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26224 FBXL3

26224

FBXL3

F-box and leucine rich repeat protein 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition F-box and leucine rich repeat protein 3

研究结论

Date Results Publications
2020-03-14 12:34:00 we conclude that homozygous FBXL3 LoF variants likely cause autosomal recessive ID, short stature, developmental delay and facial dysmorphism in humans, and that the Cys358Arg FBXL3 variant likely adds the circadian phenotype because of abnormal interaction with CRY1 and CRY2 30481285
2019-03-23 10:28:00 FBXL3 was regulated by miR-4735-3p and suppressed cell proliferation and invasion in non-small cell lung cancer. 30594330
2018-05-12 11:14:00 data indicate an oncogenic role of miR-181d in CRC by promoting glycolysis, and miR-181d/CRY2/FBXL3/c-myc feedback loop might be a therapeutic target for patients with CRC. 28749470
2017-11-04 10:38:00 These results demonstrate that CRY2 stability controlled by FBXL3 plays a key role in the regulation of human sleep wake behavior. 27529127
2017-09-02 11:21:00 CRY2 and FBXL3 cooperatively degrade c-MYC preventing the development of cancer. 27840026

名称对应

Type IDs
Synonymous FBL3, FBL3A, FBXL3A
Gene
UniProtKB-ID: FBXL3_HUMAN
UniprotKB: Q9UKT7
UniParc: UPI0000035C8B
EMBL: BC072448, AF126028, AK314442, AF129532
Ensembl: ENSG00000005812
KO: hsa:26224
Nucleutide sequences
EMBL-CDS: AAF37383.1, AAH72448.1, AAF04466.1, BAG37051.1
Ensembl_TRS: ENST00000355619
Protein sequencees
Ensembl_PRO: ENSP00000347834
RefSeq: NP_036290.1, XP_016876027.1, XP_005266393.1, XP_005266394.1
Others
UniRef100: UniRef100_Q9UKT7
UniRef90: UniRef90_Q8C4V4
UniRef50: UniRef50_Q8C4V4
UniGene: Hs.508284
CCDS: CCDS9457.1

全选

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研究热度

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