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:1094 | attention deficit hyperactivity disorder | |
DOID:114 | heart disease | |
DOID:11832 | visual epilepsy | |
DOID:12139 | dysthymic disorder | |
DOID:12351 | alcoholic hepatitis | |
DOID:12849 | autistic disorder | |
DOID:12859 | choreatic disease | |
DOID:1287 | cardiovascular system disease | |
DOID:14018 | alcoholic liver cirrhosis | |
DOID:14159 | obstructive hydrocephalus |
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 |
---|---|---|---|
115397441 | SALFA31845 | ||
105809547 | PROCO24402 | ||
109074801 | CYPCA36607 | ||
109083276 | CYPCA58662 | ||
103276457 | CARSF10927 |
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Last updated: August 19, 2024