Symbol Name ID |
Tsc1
TSC complex subunit 1 MGI:1929183 |
Darker colors indicate more annotations |
Human Phenotypes | Gastrointestinal hemorrhage |
Chylopericardium |
Cardiac rhabdomyoma |
Pulmonary lymphangiomyomatosis |
Wolff-Parkinson-White syndrome |
Abnormality of the lymphatic system |
Lymphadenopathy |
Disease(s) Associated with TSC1 | |||||||
lymphangioleiomyomatosis | |||||||
tuberous sclerosis 1 |
Mouse Phenotypes | abnormal retina vasculature morphology |
pulmonary vascular congestion |
increased angiogenesis |
abnormal myocardial fiber morphology |
increased myocardial fiber size |
abnormal fetal cardiomyocyte morphology |
enlarged heart |
pericardial effusion |
dilated cardiomyopathy |
decreased cardiac muscle contractility |
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Availability | Mouse Genotype | ||||||||||
Tsc1tm1.1Djk/Tsc1tm1.1Djk | |||||||||||
Tsc1tm1Chdl/Tsc1tm1Chdl | |||||||||||
Tsc1tm1Hin/Tsc1tm1Hin | |||||||||||
Myl2tm1(cre)Krc/Myl2+ Tsc1tm1Djk/Tsc1tm1Djk (conditional) |
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Tg(Tal1-cre/ERT)1Jrg/0 Tsc1tm1Djk/Tsc1tm1Djk (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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