GDNF-RET signalling is at the core of the signalling network in kidney development. These signalling interactions between the metanephric mesenchyme and the nephric duct are crucial to ensure the induction of the ureter from the nephric duct.This pathway was inferred from Mus musculus pathway [WP4820_109222.gpml] with a 100.0% conversion rate.GDNF-RET signalling is at the core of the signalling network in kidney development. These signalling interactions between the metanephric mesenchyme and the nephric duct are crucial to ensure the induction of the ureter from the nephric duct.
Pathway converted from original mouse pathway WP4820.c1eHomology Mapping from Mus musculus to Homo sapiens: Original ID = S:P35546Homology Mapping from Mus musculus to Homo sapiens: Original ID = S:P97785Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000037211Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000050295Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000025902Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000025932f46f55Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000063632Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000004231f46Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000031665f46f27Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000068122Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000046714Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000022144Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000015619Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000046743Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000052516Homology Mapping from Mus musculus to Homo sapiens: Original ID = S:Q61602Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000021835Homology Mapping from Mus musculus to Homo sapiens: Original ID = S:Q9D0P8Homology Mapping from Mus musculus to Homo sapiens: Original ID = S:Q9D6H2Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000018698Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000031558Homology Mapping from Mus musculus to Homo sapiens: Original ID = S:Q02248Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000074934Homology Mapping from Mus musculus to Homo sapiens: Original ID = En:ENSMUSG00000022144fdaregulatory pathwayPW:0000004Pathway Ontology15141091PubMedSIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.Proc Natl Acad Sci U S A2004Ruf RGXu PXSilvius DOtto EABeekmann FMuerb UTKumar SNeuhaus TJKemper MJRaymond RM JrBrophy PDBerkman JGattas MHyland VRuf EMSchwartz CChang EHSmith RJStratakis CAWeil DPetit CHildebrandt F9361030PubMedClustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.Hum Mol Genet1997Abdelhak SKalatzis VHeilig RCompain SSamson DVincent CLevi-Acobas FCruaud CLe Merrer MMathieu MKönig RVigneron JWeissenbach JPetit CWeil D16971658PubMedPrevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study.J Am Soc Nephrol2006Weber SMoriniere VKnüppel TCharbit MDusek JGhiggeri GMJankauskiené AMir SMontini GPeco-Antic AWühl EZurowska AMMehls OAntignac CSchaefer FSalomon R9425907PubMedMutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.Nat Genet1998Kohlhase JWischermann AReichenbach HFroster UEngel WCAKUTDOID:0080205Disease32030122PubMedDuplex kidney formation: developmental mechanisms and genetic predisposition.F1000Res2020Kozlov VMSchedl A