Symbol Name ID |
Nphp3
nephronophthisis 3 (adolescent) MGI:1921275 |
Darker colors indicate more annotations |
Human Phenotypes | Oligohydramnios |
Polyhydramnios |
Disease(s) Associated with NPHP3 | ||
Meckel syndrome 7 | ||
renal-hepatic-pancreatic dysplasia |
Mouse Phenotypes | abnormal embryo turning |
abnormal left-right axis patterning |
|
Availability | Mouse Genotype | ||
Nphp3tm1Cbe/Nphp3tm1Cbe |
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 |
|
|