About   Help   FAQ
Symbol
Name
ID
Wwox
WW domain-containing oxidoreductase
MGI:1931237
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
Increased nuchal translucency
Short neck
Growth delay
Disease(s) Associated with WWOX
autosomal recessive spinocerebellar ataxia 12
developmental and epileptic encephalopathy 28

Mouse Phenotypes
enlarged gallbladder
growth/size/body region phenotype
decreased body weight
cachexia
decreased body size
postnatal growth retardation
enlarged spleen
Availability Mouse Genotype
Wwoxem1Mald/Wwoxem1Mald *
Wwoxtm1.1Mald/Wwoxtm1.1Mald
Wwoxtm1Mald/Wwoxtm1Mald *
Wwoxtm1Ria/Wwoxtm1Ria
Wwoxtm2.1Ria/Wwoxtm2.1Ria
Wwoxtm1Ria/Wwox+

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/14/2024
MGI 6.23
The Jackson Laboratory