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Symbol
Name
ID

Pbx1
pre B cell leukemia homeobox 1
MGI:97495

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Oligohydramnios
Disease(s) Associated with PBX1	Oligohydramnios
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay

Mouse Phenotypes		abnormal second pharyngeal arch morphology	abnormal developmental patterning	abnormal dorsal-ventral axis patterning	abnormal left-right axis symmetry of the somites	abnormal proximal-distal axis patterning	abnormal embryonic tissue morphology	abnormal limb bud morphology	umbilical hernia
Availability	Mouse Genotype	abnormal second pharyngeal arch morphology	abnormal developmental patterning	abnormal dorsal-ventral axis patterning	abnormal left-right axis symmetry of the somites	abnormal proximal-distal axis patterning	abnormal embryonic tissue morphology	abnormal limb bud morphology	umbilical hernia
	Pbx1^em1Dunw/Pbx1^em1Dunw
	Pbx1^tm1Mlc/Pbx1^tm1Mlc

Contributing Projects: 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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