| hm | homozygous | ht | heterozygous | tg | involves transgenes | √ | phenotype observed |
| cn | conditional genotype | cx | complex: > 1 genome feature | ot | other: hemizygous, indeterminate,... | N | normal phenotype |
Background:
| Affected Systems | |
|---|---|
|
|
cellular
|
√ |
|
abnormal sperm flagellum morphology
|
√ |
|
abnormal sperm axoneme morphology
|
√ |
|
abnormal sperm principal piece morphology
|
√ |
|
abnormal sperm fibrous sheath morphology
|
√ |
|
abnormal sperm motility
|
√ |
|
decreased activated sperm motility
|
√ |
|
decreased sperm progressive motility
|
√ |
|
reproductive system
|
√ |
|
abnormal sperm flagellum morphology
|
√ |
|
abnormal sperm axoneme morphology
|
√ |
|
abnormal sperm principal piece morphology
|
√ |
|
abnormal sperm fibrous sheath morphology
|
√ |
|
impaired sperm capacitation
|
√ |
|
abnormal male reproductive system physiology
|
√ |
|
abnormal sperm motility
|
√ |
|
decreased activated sperm motility
|
√ |
|
decreased sperm progressive motility
|
√ |
|
reduced male fertility
|
√ |
