Symbol Name ID |
Satb2
special AT-rich sequence binding protein 2 MGI:2679336 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Brachycephaly |
Micrognathia |
Malar flattening |
Microcephaly |
Anterior tibial bowing |
Clinodactyly of the 5th finger |
Broad thumb |
Arachnodactyly |
Broad hallux phalanx |
Toe clinodactyly |
Camptodactyly |
Joint hypermobility |
Generalized osteoporosis |
Disease(s) Associated with SATB2 | ||||||||||||||
SATB2-associated syndrome |
Mouse Phenotypes | impaired osteoblast differentiation |
abnormal cranium morphology |
abnormal frontal bone morphology |
abnormal temporal bone morphology |
abnormal hyoid bone morphology |
abnormal hyoid bone body morphology |
abnormal hyoid bone lesser horn morphology |
abnormal jaw morphology |
abnormal incisor morphology |
absent incisors |
absent lower incisors |
abnormal molar morphology |
brittle teeth |
abnormal mandible morphology |
short mandible |
abnormal maxilla morphology |
abnormal premaxilla morphology |
premaxilla hypoplasia |
short maxilla |
micrognathia |
abnormal nasal bone morphology |
abnormal nasal capsule morphology |
absent thyroid cartilage |
abnormal bone structure |
decreased bone mineral density |
abnormal trabecular bone morphology |
abnormal bone ossification |
abnormal bone mineralization |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||
Satb2Mhdabap002/Satb2Mhdabap002 | |||||||||||||||||||||||||||||
Satb2tm1(cre)Vit/Satb2tm1(cre)Vit | |||||||||||||||||||||||||||||
Satb2tm1Rug/Satb2tm1Rug | |||||||||||||||||||||||||||||
Satb2tm1(cre)Vit/Satb2+ |
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 |
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