Symbol Name ID |
Pbx1
pre B cell leukemia homeobox 1 MGI:97495 |
Darker colors indicate more annotations |
Human Phenotypes | Congenital diaphragmatic hernia |
Growth delay |
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 | palatal shelf hypoplasia |
cleft secondary palate |
small snout |
abnormal outer ear morphology |
outer ear hypoplasia |
decreased body size |
abnormal embryonic growth/weight/body size |
|
Availability | Mouse Genotype | |||||||
Pbx1em1Dunw/Pbx1em1Dunw | ||||||||
Pbx1tm1.1Febe/Pbx1tm1.1Febe | ||||||||
Pbx1tm1Mlc/Pbx1tm1Mlc | ||||||||
Pbx1tm1Mlc/Pbx1+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 07/05/2024 MGI 6.24 |
|
|