About   Help   FAQ
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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
07/05/2024
MGI 6.24
The Jackson Laboratory