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Symbol Name ID |
Pbx1
pre B cell leukemia homeobox 1 MGI:97495 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
| 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 | hunched posture |
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| Availability | Mouse Genotype | |
| Pbx1em1Dunw/Pbx1em1Dunw | ||
| Pbx1tm1.1Febe/Pbx1tm1.1Febe | ||
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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