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Symbol
Name
ID
Tbx3
T-box 3
MGI:98495
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Ventricular septal defect
Arrhythmia
Disease(s) Associated with TBX3
ulnar-mammary syndrome

Mouse Phenotypes
abnormal retina vasculature morphology
abnormal retina blood vessel morphology
abnormal vitelline vasculature morphology
absent vitelline blood vessels
abnormal inferior vena cava morphology
abnormal sinoatrial node morphology
decreased sinoatrial node size
sinoatrial node hypoplasia
abnormal cardiovascular development
abnormal heart development
abnormal fetal atrioventricular canal morphology
abnormal heart looping
delayed heart looping
failure of heart looping
ventricular septal defect
pericardial edema
eye hemorrhage
increased cardiac muscle contractility
abnormal sinus arrhythmia
increased heart rate variability
decreased heart rate
sinus bradycardia
irregular heartbeat
abnormal impulse conducting system conduction
absent PR interval
shortened PR interval
atrioventricular block
abnormal P wave
absent P wave
abnormal QRS complex
prolonged QRS complex duration
Availability Mouse Genotype
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
Tbx3tm1.1Moon/Tbx3tm1.1Moon
Tbx3tm1Jcib/Tbx3tm1Jcib
Tbx3tm1Pa/Tbx3tm1Pa
Tbx3tm2.1Moon/Tbx3tm2.1Moon
Tbx3tm3.2Moon/Tbx3tm3.2Moon
Tbx3em1(IMPC)Mbp/Tbx3+
Tbx3tm1.1Moon/Tbx3+
Tbx3tm1.1Moon/Tbx3tm2Moon
Tbx3tm2Moon/Tbx3+
Tbx3tm3.1Moon/Tbx3tm3.1Moon
Tg(GATA6-cre)#Jbeb/0  (conditional)
Tbx3tm3.1Moon/Tbx3tm3.1Moon
Tg(CAG-cre/Esr1*)5Amc/0  (conditional)
Tbx3tm3.1Moon/Tbx3tm3.1Moon
Tg(Mef2c-cre)2Blk/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
05/21/2024
MGI 6.23
The Jackson Laboratory