Tubb2b - tubulin, beta 2B class IIb-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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291081 Tubb2b

基因描述

Type	Description
Definition	tubulin, beta 2B class IIb

研究结论

Date	Results	Publications
2016-02-06 10:09:00	Tubulin tail sequences and post-translational modifications regulate closure of mitochondrial voltage-dependent anion channel, VDAC.	26306046
2010-01-21 00:00:00	Distribution in developmental and adult rat tissues	12112145

名称对应

Type	IDs
Synonymous	RGD1309427, Tubb2
Gene	UniProtKB-ID: TBB2B_RAT UniprotKB: Q3KRE8 UniParc: UPI0000024E6E EMBL: BC105754, X03369 Ensembl: ENSRNOG00000017445 KO: rno:291081
Nucleutide sequences	EMBL-CDS: AAI05755.1, CAA27067.1 Ensembl_TRS: ENSRNOT00000023582, ENSRNOT00000083705
Protein sequencees	Ensembl_PRO: ENSRNOP00000073323, ENSRNOP00000023582 RefSeq: NP_001013908.2
Others	UniRef100: UniRef100_Q9BVA1 UniRef90: UniRef90_Q9BVA1 UniRef50: UniRef50_Q9BVA1 UniGene: Rn.37849

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mRNA

Protein

UniprotKB

Description

Refseq

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全选

Pubmed编号	文献信息	发表日期	相关基因
29476059	Identification and characterization of the BRI2 interactome in the brain. Sci Rep Filipa Martins , Ana M Marafona , CÃ¡tia D Pereira , Thorsten MÃ¼ller , Christina Loosse , Katharina Kolbe , Odete A B da Cruz E Silva , Sandra Rebelo	2018-02-23	-
27594048	A heterozygous mutation in tubulin, beta 2B ( Tubb2b ) causes cognitive deficits and hippocampal disorganization. Genes Brain Behav. Rolf W Stottmann , Ashley Driver , Arnold Gutierrez , Matthew R Skelton , Michael Muntifering , Christopher Stepien , Luke Knudson , Matthew Kofron , Charles V Vorhees , Michael T Williams	2017-02-01	-
28013290	Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Hum. Mol. Genet. Martin W Breuss , Thai Nguyen , Anjana Srivatsan , Ines Leca , Guoling Tian , Tanja Fritz , Andi H Hansen , Damir Musaev , Jennifer McEvoy-Venneri , Kiely N James , Rasim O Rosti , Eric Scott , Uner Tan , Richard D Kolodner , Nicholas J Cowan , David A Keays , Joseph G Gleeson	2017-01-15	-
26732629	De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy. Eur J Med Genet Annie Laquerriere , Marie Gonzales , Yoann Saillour , Mara Cavallin , Nicole JoyÄ , ChloÃ© QuÄlin , Laurent Bidat , Marc Dommergues , Ghislaine Plessis , Ferechte Encha-Razavi , Jamel Chelly , Nadia Bahi-Buisson , Karine Poirier	2016-04-01	-
26306046	Tubulin tail sequences and post-translational modifications regulate closure of mitochondrial voltage-dependent anion channel (VDAC). J Biol Chem Kely L Sheldon , Philip A Gurnev , Sergey M Bezrukov , Dan L Sackett	2015-10-30	-
23001566	An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Hum. Mol. Genet. Gustav Y Cederquist , Anna Luchniak , Max A Tischfield , Maya Peeva , Yuyu Song , Manoj P Menezes , Wai-Man Chan , Caroline Andrews , Sheena Chew , Robyn V Jamieson , Lavier Gomes , Maree Flaherty , Patricia Ellen Grant , Mohan L Gupta , Elizabeth C Engle	2012-12-15	TUBB2B
22082260	Analysis of oxygen/glucose-deprivation-induced changes in SUMO3 conjugation using SILAC-based quantitative proteomics. J. Proteome Res. Wei Yang , J Will Thompson , Zhengfeng Wang , Liangli Wang , Huaxin Sheng , Matthew W Foster , M Arthur Moseley , Wulf Paschen	2012-02-03	LOC100359916, LOC100360950, Prdx1l1, LOC100364062, Ddx39b, Phb2, Hnrnpm, Trim28, Rpl6, Hnrnpu, Rps3, Xpnpep1, Zhx1, Gbp2, Eef1a1, Atp5b, Nacc1, Akr1b1, Gnb1, Gstp1, Hspa8, Ldha, Slc25a3, Pgam1, Pgk1, Ppp2ca, Ube2i, Rpn1, Myh9l1, COX2, Hspa4, Eif4a1, Rab5c, Ddx5, Galk1, Zbtb20, Mcm7, Pa2g4, Eprs, Hnrnpc, Tubb2b, Matr3, Nars, Brd8, Nup93, Tubb5, Znhit6, Rps14, Sox6, Serpinh1, Kif22, Sox10, Eef1g, Acta1, Tars, Cct5, Ptbp1, Atn1, Cct3, Rap1a, Prpf40a, Eef2, Hnrnpa1, Gdi2, Gars, Mcm4, Usp39, LOC297756, Tardbp, Aldoart2, Hsp90aa1, Rpl3, Krt1, Arcn1, RGD1565900, Hsp90ab1, Sumo1, Chd3, Morc3, Kdm5b, Dhx9, Eif6, Ccar2, LOC306079, Tcerg1, Nfat5, Sae1, Irf2bp1, Uba2, Hnrnph2, Rsf1, Numa1, Hnrnpul2, Zeb2, Rps6ka5, Bcl11b, Uba1, Wars, Wiz
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	-
21630459	Proteomic characterization of the human sperm nucleus. Proteomics Sara de Mateo , Judit Castillo , Josep Maria Estanyol , JosÃ© Luis BallescÃ , Rafael Oliva	2011-07-01	DNAJB6, GPC6, PSME3, PSMD14, KATNB1, TUBB3, TUBB4A, TUBB4B, PRDX4, AKAP3, CENPA, C6orf10, PTGES3, ACTL7A, TOMM34, RCC1, ZPBP, NUDT5, TUBA3E, PARK7, IZUMO4, PHB2, TUBA3D, PTPMT1, HIST4H4, C16orf78, ZPBP2, HIST2H3C, TMCO2, HMGB4, HIST3H2BB, LYZL4, NUDT16, GNPDA2, EVC2, PACRG, PRSS37, DYNLL2, RPL10L, BANF2, CS, PSMA8, SLC2A14, CSNK2A1, CSNK2A2, CSNK2B, TEKT5, SLC25A10, TMEM190, FAM71A, TEKT4, CTSG, FAM81B, CYC1, FAM71B, CYLC1, CYLC2, EEF1A1P5, DNAJB8, DECR1, CRISP1, DGUOK, DLST, DSP, EEF1A1, EEF1D, EEF1G, EEF2, FAM209A, ENO1, TUBB, CT83, ALAD, ALB, ARMC12, HIST1H2AA, GPC4, ALDOA, FLG, PSME4, DNAJC9, SYNE1, SUZ12, RPL13A, DNPEP, GTPBP4, TSSK2, MTCH2, FTH1, HIST1H2BA, MPC2, DPCD, FAM205A, NIPSNAP3A, GAPDH, TKFC, TES, RIBC2, CABYR
21515572	Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse. Genetics R W Stottmann , J L Moran , A Turbe-Doan , E Driver , M Kelley , D R Beier	2011-07-01	-

研究热度

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