Lineage-specific biology revealed by a finished genome assembly of the mouse.Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L.[...], Ponting C.P.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
A tissue-specific atlas of mouse protein phosphorylation and expression.Huttlin E.L., Jedrychowski M.P., Elias J.E., Goswami T., Rad R., Beausoleil S.A., Villen J., Haas W., Sowa M.E., Gygi S.P.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
Modernizing reference genome assemblies.Church D.M., Schneider V.A., Graves T., Auger K., Cunningham F., Bouk N., Chen H.C., Agarwala R., McLaren W.M.[...], Hubbard T.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways.Park J., Chen Y., Tishkoff D.X., Peng C., Tan M., Dai L., Xie Z., Zhang Y., Zwaans B.M.[...], Zhao Y.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCMol. Cell 50:919-930 (2013)Cited in99+99+Mapped to6
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (AUG-2024)Cited in99+
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.Draptchinskaia N., Gustavsson P., Andersson B., Pettersson M., Willig T.-N.D., Dianzani I., Ball S., Tchernia G., Klar J.[...], Dahl N.View abstractCategorySequencesSourceMGI: 1333780PubMedEurope PMCNat. Genet. 21:169-175 (1999)Cited in1Mapped to19
A male germ-cell-specific ribosome controls male fertility.Li H., Huo Y., He X., Yao L., Zhang H., Cui Y., Xiao H., Xie W., Zhang D.[...], Sha J.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCNature 0:0-0 (2022)Cited in761Mapped to99+
Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling.Liu M., Deng W., Tang L., Liu M., Bao H., Guo C., Zhang C., Lu J., Wang H.[...], Kong S.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCNat Commun 13:1006-1006 (2022)Mapped to99+
Controlling tissue patterning by translational regulation of signaling transcripts through the core translation factor eIF3c.Fujii K., Zhulyn O., Byeon G.W., Genuth N.R., Kerr C.H., Walsh E.M., Barna M.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCDev Cell 56:2928-2937.e9 (2021)Mapped to85
A p53-dependent translational program directs tissue-selective phenotypes in a model of ribosomopathies.Tiu G.C., Kerr C.H., Forester C.M., Krishnarao P.S., Rosenblatt H.D., Raj N., Lantz T.C., Zhulyn O., Bowen M.E.[...], Barna M.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCDev Cell 56:2089-2102.e11 (2021)Mapped to99+
Calreticulin Deficiency Disturbs Ribosome Biogenesis and Results in Retardation in Embryonic Kidney Development.Serin N., Dihazi G.H., Tayyeb A., Lenz C., Muller G.A., Zeisberg M., Dihazi H.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCInt J Mol Sci 22:5858-5858 (2021)Mapped to46
Diamond Blackfan anemia is mediated by hyperactive Nemo-like kinase.Wilkes M.C., Siva K., Chen J., Varetti G., Youn M.Y., Chae H., Ek F., Olsson R., Lundback T.[...], Sakamoto K.M.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCNat Commun 11:3344-3344 (2020)Mapped to24
RNA-Binding Protein IGF2BP2/IMP2 is a Critical Maternal Activator in Early Zygotic Genome Activation.Liu H.B., Muhammad T., Guo Y., Li M.J., Sha Q.Q., Zhang C.X., Liu H., Zhao S.G., Zhao H.[...], Chen Z.J.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCAdv Sci (Weinh) 6:1900295-1900295 (2019)Mapped to99+
Erythroblast differentiation at spleen in Q137E mutant ribosomal protein S19 gene knock-in C57BL/6J mice.Yamanegi K., Yamada N., Nakasho K., Nishiura H.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCImmunobiology 223:118-124 (2018)Mapped to19
Structure of the human 80S ribosome.Khatter H., Myasnikov A.G., Natchiar S.K., Klaholz B.P.View abstractCategoryStructureSourceMGI: 1333780PubMedEurope PMCNature 520:640-645 (2015)Cited in13Mapped to99+
The chromatin regulator Brpf1 regulates embryo development and cell proliferation.You L., Yan K., Zou J., Zhao H., Bertos N.R., Park M., Wang E., Yang X.J.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCJ. Biol. Chem. 290:11349-11364 (2015)Cited in1Mapped to99+
Hepatic Notch2 deficiency leads to bile duct agenesis perinatally and secondary bile duct formation after weaning.Falix F.A., Weeda V.B., Labruyere W.T., Poncy A., de Waart D.R., Hakvoort T.B., Lemaigre F., Gaemers I.C., Aronson D.C., Lamers W.H.View abstractCategoryExpressionSourceMGI: 1333780PubMedEurope PMCDev Biol 396:201-213 (2014)Mapped to99+
p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia- proteins: RPS19 versus RPL5.Singh S.A., Goldberg T.A., Henson A.L., Husain-Krautter S., Nihrane A., Blanc L., Ellis S.R., Lipton J.M., Liu J.M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCPLoS One 9:e89098-e89098 (2014)Mapped to13
The phosphatase Dullard negatively regulates BMP signalling and is essential for nephron maintenance after birth.Sakaguchi M., Sharmin S., Taguchi A., Ohmori T., Fujimura S., Abe T., Kiyonari H., Komatsu Y., Mishina Y.[...], Nishinakamura R.View abstractCategoriesFunction, Interaction, Subcellular LocationSourceMGI: 1333780PubMedEurope PMCNat Commun 4:1398-1398 (2013)Mapped to99+
Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia.Jaako P., Flygare J., Olsson K., Quere R., Ehinger M., Henson A., Ellis S., Schambach A., Baum C.[...], Karlsson S.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCBlood 118:6087-6096 (2011)Mapped to10
Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome.McGowan K.A., Pang W.W., Bhardwaj R., Perez M.G., Pluvinage J.V., Glader B.E., Malek R., Mendrysa S.M., Weissman I.L.[...], Barsh G.S.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCBlood 118:3622-3633 (2011)Mapped to30
A conditional knockout resource for the genome-wide study of mouse gene function.Skarnes W.C., Rosen B., West A.P., Koutsourakis M., Bushell W., Iyer V., Mujica A.O., Thomas M., Harrow J.[...], Bradley A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCNature 474:337-342 (2011)Mapped to99+
Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.Kondrashov N., Pusic A., Stumpf C.R., Shimizu K., Hsieh A.C., Ishijima J., Shiroishi T., Barna M.View abstractCategoryFunctionSourceMGI: 1333780PubMedEurope PMCCell 145:383-397 (2011)Mapped to99+
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.Diez-Roux G., Banfi S., Sultan M., Geffers L., Anand S., Rozado D., Magen A., Canidio E., Pagani M.[...], Ballabio A.View abstractCategoryExpressionSourceMGI: 1333780PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia.Devlin E.E., Dacosta L., Mohandas N., Elliott G., Bodine D.M.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1333780PubMedEurope PMCBlood 116:2826-2835 (2010)Mapped to10