Fendrr Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fendrr
Foxf1 adjacent non-coding developmental regulatory RNA
MGI:1916040

19 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fendrr^tm1Bgh/Fendrr^tm2Bgh involves: 129S6/SvEvTac * C57BL/6	abnormal ventral body wall morphology	J:191565
	decreased fetal cardiomyocyte proliferation	J:191565
	embryonic lethality during organogenesis, complete penetrance	J:191565
	omphalocele	J:191565
	poor circulation	J:191565
	thin ventricular wall	J:191565
	ventricle myocardium hypoplasia	J:191565
Fendrr^tm1Vlcg/Fendrr^tm1Vlcg involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N	abnormal esophageal smooth muscle morphology	J:204277
	abnormal esophagus morphology	J:204277
	abnormal lung vasculature morphology	J:204277
	abnormal pulmonary alveolus morphology	J:204277
	neonatal lethality, complete penetrance	J:204277
	pulmonary hypoplasia	J:204277
	respiratory failure	J:204277
	ventricular septal defect	J:204277
Fendrr^tm1Vlcg/Fendrr^tm1Vlcg involves: 129S6/SvEvTac * C57BL/6NTac	abnormal lung development	J:233815
	abnormal lung lobe morphology	J:233815
	neonatal lethality, complete penetrance	J:233815
	respiratory distress	J:233815
	small lung	J:233815

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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