- abnormal retina morphology / IMPC
- increased circulating free fatty acids level / IMPC
- increased lean body mass / IMPC
- increased red blood cell distribution width / IMPC
- decreased circulating fructosamine level / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased fasting circulating glucose level / IMPC
C57BL/6NTac-Map3k1tm1a(KOMP)Wtsi/WtsiFlmg
Status | Available to order |
EMMA ID | EM:13176 |
International strain name | C57BL/6NTac-Map3k1tm1a(KOMP)Wtsi/WtsiFlmg |
Alternative name | EPD0287_3_A11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Map3k1tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Map3k1 |
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 EPD0287_3_A11. 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
- 46,XY complete gonadal dysgenesis / Orphanet_242
- 46,XY partial gonadal dysgenesis / Orphanet_251510
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased red blood cell distribution width / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal retina morphology / IMPC
- abnormal startle reflex / IMPC
- increased lean body mass / IMPC
- decreased fasting circulating glucose level / IMPC
- increased bone mineral content / IMPC
- increased circulating free fatty acids level / IMPC
- decreased circulating fructosamine level / IMPC
MGI phenotypes (gene matching)
- organ of Corti degeneration / MGI
- microphthalmia / MGI
- eyelids open at birth / MGI
- corneal opacity / MGI
- abnormal eyelid morphology / MGI
- abnormal pinna reflex / MGI
- heart inflammation / MGI
- abnormal eye morphology / MGI
- abnormal keratinocyte morphology / MGI
- exophthalmos / MGI
- early eyelid opening / MGI
- increased cardiomyocyte apoptosis / MGI
- abnormal retinal layer morphology / MGI
- abnormal heart left ventricle morphology / MGI
- decreased cochlear inner hair cell number / MGI
- increased cochlear outer hair cell number / MGI
- cochlear outer hair cell degeneration / MGI
- increased response of heart to induced stress / MGI
- abnormal vascular wound healing / MGI
- abnormal eye physiology / MGI
- hearing/vestibular/ear phenotype / MGI
- immune system phenotype / MGI
- abnormal vascular smooth muscle physiology / MGI
- decreased ventricle muscle contractility / MGI
- congestive heart failure / MGI
- abnormal eyelid fusion / MGI
- abnormal eyelid development / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- impaired fibroblast cell migration / MGI
- increased or absent threshold for auditory brainstem response / MGI
- abnormal eyelid margin morphology / MGI
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