abnormal sperm capacitation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the change undergone by spermatozoa in the female genital tract that enables them to penetrate and fertilize an egg (Mammalian Phenotype Ontology, MP_0013286)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013286
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12 gene mutations causing the abnormal sperm capacitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY10 adenylate cyclase 10 (soluble)
ADCY3 adenylate cyclase 3
ATP1A4 ATPase, Na+/K+ transporting, alpha 4 polypeptide
CATSPER3 cation channel, sperm associated 3
CATSPER4 cation channel, sperm associated 4
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
KCNU1 potassium channel, subfamily U, member 1
PKDREJ polycystin (PKD) family receptor for egg jelly
PVRL2 poliovirus receptor-related 2 (herpesvirus entry mediator B)
SEPT4 septin 4
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
UBE3A ubiquitin protein ligase E3A