abnormal chromosome pairing during meiosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an anomaly in the highly specific side-by-side association of homologous chromosomes during first prophase of meiosis (Mammalian Phenotype Ontology, MP_0009451)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009451
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8 gene mutations causing the abnormal chromosome pairing during meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
HORMAD1 HORMA domain containing 1
HSF1 heat shock transcription factor 1
MEI4 meiosis-specific 4 homolog (S. cerevisiae)
PRDM9 PR domain containing 9
SYCE3 synaptonemal complex central element protein 3
TRIP13 thyroid hormone receptor interactor 13
ZC3HC1 zinc finger, C3HC-type containing 1