- decreased bone mineral density / IMPC
- kyphosis / IMPC
- decreased body length / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- irregularly shaped pupil / IMPC
- abnormal iris morphology / IMPC
- increased circulating alkaline phosphatase level / IMPC
- abnormal spine curvature / IMPC
- abnormal auditory brainstem response / IMPC
- eyelids fail to open / IMPC
- narrow eye opening / IMPC
- absent pinna reflex / IMPC
- increased grip strength / IMPC
- increased circulating magnesium level / IMPC
- abnormal incisor color / IMPC
- decreased bone mineral content / IMPC
- developmental and structural abnormality / IMPC
- mineralisation / IMPC
- developmental dysplasia / IMPC
C57BL/6NTac-Slc20a2tm1a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:07119 |
International strain name | C57BL/6NTac-Slc20a2tm1a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0243_1_C06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slc20a2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Slc20a2 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
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. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
MGI allele-associated human disease models
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 (allele matching)
- abnormal mineral level / MGI
- decreased circulating phosphate level / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal thalamus morphology / MGI
- abnormal basal ganglion morphology / MGI
- microgliosis / MGI
- calcified brain / MGI
- abnormal atrioventricular cushion morphology / MGI
- abnormal forebrain morphology / MGI
- small superior cervical ganglion / MGI
- ectopic cartilage / MGI
- fusion of vertebral arches / MGI
- abnormal vena cava morphology / MGI
- arteriovenous malformation / MGI
- abnormal liver vasculature morphology / MGI
- anomalous pulmonary venous connection / MGI
- abnormal hypoglossal nerve topology / MGI
- retropleural edema / MGI
- subcutaneous edema / MGI
- multiple persisting craniopharyngeal ducts / MGI
- embryo tumor / MGI
- embryo cyst / MGI
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
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).