Symbol Name ID |
Efnb1
ephrin B1 MGI:102708 |
Darker colors indicate more annotations |
Human Phenotypes | Thickened nuchal skin fold |
Disease(s) Associated with EFNB1 | |
craniofrontonasal syndrome |
Mouse Phenotypes | abnormal cardiac neural crest cell migration |
abnormal cranial neural crest cell migration |
|
Availability | Mouse Genotype | ||
Efnb1tm1.1Sor/Efnb1tm1.1Sor |
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 |
|
|