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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Trpm1
transient receptor potential cation channel, subfamily M, member 1
MGI:1330305
13 phenotypes from 4 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
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

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory