absent sperm flagellum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the whiplike posterior filiform portion of the spermatozoon that provides sperm motility (Mammalian Phenotype Ontology, MP_0008545)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008545
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Genes

15 gene mutations causing the absent sperm flagellum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
FOXJ1 forkhead box J1
GMCL1 germ cell-less, spermatogenesis associated 1
GOLGA3 golgin A3
HOOK1 hook microtubule-tethering protein 1
MEIG1 meiosis/spermiogenesis associated 1
MKKS McKusick-Kaufman syndrome
NPC1 Niemann-Pick disease, type C1
SEPT12 septin 12
THEG theg spermatid protein
TPGS1 tubulin polyglutamylase complex subunit 1
TTLL1 tubulin tyrosine ligase-like family member 1