Xlch Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Xlch
X-linked cardiac hypertrophy
MGI:3797603

14 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Xlch/? C57BL/6J-Xlch	abnormal myocardial fiber morphology	J:136798
	abnormal ventricle papillary muscle morphology	J:136798
	aortic valve stenosis	J:136798
	cardiac hypertrophy	J:136798
	cardiac interstitial fibrosis	J:136798
	dilated sarcoplasmic reticulum	J:136798
	disorganized myocardium	J:136798
	heart left ventricle hypertrophy	J:136798
	increased cardiac muscle contractility	J:136798
	increased heart weight	J:136798
	neonatal lethality, incomplete penetrance	J:136798
	premature death	J:136798
	thick aortic valve cusps	J:136798
	thick ventricular wall	J:136798
Xlch/Xlch⁺ involves: C3H/HeJ * C57BL/6J	cardiac hypertrophy	J:136798
Xlch/Xlch⁺ involves: C3H/HeJ * C57BL/6J	neonatal lethality, incomplete penetrance	J:136798

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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