Scyl1 - SCY1-like 1 (S. cerevisiae)-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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78891 Scyl1

基因描述

Type	Description
Definition	SCY1-like 1 (S. cerevisiae)

研究结论

Date	Results	Publications
2019-07-13 12:58:00	SCYL1 and SCYL3 play overlapping roles in maintaining motor neuronal viability in vivo and confirm that SCYL family members are critical regulators of neuronal function and survival	29437892
2013-02-02 11:22:00	our results identify SCYL1 as a key regulator of motor neuron survival	23175812
2010-01-21 00:00:00	Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.	17571074

名称对应

Type	IDs
Synonymous	2810011O19Rik, C85140, Ntkl, mdf, mfd, p105
Gene	UniProtKB-ID: SCYL1_MOUSE UniprotKB: Q9EQC5 UniParc: UPI00000224B3 EMBL: AK144134, AK134356, BC034519, AK161813, AK145869, AF276514 Ensembl: ENSMUSG00000024941 KO: mmu:78891
Nucleutide sequences	EMBL-CDS: BAE25720.1, AAG17393.1, BAE22111.1, BAE36588.1, AAH34519.1, BAE26711.1 Ensembl_TRS: ENSMUST00000236978
Protein sequencees	Ensembl_PRO: ENSMUSP00000157476 RefSeq: NP_076401.1, XP_030107005.1, NP_001348850.1, NP_001348851.1
Others	UniRef100: UniRef100_Q9EQC5 UniRef90: UniRef90_Q9EQC5 UniRef50: UniRef50_Q96KG9 UniGene: Mm.276063 CCDS: CCDS29480.1

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mRNA

Protein

UniprotKB

Description

Refseq

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Pubmed编号	文献信息	发表日期	相关基因
29437892	Overlapping Role of SCYL1 and SCYL3 in Maintaining Motor Neuron Viability. J. Neurosci. Emin Kuliyev , Sebastien Gingras , Clifford S Guy , Sherie Howell , Peter Vogel , Stephane Pelletier	2018-03-07	-
28570664	SCYL1 does not regulate REST expression and turnover. PLoS ONE Sebastien Gingras , Emin Kuliyev , StÃ©phane Pelletier	2017-01-01	-
26581903	Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia. Am. J. Hum. Genet. Wolfgang M Schmidt , S Lane Rutledge , Rebecca SchÃ¼le , Benjamin Mayerhofer , Stephan ZÃ¼chner , Eugen Boltshauser , Reginald E Bittner	2015-12-03	-
24457600	The central role of EED in the orchestration of polycomb group complexes. Nat Commun Qi Cao , Xiaoju Wang , Meng Zhao , Rendong Yang , Rohit Malik , Yuanyuan Qiao , Anton Poliakov , Anastasia K Yocum , Yong Li , Wei Chen , Xuhong Cao , Xia Jiang , Arun Dahiya , Clair Harris , Felix Y Feng , Sundeep Kalantry , Zhaohui S Qin , Saravana M Dhanasekaran , Arul M Chinnaiyan	2014-01-01	-
23175812	An early onset progressive motor neuron disorder in Scyl1-deficient mice is associated with mislocalization of TDP-43. J. Neurosci. Stephane Pelletier , Sebastien Gingras , Sherie Howell , Peter Vogel , James N Ihle	2012-11-21	-
21677750	A conditional knockout resource for the genome-wide study of mouse gene function. Nature William C Skarnes , Barry Rosen , Anthony P West , Manousos Koutsourakis , Wendy Bushell , Vivek Iyer , Alejandro O Mujica , Mark Thomas , Jennifer Harrow , Tony Cox , David Jackson , Jessica Severin , Patrick Biggs , Jun Fu , Michael Nefedov , Pieter J de Jong , A Francis Stewart , Allan Bradley	2011-06-15	-
21267068	A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. Graciana Diez-Roux , Sandro Banfi , Marc Sultan , Lars Geffers , Santosh Anand , David Rozado , Alon Magen , Elena Canidio , Massimiliano Pagani , Ivana Peluso , Nathalie Lin-Marq , Muriel Koch , Marchesa Bilio , Immacolata Cantiello , Roberta Verde , Cristian De Masi , Salvatore A Bianchi , Juliette Cicchini , Elodie Perroud , Shprese Mehmeti , Emilie Dagand , Sabine Schrinner , Asja NÃ¼rnberger , Katja Schmidt , Katja Metz , Christina Zwingmann , Norbert Brieske , Cindy Springer , Ana Martinez Hernandez , Sarah Herzog , Frauke Grabbe , Cornelia Sieverding , Barbara Fischer , Kathrin Schrader , Maren Brockmeyer , Sarah Dettmer , Christin Helbig , Violaine Alunni , Marie-Annick Battaini , Carole Mura , Charlotte N Henrichsen , Raquel Garcia-Lopez , Diego Echevarria , Eduardo Puelles , Elena Garcia-Calero , Stefan Kruse , Markus Uhr , Christine Kauck , Guangjie Feng , Nestor Milyaev , Chuang Kee Ong , Lalit Kumar , MeiSze Lam , Colin A Semple , Attila Gyenesei , Stefan Mundlos , Uwe Radelof , Hans Lehrach , Paolo Sarmientos , Alexandre Reymond , Duncan R Davidson , Pascal DollÃ© , Stylianos E Antonarakis , Marie-Laure Yaspo , Salvador Martinez , Richard A Baldock , Gregor Eichele , Andrea Ballabio	2011-01-18	-
19723774	Lack of periostin leads to suppression of Notch1 signaling and calcific aortic valve disease. Physiol Genomics Tatiana V Tkatchenko , Ricardo A Moreno-Rodriguez , Simon J Conway , Jeffery D Molkentin , Roger R Markwald , Andrei V Tkatchenko	2009-11-06	-
18556652	Scyl1, mutated in a recessive form of spinocerebellar neurodegeneration, regulates COPI-mediated retrograde traffic. J Biol Chem Jonathon L Burman , Lyne Bourbonniere , Jacynthe Philie , Thomas Stroh , Selma Y Dejgaard , John F Presley , Peter S McPherson	2008-08-15	-
17571074	Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO Rep Wolfgang M Schmidt , Cornelia Kraus , Harald HÃ¶ger , Sonja Hochmeister , Felicitas Oberndorfer , Manuela Branka , Sonja Bingemann , Hans Lassmann , Markus MÃ¼ller , LÃºcia InÃªs Macedo-Souza , Mariz Vainzof , Mayana Zatz , AndrÃ© Reis , Reginald E Bittner	2007-07-01	-

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