About Help FAQ

Symbol
Name
ID

Wdr35
WD repeat domain 35
MGI:1921932

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Hydrops fetalis	Polyhydramnios
Disease(s) Associated with WDR35	Hydrops fetalis	Polyhydramnios
cranioectodermal dysplasia 2
short-rib thoracic dysplasia 7 with or without polydactyly

Mouse Phenotypes		absent embryonic cilia	abnormal embryo development	abnormal direction of embryo turning	delayed embryo turning	impaired somite development
Availability	Mouse Genotype	absent embryonic cilia	abnormal embryo development	abnormal direction of embryo turning	delayed embryo turning	impaired somite development
	Wdr35^yeti/Wdr35^yeti
	Wdr35^{tm2a(EUCOMM)Hmgu}/Wdr35^yeti

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 04/16/2024 MGI 6.23