| 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 | ||
|---|---|---|
integument
|
√ | |
|
abnormal coat/hair pigmentation
|
√ | |
|
absent coat pigmentation
|
√ | |
|
mortality/aging
|
√ | |
|
embryonic lethality, complete penetrance
|
√ | |
|
pigmentation
|
√ | |
|
abnormal coat/hair pigmentation
|
√ | |
|
absent coat pigmentation
|
√ | |
|
absent eye pigmentation
|
√ | |
|
vision/eye
|
√ | |
|
absent eye pigmentation
|
√ |
