|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly in the segment of the sperm flagellum that attaches to the implantation fossa of the nucleus in the sperm head; from the remnant of the centriole at this point, the axoneme extends throughout the length of the flagellum (Mammalian Phenotype Ontology, MP_0009830)|
|Downloads & Tools|
1 gene mutations causing the abnormal sperm connecting piece morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|NEURL1||neuralized E3 ubiquitin protein ligase 1|