Symbol Name ID |
Mcm9
minichromosome maintenance 9 homologous recombination repair factor MGI:1918817 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Primary amenorrhea |
Disease(s) Associated with MCM9 | |
ovarian dysgenesis 4 |
Mouse Phenotypes | reproductive system phenotype |
abnormal female germ cell morphology |
decreased oocyte number |
oligozoospermia |
abnormal spermatogonia morphology |
decreased male germ cell number |
decreased primordial germ cell number |
arrest of male meiosis |
abnormal male germ cell apoptosis |
abnormal ovarian follicle number |
decreased primordial ovarian follicle number |
ovary hyperplasia |
abnormal seminiferous tubule morphology |
small testis |
increased ovary tumor incidence |
premature ovarian failure |
female infertility |
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Availability | Mouse Genotype | |||||||||||||||||
Mcm9Gt(AW0655)Wtsi/Mcm9Gt(AW0655)Wtsi | ||||||||||||||||||
Mcm9Gt(XG743)Byg/Mcm9Gt(XG743)Byg | * | |||||||||||||||||
Mcm9tm1.1Geno/Mcm9tm1.1Geno | * | |||||||||||||||||
Mcm9Gt(AW0655)Wtsi/Mcm9Gt(XG743)Byg |
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 05/14/2024 MGI 6.23 |
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