Symbol Name ID |
Kirrel1
kirre like nephrin family adhesion molecule 1 MGI:1891396 |
Darker colors indicate more annotations |
Human Phenotypes | Proteinuria |
Podocyte foot process effacement |
Mesangial hypercellularity |
Focal segmental glomerulosclerosis |
Minimal change glomerulonephritis |
Steroid-resistant nephrotic syndrome |
Disease(s) Associated with KIRREL1 | ||||||
nephrotic syndrome type 23 |
Mouse Phenotypes | increased mesangial cell number |
renal glomerulus cyst |
increased urine protein level |
abnormal podocyte foot process morphology |
abnormal podocyte slit diaphragm morphology |
abnormal renal glomerulus morphology |
expanded mesangial matrix |
mesangiolysis |
dilated proximal convoluted tubule |
abnormal renal reabsorption |
|
Availability | Mouse Genotype | ||||||||||
Kirrel1Gt(VICTR20)20Lex/Kirrel1Gt(VICTR20)20Lex | |||||||||||
Kirrel1tm1.2Geno/Kirrel1tm1.2Geno |
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 08/27/2024 MGI 6.24 |
|
|