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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Hprt1
hypoxanthine phosphoribosyltransferase 1
MGI:96217
23 phenotypes from 104 alleles in 87 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Hprt1b-m1/Y
involves: 129 * 129S/SvEv 		abnormal motor coordination/balance J:115724
normal behavior/neurological phenotype J:115724
decreased dopamine level J:115724
decreased vertical activity J:115724
Hprt1b-m1/Y
involves: 129S/SvEv 		normal behavior/neurological phenotype J:3354, J:15485
Hprt1b-m2/Y
involves: 129 * 129S/SvEv 		abnormal locomotor activation J:115724
abnormal motor coordination/balance J:115724
normal behavior/neurological phenotype J:115724
decreased dopamine level J:115724
Hprt1b-m2/Y
involves: 129S/SvEv 		normal behavior/neurological phenotype J:3354, J:15485
Hprt1b-m3/Y
B6.129P2-Hprt1b-m3 		abnormal dopaminergic neuron morphology J:17798, J:107966
decreased brain choline acetyltransferase activity J:17798
decreased brain tyrosine 3-monooxygenase activity J:17798
decreased dopamine level J:17798
Hprt1b-m3/Y
involves: 129P2/OlaHsd 		abnormal sleep pattern J:3354
increased grooming behavior J:3354
Hprt1b-m3/Hprt1b-m3
B6.129P2-Hprt1b-m3 		abnormal dopaminergic neuron morphology J:17798
decreased brain choline acetyltransferase activity J:17798
decreased brain tyrosine 3-monooxygenase activity J:17798
decreased dopamine level J:17798
Hprt1tm1(CMV-GFP)Nat/Y
involves: 129P2/OlaHsd * C57BL/6 		no abnormal phenotype detected J:220411
Hprt1tm1(Nfkb1-EGFP)Cjo/Hprt1+
involves: 129P2/OlaHsd * C57BL/6 		no abnormal phenotype detected J:92020
Hprt1tm1(Nfkb1-EGFP)Cjo/Y
involves: 129P2/OlaHsd * C57BL/6 		no abnormal phenotype detected J:92020
Hprt1tm1(TG-cre)1Sasr/Y
involves: C57BL/6 		normal endocrine/exocrine gland phenotype J:208718
normal growth/size/body region phenotype J:208718
Hprt1tm1.1Pobe/?
involves: 129P2/OlaHsd 		no abnormal phenotype detected J:98881
Hprt1tm1a(EUCOMM)Hmgu/Y
C57BL/6N-Hprt1tm1a(EUCOMM)Hmgu/Ieg 		abnormal gait J:165965
Hprt1tm1a(EUCOMM)Hmgu/Hprt1tm1a(EUCOMM)Hmgu
C57BL/6N-Hprt1tm1a(EUCOMM)Hmgu/Ieg 		decreased erythrocyte cell number J:165965
decreased hemoglobin content J:165965
Hprt1tm1Dwm/Hprt1b-m3
involves: 129P2/OlaHsd 		phenotypic reversion J:161048
Hprt1tm1Isrd/Y
involves: C57BL/6 		no abnormal phenotype detected J:117658
Hprt1tm2(CMV-tdTomato)Nat/Y
involves: 129P2/OlaHsd * C57BL/6 		no abnormal phenotype detected J:220411
Hprt1tm2Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm2Detl/Hprt1tm2Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm3Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm3Detl/Hprt1tm3Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm4(Ple88-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm4(Ple88-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm4Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
abnormal reflex J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm4Detl/Hprt1tm4Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
abnormal reflex J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm5(Myh7-GFP,Myh6-CFP)Unc/Y
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J 		no abnormal phenotype detected J:139125
Hprt1tm5Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm5Detl/Hprt1tm5Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm6Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm6Detl/Hprt1tm6Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		abnormal motor capabilities/coordination/movement J:84451
decreased locomotor activity J:84451
neuronal intranuclear inclusions J:84451
premature death J:84451
seizures J:84451
Hprt1tm7(Ple185-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm7(Ple185-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm7Detl/Y
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm7Detl/Hprt1tm7Detl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J 		normal behavior/neurological phenotype J:84451
Hprt1tm8(Ple151-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm8(Ple151-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm9(Ple178-EGFP/cre)Ems/Y
B6.129P2(129S4)-Hprt1tm9(Ple178-EGFP/cre)Ems 		no abnormal phenotype detected J:145689
Hprt1tm10(Ple162-EGFP/cre)Ems/Y
B6.129P2(129S4)-Hprt1tm10(Ple162-EGFP/cre)Ems 		no abnormal phenotype detected J:145689
Hprt1tm11(Ple176-EGFP/cre)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm12(Ple177-EGFP/cre)Ems/Y
B6.129P2(129S4)-Hprt1tm12(Ple177-EGFP/cre)Ems 		no abnormal phenotype detected J:145689
Hprt1tm13(Ple54-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm13(Ple54-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm14(Ple103-EGFP/cre)Ems/Y
B6.129P2(129S4)-Hprt1tm14(Ple103-EGFP/cre)Ems 		no abnormal phenotype detected J:145689
Hprt1tm15(Ple111-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm15(Ple111-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm16(Ple167-EGFP/cre)Ems/Y
B6.129P2(129S4)-Hprt1tm16(Ple167-EGFP/cre)Ems 		no abnormal phenotype detected J:145689
Hprt1tm17(Ple48-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm17(Ple48-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm18(Ple90-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm18(Ple90-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm19(Ple88-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm19(Ple88-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm20(Ple53-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm20(Ple53-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm31(Ple67-EGFP)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm32(Ple112-EGFP)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm33(Ple183-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm33(Ple183-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm34(Ple186-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm34(Ple186-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm37(lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm38(Ple17-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm38(Ple17-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm39(Ple24-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm39(Ple24-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm40(Ple34-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm40(Ple34-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm41(Ple160-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm41(Ple160-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm42(Ple131-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm42(Ple131-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm43(Ple140-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm43(Ple140-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm44(Ple49-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm44(Ple49-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm45(Ple67-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm45(Ple67-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm50(Ple55-lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm53(CAG-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm53(CAG-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm54(Ple233-EGFP)Ems/Y
