- increased leukocyte cell number / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- abnormal gait / IMPC
- stereotypic behavior / IMPC
- trunk curl / IMPC
- impaired righting response / IMPC
- increased mean platelet volume / IMPC
- increased lean body mass / IMPC
- decreased blood urea nitrogen level / IMPC
- decreased circulating amylase level / IMPC
C57BL/6N-Atm1Brd Cybatm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:07275 |
International strain name | C57BL/6N-Atm1Brd Cybatm1a(EUCOMM)Wtsi/WtsiIeg |
Alternative name | EPD0372_5_B08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cybatm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cyba |
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 EPD0372_5_B08. 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 | 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
- Chronic granulomatous disease / Orphanet_379
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- impaired righting response / IMPC
- stereotypic behavior / IMPC
- decreased blood urea nitrogen level / IMPC
- persistence of hyaloid vascular system / IMPC
- decreased circulating amylase level / IMPC
- increased lean body mass / IMPC
- cataract / IMPC
- abnormal gait / IMPC
- increased mean platelet volume / IMPC
- trunk curl / IMPC
- increased leukocyte cell number / IMPC
- abnormal lens morphology / IMPC
MGI phenotypes (gene matching)
- impaired swimming / MGI
- impaired balance / MGI
- increased inflammatory response / MGI
- lung inflammation / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal neutrophil physiology / MGI
- absent otoliths / MGI
- absent linear vestibular evoked potential / MGI
- sepsis / MGI
- head tilt / MGI
- hearing/vestibular/ear phenotype / MGI
- abnormal intestinal goblet cell physiology / MGI
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