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Symbol
Name
ID
Sox9
SRY (sex determining region Y)-box 9
MGI:98371
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Polyhydramnios
Disease(s) Associated with SOX9
campomelic dysplasia

Mouse Phenotypes
increased trunk neural crest cell apoptosis
abnormal rostral-caudal body axis extension
abnormal limb bud morphology
failure of Mullerian duct regression
impaired cranial neural crest cell differentiation
abnormal trunk neural crest cell morphology
Availability Mouse Genotype
Tg(Prrx1-Sox9,-lacZ)1Haak/Tg(Prrx1-Sox9,-lacZ)1Haak
Sox9tm1Gsr/Sox9tm1Gsr
Krt19tm1(cre)Mmt/Krt19+  (conditional)
Sox9tm1Gsr/Sox9tm1Gsr  (conditional)
Sox9tm1Gsr/Sox9tm1Gsr
Tg(Pax3-cre)1Joe/0  (conditional)
Sox9tm2Crm/Sox9tm2Crm
Tg(Prrx1-cre)1Cjt/0  (conditional)
Sox9tm2Crm/Sox9tm2Crm
Tg(Zp3-cre)93Knw/?  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/11/2018
MGI 6.12
The Jackson Laboratory