Symbol Name ID |
Sox11
SRY (sex determining region Y)-box 11 MGI:98359 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Short distal phalanx of finger |
Clinodactyly |
Disease(s) Associated with SOX11 | |||
Coffin-Siris syndrome 9 |
Mouse Phenotypes | wide cranial sutures |
abnormal cranium morphology |
small Meckel's cartilage |
abnormal pterygoid process morphology |
abnormal mandible morphology |
mandible hypoplasia |
short mandible |
maxilla hypoplasia |
abnormal phalanx morphology |
abnormal calcaneum morphology |
abnormal talus morphology |
abnormal caudal vertebrae morphology |
abnormal sternebra morphology |
sternebra fusion |
asymmetric sternocostal joints |
abnormal sternum ossification |
abnormal xiphoid process morphology |
abnormal rib morphology |
increased rib number |
abnormal vertebrae morphology |
abnormal lumbar vertebrae morphology |
abnormal bone ossification |
abnormal bone mineralization |
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Availability | Mouse Genotype | |||||||||||||||||||||||
Sox11tm1Weg/Sox11tm1Weg | ||||||||||||||||||||||||
Sox11tm2.2Weg/Sox11tm2.2Weg | ||||||||||||||||||||||||
Sox11tm1.1Gan/Sox11tm1.1Gan Tg(EIIa-cre)C5379Lmgd/0 (conditional) |
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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