abnormal sperm nucleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the sperm head nucleus, including an abnormal nuclear shape or defects in the compaction of nuclear chromatin (Mammalian Phenotype Ontology, MP_0009232)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009232
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Genes

19 gene mutations causing the abnormal sperm nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGFG1 ArfGAP with FG repeats 1
AURKC aurora kinase C
CSNK2A2 casein kinase 2, alpha prime polypeptide
FHL5 four and a half LIM domains 5
FSHR follicle stimulating hormone receptor
GMCL1 germ cell-less, spermatogenesis associated 1
GOPC golgi-associated PDZ and coiled-coil motif containing
GPX5 glutathione peroxidase 5
H1FNT H1 histone family, member N, testis-specific
HOOK1 hook microtubule-tethering protein 1
PICK1 protein interacting with PRKCA 1
PVRL2 poliovirus receptor-related 2 (herpesvirus entry mediator B)
RIMBP3 RIMS binding protein 3
SEPT12 septin 12
T T, brachyury homolog (mouse)
THEG theg spermatid protein
TNP1 transition protein 1 (during histone to protamine replacement)
TNP2 transition protein 2 (during histone to protamine replacement)
ZPBP zona pellucida binding protein