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:14221 | abdominal obesity-metabolic syndrome 1 | |
DOID:1443 | cerebral degeneration | |
DOID:14524 | senile degeneration of brain | |
DOID:1470 | major depressive disorder | |
DOID:1573 | communicating hydrocephalus | |
DOID:1595 | melancholic depression | |
DOID:1596 | depressive disorder | |
DOID:1826 | epilepsy | |
DOID:1837 | diabetic ketoacidosis | |
DOID:1883 | hepatitis C |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000252 | Microcephaly |
HP:0000729 | Autistic behavior |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001263 | Global developmental delay |
HP:0001276 | Hypertonia |
HP:0001290 | Generalized hypotonia |
HP:0001344 | Absent speech |
HP:0001347 | Hyperreflexia |
Disease ID | Disease Name |
---|---|
OMIM:617188 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100735624 | CAVPO19408 | ||
101723338 | HETGA20675 | ||
100028484 | MONDO24617 | ||
113875929 | BOBOX11535 | ||
101061154 | TAKRU46161 | ||
102013132 | CHILA25100 | ||
105732521 | AOTNA40570 | ||
110219768 | PHACI32952 | ||
101028281 | SAIBB39184 | ||
101967081 | ICTTR14554 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024