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77087 Ankrd11

77087

Ankrd11

ankyrin repeat domain 11

protein-coding

Mus musculus

基因描述

Type Description
Definition ankyrin repeat domain 11

研究结论

Date Results Publications
2019-06-22 10:45:00 Ankrd11 knockdown delayed radial migration of cortical neurons. ANKRD11-deficient neurons displayed markedly reduced dendrite growth and branching as well as abnormal dendritic spine morphology. Ankrd11 knockdown suppressed acetylation of epigenetic molecules such as p53 and Histone H3. Furthermore, the mRNA levels of Trkb, Bdnf, and neurite growth-related genes were downregulated in ANKRD11-deficient cortical neurons. 29274743
2015-04-18 10:56:00 ANKRD11 C-terminus plays an important role in regulating the abundance of the protein, and a disturbance of the protein abundance due to the mutations leads to KBG syndrome. 25413698
2010-01-21 00:00:00 A Glu->Lys missense mutation in a highly conserved region causes osteopenia and craniofacial abnormalities. Homozygosity causes embryo death. Ankrd11 is a genetic regular of bone homeostasis. 17986521

名称对应

Type IDs
Synonymous 2410104C19Rik, 3010027A04Rik, 6330578C09Rik, 9530048I21Rik, AA930108, Gm176, Yod
Gene
UniProtKB-ID: ANR11_MOUSE
UniprotKB: E9Q4F7
UniParc: UPI0000605E52
EMBL: BC059876, BC158043, AC132287
Ensembl: ENSMUSG00000035569
KO: mmu:77087
Nucleutide sequences
EMBL-CDS: AAH59876.1, AAI58044.1
Ensembl_TRS: ENSMUST00000098334
Protein sequencees
Ensembl_PRO: ENSMUSP00000095939
RefSeq: XP_030099711.1, NP_001074848.2, XP_030099712.1, XP_036010270.1
Others
UniRef100: UniRef100_E9Q4F7
UniRef90: UniRef90_E9Q4F7
UniRef50: UniRef50_Q6UB99
UniGene: Mm.31567
CCDS: CCDS40507.2

全选

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