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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
lipin 2
Summary
- Gene Symbol
-
- LPIN2
- Aliases
-
- KIAA0249
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Congenital dyserythropoietic anemia
- Cytoplasm
- Disease variant
- Endoplasmic reticulum
- Fatty acid metabolism
- Hydrolase
- Membrane
- Nucleus
- Phosphoprotein
- Reference proteome
- Transcription regulation
- Proteins
| UniProt | Protein Name |
|---|---|
| Q92539 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| triglyceride biosynthetic process | ||
| positive regulation of transcription by RNA polymerase II | ||
| fatty acid catabolic process | ||
| lipid metabolic process | ||
| cellular response to insulin stimulus |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphatidate phosphatase activity | ||
| transcription coactivator activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:77 | gastrointestinal system disease | |
| DOID:811 | lipodystrophy | |
| DOID:8577 | ulcerative colitis | |
| DOID:8778 | Crohn's disease | |
| DOID:9351 | diabetes mellitus | |
| DOID:9352 | type 2 diabetes mellitus | |
| DOID:9360 | intrinsic asthma | |
| DOID:9415 | allergic asthma | |
| DOID:970 | tenosynovitis | |
| DOID:9970 | obesity |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000093 | Proteinuria |
| HP:0000823 | Delayed puberty |
| HP:0000969 | Edema |
| HP:0000988 | Skin rash |
| HP:0001061 | Acne |
| HP:0001371 | Flexion contracture |
| HP:0001386 | Joint swelling |
| HP:0001433 | Hepatosplenomegaly |
| HP:0001508 | Failure to thrive |
| Disease ID | Disease Name |
|---|---|
| OMIM:609628 |
|
| ORPHA:77297 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 113435499 | PSETE06507 | ||
| 103826873 | SERCA00455 | ||
| 100077278 | ORNAN22017 | ||
| 100919385 | SARHA17805 | ||
| 100414205 | CALJA09073 | ||
| 105583958 | CERAT24400 | ||
| 102121328 | MACFA16517 | ||
| 695641 | MACMU17638 | ||
| 105478818 | MACNE27729 | ||
| 101018057 | PAPAN16729 |
