Gene DeletionSequence DeletionChromosome DeletionOncogene Protein v-cblMolecular Sequence DataBase SequenceMutationAmino Acid SequenceRetroviridae Proteins, OncogenicTranscobalaminsPhenotypeCell LineVitamin B 12DNA Mutational AnalysisPlasmidsProto-Oncogene ProteinsMice, KnockoutCloning, MolecularProtein BindingChromosome MappingPolymerase Chain ReactionExonsIntrinsic FactorClonal DeletionSignal TransductionPromoter Regions, GeneticAdaptor Proteins, Signal TransducingChromosomes, Human, Pair 22DNA Primerssrc Homology DomainsTranscription, GeneticEscherichia coliBinding SitesRecombinant Fusion ProteinsProtein Structure, TertiaryMutagenesisDNA-Binding ProteinsPhosphorylationTransfectionSaccharomyces cerevisiaeBacterial ProteinsTranscription FactorsMutagenesis, Site-DirectedIn Situ Hybridization, FluorescenceRestriction MappingGenetic Complementation TestHomozygote22q11 Deletion SyndromeRecombination, GeneticAbnormalities, MultipleAllelesRNA, MessengerMice, Inbred C57BLSequence Homology, Amino AcidTyrosineBlotting, SouthernMethylmalonyl-CoA MutaseDNAPoint MutationDiGeorge SyndromeNuclear ProteinsFrameshift MutationGenes, BacterialSequence Analysis, DNARecombinant ProteinsCarrier ProteinsMutagenesis, InsertionalPedigreeGenotypeSaccharomyces cerevisiae ProteinsGene Expression RegulationMembrane ProteinsProteinsRepetitive Sequences, Nucleic AcidGRB2 Adaptor ProteinHeterozygoteKaryotypingSyndromeGene Expression Regulation, BacterialUbiquitinCells, CulturedIntellectual DisabilityINDEL MutationGenesGene DosageFungal ProteinsSequence AlignmentDNA Transposable ElementsGenes, FungalCOS CellsChromosomes, Human, Pair 9Chromosome AberrationsStructure-Activity RelationshipGene RearrangementChromosomes, Human, Pair 11Repressor ProteinsPhosphotyrosineLeukemia, Myelomonocytic, JuvenileGenes, ViralPhosphoproteins