Symbol Name ID |
Tgfbr1
transforming growth factor, beta receptor I MGI:98728 |
Darker colors indicate more annotations |
Human Phenotypes | Disproportionate tall stature |
Weight loss |
Disease(s) Associated with TGFBR1 | ||
Loeys-Dietz syndrome 1 | ||
Lynch syndrome |
Mouse Phenotypes | abnormal palatal shelf morphology |
palatal shelf hypoplasia |
cleft upper lip |
bilateral cleft upper lip |
unilateral cleft upper lip |
embryonic growth retardation |
decreased embryo size |
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Availability | Mouse Genotype | |||||||
Tgfbr1tm1Karl/Tgfbr1tm1Karl | ||||||||
Tgfbr1tm1Spo/Tgfbr1tm1Spo | ||||||||
Tgfbr1tm1.1Karl/Tgfbr1tm1.1Karl Tg(Nes-cre)1Atp/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 04/09/2024 MGI 6.23 |
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