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Symbol
Name
ID
Tgfb2
transforming growth factor, beta 2
MGI:98726
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Dolichocephaly
Retrognathia
Malar flattening
Arachnodactyly
Protrusio acetabuli
Joint hypermobility
Abnormal sternum morphology
Scoliosis
Spondylolisthesis
Disease(s) Associated with TGFB2
Loeys-Dietz syndrome 4

Mouse Phenotypes
abnormal craniofacial bone morphology
abnormal neurocranium morphology
large fontanelles
small frontal bone
small interparietal bone
absent occipital bone
small parietal bone
absent alisphenoid bone
absent pterygoid process
small temporal bone
abnormal mandible morphology
absent mandibular angle
small mandibular condyloid process
small mandibular coronoid process
short mandible
absent maxillary shelf
retrognathia
spina bifida occulta
abnormal humerus morphology
absent deltoid tuberosity
short radius
small olecranon
short ulna
abnormal femur morphology
abnormal trochanter morphology
abnormal clavicle morphology
abnormal sternum morphology
abnormal xiphoid process morphology
abnormal rib morphology
rib fusion
abnormal thoracic cage shape
Availability Mouse Genotype
Tgfb2tm1Doe/Tgfb2tm1Doe

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
04/30/2024
MGI 6.23
The Jackson Laboratory