| 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 | |
|---|---|
behavior/neurological
|
√ |
|
poor grooming
|
√ |
|
impaired coordination
|
√ |
|
paraparesis
|
√ |
|
cardiovascular system
|
√ |
|
decreased heart rate
|
√ |
|
prolonged PR interval
|
√ |
|
prolonged QRS complex duration
|
√ |
|
prolonged QT interval
|
√ |
|
growth/size/body
|
√ |
|
decreased birth body size
|
√ |
|
decreased body weight
|
√ |
|
homeostasis/metabolism
|
√ |
|
cyanosis
|
√ |
|
immune system
|
√ |
|
conjunctivitis
|
√ |
|
mortality/aging
|
√ |
|
decreased survivor rate
|
√ |
|
neonatal lethality, incomplete penetrance
|
√ |
|
muscle
|
√ |
|
dystrophic muscle
|
√ |
|
respiratory system
|
√ |
|
small lung
|
√ |
|
atelectasis
|
√ |
|
skeleton
|
√ |
|
kyphoscoliosis
|
√ |
|
vision/eye
|
√ |
|
conjunctivitis
|
√ |
