- 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
C57BL/6NTac-Coq6tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:09952 |
International strain name | C57BL/6NTac-Coq6tm1a(EUCOMM)Hmgu/IcsOrl |
Alternative name | HEPD0535_5_A07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Coq6tm1a(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 IKMC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac |
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 (gene matching)
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