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Symbol Name ID |
Pbx1
pre B cell leukemia homeobox 1 MGI:97495 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal pinna morphology |
Hypoplastic helices |
Thickened helices |
Anteverted ears |
Low-set ears |
Microtia |
Hearing impairment |
| 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 | absent oval window |
abnormal middle ear ossicle morphology |
abnormal malleus morphology |
absent stapes |
abnormal outer ear morphology |
outer ear hypoplasia |
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| Availability | Mouse Genotype | ||||||
| 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 04/23/2024 MGI 6.23 |
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