- 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 |
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)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).