- increased body weight / IMPC
C57BL/6N-Atm1Brd Mfrptm1a(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:05815 |
International strain name | C57BL/6N-Atm1Brd Mfrptm1a(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0555_1_E10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Mfrptm1a(KOMP)Wtsi |
Gene/Transgene symbol | Mfrp |
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 EPD0555_1_E10. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6N Tac |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome / Orphanet_251279
- Nanophthalmos / Orphanet_35612
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased body weight / IMPC
MGI phenotypes (gene matching)
- abnormal retina morphology / MGI
- retinal degeneration / MGI
- abnormal ocular fundus morphology / MGI
- abnormal photoreceptor outer segment morphology / MGI
- abnormal rod electrophysiology / MGI
- abnormal retinal pigment epithelium morphology / MGI
- vision/eye phenotype / MGI
- retinal photoreceptor degeneration / MGI
- thin retinal outer nuclear layer / MGI
- disorganized photoreceptor outer segment / MGI
- retinal spots / MGI
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