- persistence of hyaloid vascular system / IMPC
- small kidney / IMPC
- increased circulating iron level / IMPC
- abnormal retina blood vessel morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- process of degenerative change / IMPC
- granulation tissue / IMPC
- inflammation / IMPC
- developmental and structural abnormality / IMPC
- hydronephrosis / IMPC
C57BL/6NCrl-Fancd2em1(IMPC)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:13625 |
International strain name | C57BL/6NCrl-Fancd2em1(IMPC)Hmgu/Ieg |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Fancd2em1(IMPC)Hmgu |
Gene/Transgene symbol | Fancd2 |
Information from provider
Provider | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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 |
Animals used for archiving | heterozygous C57BL/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Fanconi anemia / Orphanet_84
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- granulation tissue / IMPC
- process of degenerative change / IMPC
- abnormal retina blood vessel morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- persistence of hyaloid vascular system / IMPC
- increased circulating iron level / IMPC
- developmental and structural abnormality / IMPC
- inflammation / IMPC
- hydronephrosis / IMPC
- small kidney / IMPC
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