Symbol Name ID |
Sox9
SRY (sex determining region Y)-box 9 MGI:98371 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cardiovascular system morphology |
Abnormal heart morphology |
Disease(s) Associated with SOX9 | ||
campomelic dysplasia |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal angiogenesis |
conotruncal ridge hypoplasia |
abnormal fetal atrioventricular canal morphology |
abnormal atrioventricular cushion morphology |
abnormal heart valve development |
abnormal atrioventricular valve development |
abnormal atrioventricular valve morphology |
abnormal mitral valve morphology |
calcified mitral valve |
abnormal tricuspid valve morphology |
abnormal interatrial septum morphology |
thick interventricular septum |
heart hypoplasia |
abnormal heart valve morphology |
abnormal semilunar valve morphology |
thick heart valve cusps |
pericardial edema |
abnormal blood circulation |
congestive heart failure |
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Availability | Mouse Genotype | ||||||||||||||||||||
Sox9tm2.1Crm/Sox9tm2.1Crm | |||||||||||||||||||||
Tg(Prrx1-Sox9,-lacZ)1Haak/? | * | ||||||||||||||||||||
Sox9tm1Gsr/Sox9tm1Gsr Krt19tm1(cre)Mmt/Krt19+ (conditional) |
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Sox9tm1Gsr/Sox9tm1Gsr Tg(Tek-cre)1Ywa/0 (conditional) |
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Sox9tm1Gsr/Sox9tm1Gsr Tg(Col2a1-cre)1Bhr/0 (conditional) |
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Sox9tm2Crm/Sox9tm2Crm Tg(Prrx1-cre)1Cjt/0 (conditional) |
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Sox9tm1Gsr/Sox9+ Tg(Col2a1-cre)1Bhr/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 04/23/2024 MGI 6.23 |
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