Symbol Name ID |
Sqstm1
sequestosome 1 MGI:107931 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Urinary incontinence |
Bone pain |
Apathy |
Personality changes |
Disinhibition |
Disease(s) Associated with SQSTM1 | |||||
frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | |||||
neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | |||||
Paget's disease of bone 3 |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
increased food intake |
decreased locomotor activity |
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Availability | Mouse Genotype | ||||
Sqstm1tm1a(KOMP)Wtsi/Sqstm1tm1a(KOMP)Wtsi | |||||
Sqstm1tm1Keta/Sqstm1tm1Keta | |||||
Sqstm1tm1.1Ewa/Sqstm1tm1.1Ewa Tg(Nes-cre)1Kag/0 (conditional) |
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Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos Tg(Fabp4-cre)1Rev/0 (conditional) |
* | ||||
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos Tg(Nes-cre)1Kln/0 (conditional) |
* | ||||
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
* |
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 04/23/2024 MGI 6.23 |
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