- 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
C57BL/6N-Otofem1(IMPC)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:14440 |
International strain name | C57BL/6N-Otofem1(IMPC)Wtsi/WtsiCnbc |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Otofem1(IMPC)Wtsi |
Gene/Transgene symbol | Otof |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6N |
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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