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93790 Nipa2

93790

Nipa2

non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)

protein-coding

Mus musculus

基因描述

Type Description
Definition non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)

研究结论

Date Results Publications
2020-11-21 13:32:00 NIPA2 regulates osteoblast function by modulating mitophagy in type 2 diabetes osteoporosis. 32080264
2010-01-21 00:00:00 indentification on mouse chromosome 7C 14508708
2010-01-21 00:00:00 The isolation and characterization of Nipa2 in mouse distal convoluted tubule cells are reported. 18667602

名称对应

Type IDs
Synonymous 2600017P10Rik, 3830408P04Rik, AB041581
Gene
UniProtKB-ID: NIPA2_MOUSE
UniprotKB: Q9JJC8
UniParc: UPI00000234D2
EMBL: AK076051, AK028734, BC038499, BK001121, AB041581, AK154755, AK041427
Ensembl: ENSMUSG00000030452
KO: mmu:93790
Nucleutide sequences
EMBL-CDS: BAC26089.1, BAA95065.1, BAC36149.1, DAA01178.1, AAH38499.1, BAC30943.1, BAE32806.1
Gene_ORFName: MNCb-2146
Ensembl_TRS: ENSMUST00000032635, ENSMUST00000119201, ENSMUST00000117812, ENSMUST00000119041
Protein sequencees
Ensembl_PRO: ENSMUSP00000113727, ENSMUSP00000032635, ENSMUSP00000114020, ENSMUSP00000112394
RefSeq: NP_001243061.1, NP_076136.2, NP_001243060.1, XP_006541387.1, NP_001243059.1, NP_001243062.1
Others
UniRef100: UniRef100_Q9JJC8
UniRef90: UniRef90_Q9JJC8
UniRef50: UniRef50_Q9JJC8
UniGene: Mm.37249, Mm.333893, Mm.486878
CCDS: CCDS21316.1

全选

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研究热度

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