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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fbln1
fibulin 1
MGI:95487
60 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fbln1Gt(XST011)Byg/Fbln1Gt(XST011)Byg
B6.129P2-Fbln1Gt(XST011)Byg 		atrial septal defect J:137690
overriding aortic valve J:137690
ventricular septal defect J:137690
Fbln1Gt(XST011)Byg/Fbln1Gt(XST011)Byg
involves: 129P2/OlaHsd * C57BL/6 		aberrant origin of the right subclavian artery J:137690
abnormal blood vessel morphology J:137690
abnormal cardiovascular system morphology J:137690
abnormal common carotid artery morphology J:137690
abnormal cranial nerve morphology J:137690
abnormal cranium morphology J:137690
abnormal frontal bone morphology J:137690
abnormal glossopharyngeal nerve morphology J:137690
abnormal heart morphology J:137690
abnormal nasal bone morphology J:137690
abnormal otic vesicle development J:137690
abnormal parietal bone morphology J:137690
abnormal premaxilla morphology J:137690
abnormal pulmonary alveolus morphology J:137690
abnormal rhombomere morphology J:137690
abnormal truncus arteriosus septation J:137690
abnormal tympanic ring morphology J:137690
abnormal vagus nerve morphology J:137690
atrial septal defect J:137690
double outlet right ventricle J:137690
eye hemorrhage J:137690
fusion of glossopharyngeal and vagus nerve J:137690
hemorrhage J:137690
increased hindbrain apoptosis J:137690
internal hemorrhage J:137690
intracerebral hemorrhage J:137690
micrognathia J:137690
muscular ventricular septal defect J:137690
neonatal lethality, complete penetrance J:137690
ostium primum atrial septal defect J:137690
ostium secundum atrial septal defect J:137690
overriding aortic valve J:137690
perimembraneous ventricular septal defect J:137690
petechiae J:137690
respiratory distress J:137690
retroesophageal right subclavian artery J:137690
small lung J:137690
small thyroid cartilage J:137690
spinal hemorrhage J:137690
thymus hypoplasia J:137690
thyroid gland hypoplasia J:137690
ventricle myocardium hypoplasia J:137690
ventricular septal defect J:137690
Fbln1Gt(XST011)Byg/Fbln1tm1Tmpl
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		atrial septal defect J:137690
double outlet right ventricle J:137690
overriding aortic valve J:137690
ventricular septal defect J:137690
Fbln1tm1Tmpl/Fbln1tm1Tmpl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal breathing pattern J:71581
abnormal capillary morphology J:71581
abnormal glomerular capillary endothelium morphology J:71581
abnormal lung development J:71581
abnormal lung interstitium morphology J:71581
abnormal podocyte foot process morphology J:71581
abnormal renal glomerulus morphology J:71581
atrial septal defect J:137690
decreased body size J:71581
decreased body weight J:71581
decreased glomerular capillary number J:71581
decreased hematocrit J:71581
dilated glomerular capillary J:71581
double outlet right ventricle J:137690
hemorrhage J:71581
impaired lung alveolus development J:71581
intracranial hemorrhage J:71581
overexpanded pulmonary alveolus J:71581
perinatal lethality, incomplete penetrance J:71581
petechiae J:71581
postnatal lethality, incomplete penetrance J:71581
thymus hypoplasia J:137690
ventricular septal defect J:137690
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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