- enlarged heart / IMPC
- increased circulating triglyceride level / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal lymph node morphology / IMPC
- abnormal brain morphology / IMPC
- abnormal adrenal gland morphology / IMPC
- increased circulating aspartate transaminase level / IMPC
- abnormal heart morphology / IMPC
- small testis / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased freezing behavior / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- increased circulating chloride level / IMPC
- small adrenal glands / IMPC
- abnormal mammary gland morphology / IMPC
- increased brain size / IMPC
- long tibia / IMPC
- abnormal retina morphology / IMPC
- increased circulating calcium level / IMPC
- abnormal testis morphology / IMPC
- enlarged lymph nodes / IMPC
- embryonic lethality prior to organogenesis / IMPC
B6NCrl;B6N-Atm1Brd Tmem237tm1a(EUCOMM)Hmgu/Ph
Status | Available to order |
EMMA ID | EM:10004 |
Citation information | RRID:IMSR_EM:10004 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 | 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
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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