Symbol Name ID |
Lamb2
laminin, beta 2 MGI:99916 |
Darker colors indicate more annotations |
Human Phenotypes | Hematuria |
Proteinuria |
Renal interstitial foam cells |
Podocyte foot process effacement |
Mesangial hypercellularity |
Diffuse mesangial sclerosis |
Focal segmental glomerulosclerosis |
Glomerulonephritis |
Hyperechogenic kidneys |
Nephrotic syndrome |
Renal insufficiency |
Stage 5 chronic kidney disease |
Disease(s) Associated with LAMB2 | ||||||||||||
nephrotic syndrome type 5 | ||||||||||||
Pierson syndrome |
Mouse Phenotypes | increased urine protein level |
albuminuria |
glomerulonephritis |
abnormal kidney morphology |
fused podocyte foot processes |
abnormal renal glomerulus basement membrane morphology |
increased renal glomerulus basement membrane thickness |
abnormal renal tubule epithelium morphology |
abnormal kidney physiology |
abnormal glomerular filtration barrier function |
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Availability | Mouse Genotype | ||||||||||
Lamb2npht/Lamb2npht | |||||||||||
Lamb2tm1Jrs/Lamb2tm1Jrs |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 07/05/2024 MGI 6.24 |
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