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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 primitive urogenital sinus morphology
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)
Shhtm1(EGFP/cre)Cjt/Shh+
Sox9tm2Crm/Sox9tm2Crm  (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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory