- increased circulating LDL cholesterol level / IMPC
- increased circulating HDL cholesterol level / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating chloride level / IMPC
- abnormal eyelid aperture / IMPC
- increased circulating cholesterol level / IMPC
- process of degenerative change / IMPC
- developmental dysplasia / IMPC
C57BL/6NTac-Ehd1tm1a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05712 |
Citation information | RRID:IMSR_EM:05712 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6NTac-Ehd1tm1a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0114_1_D05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ehd1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ehd1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0114_1_D05. 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 | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating HDL cholesterol level / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating chloride level / IMPC
- developmental dysplasia / IMPC
- increased circulating LDL cholesterol level / IMPC
- increased circulating alanine transaminase level / IMPC
- abnormal eyelid aperture / IMPC
- process of degenerative change / IMPC
MGI phenotypes (gene matching)
- malocclusion / MGI
- seminiferous tubule degeneration / MGI
- abnormal spermatogenesis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- cataract / MGI
- male infertility / MGI
- no abnormal phenotype detected / MGI
- abnormal germ cell morphology / MGI
- no phenotypic analysis / MGI
- increased circulating chloride level / MGI
- abnormal cell migration / MGI
- abnormal eyelid aperture / MGI
- abnormal spermiation / MGI
- decreased testis weight / MGI
- azoospermia / MGI
- abnormal male meiosis / MGI
- cellular phenotype / MGI
- increased mean corpuscular hemoglobin / MGI
- abnormal cell physiology / MGI
- abnormal spermatogonia morphology / MGI
- abnormal spermatocyte morphology / MGI
- abnormal spermatid morphology / MGI
- arrest of spermiogenesis / MGI
- abnormal male germ cell apoptosis / MGI
- abnormal acrosome morphology / MGI
- abnormal Sertoli cell phagocytosis / MGI
- postnatal lethality, incomplete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- decreased fibroblast cell migration / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).