- persistence of hyaloid vascular system / IMPC
- abnormal cornea morphology / IMPC
- abnormal embryo size / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal tail bud morphology / IMPC
- abnormal forebrain development / IMPC
- embryonic growth retardation / IMPC
- increased circulating sodium level / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased fasting circulating glucose level / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
C57BL/6N-Coq6tm1b(EUCOMM)Hmgu/Ics
| Status | Under development - register interest |
| EMMA ID | EM:16696 |
| Citation information | RRID:IMSR_EM:16696 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-Coq6tm1b(EUCOMM)Hmgu/Ics |
| Alternative name | HEPD0535_5_A07 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Coq6tm1b(EUCOMM)Hmgu |
| Gene/Transgene symbol | Coq6 |
| 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 | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | This mouse line originates from EUCOMM ES clone HEPD0535_5_A07. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sortm1(ACTB-cre,-EGFP)Ics). Click here for more information on EUCOMM final vectors. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Familial steroid-resistant nephrotic syndrome with sensorineural deafness / Orphanet_280406
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- embryonic growth retardation / IMPC
- abnormal embryo size / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal forebrain development / IMPC
- persistence of hyaloid vascular system / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- abnormal cornea morphology / IMPC
- abnormal tail bud morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased circulating sodium level / IMPC
- increased fasting circulating glucose level / IMPC
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