B6NCrl;B6N-Atm1Brd Tmem237tm1a(EUCOMM)Hmgu/Ph
Status | Available to order |
EMMA ID | EM:10004 |
International strain name | B6NCrl;B6N-Atm1Brd Tmem237tm1a(EUCOMM)Hmgu/Ph |
Alternative name | HEPD0752_3_B12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Tmem237tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Tmem237 |
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 | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0752_3_B12. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Joubert syndrome with oculorenal defect / Orphanet_2318
- Joubert syndrome / Orphanet_475
- Joubert syndrome with renal defect / Orphanet_220497
- Meckel syndrome / Orphanet_564
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