IMPC phenotypes (allele matching)
- absent pinna reflex / IMPC
C57BL/6N-Atm1Brd Ildr1tm1(KOMP)Wtsi/WtsiH
| Status | Available to order |
| EMMA ID | EM:08997 |
| Citation information | RRID:IMSR_EM:08997 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/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 (gene matching)
- absent pinna reflex / IMPC
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
MGI phenotypes (gene matching)
- abnormal inner ear morphology / MGI
- abnormal organ of Corti morphology / MGI
- organ of Corti degeneration / MGI
- deafness / MGI
- abnormal cochlear hair cell morphology / MGI
- abnormal endocochlear potential / MGI
- no phenotypic analysis / MGI
- absent tunnel of Corti / MGI
- cochlear inner hair cell degeneration / MGI
- cochlear outer hair cell degeneration / MGI
- abnormal outer hair cell stereociliary bundle morphology / MGI
- abnormal inner hair cell stereociliary bundle morphology / MGI
- absent distortion product otoacoustic emissions / MGI
- sensorineural hearing loss / MGI
- homeostasis/metabolism phenotype / MGI
- hearing/vestibular/ear phenotype / MGI
- growth/size/body region phenotype / MGI
- digestive/alimentary phenotype / MGI
- abnormal circulating hormone level / MGI
- increased or absent threshold for auditory brainstem response / MGI
- abnormal tunnel of Corti morphology / MGI