Symbol Name ID |
Tbx1
T-box 1 MGI:98493 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Retrognathia |
Recurrent sinusitis |
Microcephaly |
Abnormal dental enamel morphology |
Clinodactyly of the 5th finger |
Patellar dislocation |
Scoliosis |
Intervertebral disk degeneration |
Pilonidal sinus |
Cerebral calcification |
Disease(s) Associated with TBX1 | |||||||||||
DiGeorge syndrome | |||||||||||
hypoparathyroidism | |||||||||||
tetralogy of Fallot | |||||||||||
velocardiofacial syndrome |
Mouse Phenotypes | abnormal craniofacial bone morphology |
abnormal cranium morphology |
fusion of basioccipital and basisphenoid bone |
abnormal temporal bone morphology |
temporal bone hypoplasia |
abnormal zygomatic arch morphology |
absent zygomatic arch |
abnormal hyoid bone morphology |
hyoid bone hypoplasia |
abnormal upper incisor morphology |
absent upper incisors |
absent mandibular coronoid process |
short mandible |
micrognathia |
abnormal middle ear ossicle morphology |
abnormal incus morphology |
abnormal malleus morphology |
thin malleus neck |
malleus hypoplasia |
abnormal stapes morphology |
absent stapes |
absent middle ear ossicles |
small cricoid cartilage |
abnormal thyroid cartilage morphology |
small thyroid cartilage |
abnormal cervical atlas morphology |
absent arcus anterior |
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Availability | Mouse Genotype | |||||||||||||||||||||||||||
Tbx1tm1.1Dsr/Tbx1tm1.1Dsr | ||||||||||||||||||||||||||||
Tbx1tm1Dsr/Tbx1tm1Dsr | ||||||||||||||||||||||||||||
Tbx1tm1Pa/Tbx1tm1Pa | ||||||||||||||||||||||||||||
Tbx1tm2Bem/Tbx1tm2Bem | ||||||||||||||||||||||||||||
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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