abnormal x-y chromosome synapsis during male meiosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an anomaly in the process in which the side by side pairing and physical juxtaposition of X and Y chromosomes is created at the metaphase plate, usually resulting in incorrect sex chromosome disjunction (Mammalian Phenotype Ontology, MP_0011751)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011751
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Genes

4 gene mutations causing the abnormal x-y chromosome synapsis during male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCDC79 coiled-coil domain containing 79
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
M1AP meiosis 1 associated protein
SPO11 SPO11 meiotic protein covalently bound to DSB