Wdr35 - WD repeat domain 35-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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74682 Wdr35

基因描述

Type	Description
Definition	WD repeat domain 35

研究结论

Date	Results	Publications
2015-06-20 12:46:00	These results suggest that bupivacaine activates AMPK and p38 MAPK via CaMKK in Neuro2a cells, and that the CaMKK/AMPK/p38 MAPK pathway is involved in regulating WDR35 expression.	24859235
2014-09-20 11:51:00	C-Jun siRNA did not inhibit the bupivacaine-induced increase in WDR35 mRNA expression.	24466034
2011-06-18 10:35:00	In a mutation screen for developmental phenotypes, we identified a mutation in Wdr35 as the cause of midgestation lethality, with abnormalities characteristic of defects in the Hedgehog signaling pathway.	21473986

名称对应

Type	IDs
Synonymous	4930459M12Rik, 4931430C06, mKIAA1336
Gene	UniProtKB-ID: WDR35_MOUSE UniprotKB: Q8BND3 UniParc: UPI000024DABF, UPI0000434911 EMBL: BC056925, AK029896, AC110376, AK083971 Ensembl: ENSMUSG00000066643 KO: mmu:74682
Nucleutide sequences	EMBL-CDS: AAH56925.1, BAC26663.1, BAC39081.1 Ensembl_TRS: ENSMUST00000085745, ENSMUST00000111113
Protein sequencees	Ensembl_PRO: ENSMUSP00000106742, ENSMUSP00000082895 RefSeq: XP_036013526.1, NP_001152999.1, NP_766058.3
Others	UniRef100: UniRef100_Q8BND3 UniRef90: UniRef90_Q8BND3 UniRef50: UniRef50_Q9P2L0 UniGene: Mm.87389 CCDS: CCDS49027.1, CCDS25807.1

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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
30995482	Overlapping Activities of Two Neuronal Splicing Factors Switch the GABA Effect from Excitatory to Inhibitory by Regulating REST. Cell Rep Yoko Nakano , Susan Wiechert , Botond BÃ¡nfi	2019-04-16	-
27103069	Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death. EMBO J Chantal Sellier , Maria-Letizia Campanari , Camille Julie Corbier , Angeline Gaucherot , Isabelle Kolb-Cheynel , Mustapha Oulad-Abdelghani , Frank Ruffenach , Adeline Page , Sorana Ciura , Edor Kabashi , Nicolas Charlet-Berguerand	2016-06-15	-
25908617	Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium. Hum. Mol. Genet. JosÃ© A CaparrÃ³s-MartÃn , Alessandro De Luca , FranÃ§ois Cartault , Mona Aglan , Samia Temtamy , Ghada A Otaify , Mennat Mehrez , MarÃa Valencia , Laura VÃ¡zquez , Jean-Luc Alessandri , JuliÃ¡n Nevado , Inmaculada Rueda-Arenas , Karen E Heath , Maria Cristina Digilio , Bruno Dallapiccola , Judith A Goodship , Pleasantine Mill , Pablo Lapunzina , Victor L Ruiz-Perez	2015-07-15	-
24859235	Enhanced expression of WD repeat-containing protein 35 via CaMKK/AMPK activation in bupivacaine-treated Neuro2a cells. PLoS ONE Lei Huang , Fumio Kondo , Masahiko Gosho , Guo-Gang Feng , Misako Harato , Zhong-yuan Xia , Naohisa Ishikawa , Yoshihiro Fujiwara , Shoshiro Okada	2014-01-01	Wdr35
24466034	Enhanced expression of WD repeat-containing protein 35 via nuclear factor-kappa B activation in bupivacaine-treated Neuro2a cells. PLoS ONE Lei Huang , Fumio Kondo , Misako Harato , Guo-Gang Feng , Naoshisa Ishikawa , Yoshihiro Fujiwara , Shoshiro Okada	2014-01-01	Nfkb1, Wdr35
22326026	Proteomic analysis of mammalian primary cilia. Curr. Biol. Hiroaki Ishikawa , James Thompson , John R Yates , Wallace F Marshall	2012-03-06	-
23055939	A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse. PLoS Genet Yoko Nakano , Israt Jahan , Gregory Bonde , Xingshen Sun , Michael S Hildebrand , John F Engelhardt , Richard J H Smith , Robert A Cornell , Bernd Fritzsch , Botond BÃ¡nfi	2012-01-01	-
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
21565611	Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways. Cell Liyun Sang , Julie J Miller , Kevin C Corbit , Rachel H Giles , Matthew J Brauer , Edgar A Otto , Lisa M Baye , Xiaohui Wen , Suzie J Scales , Mandy Kwong , Erik G Huntzicker , Mindan K Sfakianos , Wendy Sandoval , J Fernando Bazan , Priya Kulkarni , Francesc R Garcia-Gonzalo , Allen D Seol , John F O'Toole , Susanne Held , Heiko M Reutter , William S Lane , Muhammad Arshad Rafiq , Abdul Noor , Muhammad Ansar , Akella Radha Rama Devi , Val C Sheffield , Diane C Slusarski , John B Vincent , Daniel A Doherty , Friedhelm Hildebrandt , Jeremy F Reiter , Peter K Jackson	2011-05-13	-
21473986	Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. Am J Hum Genet Pleasantine Mill , Paul J Lockhart , Elizabeth Fitzpatrick , Hayley S Mountford , Emma A Hall , Martin A M Reijns , Margaret Keighren , Melanie Bahlo , Catherine J Bromhead , Peter Budd , Salim Aftimos , Martin B Delatycki , Ravi Savarirayan , Ian J Jackson , David J Amor	2011-04-08	-

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