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: 2153480PubMedEurope 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: 2153480PubMedEurope PMCNucleic Acids Res 42:D802-9 (2014)Mapped to99+
Deletion of the prorenin receptor from the ureteric bud causes renal hypodysplasia.Song R., Preston G., Ichihara A., Yosypiv I.V.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2153480PubMedEurope PMCPLoS One 8:e63835-e63835 (2013)Mapped to72
Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear.Lorente-Canovas B., Ingham N., Norgett E.E., Golder Z.J., Karet Frankl F.E., Steel K.P.View abstractAnnotationThe first detailed analysis of the structure and function of the auditory system in Atp6v0a4(-/-) knockout mice is reported.CategoriesFunction, Phenotypes & VariantsSourceGeneRif: 140494, MGI: 2153480PubMedEurope PMCDis Model Mech 6:434-442 (2013)Mapped to5
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: 2153480PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+