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93757 Immp2l

93757

Immp2l

IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)

protein-coding

Mus musculus

基因描述

Type Description
Definition IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)

研究结论

Date Results Publications
2021-01-09 13:30:00 The Immp2l Mutation Causes Ovarian Aging Through Pathway: Preventive Effect of Melatonin. 32652035
2019-11-09 11:25:00 IMP2-deficient muscle exhibits reduced fatty acid oxidation, due to a reduced abundance of mRNA of peroxisome proliferator-activated receptor alpha (PPARalpha), an IMP2 client, and PPARalpha protein. IMP2-deficient muscle fibers treated with a mitochondrial uncoupler to increase electron flux, as occurs with exercise, exhibit reduced oxygen consumption from fatty acids, with higher oxygen consumption from glucose. 30692269
2019-05-25 10:25:00 Data indicates that overexpression of IMP2 alters the regulatory capacity of many miRNAs and conclude that IMP2 competes with miRNAs for binding sites on thousands of transcripts. As a result, data implicates that overexpression of IMP2 has distinct effects to the regulatory capacity of miRNAs with yet unknown consequences for translational efficiency. 29859241
2018-05-19 10:25:00 The results indicate that IMP2 deficiency delayed bone remodeling by significantly inhibiting the activity of osteoclasts and impairing their adhesion. 29322325
2018-01-13 10:23:00 data suggest that respiratory deficiency is not the cause of the observed Immp2l mutant phenotypes. 25460737

名称对应

Type IDs
Synonymous AI853880, IMP2, Tg(HLA-A/H2-D)2Enge
Gene
UniProtKB-ID: IMP2L_MOUSE
UniprotKB: Q8BPT6
UniParc: UPI0000025AAE
EMBL: BC100557, AK161351, AF359564, AK053361
Ensembl: ENSMUSG00000056899
KO: mmu:93757
Nucleutide sequences
EMBL-CDS: AAK52906.1, BAE36343.1, AAI00558.1, BAC35362.1
Ensembl_TRS: ENSMUST00000132121, ENSMUST00000134965
Protein sequencees
Ensembl_PRO: ENSMUSP00000118779, ENSMUSP00000116441
RefSeq: NP_444352.2, XP_030102864.1, XP_017170750.1, XP_017170751.1, XP_036013583.1
Others
UniRef100: UniRef100_Q8BPT6
UniRef90: UniRef90_Q8BPT6
UniRef50: UniRef50_Q8BPT6
UniGene: Mm.363813
CCDS: CCDS83961.1

全选

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