| 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 | |
|---|---|
cardiovascular system
|
√ |
|
ventricular septal defect
|
√ |
|
cellular
|
√ |
|
abnormal embryonic cilium location or orientation
|
√ |
|
abnormal motile primary cilium physiology
|
√ |
|
embryo
|
√ |
|
abnormal embryonic cilium location or orientation
|
√ |
|
abnormal motile primary cilium physiology
|
√ |
|
growth/size/body
|
√ |
|
situs ambiguus
|
√ |
|
situs inversus
|
√ |
|
mortality/aging
|
√ |
|
postnatal lethality, complete penetrance
|
√ |
|
prenatal lethality, incomplete penetrance
|
√ |
|
renal/urinary system
|
√ |
|
kidney failure
|
√ |
