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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc20a2
solute carrier family 20, member 2
MGI:97851
44 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2+
C57BL/6N-Slc20a2tm1a(EUCOMM)Wtsi/Wtsi
increased grip strength J:211773
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2tm1a(EUCOMM)Wtsi
C57BL/6N-Slc20a2tm1a(EUCOMM)Wtsi/Wtsi
abnormal atrioventricular cushion morphology J:239583
abnormal auditory brainstem response J:211773
abnormal forebrain morphology J:239583
abnormal hypoglossal nerve topology J:239583
abnormal incisor color J:211773
abnormal iris morphology J:211773
abnormal lens morphology J:211773
abnormal liver vasculature morphology J:239583
abnormal spine curvature J:211773
abnormal vena cava morphology J:239583
absent pinna reflex J:211773
anomalous pulmonary venous connection J:239583
arteriovenous malformation J:239583
cataract J:211773
decreased body length J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
ectopic cartilage J:239583
embryo cyst J:239583
embryo tumor J:239583
eyelids fail to open J:211773
fusion of vertebral arches J:239583
increased circulating alkaline phosphatase level J:211773
increased circulating magnesium level J:211773
increased hemangioma incidence J:239583
irregularly shaped pupil J:211773
kyphosis J:211773
multiple persisting craniopharyngeal ducts J:239583
narrow eye opening J:211773
small superior cervical ganglion J:239583
subcutaneous edema J:239583
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2tm1a(EUCOMM)Wtsi
C57BL/6NTac-Slc20a2tm1a(EUCOMM)Wtsi/Ieg
abnormal basal ganglion morphology J:223197
abnormal cerebral cortex morphology J:223197
abnormal mineral level J:234034
abnormal thalamus morphology J:223197
calcified brain J:223197
decreased circulating phosphate level J:234034
microgliosis J:223197
Slc20a2tm1b(EUCOMM)Wtsi/Slc20a2+
C57BL/6N-Slc20a2tm1b(EUCOMM)Wtsi/Ieg
abnormal lens morphology J:211773
abnormal motor coordination/balance J:211773
abnormal vocalization J:211773
impaired glucose tolerance J:211773
increased total body fat amount J:211773
Slc20a2tm1b(EUCOMM)Wtsi/Slc20a2tm1b(EUCOMM)Wtsi
C57BL/6N-Slc20a2tm1b(EUCOMM)Wtsi/Ieg
abnormal lens morphology J:211773
cataract J:211773
preweaning lethality, incomplete penetrance J:211773

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory