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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fuz
fuzzy planar cell polarity protein
MGI:1917550
73 phenotypes from 4 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fuzb2b1273Clo/Fuzb2b1273Clo
C57BL/6J-Fuzb2b1273Clo 		abnormal liver morphology J:175213
anophthalmia J:175213
atrioventricular septal defect J:175213
diaphragmatic hernia J:175213
dual inferior vena cava J:175213
multiple major aortopulmonary collateral arteries J:175213
polydactyly J:175213
pulmonary hypoplasia J:175213
pulmonary valve atresia J:175213
right aortic arch J:175213
tracheoesophageal fistula J:175213
Fuzem1(IMPC)Mbp/Fuz+
C57BL/6N-Fuzem1(IMPC)Mbp/MbpMmucd 		abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
Fuzem1(IMPC)Mbp/Fuzem1(IMPC)Mbp
C57BL/6N-Fuzem1(IMPC)Mbp/MbpMmucd 		abnormal blood vessel morphology J:211773
abnormal craniofacial morphology J:211773
abnormal facial morphology J:211773
abnormal heart looping J:211773
abnormal heart morphology J:211773
abnormal limb morphology J:211773
abnormal neural tube closure J:211773
abnormal neural tube morphology J:211773
abnormal optic vesicle formation J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
abnormal tail morphology J:211773
anophthalmia J:211773
cleft palate J:211773
edema J:211773
facial cleft J:211773
hemorrhage J:211773
polydactyly J:211773
preweaning lethality, complete penetrance J:211773
syndactyly J:211773
FuzGt(AN0439)Wtsi/FuzGt(AN0439)Wtsi
involves: 129P2/OlaHsd * C3H 		abnormal apical ectodermal ridge morphology J:154370
abnormal developmental patterning J:154370
abnormal midbrain morphology J:154370
abnormal motor neuron morphology J:154370
abnormal neural tube closure J:154370
abnormal primary cilium morphology J:154370
abnormal spinal cord morphology J:154370
abnormal ventral interneuron 3 morphology J:154370
absent eye pigmentation J:154370
edema J:154370
lethality throughout fetal growth and development, complete penetrance J:154370
microphthalmia J:154370
pericardial edema J:154370
polydactyly J:154370
small floor plate J:154370
FuzGt(OSTGST001398)Lex/FuzGt(OSTGST001398)Lex
involves: 129S5/SvEvBrd * C57BL/6 		abnormal brain development J:177881
abnormal cochlea morphology J:177881
abnormal craniofacial morphology J:177881
abnormal diencephalon morphology J:177881
abnormal head mesenchyme morphology J:177881
abnormal mandible morphology J:177881
abnormal Meckel's cartilage morphology J:177881
abnormal palate development J:177881
abnormal pituitary diverticulum morphology J:177881
abnormal striatum morphology J:177881
abnormal tongue morphology J:177881
abnormal tooth development J:177881
absent choroid plexus J:177881
absent incisors J:177881
anophthalmia J:177881
cleft secondary palate J:177881
delayed bone ossification J:177881
delayed intramembranous bone ossification J:177881
delayed palatal shelf elevation J:177881
mandible hypoplasia J:177881
maxilla hypoplasia J:177881
Meckel's cartilage hyperplasia J:177881
neonatal lethality, complete penetrance J:177881
tongue ankylosis J:177881
FuzGt(OSTGST001398)Lex/FuzGt(OSTGST001398)Lex
involves: 129S5/SvEvBrd * C57BL/6N 		abnormal cardiac outflow tract development J:158243
abnormal craniofacial morphology J:158243
abnormal eye morphology J:158243
abnormal long bone morphology J:158243
abnormal Meckel's cartilage morphology J:158243
abnormal rib morphology J:158243
abnormal sternum morphology J:158243
abnormal truncus arteriosus septation J:158243
anophthalmia J:158243
dilated brain ventricle J:158243
encephalomeningocele J:158243
exencephaly J:158243
persistent truncus arteriosus J:158243
polydactyly J:158243
pulmonary hypoplasia J:158243
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
11/19/2024
MGI 6.24 		The Jackson Laboratory