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Symbol
Name
ID

Kirrel1
kirre like nephrin family adhesion molecule 1
MGI:1891396

Phenotype annotations related to renal/urinary system

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	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
	Kirrel1^{Gt(VICTR20)20Lex}/Kirrel1^{Gt(VICTR20)20Lex}
	Kirrel1^tm1.2Geno/Kirrel1^tm1.2Geno

Contributing Projects: 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 04/23/2024 MGI 6.23