Cm Phenotype Annotations - Multigenic Genotypes

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cm
coloboma deletion region
MGI:88424

10 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cm/+ Drd2^tm1Low/Drd2^tm1Low involves: 101/H * 129S2/SvPas * C3H/HeH * C3H/HeSn * C57BL/6J	normal behavior/neurological phenotype	J:156905
	decreased dopamine level	J:156905
	decreased locomotor activity	J:156905
	normal nervous system phenotype	J:156905
Cm/+ Drd3^tm1Stl/Drd3^tm1Stl involves: 101/H * 129S2/SvPas * C3H/HeH * C3H/HeSn * C57BL/6J	abnormal behavioral response to addictive substance	J:156905
Cm/+ Tg(Snap25)40Micw/0 involves: C3H/HeJ * C57BL/6J	hyperactivity	J:32588
Cm/+ Tg(Snap25)40Micw/Tg(Snap25)40Micw involves: C3H/HeJ * C57BL/6J	abnormal eye development	J:32588
	normal behavior/neurological phenotype	J:32588, J:58598
	coloboma	J:32588
	head bobbing	J:32588
Jag1^tm1Grid/Cm involves: 101/H * 129S1/Sv * C3H/He * C57BL/6 * FVB/N	intracranial hemorrhage	J:54907

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 04/16/2024 MGI 6.23