ABTB2 - ankyrin repeat and BTB domain containing 2-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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25841 ABTB2

基因描述

Type	Description
Definition	ankyrin repeat and BTB domain containing 2

研究结论

Date	Results	Publications
2010-06-30 22:06:00	Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)	20379614

名称对应

Type	IDs
Synonymous	ABTB2A, BTBD22
Gene	UniProtKB-ID: ABTB2_HUMAN UniprotKB: Q8N961 UniParc: UPI0001DD21BB, UPI000006EA95 EMBL: AL133294, AK091560, AK291744, AC090469, AL139174, AK095632, BC093968, AL035079, BX640841 Ensembl: ENSG00000166016 KO: hsa:25841
Nucleutide sequences	EMBL-CDS: CAE45913.3, AAH93968.1, BAF84433.1, BAC04595.1, BAC03697.1 Ensembl_TRS: ENST00000435224
Protein sequencees	Ensembl_PRO: ENSP00000410157 RefSeq: NP_665803.2
Others	UniRef100: UniRef100_Q8N961 UniRef90: UniRef90_Q8N961 UniRef50: UniRef50_Q8N961 UniGene: Hs.23361 CCDS: CCDS7890.2

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mRNA

Protein

UniprotKB

Description

Refseq

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Location

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31586073	The midbody interactome reveals unexpected roles for PP1 phosphatases in cytokinesis. Nat Commun Luisa Capalbo , Zuni I Bassi , Marco Geymonat , Sofia Todesca , Liviu Copoiu , Anton J Enright , Giuliano Callaini , Maria Giovanna Riparbelli , Lu Yu , Jyoti S Choudhary , Enrico Ferrero , Sally Wheatley , Max E Douglas , Masanori Mishima , Pier Paolo D'Avino	2019-10-04	-
30404837	Cullin-3-KCTD10-mediated CEP97 degradation promotes primary cilium formation. J. Cell. Sci. Tomoaki Nagai , Sachiho Mukoyama , Harumi Kagiwada , Naoki Goshima , Kensaku Mizuno	2018-12-12	-
29507755	VIRMA mediates preferential m⁶A mRNA methylation in 3'UTR and near stop codon and associates with alternative polyadenylation. Cell Discov Yanan Yue , Jun Liu , Xiaolong Cui , Jie Cao , Guanzheng Luo , Zezhou Zhang , Tao Cheng , Minsong Gao , Xiao Shu , Honghui Ma , Fengqin Wang , Xinxia Wang , Bin Shen , Yizhen Wang , Xinhua Feng , Chuan He , Jianzhao Liu	2018-01-01	-
29117863	RNA-binding activity of TRIM25 is mediated by its PRY/SPRY domain and is required for ubiquitination. BMC Biol Nila Roy Choudhury , Gregory Heikel , Maryia Trubitsyna , Peter Kubik , Jakub Stanislaw Nowak , Shaun Webb , Sander Granneman , Christos Spanos , Juri Rappsilber , Alfredo Castello , Gracjan Michlewski	2017-11-08	-
28675297	A Human Tyrosine Phosphatase Interactome Mapped by Proteomic Profiling. J Proteome Res Parveen Kumar , Prathyusha Munnangi , Kvs Rammohan Chowdary , Varun J Shah , Swapnil R Shinde , Nanci R Kolli , Rachita R Halehalli , Hampapathalu A Nagarajaram , Subbareddy Maddika	2017-08-04	-
28514442	Architecture of the human interactome defines protein communities and disease networks. Nature Edward L Huttlin , Raphael J Bruckner , Joao A Paulo , Joe R Cannon , Lily Ting , Kurt Baltier , Greg Colby , Fana Gebreab , Melanie P Gygi , Hannah Parzen , John Szpyt , Stanley Tam , Gabriela Zarraga , Laura Pontano-Vaites , Sharan Swarup , Anne E White , Devin K Schweppe , Ramin Rad , Brian K Erickson , Robert A Obar , K G Guruharsha , Kejie Li , Spyros Artavanis-Tsakonas , Steven P Gygi , J Wade Harper	2017-05-25	-
27432908	Defining the Protein-Protein Interaction Network of the Human Protein Tyrosine Phosphatase Family. Mol Cell Proteomics Xu Li , Kim My Tran , Kathryn E Aziz , Alexey V Sorokin , Junjie Chen , Wenqi Wang	2016-09-01	-
26760575	High-throughput analyses of hnRNP H1 dissects its multi-functional aspect. RNA Biol Philip J Uren , Emad Bahrami-Samani , Patricia Rosa de Araujo , Christine Vogel , Mei Qiao , Suzanne C Burns , Andrew D Smith , Luiz O F Penalva	2016-01-01	-
26673895	A deep proteomics perspective on CRM1-mediated nuclear export and nucleocytoplasmic partitioning. Elife Koray KÄ±rlÄ± , Samir Karaca , Heinz JÃ¼rgen Dehne , Matthias Samwer , Kuan Ting Pan , Christof Lenz , Henning Urlaub , Dirk GÃ¶rlich	2015-01-01	CHA1, KRR1, SRO9, STE50, RRP7, RNQ1, DCC1, GBP2, SAT4, RVS161, YCR016W, PWP2, SSK22, SOL2, PAT1, YCR087C-A, OCA4, MOB2, EPL1, BUD27, FRS2, LOC1, YFR016C, LSB3, RPL2A, PHO4, SAP155, IRC6, ENT4, PRP19, RIX7, YLL032C, FRA1, ISA1, SPA2, PUF3, RPL8B, NOC3, SSL1, SSK1, NSE1, RLP24, SDO1, ADE16, RPL15A, STU2, RPS0B, FRS1, BMT6, KIN2, HRT3, REX3, YLR108C, CFT2, MSL5, ACE2, STM1, YLR157C-A, APS1, CBF5, SWI6, SKG3, HCR1, PWP1, NOP56, BUR2, GPN3, DBP9, GCD7, SGD1, STE11, NMD4, RPS22B, ROM2, STP3, IKI3, REH1, AFG2, UTP21, ATG17, TUS1, MAG2, ATG23, RPS1A, FPR4, PDP3, CDC24, RBG1, FUN12, MTW1, PRP45, MAK16, ECM1, GPB2, VPS8, KIN3, CDC15, YAT1, WHI4
24623842	GABRA1 and STXBP1: novel genetic causes of Dravet syndrome. Neurology Gemma L Carvill , Sarah Weckhuysen , Jacinta M McMahon , Corinna Hartmann , Rikke S MÃ¸ller , Helle Hjalgrim , Joseph Cook , Eileen Geraghty , Brian J O'Roak , Steve Petrou , Alison Clarke , Deepak Gill , Lynette G Sadleir , Hiltrud Muhle , Sarah von Spiczak , Marina Nikanorova , Bree L Hodgson , Elena V Gazina , Arvid Suls , Jay Shendure , Leanne M Dibbens , Peter De Jonghe , Ingo Helbig , Samuel F Berkovic , Ingrid E Scheffer , Heather C Mefford	2014-04-08	SPATA13, CLSTN1, KIF1B, GABRA1, ABTB2, NOL11, NKAIN3, ATP6V0C, STK31, SCN1A, SCN1B, SLC8A1, STXBP1, KDM2B, RIMS2

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