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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:2361 | macrocytic anemia | |
| DOID:2703 | synovitis | |
| DOID:2723 | dermatitis | |
| DOID:2734 | keratosis follicularis | |
| DOID:2738 | pseudoxanthoma elasticum | |
| DOID:2841 | asthma | |
| DOID:2921 | glomerulonephritis | |
| DOID:2987 | familial mediterranean fever | |
| DOID:3146 | lipid metabolism disorder | |
| DOID:423 | myopathy |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004326 | Cachexia |
| HP:0004810 | Congenital hypoplastic anemia |
| HP:0004840 | Hypochromic microcytic anemia |
| HP:0005561 | Abnormal bone marrow cell morphology |
| HP:0010972 | Anemia of inadequate production |
| HP:0011001 | Increased bone mineral density |
| HP:0011123 | Inflammatory abnormality of the skin |
| HP:0012132 | Erythroid hyperplasia |
| HP:0012647 | Abnormal inflammatory response |
| HP:0012735 | Cough |
| 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 |
|---|---|---|---|
| 101087178 | FELCA28732 | ||
| 118880208 | BALMU02537 | ||
| 100661234 | LOXAF18584 | ||
| 100187579 | PIGXX29811 | ||
| 514448 | BOVIN19598 | ||
| 102173798 | CAPHI16177 | ||
| 101123258 | SHEEP11892 | ||
| 100348321 | RABIT13073 | ||
| 105993809 | DIPOR15459 | ||
| 100769904 | CRIGR21892 |
