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: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 |
---|---|---|---|
100408143 | CALJA24453 | ||
693742 | MACMU19723 | ||
101146063 | GORGO17075 | ||
100981053 | PANPA21365 | ||
107969800 | PANTR19266 | ||
100457310 | PONAB14621 | ||
100683790 | CANLF00666 | ||
112909412 | VULVU35427 | ||
123786964 | URSAM28682 | ||
100464529 | AILME03788 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024