C57BL/6N-Atm1Brd Ildr1tm1(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:08997 |
International strain name | C57BL/6N-Atm1Brd Ildr1tm1(KOMP)Wtsi/WtsiH |
Alternative name | EPD0384_1_C10 |
Strain type | |
Allele/Transgene symbol | Ildr1tm1(KOMP)Wtsi, |
Gene/Transgene symbol | Ildr1 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0384_1_C10. 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
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- abnormal organ of Corti morphology / MGI
- deafness / MGI
- abnormal endocochlear potential / MGI
- cochlear inner hair cell degeneration / MGI
- cochlear outer hair cell degeneration / MGI
- abnormal inner hair cell stereociliary bundle morphology / MGI
- sensorineural hearing loss / MGI
- hearing/vestibular/ear phenotype / MGI
- increased or absent threshold for auditory brainstem response / MGI
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