abnormal corpus epididymis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the body of the epididymis (Mammalian Phenotype Ontology, MP_0002661)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002661
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5 gene mutations causing the abnormal corpus 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)
PAX8 paired box 8
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
SLC4A2 solute carrier family 4 (anion exchanger), member 2