Excel File Text File All mouse models of purine-pyrimidine metabolic disorder with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      adenine phosphoribosyltransferase deficiency Aprttm1Dwm/Aprttm1Dwm involves: 129P2/OlaHsd * BALB/c J:38450 View
adenine phosphoribosyltransferase deficiency Aprttm1Jat/Aprttm1Jat involves: 129S2/SvPas * Black Swiss J:33255 View
adenine phosphoribosyltransferase deficiency Aprttm1Jat/Aprttm1Jat involves: 129S2/SvPas * C57BL/6J J:33255 View
Lesch-Nyhan syndrome Hprt1b-m3/Hprt1b-m3 B6.129P2-Hprt1b-m3 J:17798 View
Lesch-Nyhan syndrome Hprt1b-m3/Y B6.129P2-Hprt1b-m3 J:17798, J:107966 View
xanthinuria type II Mocosem2(IMPC)Ics/Mocosem2(IMPC)Ics involves: C57BL/6N J:336718 View