C57BL/6N-F10tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:06365 |
International strain name | C57BL/6N-F10tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0602_2_G07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | F10tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | F10 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0602_2_G07. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Congenital factor X deficiency / Orphanet_328
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- internal hemorrhage / MGI
- decreased litter size / MGI
- neonatal lethality / MGI
- cardiac fibrosis / MGI
- cardiovascular system phenotype / MGI
- increased bleeding time / MGI
- mortality/aging / MGI
- postnatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- increased heart iron level / MGI
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