Cltrn Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cltrn
collectrin, amino acid transport regulator
MGI:1926234

22 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cltrn^tm1.1Pngr/Cltrn^tm1.1Pngr involves: 129P2/OlaHsd * C57BL/6J	abnormal homeostasis	J:117490
	abnormal renal transport	J:117490
	increased urine osmolality	J:117490
	polyuria	J:117490
Cltrn^tm1Thu/Y involves: 129S/SvEv * C57BL/6	abnormal amino acid level	J:148522
	abnormal muscle physiology	J:148522
	abnormal tricarboxylic acid cycle	J:148522
	abnormal urine homeostasis	J:148522
	aminoaciduria	J:148752
	crystalluria	J:148752
	decreased body weight	J:148522
	decreased circulating carnitine level	J:148522
	decreased percent body fat/body weight	J:148522
	decreased urine osmolality	J:148752
	decreased urine sodium level	J:148752
	decreased urine urea nitrogen level	J:148752
	increased circulating ketone body level	J:148522
	increased circulating methionine level	J:148752
	increased circulating sodium level	J:148752
	increased circulating tyrosine level	J:148752
	increased insulin sensitivity	J:148522
	polyphagia	J:148752
	polyuria	J:148752

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 04/23/2024 MGI 6.23