Symbol Name ID |
Trip13
thyroid hormone receptor interactor 13 MGI:1916966 |
Darker colors indicate more annotations |
Human Phenotypes | Premature chromatid separation |
Disease(s) Associated with TRIP13 | |
mosaic variegated aneuploidy syndrome 3 |
Mouse Phenotypes | decreased oocyte number |
abnormal chiasmata formation |
abnormal chromosomal synapsis |
abnormal female meiosis |
arrest of male meiosis |
abnormal synaptonemal complex |
immotile sperm |
abnormal DNA repair |
abnormal double-strand DNA break repair |
|
Availability | Mouse Genotype | |||||||||
Trip13Gt(CH0621)Wtsi/Trip13Gt(CH0621)Wtsi | ||||||||||
Trip13Gt(RRB047)Byg/Trip13Gt(RRB047)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 08/02/2024 MGI 6.24 |
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