No title available.Markus J., Feikova S., Sramko M., Wolff L., Bies J.Cited forNUCLEOTIDE SEQUENCEStrainSwiss WebsterCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (FEB-2003)Cited in2
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/6JCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
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/6JCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (JUN-2024)Cited in99+
Genetic determinants of micronucleus formation in vivo.Adams D.J., Barlas B., McIntyre R.E., Salguero I., van der Weyden L., Barros A., Vicente J.R., Karimpour N., Haider A.[...], White J.K.View abstractSourceMGI: 2443584PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.Ingham N.J., Pearson S.A., Vancollie V.E., Rook V., Lewis M.A., Chen J., Buniello A., Martelletti E., Preite L.[...], Steel K.P.View abstractSourceMGI: 2443584PubMedEurope PMCPLoS Biol. 17:E3000194-E3000194 (2019)Cited in4Mapped to99+
L3MBTL2 regulates chromatin remodeling during spermatogenesis.Meng C., Liao J., Zhao D., Huang H., Qin J., Lee T.L., Chen D., Chan W.Y., Xia Y.View abstractAnnotationL3MBTL2 regulates chromatin remodeling during spermatogenesis.CategoriesFunctionSourceGeneRif: 214669, MGI: 2443584PubMedEurope PMCCell Death Differ 26:2194-2207 (2019)Mapped to7
Placentation defects are highly prevalent in embryonic lethal mouse mutants.Perez-Garcia V., Fineberg E., Wilson R., Murray A., Mazzeo C.I., Tudor C., Sienerth A., White J.K., Tuck E.[...], Hemberger M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2443584PubMedEurope PMCNature 555:463-468 (2018)Cited in1Mapped to99+
Lethal (3) malignant brain tumor-like 2 (L3MBTL2) protein protects against kidney injury by inhibiting the DNA damage-p53-apoptosis pathway in renal tubular cells.Huang H., Xu C., Wang Y., Meng C., Liu W., Zhao Y., Huang X.R., You W., Feng B.[...], Xia Y.View abstractAnnotationL3MBTL2 plays a protective role in kidney injury in part by inhibiting the DNA damage-p53-apoptosis pathway.CategoriesFunction, InteractionSourceGeneRif: 214669PubMedEurope PMCKidney Int 93:855-870 (2018)Mapped to27
Kdm2b Regulates Somatic Reprogramming through Variant PRC1 Complex- Dependent Function.Zhou Z., Yang X., He J., Liu J., Wu F., Yu S., Liu Y., Lin R., Liu H.[...], Chen J.View abstractAnnotationthat PRC1 complex participates in the establishment of pluripotency and identify BMP4 signaling as a modulator of PRC1.1 functionCategoriesFunction, InteractionSourceGeneRif: 214669PubMedEurope PMCCell Rep 21:2160-2170 (2017)Mapped to6
Characterization of non-canonical Polycomb Repressive Complex 1 subunits during early mouse embryogenesis.Eid A., Torres-Padilla M.E.View abstractCategoriesFunctionSourceMGI: 2443584PubMedEurope PMCEpigenetics 11:389-397 (2016)Mapped to17
The polycomb group protein L3mbtl2 assembles an atypical PRC1-family complex that is essential in pluripotent stem cells and early development.Qin J., Whyte W.A., Anderssen E., Apostolou E., Chen H.H., Akbarian S., Bronson R.T., Hochedlinger K., Ramaswamy S.[...], Hock H.View abstractAnnotationDisruption of L3mbtl2 results in embryonic lethality with failure of gastrulation.CategoriesInteractionSourceGeneRif: 214669, MGI: 2443584PubMedEurope PMCCell Stem Cell 11:319-332 (2012)Mapped to99+
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: 2443584PubMedEurope PMCNature 474:337-342 (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 abstractCategoriesExpressionSourceMGI: 2443584PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58.Yokoyama S., Ito Y., Ueno-Kudoh H., Shimizu H., Uchibe K., Albini S., Mitsuoka K., Miyaki S., Kiso M.[...], Asahara H.View abstractCategoriesFunctionSourceMGI: 2443584PubMedEurope PMCDev. Cell 17:836-848 (2009)Cited in1Mapped to99+
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.Hansen G.M., Markesich D.C., Burnett M.B., Zhu Q., Dionne K.M., Richter L.J., Finnell R.H., Sands A.T., Zambrowicz B.P., Abuin A.View abstractCategoriesSequencesSourceMGI: 2443584PubMedEurope PMCGenome Res 18:1670-1679 (2008)Mapped to99+
EUCOMM--the European conditional mouse mutagenesis program.Friedel R.H., Seisenberger C., Kaloff C., Wurst W.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2443584PubMedEurope PMCBrief Funct Genomic Proteomic 6:180-185 (2007)Mapped to99+
The transcriptional landscape of the mammalian genome.Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B.[...], Hayashizaki Y.View abstractCategoriesSequencesSourceMGI: 2443584PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+
Impaired maturation of myeloid progenitors in mice lacking novel Polycomb group protein MBT-1.Arai S., Miyazaki T.View abstractCategoriesFunctionSourceMGI: 2443584PubMedEurope PMCEMBO J. 24:1863-1873 (2005)Cited in1Mapped to19
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A.[...], Sands A.T.View abstractCategoriesPhenotypes & VariantsSourceMGI: 2443584PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+
Proliferation-linked expression of the novel murine gene m4mbt encoding a nuclear zinc finger protein with four mbt domains.Markus J., Feikova S., Sramko M., Wolff L., Bies J.View abstractCategoriesSequences, Subcellular LocationSourceMGI: 2443584PubMedEurope PMCGene 319:117-126 (2003)Cited in1Mapped to6
A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome.Hansen J., Floss T., Van Sloun P., Fuchtbauer E.M., Vauti F., Arnold H.H., Schnutgen F., Wurst W., von Melchner H., Ruiz P.View abstractCategoriesSequencesSourceMGI: 2443584PubMedEurope PMCProc Natl Acad Sci U S A 100:9918-9922 (2003)Mapped to99+
BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.Stryke D., Kawamoto M., Huang C.C., Johns S.J., King L.A., Harper C.A., Meng E.C., Lee R.E., Yee A.[...], Ferrin T.E.View abstractCategoriesSequencesSourceMGI: 2443584PubMedEurope PMCNucleic Acids Res 31:278-281 (2003)Mapped to99+
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R.[...], Hayashizaki Y.View abstractCategoriesSequencesSourceMGI: 2443584PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+