abnormal stapedial artery morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the small artery that passes through the ring of the stapes; while the stapedial artery is a temporary artery thought to disappear at late embryonic stage in humans, the mouse stapedial artery is complete by E13 and persists into adulthood (Mammalian Phenotype Ontology, MP_0004665)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004665
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Genes

6 gene mutations causing the abnormal stapedial artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX1 distal-less homeobox 1
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
HOXA2 homeobox A2
PAX8 paired box 8
SIX1 SIX homeobox 1