- organ of Corti degeneration / MGI
- abnormal stria vascularis morphology / MGI
- abnormal sebaceous gland morphology / MGI
- enlarged sebaceous gland / MGI
- abnormal epidermal layer morphology / MGI
- hyperkeratosis / MGI
- increased anxiety-related response / MGI
- deafness / MGI
- decreased vertical activity / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- abnormal nervous system physiology / MGI
- greasy coat / MGI
- abnormal hair cell physiology / MGI
- cochlear hair cell degeneration / MGI
- abnormal stria vascularis vasculature morphology / MGI
- cochlear inner hair cell degeneration / MGI
- cochlear outer hair cell degeneration / MGI
- absent endocochlear potential / MGI
- decreased endocochlear potential / MGI
- sensorineural hearing loss / MGI
- abnormal blood-inner ear barrier function / MGI
- abnormal amino acid level / MGI
- hearing/vestibular/ear phenotype / MGI
- immune system phenotype / MGI
- decreased dopamine level / MGI
- impaired hearing / MGI
- abnormal cochlear potential / MGI
- absent pinna reflex / MGI
- abnormal cochlear endolymph ionic homeostasis / MGI
- increased or absent threshold for auditory brainstem response / MGI
- decreased threshold for auditory brainstem response / MGI
- increased sebocyte number / MGI
C57BL/6NCrl-Gjb6em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15734 |
Citation information | RRID:IMSR_EM:15734 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 | C57BL/6NCrl-Gjb6em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Gjb6em1(IMPC)Ccpcz |
Gene/Transgene symbol | Gjb6 |
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
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
- Hidrotic ectodermal dysplasia / Orphanet_189
- KID syndrome / Orphanet_477
- Autosomal dominant non-syndromic sensorineural deafness type DFNA / Orphanet_90635
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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