C57BL/6N-Kcnj10tm1a(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:09266 |
International strain name | C57BL/6N-Kcnj10tm1a(KOMP)Wtsi/H |
Alternative name | EPD0528_2_E06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Kcnj10tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Kcnj10 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from KOMP ES clone EPD0528_2_E06. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Pendred syndrome / Orphanet_705
- EAST syndrome / Orphanet_199343
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal cochlea morphology / MGI
- organ of Corti degeneration / MGI
- abnormal stria vascularis morphology / MGI
- tremors / MGI
- weakness / MGI
- hindlimb paralysis / MGI
- abnormal myelination / MGI
- abnormal oligodendrocyte morphology / MGI
- abnormal spinal cord morphology / MGI
- decreased body weight / MGI
- decreased body size / MGI
- dehydration / MGI
- abnormal posture / MGI
- abnormal motor coordination/balance / MGI
- impaired righting response / MGI
- impaired balance / MGI
- postnatal growth retardation / MGI
- polyuria / MGI
- abnormal motor capabilities/coordination/movement / MGI
- abnormal nervous system electrophysiology / MGI
- abnormal renal tubule morphology / MGI
- cochlear ganglion degeneration / MGI
- decreased urine calcium level / MGI
- abnormal tectorial membrane morphology / MGI
- abnormal scala media morphology / MGI
- vestibular ganglion degeneration / MGI
- vestibular hair cell degeneration / MGI
- vestibular saccular macula degeneration / MGI
- utricular macular degeneration / MGI
- cochlear inner hair cell degeneration / MGI
- cochlear outer hair cell degeneration / MGI
- abnormal crista ampullaris neuroepithelium morphology / MGI
- absent endocochlear potential / MGI
- abnormal cochlear nerve morphology / MGI
- abnormal eye physiology / MGI
- hearing/vestibular/ear phenotype / MGI
- vision/eye phenotype / MGI
- axon degeneration / MGI
- jerky movement / MGI
- abnormal eye electrophysiology / MGI
- abnormal Reissner membrane morphology / MGI
- collapsed Reissner membrane / MGI
- distended Reissner membrane / MGI
- increased urine sodium level / MGI
- impaired hearing / MGI
- absent pinna reflex / MGI
- absent startle reflex / MGI
- abnormal cochlear endolymph ionic homeostasis / MGI
- abnormal spinal cord white matter morphology / MGI
- postnatal lethality, complete penetrance / MGI
- decreased urine creatinine level / MGI
- increased or absent threshold for auditory brainstem response / MGI
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