abnormal chiasmata formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical contact between nonsister chromatids of homologous chromosomes during meiosis I, precluding formation of the expected number of cross-shaped configurations representing recombination events (Mammalian Phenotype Ontology, MP_0008966)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008966
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8 gene mutations causing the abnormal chiasmata formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCNB1IP1 cyclin B1 interacting protein 1, E3 ubiquitin protein ligase
EXO1 exonuclease 1
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
HORMAD1 HORMA domain containing 1
HORMAD2 HORMA domain containing 2
TEX12 testis expressed 12
TRIP13 thyroid hormone receptor interactor 13
UBE2B ubiquitin-conjugating enzyme E2B