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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gys1
glycogen synthase 1, muscle
MGI:101805
44 phenotypes from 6 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gys1em1(IMPC)Bay/Gys1+
C57BL/6N-Gys1em1(IMPC)Bay/BayMmucd
decreased body length J:211773
increased bone mineral content J:211773
Gys1em1(IMPC)Bay/Gys1em1(IMPC)Bay
C57BL/6N-Gys1em1(IMPC)Bay/BayMmucd
abnormal embryo size J:211773
abnormal skin coloration J:211773
edema J:211773
preweaning lethality, complete penetrance J:211773
preweaning lethality, incomplete penetrance J:211773
Gys1Gt(OST33395)Lex/Gys1Gt(OST33395)Lex
involves: 129S5/SvEvBrd * 129X1/SvJ * C57BL/6J
abnormal blood circulation J:92245
abnormal fetal cardiomyocyte proliferation J:92245
abnormal heart ventricle morphology J:92245
abnormal interventricular septum morphology J:92245
abnormal pericardial cavity morphology J:92245
blood vessel congestion J:92245
cardiac fibrosis J:92245
decreased glycogen level J:92245
dilated heart atrium J:92245
increased heart weight J:92245
liver hemorrhage J:92245
neonatal lethality, incomplete penetrance J:92245
pulmonary vascular congestion J:92245
thin ventricular wall J:92245
trabecula carnea hypoplasia J:92245
Gys1tm1.1Arte/Gys1+
involves: C57BL/6J
abnormal glycogen homeostasis J:167911
decreased skeletal muscle glycogen level J:167911
Gys1tm1.1Arte/Gys1tm1.1Arte
involves: C57BL/6J
abnormal glycogen homeostasis J:167911
abnormal muscle cell glucose uptake J:167911
decreased skeletal muscle glycogen level J:167911
normal growth/size/body region phenotype J:167911
normal homeostasis/metabolism phenotype J:167911
increased glycogen catabolism rate J:167911
Gys1tm1a(EUCOMM)Wtsi/Gys1tm1a(EUCOMM)Wtsi
involves: C57BL/6J * C57BL/6NTac
normal nervous system phenotype J:216806
perinatal lethality, incomplete penetrance J:216806
Gys1tm1a(EUCOMM)Wtsi/Gys1tm1a(EUCOMM)Wtsi
involves: C57BL/6N
abnormal lung morphology J:300001
decreased lung glycogen level J:300001
Gys1tm1c(EUCOMM)Wtsi/Gys1tm1c(EUCOMM)Wtsi
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL
abnormal operant conditioning behavior J:218886
decreased brain glycogen level J:218886
enhanced paired-pulse facilitation J:218886
impaired synaptic plasticity J:218886
normal nervous system phenotype J:218886
reduced long-term potentiation J:218886
Hprt1tm1(CAG-Gys1*)Jjg/?
Myl1tm1(cre)Sjb/Myl1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
abnormal cellular respiration J:244440
abnormal response to exercise J:244440
decreased aerobic running capacity J:244440
impaired exercise endurance J:244440
increased skeletal muscle glycogen level J:244440
Hprt1tm1(CAG-Gys1*)Jjg/?
Tg(Nes-cre)1Kag/?
involves: 129P2/OlaHsd
impaired autophagy J:210491
increased brain glycogen level J:210491

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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
04/30/2024
MGI 6.23
The Jackson Laboratory