- abnormal skin pigmentation / IMPC
C57BL/6N-Atm1Brd Fryltm1a(KOMP)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:14086 |
International strain name | C57BL/6N-Atm1Brd Fryltm1a(KOMP)Wtsi/WtsiPh |
Alternative name | EPD0553_3_A01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Fryltm1a(KOMP)Wtsi |
Gene/Transgene symbol | Fryl |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0553_3_A01. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- abnormal skin pigmentation / MGI
MGI phenotypes (gene matching)
- hydronephrosis / MGI
- kidney cortex cysts / MGI
- abnormal kidney development / MGI
- decreased body weight / MGI
- postnatal growth retardation / MGI
- kidney inflammation / MGI
- premature death / MGI
- abnormal skin pigmentation / MGI
- abnormal renal tubule morphology / MGI
- enlarged kidney / MGI
- renal interstitial fibrosis / MGI
- kidney cysts / MGI
- abnormal kidney collecting duct morphology / MGI
- dilated kidney collecting duct / MGI
- pale kidney / MGI
- postnatal lethality, incomplete penetrance / MGI
- kidney medulla cysts / MGI
- increased kidney apoptosis / MGI
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