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79443 FYCO1

79443

FYCO1

FYVE and coiled-coil domain containing 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition FYVE and coiled-coil domain containing 1

研究结论

Date Results Publications
2018-08-04 11:52:00 FYCO1 regulates accumulation of post-mitotic midbodies by mediating LC3-dependent midbody degradation 29196475
2018-01-06 10:16:00 FYCO1 and MAP1LC3A interact through a novel binding mode that involves Atg8-family proteins 27246247
2017-07-01 10:54:00 Rare missense variants in FYCO1 are overrepresented in sporadic inclusion body myositis patients. 28009083
2016-04-23 10:55:00 FYCO1 requires a functional LC3A/B-preferring LC3-interacting Region (LIR) motif to facilitate efficient maturation of autophagosomes under basal conditions, whereas starvation-induced autophagy was unaffected 26468287
2011-08-20 10:49:00 FYCO1 is involved in lens development and transparency in humans, and mutations in this gene are one of the most common causes of autosomal-recessive congenital cataracts in the Pakistani population. 21636066

名称对应

Type IDs
Synonymous CATC2, CTRCT18, RUFY3, ZFYVE7
Gene
UniProtKB-ID: FYCO1_HUMAN
UniprotKB: Q9BQS8
UniParc: UPI0001F4E01A, UPI000013E307, UPI000189A737, UPI00004122EB
EMBL: AK074165, BC007218, AL832358, BC143368, AJ292348, BC101468, AC099782, BC101470, AK023397, AL833308
Ensembl: ENSG00000163820
KO: hsa:79443
Nucleutide sequences
EMBL-CDS: AAI43369.1, AAI01469.1, CAD91151.1, BAB84991.1, BAB14559.1, CAC33883.1, AAH07218.1, AAI01471.1, CAD89924.1
Ensembl_TRS: ENST00000535325, ENST00000296137
Protein sequencees
Ensembl_PRO: ENSP00000441178, ENSP00000296137
RefSeq: NP_001373352.1, NP_001373354.1, NP_001373357.1, NP_001373356.1, NP_001373355.1, NP_001373353.1, NP_001373358.1, NP_001373350.1, NP_001373351.1, XP_006713396.1, NP_001373359.1, NP_078789.2
Others
UniRef100: UniRef100_Q9BQS8
UniRef90: UniRef90_Q9BQS8
UniRef50: UniRef50_Q9BQS8
UniGene: Hs.200227, Hs.739775
CCDS: CCDS2734.1

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