Excel File Text File All mouse models of congenital disorder of glycosylation with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      alacrima, achalasia, and impaired intellectual development syndrome Gmppatm1d(EUCOMM)Wtsi/Gmppatm1d(EUCOMM)Wtsi involves: C57BL/6N J:305791 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:80661 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * ICR J:80661 View
congenital disorder of glycosylation type IIc Slc35c1tm1Cknr/Slc35c1tm1Cknr involves: 129/Sv * 129P2/OlaHsd * C57BL/6 J:121151 View
      congenital disorder of glycosylation type I Pmm2tm1.1Jins/Pmm2tm2.1Jins involves: 129S6/SvEvTac * C57BL/6J J:23604 View

       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      congenital disorder of glycosylation type I MpiGt(OST90588)Lex/MpiGt(OST90588)Lex involves: 129S5/SvEvBrd * C57BL/6 J:109220 View