Symbol Name ID |
Smad3
SMAD family member 3 MGI:1201674 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Cystocele |
Ovarian neoplasm |
Ovarian carcinoma |
Endometrial carcinoma |
Uterine prolapse |
Disease(s) Associated with SMAD3 | |||||
Loeys-Dietz syndrome 3 | |||||
Lynch syndrome | |||||
pancreatic cancer |
Mouse Phenotypes | reproductive system phenotype |
decreased primary ovarian follicle number |
increased primordial ovarian follicle number |
decreased secondary ovarian follicle number |
decreased tertiary ovarian follicle number |
impaired ovarian folliculogenesis |
reduced female fertility |
abnormal fertility/fecundity |
|
Availability | Mouse Genotype | ||||||||
Smad3tm1Cxd/Smad3tm1Cxd | |||||||||
Smad3tm1Par/Smad3tm1Par | |||||||||
Amhr2tm3(cre)Bhr/Amhr2+ Smad3tm1Par/Smad3tm1Zuk (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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