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Symbol
Name
ID
Tbx1
T-box 1
MGI:98493
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Retinal vascular tortuosity
Posterior embryotoxon
Sclerocornea
Cataract
Hypertelorism
Proptosis
Esophoria
Esotropia
Accommodative esotropia
Exotropia
Amblyopia
Disease(s) Associated with TBX1
DiGeorge syndrome
hypoparathyroidism
tetralogy of Fallot
velocardiofacial syndrome

Mouse Phenotypes
abnormal eye morphology
abnormal optic vesicle formation
persistence of hyaloid vascular system
microphthalmia
anophthalmia
Availability Mouse Genotype
Tbx1em1(IMPC)Mbp/Tbx1+
Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+
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
05/07/2024
MGI 6.23
The Jackson Laboratory