Mus musculus Gene: Lpin3
Summary
InnateDB Gene IDBG-211662.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Lpin3
Gene Name lipin 3
Synonyms 9130206L11Rik; AA438110; AV236139; mKIAA4023
Species Mus musculus
Ensembl Gene ENSMUSG00000027412
Encoded Proteins
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 2:160880670-160906002
Strand Forward strand
Band H2
Transcripts
ENSMUST00000040872 ENSMUSP00000043053
ENSMUST00000109457 ENSMUSP00000105083
ENSMUST00000109456 ENSMUSP00000105082
ENSMUST00000109455 ENSMUSP00000105081
ENSMUST00000124920
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
Accession GO Term
GO:0008195 phosphatidate phosphatase activity
Biological Process
GO:0006631 fatty acid metabolic process
GO:0016311 dephosphorylation
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
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
INOH
PID NCI
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
KEGG
Glycerophospholipid metabolism pathway
Glycerolipid metabolism pathway
INOH
PID NCI
Cross-References
SwissProt Q99PI4
TrEMBL Q149B0 Q571G1
UniProt Splice Variant
Entrez Gene 64899
UniGene Mm.292111 Mm.404269 Mm.488657
RefSeq NM_001199118 NM_022883
OMIM
CCDS CCDS16998
HPRD
IMGT
MGI ID MGI:1891342
MGI Symbol Lpin3
EMBL AF286724 AK049363 AK163833 AK220228 BC117882 BC117883 CH466551
GenPept AAG52762 AAI17883 AAI17884 BAC33710 BAD90153 BAE37510 EDL06298
RNA Seq Atlas 64899