abnormal manchette morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the conic array of microtubules that invests the posterior nucleus of a spermatid, and is believed to play a role in definitive posterior head-shaping events during spermiogenesis (Mammalian Phenotype Ontology, MP_0009376)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009376
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7 gene mutations causing the abnormal manchette morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLIP1 CAP-GLY domain containing linker protein 1
DPY19L2 dpy-19-like 2 (C. elegans)
HOOK1 hook microtubule-tethering protein 1
KATNB1 katanin p80 (WD repeat containing) subunit B 1
KRT19 keratin 19, type I
RIMBP3 RIMS binding protein 3
T T, brachyury homolog (mouse)