Symbol Name ID |
Ift122
intraflagellar transport 122 MGI:1932386 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal dystrophy |
Hypotelorism |
Nystagmus |
Myopia |
Disease(s) Associated with IFT122 | ||||
cranioectodermal dysplasia 1 |
Mouse Phenotypes | abnormal eye morphology |
abnormal eye development |
|
Availability | Mouse Genotype | ||
Ift122sopb/Ift122sopb | |||
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc |
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 08/21/2024 MGI 6.24 |
![]() |
|