Symbol Name ID |
Tbx1
T-box 1 MGI:98493 |
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) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/07/2024 MGI 6.23 |
|
|