- increased circulating calcium level / IMPC
- abnormal retina morphology / IMPC
- increased startle reflex / IMPC
- increased circulating phosphate level / IMPC
- abnormal eye morphology / 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
- increased circulating amylase level / IMPC
- preweaning lethality, complete penetrance / IMPC
C57BL/6NTac-Grhl3tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07681 |
Citation information | RRID:IMSR_EM:07681 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/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 males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Van der Woude syndrome / Orphanet_888
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased startle reflex / IMPC
- increased circulating phosphate level / IMPC
- increased circulating glucose level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- decreased blood urea nitrogen level / IMPC
- abnormal eye morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal retina morphology / IMPC
- increased circulating amylase level / IMPC
- increased circulating calcium level / IMPC
- decreased circulating triglyceride level / IMPC
- abnormal locomotor activation / IMPC
MGI phenotypes (gene matching)
- cleft palate / MGI
- abnormal vertebrae morphology / MGI
- kyphosis / MGI
- gastrointestinal hemorrhage / MGI
- abnormal stomach epithelium morphology / MGI
- abnormal intestine morphology / MGI
- kinked tail / MGI
- abnormal brain development / MGI
- exencephaly / MGI
- open neural tube / MGI
- scaly skin / MGI
- skin lesions / MGI
- abnormal epidermal layer morphology / MGI
- thick epidermis / MGI
- epidermal hyperplasia / MGI
- abnormal epidermis stratum basale morphology / MGI
- abnormal epidermis stratum granulosum morphology / MGI
- abnormal epidermis stratum corneum morphology / MGI
- eyelids open at birth / MGI
- excessive scratching / MGI
- abnormal lipid level / MGI
- decreased embryo size / MGI
- abnormal dorsal-ventral axis patterning / MGI
- anencephaly / MGI
- neoplasm / MGI
- abnormal neural tube morphology / MGI
- no abnormal phenotype detected / MGI
- delayed neural tube closure / MGI
- abnormal keratinocyte differentiation / MGI
- impaired skin barrier function / MGI
- curly tail / MGI
- spina bifida / MGI
- abnormal neural tube closure / MGI
- abnormal craniofacial development / MGI
- fetal growth retardation / MGI
- abnormal vertebral spinous process morphology / MGI
- absent vertebral arch / MGI
- split vertebrae / MGI
- thick epidermis stratum spinosum / MGI
- increased keratinocyte proliferation / MGI
- abnormal corneocyte envelope morphology / MGI
- abnormal palate development / MGI
- perinatal lethality, complete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- lethality during fetal growth through weaning, complete penetrance / MGI
- spina bifida cystica / MGI
- abnormal periderm development / MGI
- abnormal corneocyte morphology / MGI
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