Protein family
Protein sequence
Protein function
GO ontology
| GO term | GO description |
---|---|---|
Biological Process | GO:0036155 | acylglycerol acyl-chain remodeling |
Biological Process | GO:0006651 | diacylglycerol biosynthetic process |
Biological Process | GO:1905691 | lipid droplet disassembly |
Biological Process | GO:0055088 | lipid homeostasis |
Biological Process | GO:0019915 | lipid storage |
Biological Process | GO:0010891 | negative regulation of sequestering of triglyceride |
Biological Process | GO:0010898 | positive regulation of triglyceride catabolic process |
Biological Process | GO:0019433 | triglyceride catabolic process |
Cellular Component | GO:0005737 | cytoplasm |
Cellular Component | GO:0005829 | cytosol |
Reactome
| Reactome Name | Node type
| Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-1482883 | Acyl chain remodeling of DAG and TAG | Leaf | R-HSA-1430728 | Metabolism |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | Leaf | R-HSA-392499 | Metabolism of proteins |
R-HSA-8957275 | Post-translational protein phosphorylation | Leaf | R-HSA-392499 | Metabolism of proteins |
Location
| ECO term
| Pubmed |
---|---|---|
Cell membrane | ECO:0000269 | PubMed:17032652 |
Cytoplasm | ECO:0000250 | |
Lipid droplet | ECO:0000269 | PubMed:16239926 |
Lipid droplet | ECO:0000269 | PubMed:34903883 |
HPO ID
| HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000407 | Sensorineural hearing impairment |
HP:0000467 | Neck muscle weakness |
HP:0000478 | Abnormality of the eye |
HP:0000819 | Diabetes mellitus |
HP:0001082 | Cholecystitis |
HP:0001249 | Intellectual disability |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
HP:0001270 | Motor delay |
Disease name | MONDO ID
| ICD10
| ICD10 chapter
| OMIM
| Orphanet
|
---|---|---|---|---|---|
neutral lipid storage myopathy | MONDO:0012545 | E75 | chapter4, Endocrine, nutritional and metabolic diseases | OMIM:610717 | Orphanet:98908 |