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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:0110892 | inflammatory bowel disease 1 | |
| DOID:0110946 | autosomal recessive osteopetrosis 7 | |
| DOID:0111135 | congenital generalized lipodystrophy type 1 | |
| DOID:0111136 | congenital generalized lipodystrophy type 2 | |
| DOID:0111137 | congenital generalized lipodystrophy type 3 | |
| DOID:0111138 | congenital generalized lipodystrophy type 4 | |
| DOID:0111414 | trichohepatoenteric syndrome | |
| DOID:0111415 | trichohepatoenteric syndrome 1 | |
| DOID:1019 | osteomyelitis | |
| DOID:10283 | prostate cancer |
- 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 |
|---|---|---|---|
| 64898 | MGI:1891341 | MOUSE20909 | |
| 316737 | RGD:1304588 | RATNO43271 | |
| 100716519 | CAVPO20689 | ||
| 101581300 | OCTDE14554 | ||
| 101714530 | HETGA08362 | ||
| 101875504 | MELUD01029 | ||
| 100012110 | MONDO20095 | ||
| 102459696 | PELSI14647 | ||
| 100566027 | ANOCA05592 | ||
| 107098292 | CYPVA23862 |
