- decreased startle reflex / MGI
- deafness / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- abnormal cochlear inner hair cell morphology / MGI
- abnormal cochlear inner hair cell physiology / MGI
- abnormal cochlear hair cell stereociliary bundle morphology / MGI
- abnormal inner hair cell synaptic ribbon morphology / MGI
- abnormal miniature excitatory postsynaptic currents / MGI
- hearing/vestibular/ear phenotype / MGI
- absent pinna reflex / MGI
- increased or absent threshold for auditory brainstem response / MGI
B6D2F1 x B6-Otofem1(IMPC)Cnrm/Cnrm
Status | Available to order |
EMMA ID | EM:11955 |
Citation information | RRID:IMSR_EM:11955 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | B6D2F1 x B6-Otofem1(IMPC)Cnrm/Cnrm |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Otofem1(IMPC)Cnrm |
Gene/Transgene symbol | Otof |
Information from provider
Provider | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
MGI phenotypes (gene matching)
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