- abnormal lens morphology / IMPC
- cataract / IMPC
- abnormal retina morphology / IMPC
- abnormal motor coordination/balance / IMPC
- abnormal vocalization / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal retina vasculature morphology / IMPC
- narrow eye opening / IMPC
- impaired glucose tolerance / IMPC
- increased total body fat amount / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased total retina thickness / IMPC
C57BL/6N-Slc20a2tm1b(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:08067 |
International strain name | C57BL/6N-Slc20a2tm1b(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0243_1_C06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slc20a2tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Slc20a2 |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0243_1_C06. 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)26Sor |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTacUSA |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- eyelids fail to open / IMPC
- decreased total retina thickness / IMPC
- cataract / IMPC
- abnormal incisor color / IMPC
- abnormal lens morphology / IMPC
- decreased bone mineral density / IMPC
- decreased bone mineral content / IMPC
- impaired glucose tolerance / IMPC
- abnormal vitreous body morphology / IMPC
- increased circulating magnesium level / IMPC
- developmental and structural abnormality / IMPC
- increased total body fat amount / IMPC
- developmental dysplasia / IMPC
- decreased body length / IMPC
- narrow eye opening / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal vocalization / IMPC
- abnormal spine curvature / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal retina vasculature morphology / IMPC
- mineralisation / IMPC
- irregularly shaped pupil / IMPC
- increased grip strength / IMPC
- kyphosis / IMPC
- absent pinna reflex / IMPC
- abnormal retina morphology / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal iris morphology / IMPC
- abnormal motor coordination/balance / IMPC
MGI phenotypes (gene matching)
- abnormal mineral level / MGI
- decreased circulating phosphate level / MGI
- abnormal atrioventricular cushion morphology / MGI
- abnormal forebrain morphology / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal thalamus morphology / MGI
- small superior cervical ganglion / MGI
- ectopic cartilage / MGI
- fusion of vertebral arches / MGI
- abnormal basal ganglion morphology / MGI
- abnormal vena cava morphology / MGI
- arteriovenous malformation / MGI
- microgliosis / MGI
- abnormal liver vasculature morphology / MGI
- anomalous pulmonary venous connection / MGI
- abnormal hypoglossal nerve topology / MGI
- subcutaneous edema / MGI
- multiple persisting craniopharyngeal ducts / MGI
- embryo tumor / MGI
- embryo cyst / MGI
- hemangioma / MGI
- calcified brain / MGI
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