Fndc3b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fndc3b
fibronectin type III domain containing 3B
MGI:1919257

14 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fndc3b^{tm1.1(KOMP)Vlcg}/Fndc3b⁺ C57BL/6N-Fndc3b^{tm1.1(KOMP)Vlcg}/Tcp	abnormal coat/hair pigmentation	J:211773
	abnormal eye morphology	J:211773
	abnormal heart morphology	J:211773
	enlarged heart	J:211773
	increased heart weight	J:211773
	urinary bladder obstruction	J:211773
Fndc3b^{tm1.1(KOMP)Vlcg}/Fndc3b^{tm1.1(KOMP)Vlcg} C57BL/6N-Fndc3b^{tm1.1(KOMP)Vlcg}/Tcp	preweaning lethality, complete penetrance	J:211773
Fndc3b^tm1Maim/Fndc3b^tm1Maim B6.129S2-Fndc3b^tm1Maim	abnormal cell adhesion	J:163660
	abnormal cell differentiation	J:163660
	decreased fibroblast cell migration	J:163660
	decreased fibroblast proliferation	J:163660
	normal homeostasis/metabolism phenotype	J:163660
	neonatal lethality, complete penetrance	J:163660
Fndc3b^tm1Maim/Fndc3b^tm1Maim involves: 129S2/SvPas	abnormal cell differentiation	J:162425
Fndc3b^tm1Maim/Fndc3b^tm1Maim involves: 129S2/SvPas	increased bone ossification	J:162425

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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