- mammalian phenotype / IMPC
- increased circulating calcium level / IMPC
- abnormal retina morphology / IMPC
- abnormal eye morphology / IMPC
- decreased IgE level / IMPC
- decreased circulating triglyceride level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- abnormal locomotor activation / IMPC
- increased circulating glucose level / IMPC
- decreased blood urea nitrogen level / IMPC
C57BL/6NTac-Grhl3tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07681 |
International strain name | C57BL/6NTac-Grhl3tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0039_3_C02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Grhl3tm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Grhl3 |
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 EPD0039_3_C02. 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 | 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
- Van der Woude syndrome / Orphanet_888
IMPC phenotypes (allele matching)
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