Symbol Name ID |
Kifbp
kinesin family binding protein MGI:1919570 |
Darker colors indicate more annotations |
Human Phenotypes | Ventricular septal defect |
Aortic regurgitation |
Disease(s) Associated with KIFBP | ||
Goldberg-Shprintzen syndrome |
Mouse Phenotypes | absent extracranial vertebral artery segment |
absent posterior communicating artery |
dilated liver sinusoidal space |
abnormal placental labyrinth vasculature morphology |
abnormal ductus venosus morphology |
abnormal ductus venosus topology |
placenta hemorrhage |
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Availability | Mouse Genotype | |||||||
Kifbptm1a(KOMP)Wtsi/Kifbptm1a(KOMP)Wtsi |
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 05/21/2024 MGI 6.23 |
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