UniProt | Protein Name |
---|---|
Q96N66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
regulation of triglyceride metabolic process | ||
phosphatidylinositol acyl-chain remodeling |
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 |
---|---|---|---|
111824266 | MYOLU17900 | ||
117034505 | RHIFE00735 | ||
104676014 | RHIRO33124 | ||
100605511 | NOMLE02336 | ||
114581856 | PODMU02240 | ||
107552840 | SINGR57979 | ||
107587783 | SINGR15182 | ||
106840873 | EQUAS24217 | ||
105309472 | PTEVA06253 | ||
115045038 | ECHNA27702 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024