Symbol Name ID |
Tgfbr1
transforming growth factor, beta receptor I MGI:98728 |
Darker colors indicate more annotations |
Human Phenotypes | Flexion contracture |
Camptodactyly |
Hypertonia |
Hypotonia |
Disease(s) Associated with TGFBR1 | ||||
Loeys-Dietz syndrome 1 | ||||
Lynch syndrome |
Mouse Phenotypes | abnormal vascular smooth muscle morphology |
dilated cardiomyopathy |
decreased cardiac muscle contractility |
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Availability | Mouse Genotype | |||
Tgfbr1tm1Spo/Tgfbr1tm1Spo | ||||
Tgfbr1tm1.1Karl/Tgfbr1tm1.1Karl A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (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 03/19/2024 MGI 6.23 |
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