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Symbol
Name
ID
Tbx1
T-box 1
MGI:98493
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Drooling
Cerebral calcification
Hemiparesis
Delayed speech and language development
Emotional lability
Paranoia
Schizophrenia
Bipolar affective disorder
Aggressive behavior
Attention deficit hyperactivity disorder
Intellectual disability
Global developmental delay
Specific learning disability
Seizure
Disease(s) Associated with TBX1
DiGeorge syndrome
hypoparathyroidism
velocardiofacial syndrome

Mouse Phenotypes
abnormal neuron differentiation
abnormal forebrain morphology
abnormal vestibulocochlear ganglion morphology
abnormal cochlear ganglion morphology
cochlear ganglion degeneration
abnormal geniculate ganglion morphology
abnormal glossopharyngeal ganglion morphology
abnormal trigeminal ganglion morphology
abnormal vagus ganglion morphology
vestibular ganglion degeneration
abnormal cranial nerve morphology
abnormal accessory nerve morphology
abnormal facial nerve morphology
abnormal glossopharyngeal nerve morphology
fusion of glossopharyngeal and vagus nerve
glossopharyngeal nerve hypoplasia
abnormal trigeminal nerve morphology
abnormal mandibular nerve branching
abnormal vagus nerve morphology
abnormal vestibulocochlear nerve morphology
decreased prepulse inhibition
Availability Mouse Genotype
Tbx1nmf219/Tbx1nmf219
Tbx1tm1Bem/Tbx1tm1Bem
Tbx1tm1Bld/Tbx1tm1Bld
Tbx1tm1Pa/Tbx1tm1Pa
Tbx1tm1Bem/Tbx1+
Tbx1tm1Bld/Tbx1+
Tbx1tm2.1Bem/Tbx1tm2.2Bem
Foxg1tm1(cre)Skm/Foxg1+  (conditional)
Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+
Foxg1tm1(cre)Skm/Foxg1+  (conditional)
Mesp1tm2(cre)Ysa/Mesp1+
Tbx1tm1Bld/Tbx1tm3Bld  (conditional)
Tbx1tm2.1Bem/Tbx1tm2.2Bem
Tg(Pax2-cre)1Akg/0  (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