- 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 |
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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