Symbol Name ID |
Sirt1
sirtuin 1 MGI:2135607 |
Darker colors indicate more annotations |
Human Phenotypes | Gliosis |
Cerebellar atrophy |
Neuronal loss in central nervous system |
Gait ataxia |
Bradykinesia |
Chorea |
Depression |
Personality changes |
Dementia |
Hyperreflexia |
Seizure |
Disease(s) Associated with SIRT1 | |||||||||||
Huntington's disease |
Mouse Phenotypes | decreased pituitary gland weight |
small pituitary gland |
abnormal pituitary gland physiology |
decreased brain weight |
exencephaly |
abnormal retina photoreceptor morphology |
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Availability | Mouse Genotype | ||||||
Sirt1tm1Fwa/Sirt1tm1Fwa | |||||||
Sirt1tm1Mcby/Sirt1tm1Mcby | |||||||
Sirt1tm1.1Cxd/Sirt1+ | |||||||
Sirt1tm3Fwa/Sirt1tm3Fwa Tg(Nes-cre)1Kln/0 (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 04/30/2024 MGI 6.23 |
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