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Symbol
Name
ID
Tbx1
T-box 1
MGI:98493
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Tbx1tm1Bem/Tbx1tm1Bem
Tbx1tm1Pa/Tbx1tm1Pa
Tbx1tm2.2Bem/Tbx1tm2.2Bem
Tbx1tm1Bld/Tbx1+
Tbx1tm2.1Bem/Tbx1tm2.2Bem
Foxg1tm1(cre)Skm/Foxg1+  (conditional)

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory