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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Adar
adenosine deaminase, RNA-specific
MGI:1889575
54 phenotypes from 11 alleles in 12 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Adarem1Stsn/Adarem1Stsn
involves: C57BL/6J
normal embryo phenotype J:308678
normal growth/size/body region phenotype J:308678
normal mortality/aging J:308678
Adarem1Stsn/Adartm1.1Phs
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J
decreased body size J:308678
lethality, complete penetrance J:308678
Adarem1Stsn/Adartm1Olds
involves: 129S/SvEv * C57BL/6J
abnormal homeostasis J:308678
abnormal liver morphology J:308678
abnormal renal glomerulus morphology J:308678
abnormal spleen morphology J:308678
decreased body size J:308678
decreased circulating serum albumin level J:308678
expanded mesangial matrix J:308678
increased circulating alkaline phosphatase level J:308678
lethality, complete penetrance J:308678
Adarem2Qwan/Adarem2Qwan
Not Specified
normal growth/size/body region phenotype J:325221
normal immune system phenotype J:325221
Adarem3Qwan/Adarem3Qwan
Not Specified
abnormal chemokine level J:325221
decreased body size J:325221
decreased body weight J:325221
normal immune system phenotype J:325221
increased circulating interleukin-1 level J:325221
increased circulating interleukin-6 level J:325221
increased circulating interleukin-17 level J:325221
increased CXCL10 level J:325221
Adartm1.1Knk/Adar+
involves: 129S1/Sv * 129X1/SvJ
normal mortality/aging J:87714
Adartm1.1Knk/Adartm1.1Knk
involves: 129S1/Sv * 129X1/SvJ
abnormal apoptosis J:87714
embryonic lethality during organogenesis, complete penetrance J:87714
normal hematopoietic system phenotype J:87714
increased embryonic tissue cell apoptosis J:87714
increased hepatocyte apoptosis J:87714
increased sensitivity to induced cell death J:87714
internal hemorrhage J:87714
pale yolk sac J:87714
Adartm1.1Phs/Adartm2Phs
Tg(Mx1-cre)1Cgn/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
abnormal definitive hematopoiesis J:142338
liver hypoplasia J:142338
postnatal lethality, complete penetrance J:142338
Adartm1.1Phs/Adartm2Phs
Tg(Tal1-cre/ERT)42-056Jrg/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal hematopoietic stem cell morphology J:142338
decreased bone marrow cell number J:142338
Adartm1b(EUCOMM)Wtsi/Adar+
B6N(Cg)-Adartm1b(EUCOMM)Wtsi/J
decreased circulating glucose level J:211773
Adartm1b(EUCOMM)Wtsi/Adartm1b(EUCOMM)Wtsi
B6N(Cg)-Adartm1b(EUCOMM)Wtsi/J
abnormal embryo size J:211773
abnormal neural tube closure J:211773
abnormal placenta size J:211773
pale yolk sac J:211773
pallor J:211773
preweaning lethality, complete penetrance J:211773
Adartm1Knk/Adartm1Knk
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA
abnormal circulating enzyme level J:87714
abnormal liver morphology J:87714
decreased body size J:87714
normal hematopoietic system phenotype J:87714
hyperglycemia J:87714
increased circulating alanine transaminase level J:87714
increased circulating alkaline phosphatase level J:87714
increased circulating aspartate transaminase level J:87714
increased circulating lactate dehydrogenase level J:87714
increased hepatocyte apoptosis J:87714
Adartm1Olds/Adartm1Olds
involves: 129S/SvEv * C57BL/6J
abnormal cell physiology J:169014
embryonic lethality during organogenesis, complete penetrance J:169014
increased susceptibility to Orthomyxoviridae infection J:169014
increased susceptibility to Paramyxoviridae infection J:169014
Adartm1Phs/Adartm1Phs
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal liver development J:87715
absent common myeloid progenitor cells J:87715
embryonic growth retardation J:87715
embryonic lethality during organogenesis, complete penetrance J:87715
impaired hematopoiesis J:87715
small liver J:87715
Adartm1Phs/Adartm1Phs
involves: 129S1/Sv * 129X1/SvJ * NMRI
abnormal liver development J:87715
absent common myeloid progenitor cells J:87715
embryonic growth retardation J:87715
embryonic lethality during organogenesis, complete penetrance J:87715
impaired hematopoiesis J:87715
small liver J:87715
Adartm2Knk/Adar+
chimera involves: 129S1/Sv * 129X1/SvJ * FVB/N
abnormal embryonic erythropoiesis J:65981
abnormal liver development J:65981
embryonic lethality during organogenesis, complete penetrance J:65981
Adartm2Phs/Adartm2Phs
B6.Cg-Adartm2Phs
abnormal circulating interferon-beta level J:142338
abnormal hematopoietic stem cell morphology J:142338
increased circulating interferon-alpha level J:142338
Adartm2Phs/Adartm2Phs
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal liver development J:87715
absent common myeloid progenitor cells J:87715
embryonic growth retardation J:87715
embryonic lethality during organogenesis, complete penetrance J:87715
impaired hematopoiesis J:87715
small liver J:87715
Adartm2Phs/Adartm2Phs
involves: 129S1/Sv * 129X1/SvJ * NMRI
abnormal liver development J:87715
absent common myeloid progenitor cells J:87715
embryonic growth retardation J:87715
embryonic lethality during organogenesis, complete penetrance J:87715
impaired hematopoiesis J:87715
small liver J:87715

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory