Symbol Name ID |
Wdr62
WD repeat domain 62 MGI:1923696 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Failure to thrive |
Growth delay |
Disease(s) Associated with WDR62 | |||
primary autosomal recessive microcephaly | |||
primary autosomal recessive microcephaly 2 with or without cortical malformations |
Mouse Phenotypes | growth/size/body region phenotype |
microcephaly |
proportional dwarf |
fetal growth retardation |
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Availability | Mouse Genotype | ||||
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 05/21/2024 MGI 6.23 |
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