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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc4a3
solute carrier family 4 (anion exchanger), member 3
MGI:109350
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc4a3tm1Cahb/Slc4a3tm1Cahb
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal pH regulation J:104157
increased susceptibility to pharmacologically induced seizures J:104157
Slc4a3tm1Ges/Slc4a3tm1Ges
involves: 129X1/SvJ
abnormal astrocyte morphology J:129363
abnormal eye electrophysiology J:129363
abnormal optic nerve morphology J:129363
abnormal retina rod bipolar cell morphology J:129363
abnormal retina vasculature morphology J:129363
blindness J:129363
increased retina apoptosis J:129363

Contributing Projects:
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
04/30/2024
MGI 6.23
The Jackson Laboratory