 3 months to 6 years) |
HP:0002540 | Inability to walk |
HP:0003593 | Infantile onset |
HP:0007359 | Focal-onset seizure |
HP:0008936 | Axial hypotonia |
Disease ID | Disease Name |
---|---|
OMIM:617188 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
106577207 | SALSA107762 | ||
115176351 | SALTR83687 | ||
115553956 | GADMO03503 | ||
101161994 | ORYLA05799 | ||
100696020 | ORENI06139 | ||
115567825 | SPAAU60034 | ||
495497 | Xenbase:XB-GENE-978831 | ||
100380044 | Xenbase:XB-GENE-978827 | ||
101944171 | CHRPI26597 | ||
100088576 | ORNAN01567 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024