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)
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