Cm Phenotype Annotations - Multigenic Genotypes

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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)
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