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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fat1
FAT atypical cadherin 1
MGI:109168
46 phenotypes from 6 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fat1Gt(GST070)Byg/Fat1Gt(GST070)Byg
involves: 129P2/OlaHsd * C57BL/6 		neonatal lethality, complete penetrance J:70273
Fat1Gt(KST249)Byg/Fat1Gt(KST249)Byg
Tg(Myl1-lacZ)1Ibdml/0
involves: 129P2/OlaHsd 		abnormal muscle development J:199157
abnormal neuromuscular synapse morphology J:199157
abnormal posture J:199157
abnormal retina vasculature morphology J:199157
abnormal skeletal muscle morphology J:199157
aniridia J:199157
decreased skeletal muscle fiber diameter J:199157
decreased skeletal muscle mass J:199157
ectopic skeletal muscle J:199157
impaired coordination J:199157
kidney cyst J:199157
kyphosis J:199157
lymphangiectasis J:199157
microphthalmia J:199157
myositis J:199157
premature death J:199157
retina detachment J:199157
retina microaneurysm J:199157
skeletal muscle atrophy J:199157
skeletal muscle fiber necrosis J:199157
normal skeleton phenotype J:199157
weight loss J:199157
Fat1tm1.1Nsib/Fat1+
Tg(NPHS2-cre)295Lbh/0
involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * C57BL/6J * SJL 		abnormal glomerular mesangium morphology J:234732
albuminuria J:234732
Fat1tm1.1Nsib/Fat1tm1.1Nsib
Tg(NPHS2-cre)295Lbh/0
involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * C57BL/6J * SJL 		abnormal podocyte morphology J:234732
abnormal podocyte slit diaphragm morphology J:234732
albuminuria J:234732
glomerulosclerosis J:234732
increased urine protein level J:234732
podocyte foot process effacement J:234732
podocyte microvillus transformation J:234732
Fat1tm1.2Fhel/Fat1tm1.2Fhel
Tg(Myl1-lacZ)1Ibdml/0
involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J * SJL 		abnormal behavior J:199157
abnormal facial muscle morphology J:199157
abnormal muscle development J:199157
abnormal neuromuscular synapse morphology J:199157
abnormal skeletal muscle morphology J:199157
decreased skeletal muscle fiber diameter J:199157
ectopic skeletal muscle J:199157
myositis J:199157
neonatal lethality, incomplete penetrance J:199157
short endolymphatic duct J:199157
skeletal muscle fiber necrosis J:199157
Fat1tm1Cfc/Fat1tm1Cfc
either: 129/Sv or (involves: 129/Sv * C57BL/6) 		abnormal podocyte slit junction morphology J:83058
abnormal retina neuronal layer morphology J:83058
anophthalmia J:83058
aphakia J:83058
cyclopia J:83058
fused podocyte foot processes J:83058
holoprosencephaly J:83058
normal integument phenotype J:83058
microphthalmia J:83058
postnatal lethality, complete penetrance J:83058
proboscis J:83058
retina pigment epithelium atrophy J:83058
Fat1tm1Fhel/Fat1tm1Fhel
Pax3tm1(cre)Joe/Pax3+
Tg(Myl1-lacZ)1Ibdml/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL 		abnormal muscle development J:199157
abnormal skeletal muscle morphology J:199157
ectopic skeletal muscle J:199157
Fat1tm1Fhel/Fat1tm1Fhel
Tg(Myl1-lacZ)1Ibdml/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL 		abnormal muscle development J:199157
abnormal skeletal muscle morphology J:199157
ectopic skeletal muscle J:199157
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
12/10/2024
MGI 6.24 		The Jackson Laboratory