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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Sqstm1
sequestosome 1
MGI:107931
70 phenotypes from 10 alleles in 14 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Sqstm1em1Kmts/Sqstm1+
involves: C57BL/6N
abnormal forestomach morphology J:342766
enlarged liver J:342766
esophagus hyperplasia J:342766
hyperkeratosis J:342766
hypoglycemia J:342766
increased blood urea nitrogen level J:342766
increased circulating aspartate transaminase level J:342766
increased circulating cholesterol level J:342766
increased circulating creatinine level J:342766
postnatal growth retardation J:342766
Sqstm1em2Kmts/Sqstm1em2Kmts
involves: C57BL/6N
normal growth/size/body region phenotype J:342766
normal reproductive system phenotype J:342766
Sqstm1tm1.1Ewa/Sqstm1tm1.1Ewa
Tg(Nes-cre)1Kag/0
involves: C57BL/6J
increased abdominal adipose tissue amount J:201732
increased body weight J:201732
increased food intake J:201732
Sqstm1tm1.1Sral/Sqstm1+
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
abnormal bone structure J:173755
abnormal osteoclast differentiation J:173755
increased osteoclast cell number J:173755
Sqstm1tm1.1Sral/Sqstm1tm1.1Sral
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
abnormal bone mineralization J:173755
abnormal bone ossification J:173755
abnormal bone structure J:173755
abnormal compact bone morphology J:173755
abnormal osteoclast differentiation J:173755
abnormal osteoclast morphology J:173755
abnormal trabecular bone morphology J:173755
increased osteoclast cell number J:173755
Sqstm1tm1a(KOMP)Wtsi/Sqstm1tm1a(KOMP)Wtsi
B6JTyr;B6N-Sqstm1tm1a(KOMP)Wtsi/Wtsi
abnormal behavior J:175295
decreased circulating glucose level J:175295
decreased mean corpuscular hemoglobin J:175295
increased body length J:175295
Sqstm1tm1Hwl/Sqstm1tm1Hwl
B6.129P2-Sqstm1tm1Hwl
abnormal mitochondrial physiology J:181228
abnormal respiratory electron transport chain J:181228
decreased oxygen consumption J:181228
decreased subcutaneous adipose tissue amount J:181228
lordokyphosis J:181228
oxidative stress J:181228
premature aging J:181228
premature death J:181228
rough coat J:181228
Sqstm1tm1Jjw/Sqstm1tm1Jjw
involves: 129 * C57BL/6
abnormal osteoclast differentiation J:141179
abnormal osteoclast physiology J:141179
normal skeleton phenotype J:141179
Sqstm1tm1Jmos/Sqstm1tm1Jmos
involves: 129S1/Sv * 129X1/SvJ
abnormal aerobic respiration J:194291
Sqstm1tm1Jmos/Sqstm1tm1Jmos
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal osteoclast differentiation J:90010
decreased interleukin-6 secretion J:90010
decreased osteoclast cell number J:90010
Sqstm1tm1Keta/Sqstm1tm1Keta
B6.129-Sqstm1tm1Keta
impaired glucose tolerance J:201732
increased body weight J:201732
increased circulating leptin level J:201732
increased food intake J:201732
increased neuron number J:201732
Sqstm1tm1Keta/Sqstm1tm1Keta
involves: 129
hyperglycemia J:130839
increased susceptibility to age related obesity J:130839
Sqstm1tm1Keta/Sqstm1tm1Keta
involves: 129 * C57BL/6N
abnormal bone remodeling J:264183
abnormal bone structure J:264183
abnormal osteoblast physiology J:264183
abnormal osteoclast differentiation J:264183
abnormal osteoclast physiology J:264183
abnormal trabecular bone morphology J:264183
decreased bone trabecular spacing J:264183
increased bone mineral density of femur J:264183
increased bone trabecula number J:264183
increased bone volume J:264183
obese J:264183
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos
Lyz2tm1(cre)Ifo/Lyz2+
involves: 129P2/OlaHsd
normal cellular phenotype J:194291
normal growth/size/body region phenotype J:194291
normal homeostasis/metabolism phenotype J:194291
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: C57BL/6 * DBA
normal behavior/neurological phenotype J:194291
normal growth/size/body region phenotype J:194291
normal homeostasis/metabolism phenotype J:194291
normal liver/biliary system phenotype J:194291
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos
Tg(Fabp4-cre)1Rev/0
Not Specified
abnormal brown adipose tissue thermogenesis J:194291
abnormal mitochondrial ATP synthesis coupled electron transport J:194291
abnormal mitochondrial crista morphology J:194291
normal behavior/neurological phenotype J:194291
decreased core body temperature J:194291
decreased energy expenditure J:194291
decreased locomotor activity J:194291
disorganized mitochondrial cristae J:194291
hepatic steatosis J:194291
impaired glucose tolerance J:194291
increased body weight J:194291
increased brown fat cell lipid droplet size J:194291
increased lean body mass J:194291
increased total body fat amount J:194291
increased white fat cell size J:194291
insulin resistance J:194291
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * DBA
normal behavior/neurological phenotype J:194291
normal growth/size/body region phenotype J:194291

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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