The T-box gene Tbx10 exhibits a uniquely restricted expression pattern during mouse embryogenesis.Bush J.O., Maltby K.M., Cho E.-S., Jiang R.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)StrainC57BL/6JCategorySequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGene Expr. Patterns 3:533-538 (2003)Cited in2Mapped to10
The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.Bush J.O., Lan Y., Jiang R.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2), DISEASEStrainC3H/HeJCategoriesSequences, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 101:7022-7027 (2004)Cited in1Mapped to4
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)CategorySequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
A combined analysis of genomic and primary protein structure defines the phylogenetic relationship of new members of the T-box family.Wattler S., Russ A., Evans M., Nehls M.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 74-251CategorySequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenomics 48:24-33 (1998)Cited in31Mapped to24
A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles.Stankewich M.C., Tse W.T., Peters L.L., Ch'ng Y., John K.M., Stabach P.R., Devarajan P., Morrow J.S., Lux S.E.View abstractCategoriesSequences, Subcellular LocationSourceMGI: 1261436PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 95:14158-14163 (1998)Cited in11Mapped to27
TBX10, a member of the Tbx1-subfamily of conserved developmental genes, is located at human chromosome 11q13 and proximal mouse chromosome 19.Law D.J., Garvey N., Agulnik S.I., Perlroth V., Hahn O.M., Rhinehart R.E., Gebuhr T.C., Silver L.M.CategorySequencesSourceMGI: 1261436PubMedEurope PMCMamm. Genome 9:397-399 (1998)Cited in1Mapped to1
Expression of the winged helix genes fkh-4 and fkh-5 defines domains in the central nervous system.Kaestner K.H., Schuetz G., Monaghan A.P.View abstractCategorySequencesSourceMGI: 1261436PubMedEurope PMCMech. Dev. 55:221-230 (1996)Cited in2Mapped to53
Identification of a member of the MAPKKK family as a potential mediator of TGF-beta signal transduction.Yamaguchi K., Shirakabe K., Shibuya H., Irie K., Ohishi I., Ueno N., Taniguchi T., Nishida E., Matsumoto K.View abstractCategoryFunctionSourceMGI: 1261436PubMedEurope PMCScience 270:2008-2011 (1995)Cited in1Mapped to27
Mitotic index in mouse embryos with 6-aminonicotinamide-induced and inherited cleft lip.Trasler D.G., Leong S.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCTeratology 25:259-265 (1982)Mapped to4
Increased susceptibility to 6-aminonicotinamide-induced cleft lip of heterozygote Dancer mice.Trasler D.G., Kemp D., Trasler T.A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCTeratology 29:101-104 (1984)Mapped to1
A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse.Deol M.S., Lane P.W.CategoriesFunction, SequencesSourceMGI: 1261436PubMedEurope PMCJ Embryol Exp Morphol 16:543-558 (1966)Mapped to10
The identification of the chromosome bearing linkage group XII in the mouse.Eicher E.M.CategorySequencesSourceMGI: 1261436PubMedEurope PMCGenetics 69:267-271 (1971)Mapped to1
Chromosome 19 of the house mouse.Lane P.W., Eicher E.M., Southard J.L.CategorySequencesSourceMGI: 1261436PubMedEurope PMCJ Hered 65:297-300 (1974)Mapped to21
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: 1261436PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Age-related auditory brainstem response (ABR) threshold changes in the dancer mouse mutant.Wenngren B.I., Anniko M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCActa Otolaryngol 106:386-392 (1988)Mapped to1
Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis.Suzuki A., Abdallah N., Gajera M., Jun G., Jia P., Zhao Z., Iwata J.View abstractCategoryFunctionSourceMGI: 1261436PubMedEurope PMCMech Dev 150:21-27 (2018)Mapped to99+
Vestibular hair cell pathology in the dancer mouse mutant.Wenngren B.I., Anniko M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCActa Otolaryngol 107:182-190 (1989)Mapped to1
High-throughput discovery of novel developmental phenotypes.International Mouse Phenotyping ConsortiumDickinson M.E., Flenniken A.M., Ji X., Teboul L., Wong M.D., White J.K., Meehan T.F., Weninger W.J., Westerberg H.[...], Murakami A.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCNature 537:508-514 (2016)Mapped to99+
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data.Koscielny G., Yaikhom G., Iyer V., Meehan T.F., Morgan H., Atienza-Herrero J., Blake A., Chen C.K., Easty R.[...], Parkinson H.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCNucleic Acids Res 42:D802-9 (2014)Mapped to99+
Aberrant frequency tuning and early stereociliary derangement in genetic inner ear disease.Wenngren B.I., Anniko M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1261436PubMedEurope PMCActa Otolaryngol 109:202-212 (1990)Mapped to1
A genome-wide screen to identify transcription factors expressed in pelvic Ganglia of the lower urinary tract.Wiese C.B., Ireland S., Fleming N.L., Yu J., Valerius M.T., Georgas K., Chiu H.S., Brennan J., Armstrong J.[...], Southard-Smith E.M.View abstractCategoryExpressionSourceMGI: 1261436PubMedEurope PMCFront Neurosci 6:130-130 (2012)Mapped to99+
SOX2 regulates the hypothalamic-pituitary axis at multiple levels.Jayakody S.A., Andoniadou C.L., Gaston-Massuet C., Signore M., Cariboni A., Bouloux P.M., Le Tissier P., Pevny L.H., Dattani M.T., Martinez-Barbera J.P.View abstractCategorySequencesSourceMGI: 1261436PubMedEurope PMCJ Clin Invest 122:3635-3646 (2012)Mapped to96
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: 1261436PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
A unique expression pattern of Tbx10 in the hindbrain as revealed by Tbx10(LacZ) allele.Xue X.D., Kimura W., Wang B., Hikosaka K., Itakura T., Uezato T., Matsuda M., Koseki H., Miura N.View abstractAnnotationData show that the LacZ-marked Tbx10 expressing cells are likely to be a subpopulation of interneurons in the ventral pons.CategoryExpressionSourceGeneRif: 109575, MGI: 1261436PubMedEurope PMCGenesis 48:295-302 (2010)Mapped to19
Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse.Sweet H.O., Bronson R.T.View abstractCategorySequencesSourceMGI: 1261436PubMedEurope PMCJ Hered 82:140-144 (1991)Mapped to6