- 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 |
Citation information | RRID:IMSR_EM:07119 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-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
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