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)
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