- abnormal kidney cortex morphology / MGI
- cortical renal glomerulopathies / MGI
- kidney hemorrhage / MGI
- decreased body size / MGI
- abnormal renal tubule morphology / MGI
- dilated renal tubules / MGI
- abnormal renal glomerular capsule morphology / MGI
- albuminuria / MGI
- increased urine protein level / MGI
- kidney failure / MGI
- abnormal proximal convoluted tubule morphology / MGI
- glomerulosclerosis / MGI
- abnormal renal glomerulus morphology / MGI
- abnormal podocyte morphology / MGI
- renal/urinary system phenotype / MGI
- increased circulating creatinine level / MGI
- increased blood urea nitrogen level / MGI
- abnormal podocyte foot process morphology / MGI
- absent podocyte slit diaphragm / MGI
- podocyte foot process effacement / MGI
- dilated proximal convoluted tubules / MGI
- abnormal renal tubule epithelium morphology / MGI
- postnatal lethality, complete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- renal glomerulus hypertrophy / MGI
- abnormal kidney arterial blood vessel morphology / MGI
- abnormal glomerular capillary morphology / MGI
- abnormal peritubular capillary morphology / MGI
- abnormal renal glomerulus basement membrane morphology / MGI
- expanded mesangial matrix / MGI
- renal cast / MGI
- mesangiolysis / MGI
- abnormal glomerular capillary endothelium morphology / MGI
- abnormal glomerular endothelium fenestra morphology / MGI
- glomerular crescent / MGI
- dilated glomerular capillary / MGI
- podocyte microvillus transformation / MGI
- podocyte hypertrophy / MGI
C57BL/6NTac-Nphs2tm2(EGFP/cre/ERT2)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:10065 |
International strain name | C57BL/6NTac-Nphs2tm2(EGFP/cre/ERT2)Wtsi/WtsiIeg |
Alternative name | CEPD0091_1_C09 |
Strain type | |
Allele/Transgene symbol | Nphs2tm2(EGFP/cre/ERT2)Wtsi |
Gene/Transgene symbol | Nphs2 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone CEPD0091_1_C09. For further details on the construction of this clone see the page at the IMPC portal. Quality Control/Disclaimer: The structure of the targeted mutation is not fully verified. It is recommended that the recipient confirms the mutation structure by Southern blotting. The Cre expression pattern is expected to mirror that of the host gene, but this may not be fully described and/or may be modified in the targeted allele. Although characterisation of the Cre expression pattern is an objective of EUCOMMTools this is an ongoing process which may be incomplete. It is therefore recommended that the recipient verifies the Cre expression pattern. For the tm2(EGFP/Cre/ERT2) type allele, if the promoter-driven selection cassette is flanked with Rox sites, it may be removed using Dre recombinase. Please be aware that the strain description may be subject to change. For the most recent description please consult the information pages for the appropriate product details at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Genetic steroid-resistant nephrotic syndrome / Orphanet_656
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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