|
Symbol Name ID |
Kifbp
kinesin family binding protein MGI:1919570 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sparse scalp hair |
Hypoplasia of the maxilla |
Microcephaly |
Pointed chin |
Sloping forehead |
Everted lower lip vermilion |
Short philtrum |
Thick vermilion border |
Cleft palate |
Oligodontia |
Bulbous nose |
Prominent nasal bridge |
Wide nasal bridge |
Sparse eyebrow |
Highly arched eyebrow |
Synophrys |
Thick eyebrow |
Downslanted palpebral fissures |
Telecanthus |
| Disease(s) Associated with KIFBP | |||||||||||||||||||
| Goldberg-Shprintzen syndrome |
| Mouse Phenotypes | cleft palate |
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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 04/16/2024 MGI 6.23 |
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