Slc17a9 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23