B6.129P2(Cg)-Hprt1tm54(Ple233-EGFP)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm56(Ple25-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm56(Ple25-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm57(Ple26-lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm58(Ple119-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm58(Ple119-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm59(Ple123-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm59(Ple123-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm62(Ple153-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm62(Ple153-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm63(Ple12-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm63(Ple12-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm64(Ple170-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm64(Ple170-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm65(Ple53-lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm66(Ple5-lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm67(Ple238-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm67(Ple238-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm68(Ple127-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm68(Ple127-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm69(Ple134-lacZ)Ems/Y
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J 		no abnormal phenotype detected J:145689
Hprt1tm70(Ple240-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm70(Ple240-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm71(Ple155-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm71(Ple155-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm72(Ple158-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm72(Ple158-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm73(Ple142-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm73(Ple142-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm74(Ple232-lacZ)Ems/Y
B6.129P2(Cg)-Hprt1tm74(Ple232-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm75(Ple143-lacZ)Ems/Y
B6.Cg-Hprt1tm75(Ple143-lacZ)Ems/Mmjax 		no abnormal phenotype detected J:145689
Hprt1tm331a(Ple275-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm331a(Ple275-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm332(Ple272-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm332(Ple272-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm333(Ple281-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm333(Ple281-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm334a(Ple279-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm334a(Ple279-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm335(Ple277-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm335(Ple277-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm336a(Ple134-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm336a(Ple134-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm337a(Ple285-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm337a(Ple285-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm338a(Ple284-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm338a(Ple284-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm339a(Ple280-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm339a(Ple280-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm340(Ple252-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm340(Ple252-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm341a(Ple273-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm341a(Ple273-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm342a(Ple282-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm342a(Ple282-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm343(Ple270-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm343(Ple270-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm344a(Ple5-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm344a(Ple5-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm345a(icre/ERT2)Ems/Y
B6.Cg-Hprt1tm345a(icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm346a(Ple264-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm346a(Ple264-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm347a(Ple155-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm347a(Ple155-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm348a(Ple265-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm348a(Ple265-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm349a(hs671-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm349a(hs671-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm350a(Ple232-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm350a(Ple232-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm351a(Ple198-icre/ERT2)Ems/Y
B6.Cg-Hprttm351a(Ple198-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm352a(Hspa1a-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm352a(Hspa1a-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm353(Ple274-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm353(Ple274-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm354(Ple283-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm354(Ple283-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm355(Ple286-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm355(Ple286-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm356a(Ple271-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm356a(Ple271-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm357(Ple278-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm357(Ple278-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm358(Ple287-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm358(Ple287-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm359a(Ple94-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm359a(Ple94-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm360a(Ple253-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm360a(Ple253-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm361a(Ple267-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm361a(Ple267-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm362a(Ple304-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm362a(Ple304-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm363a(hs1218-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm363a(hs1218-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm364a(CAG-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm364a(CAG-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm365a(Ple266-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm365a(Ple266-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm366a(Ple67-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm366a(Ple67-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
Hprt1tm367a(Ple251-icre/ERT2)Ems/Y
B6.Cg-Hprt1tm367a(Ple251-icre/ERT2)Ems 		no abnormal phenotype detected J:204202
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory