Version 5.4
| Bos taurus Gene: LPIN3 | |||||
|---|---|---|---|---|---|
| Summary | |||||
| InnateDB Gene | IDBG-642701.3 | ||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||
| Gene Symbol | LPIN3 | ||||
| Gene Name | phosphatidate phosphatase LPIN3 | ||||
| Synonyms | |||||
| Species | Bos taurus | ||||
| Ensembl Gene | ENSBTAG00000009165 | ||||
| Encoded Proteins |
lipin 3
|
||||
| Protein Structure | |||||
| Useful resources | Stemformatics EHFPI ImmGen | ||||
| Entrez Gene | |||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000132793:
Humans lipodystrophy is characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mice carrying mutations in the fatty liver dystrophy (fld) gene have similar phenotypes. Through positional cloning, the mouse gene responsible for fatty liver dystrophy was isolated and designated Lpin1. The nuclear protein encoded by Lpin1 was named lipin. Lpin1 mRNA was expressed at high levels in adipose tissue and was induced during differentiation of preadipocytes. These results indicated that lipin is required for normal adipose tissue development and provided a candidate gene for human lipodystrophy. Through database searches, mouse and human EST and genomic sequences with similarities to Lpin1 were identified. These included two related mouse genes (Lpin2 and Lpin3) and three human homologs (LPIN1, LPIN2, and LPIN3). Human LPIN1 gene has been mapped to 2p25.; linkages of fat mass and serum leptin levels to this same region have been noted. Human LPIN2 and LPIN3 mapped to chromosomes 18p11 and 20q11-q12, respectively. The mouse genes encoding Lpin1, Lpin2, and Lpin3 mapped to chromosome 12, 17, and 2, respectively. [provided by RefSeq, Jul 2008] |
||||
| Gene Information | |||||
| Type | Protein coding | ||||
| Genomic Location | Chromosome 13:70666141-70683589 | ||||
| Strand | Forward strand | ||||
| Band | |||||
| Transcripts |
|
||||
| Interactions | |||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
|
||||
| Gene Ontology | |||||
Molecular Function |
|
||||
| Biological Process |
|
||||
| Cellular Component |
|
||||
| Orthologs | |||||
|
Species
Homo sapiens
Mus musculus
|
Gene ID
Gene Order
|
||||
| Pathway Predictions based on Human Orthology Data | |||||
| NETPATH | |||||
| REACTOME |
Synthesis of PC pathway
Synthesis of PE pathway
Triglyceride Biosynthesis pathway
Fatty acid, triacylglycerol, and ketone body metabolism pathway
Metabolism of lipids and lipoproteins pathway
Glycerophospholipid biosynthesis pathway
Cell Cycle pathway
M Phase pathway
Phospholipid metabolism pathway
Mitotic Prophase pathway
Cell Cycle, Mitotic pathway
Metabolism pathway
Depolymerisation of the Nuclear Lamina pathway
Nuclear Envelope Breakdown pathway
Synthesis of PE pathway
Synthesis of PC pathway
Metabolism pathway
Metabolism of lipids and lipoproteins pathway
Glycerophospholipid biosynthesis pathway
Phospholipid metabolism pathway
|
||||
| KEGG |
Glycerophospholipid metabolism pathway
Glycerolipid metabolism pathway
Glycerophospholipid metabolism pathway
Glycerolipid metabolism pathway
|
||||
| INOH | |||||
| PID NCI | |||||
| Cross-References | |||||
| SwissProt | |||||
| TrEMBL | E1BLQ9 | ||||
| UniProt Splice Variant | |||||
| Entrez Gene | 521637 | ||||
| UniGene | Bt.96808 | ||||
| RefSeq | NM_001192540 XM_005214717 XM_005214718 XM_005214719 | ||||
| HUGO | HGNC:14451 | ||||
| OMIM | |||||
| CCDS | |||||
| HPRD | |||||
| IMGT | |||||
| EMBL | DAAA02036650 | ||||
| GenPept | |||||
| RNA Seq Atlas | 521637 | ||||