Symbol Name ID |
Tbx1
T-box 1 MGI:98493 |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Tetany |
Myopathy |
Disease(s) Associated with TBX1 | |||
DiGeorge syndrome | |||
hypoparathyroidism | |||
velocardiofacial syndrome |
Mouse Phenotypes | vascular smooth muscle hypoplasia |
increased vascular smooth muscle cell proliferation |
absent masseter muscle |
absent pterygoid muscle |
absent facial muscle |
abnormal laryngeal muscle morphology |
abnormal myogenesis |
abnormal hypoglossal cord morphology |
abnormal pharyngeal muscle morphology |
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Availability | Mouse Genotype | |||||||||
Tbx1tm1Bem/Tbx1tm1Bem | ||||||||||
Tbx1tm1Pa/Tbx1tm1Pa | ||||||||||
Tbx1tm2.2Bem/Tbx1tm2.2Bem | ||||||||||
Tbx1tm1Bld/Tbx1+ | ||||||||||
Tbx1tm2.1Bem/Tbx1tm2.2Bem Foxg1tm1(cre)Skm/Foxg1+ (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 05/14/2024 MGI 6.23 |
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