C57BL/6NTac-Cdh23ahl+em3H Ush2aem1H/H
Status | Available to order |
EMMA ID | EM:14656 |
International strain name | C57BL/6NTac-Cdh23ahl+em3H Ush2aem1H/H |
Alternative name | USH2A-W3947X-EM1-CDH23-B6 |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Ush2aem1H, |
Gene/Transgene symbol | Ush2a |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mammalian Genetics Unit, Mary Lyon Centre at MRC Harwell |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Phenotypic information | Homozygous:not knownHeterozygous:None reported |
Breeding history | Co-isogenic on original background |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
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
- Usher syndrome type 1 / Orphanet_231169
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
- Retinitis pigmentosa / Orphanet_791
- Usher syndrome type 2 / Orphanet_231178
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