Type | Description |
---|---|
Definition | lipin 2 |
Date | Results | Publications |
---|---|---|
2020-07-25 12:47:00 | Data reveal that LPIN2 silencing interferes with HCV virion secretion at late stages of the infection, without significantly LPIN2-deficient cells display alterations in mitochondrial and Golgi apparatus morphology, suggesting that LPIN2 contributes to the maintenance of the overall organelle architecture. These data suggest a broader function of LPIN2 for replication of HCV and other RNA viruses. | 31752156 |
2017-12-16 12:33:00 | we proposed that four newly identified peripheral blood mononuclear cells-derived genes( DHRS3, TTC38, SAP30BP and LPIN2 )could be integrated with previously reported rheumatoid arthritis (RA)-associated genes to monitor and/or diagnose RA. | 28371410 |
2015-05-16 10:52:00 | Structural variants unique to the malignant cell line inactivated: LPIN2, a phosphatidic acid phosphatase and a co-factor of PGC1a that is important for lipid metabolism and for suppressing autoinflammation. | 23792589 |
2013-04-20 12:11:00 | We describe two brothers with Majeed syndrome, homozygous novel 2-base pair deletion in LPIN2 (c.1312_1313delCT; p.Leu438fs+16X) | 23087183 |
2013-04-06 10:51:00 | LPIN1-related myolysis constitutes a major cause of early-onset rhabdomyolysis and occasionally in adults. Heterozygous LPIN1 mutations may cause mild muscular symptoms. No major defects of LPIN2 or LPIN3 genes were associated with muscle manifestations. | 22481384 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
LPIN2_HUMAN
UniprotKB:
Q92539
UniParc:
UPI000012E865
EMBL:
D87436,
BC152448,
CH471113
Ensembl:
ENSG00000101577
KO:
hsa:9663
|
Nucleutide sequences |
EMBL-CDS:
EAX01687.1,
AAI52449.1,
BAA13380.2,
EAX01686.1
Ensembl_TRS:
ENST00000261596
|
Protein sequencees |
Ensembl_PRO:
ENSP00000261596
RefSeq:
NP_001362738.1,
NP_001362737.1,
NP_055461.1,
XP_016881587.1,
XP_016881588.1,
XP_005258234.1
|
Others |
UniRef100:
UniRef100_Q92539
UniRef90:
UniRef90_Q92539
UniRef50:
UniRef50_Q92539
UniGene:
Hs.132342
CCDS:
CCDS11829.1
|
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Refseq |
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