Key:

hm	homozygous	ht	heterozygous	tg	involves transgenes	√	phenotype observed
cn	conditional genotype	cx	complex: > 1 genome feature	ot	other: hemizygous, indeterminate,...	N	normal phenotype

Genotype/
Background:

Phenotypes:

Affected Systems	hm1	cx2		cx3	cx4	cx5	cx6
show or hide all annotated terms Sex:
cellular			√					√
abnormal sperm head morphology								√
impaired sperm migration in female genital tract								√
asthenozoospermia			√					√
reproductive system		√	√	N	√	√	√	√
reproductive system phenotype				N
abnormal sperm head morphology								√
impaired sperm migration in female genital tract								√
asthenozoospermia			√					√
male infertility			√			√
reduced male fertility					√			√
impaired fertilization		√	√				√	√
impaired sperm penetration of zona pellucida			√
impaired binding of sperm to zona pellucida								√
normal phenotype	√
no abnormal phenotype detected	√