Symbol Name ID |
Ift27
intraflagellar transport 27 MGI:1914292 |
Darker colors indicate more annotations |
Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Partial atrioventricular canal defect |
Hypoplastic left heart |
Patent ductus arteriosus |
Disease(s) Associated with IFT27 | |||||
Bardet-Biedl syndrome 19 |
Mouse Phenotypes | abnormal blood vessel morphology |
pulmonary trunk hypoplasia |
abnormal aortic arch morphology |
double aortic arch |
dual inferior vena cava |
abnormal atrioventricular cushion morphology |
double outlet right ventricle with atrioventricular septal defect |
common atrium |
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Availability | Mouse Genotype | ||||||||
Ift27tm1b(EUCOMM)Hmgu/Ift27tm1b(EUCOMM)Hmgu |
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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last database update 04/23/2024 MGI 6.23 |
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