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Organism Name
FVB.Cg-Tbx1tm1Bem/Mmucd
RRID:MMRRC_036811-UCD RRID Copied  
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RRID:MMRRC_036811-UCD
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Organism Information

URL: https://www.mmrrc.org/catalog/sds.php?mmrrc_id=36811

Proper Citation: RRID:MMRRC_036811-UCD

Description: Mus musculus with name FVB.Cg-Tbx1tm1Bem/Mmucd from MMRRC.

Species: Mus musculus

Notes: Research areas: Cardiovascular, Developmental Biology, Models for Human Disease, Sensorineural; Mutation Type: Targeted Mutation ; Collection:

Phenotype: abnormal inner ear morphology [MP:0000026]| abnormal middle ear morphology [MP:0000049]| cleft palate [MP:0000111]| abnormal heart morphology [MP:0000266]| abnormal heart shape [MP:0000277]| double outlet right ventricle [MP:0000284]| absent parathyroid glands [MP:0000680]| athymia [MP:0000705]| cyanosis [MP:0001575]| thymus hypoplasia [MP:0001823]| increased susceptibility to otitis media [MP:0001850]| abnormal motor capabilities/coordination/movement [MP:0002066]| abnormal cardiovascular system morphology [MP:0002127]| abnormal social/conspecific interaction [MP:0002557]| persistent truncus arteriosis [MP:0002633]| abnormal atrioventricular valve morphology [MP:0002745]| increased thigmotaxis [MP:0002797]| abnormal cochlear ganglion morphology [MP:0002855]| abnormal cardiovascular development [MP:0002925]| anotia [MP:0003142]| abnormal response to novel object [MP:0003461]| interrupted aortic arch [MP:0004157]| right aortic arch [MP:0004158]| retroesophageal right subclavian artery [MP:0004160]| cervical aortic arch [MP:0004161]| absent masseter muscle [MP:0004236]| absent pterygoid muscle [MP:0004238]| otic vesicle hypoplasia [MP:0004311]| absent ultimobranchial body [MP:0004914]| abnormal heart ventricle morphology [MP:0005294]| abnormal pharyngeal pouch morphology [MP:0006031]| abnormal fetal atrioventricular canal morphology [MP:0006107]| abnormal cardiac outflow tract development [MP:0006126]| abnormal fourth pharyngeal arch morphology [MP:0006340]| small pharyngeal arch [MP:0006346]| abnormal spatial working memory [MP:0008428]| palatal shelves fail to meet at midline [MP:0009888]| abnormal neuron differentiation [MP:0009937]| ventricular septal defect [MP:0010402]| atrial septal defect [MP:0010403]| abnormal heart and great vessel attachment [MP:0010425]| anomalous pulmonary venous connection [MP:0010440]| supravalvar pulmonary trunk stenosis [MP:0010459]| aberrant origin of the right subclavian artery [MP:0010465]| abnormal coronary vessel morphology [MP:0010551]| common atrioventricular valve [MP:0010607]| neonatal lethality [MP:0011087]| complete penetrance [MP:0011967]| increased or absent threshold for auditory brainstem response [MP:0020351]

Affected Gene: Tbx1

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Data and Source Information

Source: Integrated Animals

Source Database: Mutant Mouse Resource and Research Center (MMRRC)