Slc17a9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc17a9
solute carrier family 17, member 9
MGI:1919107

14 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc17a9^{tm1.1(KOMP)Vlcg}/Slc17a9^{tm1.1(KOMP)Vlcg} C57BL/6N-Slc17a9^{tm1.1(KOMP)Vlcg}/Ucd	abnormal eye morphology	J:211773
	abnormal skin morphology	J:211773
Slc17a9^tm1.1Rpa/Slc17a9^tm1.1Rpa B6.Cg-Slc17a9^tm1.1Rpa	no abnormal phenotype detected	J:167972
Slc17a9^tm1Nomu/Slc17a9^tm1Nomu involves: 129 * C57BL/6J	abnormal adrenal gland physiology	J:256580
	abnormal catecholamine level	J:256580
	abnormal neuroendocrine gland physiology	J:256580
	normal behavior/neurological phenotype	J:256580
	decreased circulating insulin level	J:256580
	normal growth/size/body region phenotype	J:256580
	normal homeostasis/metabolism phenotype	J:256580
	hypoglycemia	J:256580
	improved glucose tolerance	J:256580
	increased insulin sensitivity	J:256580
	normal respiratory system phenotype	J:256580

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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