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Symbol
Name
ID
Wdr62
WD repeat domain 62
MGI:1923696
Phenotype annotations related to growth/size/body
*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
Availability Mouse Genotype
Wdr62Gt(AF0003)Wtsi/Wdr62Gt(AF0003)Wtsi
Wdr62tm3a(EUCOMM)Hmgu/Wdr62tm3a(EUCOMM)Hmgu *

Contributing Projects:
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
The Jackson Laboratory