C57BL/6NCrl-Wfs1em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15045 |
International strain name | C57BL/6NCrl-Wfs1em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Wfs1em1(IMPC)Ccpcz |
Gene/Transgene symbol | Wfs1 |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Wolfram syndrome / Orphanet_3463
- Wolfram-like syndrome / Orphanet_411590
- Autosomal dominant non-syndromic sensorineural deafness type DFNA / Orphanet_90635
- Early-onset nuclear cataract / Orphanet_98991
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