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101401 Adamts9

101401

Adamts9

a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 9

protein-coding

Mus musculus

基因描述

Type Description
Definition a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 9

研究结论

Date Results Publications
2020-06-27 10:18:00 Results provide compelling evidence that ADAMTS9 and ADAMTS20 were differentially sensitive to B3GLCT inactivation and suggest that the developmental defects in PTRPLS result from disruption of a subset of highly sensitive POFUT2/B3GLCT targets such as ADAMTS20. 31600785
2019-08-31 10:38:00 ADAMTS9 Regulates Skeletal Muscle Insulin Sensitivity Through Alterations. 30626608
2019-04-13 10:38:00 ADAMTS9 or ADAMTS20 mutagenesis impaired neural and yolk sac ciliogenesis, leading to morphogenetic anomalies resulting from impaired hedgehog signaling, which is transduced by primary cilia. 30814516
2019-04-13 10:20:00 there is a melanocyte cell-autonomous requirement for Adamts9. 29781574
2016-03-26 10:43:00 Extracellular matrix dynamics is a major influence on umbilical vascular SMC fate, with ADAMTS9 acting as its principal mediator. 26027930

名称对应

Type IDs
Synonymous 1810011L16Rik, 8430403M15Rik, AW743315, E030027K14Rik, Gsfund3, Mhdaund3, Mhdaund4, UND3, UND4
Gene
UniProtKB-ID: E9PYV8_MOUSE
UniprotKB: E9PYV8
UniParc: UPI00015E16A9
EMBL: AC110378, AC166101
Ensembl: ENSMUSG00000030022
KO: mmu:101401
Nucleutide sequences
Ensembl_TRS: ENSMUST00000167391
Protein sequencees
Ensembl_PRO: ENSMUSP00000126498
RefSeq: XP_006505326.1, NP_780523.3, XP_036021607.1, XP_006505324.1, XP_036021608.1, XP_036021606.1, XP_006505325.1
Others
UniRef100: UniRef100_E9PUN6
UniRef90: UniRef90_E9PUN6
UniRef50: UniRef50_Q9P2N4-4
UniGene: Mm.158235, Mm.257557

全选

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