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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Wnt3a
wingless-type MMTV integration site family, member 3A
MGI:98956
29 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fzd2tm1.1Nat/Fzd2+
Fzd7tm1.1Nat/Fzd7tm1.1Nat
Wnt3atm1Amc/Wnt3a+
involves: 129 * C57BL/6 		abnormal heart morphology J:189062
cleft palate J:189062
ventricular septal defect J:189062
Fzd7tm1.1Nat/Fzd7tm1.1Nat
Wnt3atm1Amc/Wnt3a+
involves: 129 * C57BL/6 		abnormal heart morphology J:189062
ventricular septal defect J:189062
Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+
Relnrl/Reln+
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ 		decreased Cajal-Retzius cell number J:153209
Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+
Relnrl/Reln+
Trp73tm1(cre)Agof/Trp73+
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ 		decreased Cajal-Retzius cell number J:153209
Itgb1tm1Mll/Itgb1tm1Mll
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129X1/SvJ 		normal nervous system phenotype J:170581
Lrp6Gt(Ex187)Byg/Lrp6+
Wnt3avt/Wnt3a+
involves: 129P2/OlaHsd * C57BL/6 * C57BR 		kinked tail J:64989
Lrp6Gt(Ex187)Byg/Lrp6+
Wnt3avt/Wnt3avt
involves: 129P2/OlaHsd * C57BL/6 * C57BR 		vestigial tail J:64989
Tbx6tm2Pa/Tbx6+
Wnt3atm1Amc/Wnt3a+
involves: 129 * 129S1/Sv * 129X1/SvJ * ICR 		normal cardiovascular system phenotype J:137163
normal embryo phenotype J:137163
Wnt1tm1Brd/Wnt1tm1Brd
Wnt3atm1Amc/Wnt3atm1Amc
involves: 129S1/Sv * 129S7/SvEvBrd 		abnormal dermomyotome development J:50279
abnormal dorsal-ventral axis patterning J:44094
abnormal forebrain development J:44094
abnormal melanoblast morphology J:44094
abnormal metencephalon morphology J:44094
abnormal midbrain development J:44094
abnormal myotome development J:50279
abnormal neural crest cell morphology J:44094
abnormal thyroid cartilage morphology J:44094
absent hyoid bone J:44094
absent stapes J:44094
caudal body truncation J:44094
embryonic lethality during organogenesis, incomplete penetrance J:44094
lethality throughout fetal growth and development, incomplete penetrance J:44094
small alisphenoid bone J:44094
small basisphenoid bone J:44094
small dorsal root ganglion J:44094
small otic capsule J:44094
small presphenoid bone J:44094
small temporal bone squamous part J:44094
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory