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Symbol
Name
ID
Kifbp
kinesin family binding protein
MGI:1919570
Phenotype annotations related to cardiovascular system
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
Availability Mouse Genotype
Kifbptm1a(KOMP)Wtsi/Kifbptm1a(KOMP)Wtsi

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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last database update
05/21/2024
MGI 6.23
The Jackson Laboratory