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121512 FGD4

121512

FGD4

FYVE, RhoGEF and PH domain containing 4

protein-coding

Homo sapiens

基因描述

Type Description
Definition FYVE, RhoGEF and PH domain containing 4

研究结论

Date Results Publications
2021-02-06 13:58:00 Circular RNA circFGD4 suppresses gastric cancer progression via modulating miR-532-3p/APC/beta-catenin signalling pathway. 32633323
2020-10-10 12:57:00 Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease. 31852984
2019-03-30 11:49:00 Results show that the expression of FGD4 is upregulated in cancerous prostates compared to the luminal cells in benign prostatic hyperplasia and demonstrate a tumor promoting and a cell migratory function of FGD4 in prostate cancer cells. Its inhibition enhances the response for both androgen-dependent and independent prostate cancer cells towards currently used prostate cancer drugs. 30558664
2017-05-27 11:55:00 FGD4 c.2044-236 A-allele carriers had an increased risk of paclitaxel dose reduction (HR per A-allele=1.38, P=0.036) when adjusted for total cumulative paclitaxel dose 27736846
2016-01-30 12:13:00 identified two different pairs of novel compound heterozygous mutations in the FGD4 gene from nonconsanguineous Korean Charcot-Marie-Tooth disease type 4H families 26400421

名称对应

Type IDs
Synonymous CMT4H, FRABP, ZFYVE6
Gene
UniProtKB-ID: FGD4_HUMAN, F8W1R0_HUMAN, E9PJX4_HUMAN, B7Z493_HUMAN, B7Z8F9_HUMAN, Q49A55_HUMAN
UniprotKB: Q96M96, F8W1R0, E9PJX4, B7Z493, B7Z8F9, Q49A55
UniParc: UPI0001915010, UPI00019152FD, UPI00020CE036, UPI0000037D64, UPI000004CCA6, UPI000056F1E0, UPI0001F78470, UPI00004E1942
EMBL: AK057294, AC087245, BC045552, AY367054, AL713762, AK303334, AK297025, AC084824, AC090677, AC090440
Ensembl: ENSG00000139132
KO: hsa:121512
Nucleutide sequences
EMBL-CDS: CAD28532.1, BAB71413.1, AAQ72372.1, BAH12479.1, BAH13945.1, AAH45552.1
Ensembl_TRS: ENST00000427716, ENST00000546442, ENST00000525053, ENST00000531134
Protein sequencees
Ensembl_PRO: ENSP00000394487, ENSP00000446695, ENSP00000433666, ENSP00000431323
RefSeq: NP_001291410.1, NP_001317302.1, NP_001371057.1, XP_011518861.1, XP_024304607.1, NP_001371060.1, XP_024304608.1, XP_024304605.1, XP_011518856.1, NP_001372047.1, XP_011518860.1, NP_001291413.1, NP_001371055.1, NP_001291412.1, XP_011518857.1, NP_001357227.2, XP_011518858.1, NP_001371056.1, XP_011518859.1, NP_001371061.1, NP_001371059.1, NP_640334.2, XP_024304606.1, XP_005253367.1, NP_001291409.1, NP_001357226.1, NP_001317303.1, XP_005253366.1
Others
UniRef100: UniRef100_B7Z8F9, UniRef100_Q96M96, UniRef100_E9PJX4, UniRef100_Q49A55, UniRef100_B7Z493
UniRef90: UniRef90_E9PJX4, UniRef90_Q49A55, UniRef90_Q96M96
UniRef50: UniRef50_A0A3Q2TZP0, UniRef50_Q49A55, UniRef50_Q96M96
UniGene: Hs.117835
CCDS: CCDS8727.1

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