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11116 FGFR1OP

11116

FGFR1OP

FGFR1 oncogene partner

protein-coding

Homo sapiens

基因描述

Type Description
Definition FGFR1 oncogene partner

研究结论

Date Results Publications
2019-03-30 11:53:00 We show that Fop mutation perturbs ciliogenesis in vivo and that this leads to the alteration of the Hedgehog signaling pathway. Fop mutation reduces CSs movements and affects pericentriolar material composition, which probably participates to the ciliogenesis defect. 29982567
2016-08-13 10:45:00 The rs151606 T>G was associated with an increased risk of lung cancer and rs12212247 T>C was associated with a decreased risk of lung cancer 26905588
2016-08-04 18:13:00 This study was designed to determine the association of CCR6 and FGFR10P (tag)single nucleotide polymorphisms with Vogt-Koyanagi-Harada (VKH) syndrome, in two independent Chinese Han populations. 23935994
2013-10-19 13:44:00 FOP is a centriolar satellite protein involved in ciliogenesis. 23554904
2010-06-30 22:05:00 Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) 20526339

名称对应

Type IDs
Synonymous FOP
Gene
UniProtKB-ID: CEP43_HUMAN, B4DH64_HUMAN, A0A087WV25_HUMAN
UniprotKB: O95684, B4DH64, A0A087WV25
UniParc: UPI00017A703C, UPI000013C927, UPI000056F185, UPI0001AE7311, UPI0000071446
EMBL: AK289846, CH471051, AK294950, Y18046, Z94721, BC037785, BC011902, AK312791
Ensembl: ENSG00000213066
KO: hsa:11116
Nucleutide sequences
EMBL-CDS: BAG35652.1, AAH11902.1, EAW47509.1, CAA77020.1, EAW47510.1, BAF82535.1, AAH37785.1, BAG58025.1
Ensembl_TRS: ENST00000366847, ENST00000349556, ENST00000622353
Protein sequencees
Ensembl_PRO: ENSP00000230248, ENSP00000355812, ENSP00000479115
RefSeq: NP_919410.1, NP_001265619.1, NP_008976.1
Others
UniRef100: UniRef100_A0A087WV25, UniRef100_O95684, UniRef100_O95684-3
UniRef90: UniRef90_O95684, UniRef90_O95684-3
UniRef50: UniRef50_O95684, UniRef50_O95684-3
UniGene: Hs.487175
CCDS: CCDS5297.1, CCDS5296.1

全选

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研究热度

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