Symbol Name ID |
Wnt5a
wingless-type MMTV integration site family, member 5A MGI:98958 |
Darker colors indicate more annotations |
Human Phenotypes | Short neck |
Rhizomelia |
Inguinal hernia |
Umbilical hernia |
Short stature |
Disease(s) Associated with WNT5A | |||||
autosomal dominant Robinow syndrome 1 |
Mouse Phenotypes | cleft upper lip |
cleft palate |
decreased tongue size |
short snout |
small ears |
abnormal thoracic cavity morphology |
decreased body length |
decreased body size |
enlarged liver |
|
Availability | Mouse Genotype | |||||||||
Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo | ||||||||||
Wnt5atm1Amc/Wnt5atm1Amc |
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 04/30/2024 MGI 6.23 |
|
|