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55137 FIGN

55137

FIGN

fidgetin, microtubule severing factor

protein-coding

Homo sapiens

基因描述

Type Description
Definition fidgetin, microtubule severing factor

研究结论

Date Results Publications
2017-09-16 12:23:00 FIGN might play an important role in decreased congenital heart defect risk by upregulating plasma folate concentration during embryo heart development 28534241
2017-08-19 12:38:00 FIGN +94762G>C polymorphism reduced the risk of congenital heart defects by activating the transcription of an alternative FIGN isoform, inhibiting proteasome activity and allowing the accumulation of RFC1 and DHFR, promoting folate transmembrane transport and utilization. 28302752
2012-10-20 10:51:00 The loss of Fidgetin induces a microtubule-dependent enlargement of mitotic centrosomes and an increase in the number and length of astral microtubules. 22672901
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086

名称对应

Type IDs
Gene
UniProtKB-ID: FIGN_HUMAN
UniprotKB: Q5HY92
UniParc: UPI000022BD13
EMBL: BX649105, AC093727, AK001267, AK025747, AK125324
Ensembl: ENSG00000182263
KO: hsa:55137
Nucleutide sequences
EMBL-CDS: AAX81992.1, BAB15231.1, CAI45980.1, BAA91590.1, BAG54182.1
Ensembl_TRS: ENST00000333129
Protein sequencees
Ensembl_PRO: ENSP00000333836
RefSeq: XP_016859908.1, NP_001308754.1, XP_011509691.1, NP_060556.2
Others
UniRef100: UniRef100_Q5HY92
UniRef90: UniRef90_Q9ERZ6
UniRef50: UniRef50_Q9ERZ6
UniGene: Hs.593650
CCDS: CCDS2221.2

全选

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研究热度

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