Fzd7 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fzd7
frizzled class receptor 7
MGI:108570

18 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Dvl3^tm1Awb/Dvl3⁺ Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	ventricular septal defect	J:189062
Dvl3^tm1Awb/Dvl3⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	ventricular septal defect	J:189062
Dvl3^tm1Awb/Dvl3^tm1Awb Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	ventricular septal defect	J:189062
Fzd1^tm1.1Nat/Fzd1^tm1.1Nat Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	diluted coat color	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	normal craniofacial phenotype	J:189062
	double outlet right ventricle	J:189062
	postnatal lethality, incomplete penetrance	J:189062
	ventricular septal defect	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6 * LPT/LeJ	cleft palate	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Vangl2^Lp/Vangl2⁺ involves: 129 * C57BL/6 * LPT/LeJ	abnormal heart morphology	J:189062
	cleft palate	J:189062
	ventricular septal defect	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt3a^tm1Amc/Wnt3a⁺ involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	cleft palate	J:189062
	ventricular septal defect	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt5a^tm1Amc/Wnt5a⁺ involves: 129 * C57BL/6	embryonic growth retardation	J:189062
	embryonic lethality during organogenesis, complete penetrance	J:189062
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt11^tm1Amc/Wnt11⁺ involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	cleft palate	J:189062
	ventricular septal defect	J:189062
Fzd2^tm1.1Nat/Fzd2^tm1.1Nat Fzd7^tm1.1Nat/Fzd7^tm1.1Nat involves: 129 * C57BL/6	abnormal embryonic tissue morphology	J:189062
	abnormal heart development	J:189062
	abnormal parietal yolk sac morphology	J:189062
	decreased angiogenesis	J:189062
	decreased embryo size	J:189062
	disorganized yolk sac vascular plexus	J:189062
	embryonic growth retardation	J:189062
	embryonic lethality during organogenesis, complete penetrance	J:189062
	incomplete embryo turning	J:189062
	open neural tube	J:189062
Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Vangl2^Lp/Vangl2⁺ involves: 129 * C57BL/6 * LPT/LeJ	abnormal heart morphology	J:189062
	cleft palate	J:189062
	ventricular septal defect	J:189062
Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt3a^tm1Amc/Wnt3a⁺ involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	ventricular septal defect	J:189062
Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt5a^tm1Amc/Wnt5a⁺ involves: 129 * C57BL/6	short tail	J:189062

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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