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Symbol Name ID |
Wdr62
WD repeat domain 62 MGI:1923696 |
| Darker colors indicate more annotations |
| Human Phenotypes | Premature birth |
Cryptorchidism |
| Disease(s) Associated with WDR62 | ||
| primary autosomal recessive microcephaly 2 with or without cortical malformations |
| Mouse Phenotypes | absent oocytes |
oligozoospermia |
teratozoospermia |
abnormal sperm head morphology |
abnormal manchette disassembly |
decreased sperm progressive motility |
asthenozoospermia |
small seminal vesicle |
abnormal seminiferous tubule morphology |
decreased testis weight |
small testis |
abnormal male meiosis |
female infertility |
male infertility |
reduced fertility |
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| Availability | Mouse Genotype | |||||||||||||||
| Wdr62em1(IMPC)Tcp/Wdr62em1(IMPC)Tcp | ||||||||||||||||
| Wdr62Gt(AF0003)Wtsi/Wdr62Gt(AF0003)Wtsi | ||||||||||||||||
| Wdr62tm3a(EUCOMM)Hmgu/Wdr62tm3a(EUCOMM)Hmgu | ||||||||||||||||
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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