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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pax7
paired box 7
MGI:97491
33 phenotypes from 9 alleles in 12 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
\Pax7tm1(cre)Mrc/\Pax7tm1(cre)Mrc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
no abnormal phenotype detected J:93443
\Pax7tm1(cre/Esr1*)Cklr/\Pax7tm1(cre/Esr1*)Cklr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
no abnormal phenotype detected J:157754
\Pax7tm1.1(KOMP)Vlcg/\Pax7+
C57BL/6N-Pax7tm1.1(KOMP)Vlcg/J
decreased circulating triglyceride level J:211773
\Pax7tm1.1(KOMP)Vlcg/\Pax7tm1.1(KOMP)Vlcg
C57BL/6N-Pax7tm1.1(KOMP)Vlcg/J
preweaning lethality, incomplete penetrance J:211773
\Pax7tm1.1(KOMP)Vlcg/\Pax7tm1.1(KOMP)Vlcg
C57BL/6N-Pax7tm1.1(KOMP)Vlcg/Ucd
preweaning lethality, complete penetrance J:211773
\Pax7tm1.1(rtTA)Sjl/\Pax7tm1.1(rtTA)Sjl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
cachexia J:188599
decreased body size J:188599
decreased skeletal muscle weight J:188599
postnatal lethality, incomplete penetrance J:188599
\Pax7tm1.1Thbr/\Pax7tm1.1Thbr
Not Specified
abnormal skeletal muscle satellite cell proliferation J:202693
\Pax7tm1.1Thbr/\Pax7tm1.1Thbr
\Myf5tm1(cre)Mrc/\Myf5+
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
decreased satellite cell number J:202693
\Pax7tm1.1Thbr/\Pax7tm1.1Thbr
\Myf5tm3(cre)Sor/\Myf5+
involves: 129S4/SvJaeSor
decreased body size J:202693
decreased satellite cell number J:202693
decreased skeletal muscle fiber diameter J:202693
decreased skeletal muscle fiber number J:202693
impaired skeletal muscle regeneration J:202693
\Pax7tm1.1Thbr/\Pax7tm1.1Thbr
\Tg(CMV-cre)1Cgn/0
involves: BALB/cJ
abnormal muscle morphology J:202693
decreased satellite cell number J:202693
\Pax7tm1.1Thbr/\Pax7tm2.1(cre/ERT2)Fan
involves: 129S1/Sv * 129X1/SvJ
abnormal muscle regeneration J:202693
abnormal skeletal muscle morphology J:202693
abnormal skeletal muscle satellite cell proliferation J:202693
decreased satellite cell number J:202693
decreased skeletal muscle size J:202693
normal muscle phenotype J:202693
skeletal muscle fibrosis J:202693
skeletal muscle necrosis J:202693
\Pax7tm1.2Fan/\Pax7tm1.2Fan
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
impaired skeletal muscle regeneration J:150962
skeletal muscle fibrosis J:150962
\Pax7tm1Pgr/\Pax7tm1Pgr
involves: 129S2/SvPas
abnormal muscle regeneration J:64793
abnormal nasal capsule morphology J:32018
abnormal serous gland morphology J:32018
normal cellular phenotype J:64793
decreased skeletal muscle fiber diameter J:64793
normal digestive/alimentary phenotype J:32018
normal embryo phenotype J:32018
normal muscle phenotype J:32018
muscle weakness J:64793
normal nervous system phenotype J:32018
pointed snout J:32018
postnatal growth retardation J:32018, J:64793
postnatal lethality, incomplete penetrance J:32018
premature death J:32018
short maxilla J:32018
thin diaphragm muscle J:64793
\Pax7tm2Pgr/\Pax7tm2Pgr
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S2/SvPas * C57BL/6)
abnormal muscle regeneration J:92280
decreased satellite cell number J:92280
\Pax7tm2Pgr/\Pax7tm2Pgr
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S2/SvPas)
abnormal nasal capsule morphology J:32018
abnormal serous gland morphology J:32018
abnormal small intestine morphology J:32018
pointed snout J:32018
postnatal growth retardation J:32018
postnatal lethality, incomplete penetrance J:32018
short maxilla J:32018

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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
03/25/2025
MGI 6.24
The Jackson Laboratory