- myopathy / MGI
- microphthalmia / MGI
- cataract / MGI
- small lens / MGI
- abnormal cornea morphology / MGI
- disorganized secondary lens fibers / MGI
- abnormal lens fiber morphology / MGI
- abnormal lens epithelium morphology / MGI
- abnormal autophagy / MGI
- centrally nucleated skeletal muscle fibers / MGI
- skeletal muscle fiber necrosis / MGI
- skeletal muscle fibrosis / MGI
- decreased grip strength / MGI
C57BL/6N-Atm1Brd Cryabtm1a(EUCOMM)Hmgu/WtsiFlmg
Status | Available to order |
EMMA ID | EM:13173 |
International strain name | C57BL/6N-Atm1Brd Cryabtm1a(EUCOMM)Hmgu/WtsiFlmg |
Alternative name | HEPD0724_3_H06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cryabtm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cryab |
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 EUCOMM ES clone HEPD0724_3_H06. 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 | B.S.R.C. Alexander Fleming, Vari, Greece |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Alpha-B crystallin-related late-onset myopathy / Orphanet_399058
- Fatal infantile hypertonic myofibrillar myopathy / Orphanet_280553
- Familial isolated dilated cardiomyopathy / Orphanet_154
- Early-onset posterior polar cataract / Orphanet_98993
- Early-onset lamellar cataract / Orphanet_441452
- Early-onset nuclear cataract / Orphanet_98991
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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