19 phenotypes from 6 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Trpm1nob11/Trpm1nob11 B6.Cg-Trpm1nob11/BocJ	abnormal cone electrophysiology	J:347037
	abnormal electroretinogram waveform feature	J:347037
	abnormal eye electrophysiology	J:347037
	abnormal rod electrophysiology	J:347037
	absent b-wave	J:347037
	retina spots	J:347037
Trpm1rd15/Trpm1rd15 B6.Cg-Trpm1rd15/BocJ	abnormal cone electrophysiology	J:346902
	abnormal retina outer plexiform layer morphology	J:346902
	abnormal rod electrophysiology	J:346902
	absent b-wave	J:346902
	retina degeneration	J:346902
	thin retina outer plexiform layer	J:346902
Trpm1rd15/Trpm1rd15 Not Specified	abnormal cone electrophysiology	J:167193
	abnormal retina outer plexiform layer morphology	J:166679, J:167193
	abnormal rod electrophysiology	J:167193
	retina degeneration	J:166679, J:167193
Trpm1tm1b(KOMP)Wtsi/Trpm1tm1b(KOMP)Wtsi C57BL/6N-Trpm1tm1b(KOMP)Wtsi/H	impaired glucose tolerance	J:211773
	impaired pupillary reflex	J:211773
	increased circulating creatine kinase level	J:211773
	increased circulating HDL cholesterol level	J:211773
	limb grasping	J:211773
	mydriasis	J:211773
Trpm1tm1Lex/Trpm1tm1Lex involves: 129S/SvEvBrd	abnormal cone electrophysiology	J:154776
	abnormal eye electrophysiology	J:154776
	abnormal eye physiology	J:154776
	abnormal rod electrophysiology	J:154776
	abnormal vision	J:154776
Trpm1tm1Lex/Trpm1tvrm27 involves: 129S/SvEvBrd * C57BL/6J	abnormal rod electrophysiology	J:209941
Trpm1tm1Tfur/Trpm1tm1Tfur involves: 129S6/SvEvTac	abnormal cone electrophysiology	J:156502
	abnormal rod electrophysiology	J:156502
Trpm1tvrm27/Trpm1+ involves: C57BL/6J	abnormal channel response	J:209941
	abnormal rod electrophysiology	J:209941
Trpm1tvrm27/Trpm1tvrm27 involves: C57BL/6J	abnormal channel response	J:209941
	abnormal eye electrophysiology	J:166679
	abnormal rod electrophysiology	J:209941
	normal vision/eye phenotype	J:209941