Calcrl Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Calcrl
calcitonin receptor-like
MGI:1926944

19 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Calcrl^tm1Kmca/Calcrl^tm1Kmca 129S6/SvEvTac-Calcrl^tm1Kmca	abnormal fetal cardiomyocyte proliferation	J:106927
	abnormal lymph organ development	J:130930
	abnormal myocardium compact layer morphology	J:106927
	abnormal myocardium layer morphology	J:106927
	abnormal skin condition	J:106927
	abnormal vascular smooth muscle morphology	J:106927
	disorganized myocardium	J:106927
	edema	J:130930
	hydrops fetalis	J:106927
	increased cardiomyocyte apoptosis	J:106927
	intestinal edema	J:106927
	lethality throughout fetal growth and development, complete penetrance	J:106927, J:130930
	lymphedema	J:130930
	small heart	J:106927
	thin myocardium compact layer	J:106927
	vascular smooth muscle hypoplasia	J:106927
Calcrl^tm1Kmca/Calcrl^tm1Kmca involves: 129S6/SvEvTac	abnormal placenta labyrinth morphology	J:201446
	abnormal uterine spiral artery remodeling	J:201446
	decreased uterine NK cell number	J:201446
Calcrl^tm1Kmca/Calcrl^tm2Kmca Tg(Tek-cre)12Flv/0 involves: 129P2/OlaHsd * 129S6/SvEvTac * C3H * C57BL/6 * C57BL/6J	edema	J:130930
	lethality throughout fetal growth and development, complete penetrance	J:130930

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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