| 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
|
√ | ||
|
lethargy
|
√ | ||
|
cardiovascular system
|
√ | ||
|
thin myocardium
|
√ | ||
|
enlarged heart
|
√ | ||
|
dilated heart left ventricle
|
√ | ||
|
dilated heart right ventricle
|
√ | ||
|
dilated cardiomyopathy
|
√ | ||
|
growth/size/body
|
√ | ||
|
enlarged heart
|
√ | ||
|
homeostasis/metabolism
|
√ | ||
|
abnormal atrial thrombosis
|
√ | ||
|
edema
|
√ | ||
|
integument
|
√ | ||
|
disheveled coat
|
√ | ||
|
liver/biliary system
|
N | ||
|
liver/biliary system phenotype
|
N | ||
|
mortality/aging
|
√ | ||
|
premature death
|
√ | ||
|
muscle
|
√ | ||
|
thin myocardium
|
√ | ||
|
dilated cardiomyopathy
|
√ | ||
|
vision/eye
|
√ | ||
|
vision/eye phenotype
|
N | ||
|
thin retina outer nuclear layer
|
√ | ||
|
retina outer nuclear layer degeneration
|
√ | ||
|
decreased a-wave amplitude
|
√ | ||
|
decreased b-wave amplitude
|
√ |
