Symbol
Name
ID

Sox11
SRY (sex determining region Y)-box 11
MGI:98359

Phenotype annotations related to skeleton

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

Availability

Mouse Genotype

Sox11^tm1Weg/Sox11^tm1Weg

Sox11^tm2.2Weg/Sox11^tm2.2Weg

Sox11^tm1.1Gan/Sox11^tm1.1Gan
Tg(EIIa-cre)C5379Lmgd/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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