abnormal caput epididymis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the head of the epididymis (Mammalian Phenotype Ontology, MP_0002660)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002660
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Genes

10 gene mutations causing the abnormal caput epididymis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FSHR follicle stimulating hormone receptor
HEXB hexosaminidase B (beta polypeptide)
IDO1 indoleamine 2,3-dioxygenase 1
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LHCGR luteinizing hormone/choriogonadotropin receptor
PAX8 paired box 8
PLA2G3 phospholipase A2, group III
PLTP phospholipid transfer protein
ROS1 ROS proto-oncogene 1 , receptor tyrosine kinase
SLC4A2 solute carrier family 4 (anion exchanger), member 2