Slc26a11 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc26a11
solute carrier family 26, member 11
MGI:2444589

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc26a11^em1(IMPC)Mbp/Slc26a11^em1(IMPC)Mbp C57BL/6NCrl-Slc26a11^em1(IMPC)Mbp/MbpMmucd	abnormal gait	J:211773
	hyperactivity	J:211773
Slc26a11^tm1.1Cidz/Slc26a11^tm1.1Cidz Tg(Pcp2-cre)2Mpin/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal action potential	J:240359
	abnormal afterhyperpolarization	J:240359
	abnormal chloride level	J:240359
	abnormal GABA-mediated receptor currents	J:240359
	normal behavior/neurological phenotype	J:240359
	impaired coordination	J:240359
	increased miniature inhibitory postsynaptic current frequency	J:240359

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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