Slc26a9 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc26a9
solute carrier family 26, member 9
MGI:2444594

17 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc26a9^em1(IMPC)Mbp/Slc26a9⁺ C57BL/6N-Slc26a9^em1(IMPC)Mbp/MbpMmucd	abnormal cornea morphology	J:211773
	abnormal kidney morphology	J:211773
	cornea opacity	J:211773
	enlarged kidney	J:211773
	no spontaneous movement	J:211773
Slc26a9^em1(IMPC)Mbp/Slc26a9^em1(IMPC)Mbp C57BL/6N-Slc26a9^em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	hemorrhage	J:211773
	no spontaneous movement	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Slc26a9^tm1Sole/Slc26a9⁺ involves: 129S/SvEv	decreased digestive secretion	J:142516
Slc26a9^tm1Sole/Slc26a9^tm1Sole involves: 129S/SvEv	abnormal gastric chief cell morphology	J:142516
	abnormal gastric parietal cell morphology	J:142516
	abnormal gastric surface mucous cell morphology	J:142516
	abnormal stomach epithelium morphology	J:142516
	abnormal stomach glandular epithelium morphology	J:142516
	absent digestive secretion	J:142516
	decreased digestive secretion	J:142516
	dilated gastric gland	J:142516
	increased stomach pH	J:142516

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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