Symbol Name ID |
Pbx1
pre B cell leukemia homeobox 1 MGI:97495 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal facial shape |
Long face |
Narrow face |
Deep philtrum |
Thin upper lip vermilion |
Anteverted nares |
Wide nasal bridge |
Epicanthus |
Disease(s) Associated with PBX1 | ||||||||
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay |
Mouse Phenotypes | abnormal craniofacial bone morphology |
absent oval window |
abnormal styloid process morphology |
short styloid process |
abnormal hyoid bone lesser horn morphology |
abnormal middle ear ossicle morphology |
abnormal malleus morphology |
absent stapes |
palatal shelf hypoplasia |
abnormal second pharyngeal arch morphology |
cleft secondary palate |
small snout |
abnormal outer ear morphology |
outer ear hypoplasia |
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Availability | Mouse Genotype | ||||||||||||||
Pbx1em1Dunw/Pbx1em1Dunw | |||||||||||||||
Pbx1tm1Mlc/Pbx1tm1Mlc |
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 07/05/2024 MGI 6.24 |
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