- 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 |
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)
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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