C57BL/6N-Frs2tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:05929 |
International strain name | C57BL/6N-Frs2tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0471_4_B06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Frs2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Frs2 |
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 EPD0471_4_B06. 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
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal heart morphology / MGI
- microcephaly / MGI
- decreased brain size / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal cerebellum development / MGI
- abnormal cerebellar plate morphology / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- decreased embryo size / MGI
- abnormal limb morphology / MGI
- abnormal pharyngeal arch morphology / MGI
- nervous system phenotype / MGI
- embryonic growth retardation / MGI
- decreased fetal size / MGI
- abnormal embryonic/fetal subventricular zone morphology / MGI
- abnormal trophoblast giant cell morphology / MGI
- abnormal rostral-caudal axis patterning / MGI
- craniofacial phenotype / MGI
- vision/eye phenotype / MGI
- thin cerebral cortex / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal visceral endoderm morphology / MGI
- abnormal primitive streak elongation / MGI
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