Slc4a3 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Slc4a3^tm1Cahb/Slc4a3^tm1Cahb involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal pH regulation	J:104157
	increased susceptibility to pharmacologically induced seizures	J:104157
Slc4a3^tm1Ges/Slc4a3^tm1Ges 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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