| Gene |
Phenotypes |
| coatomer protein complex, subunit alpha |
-
developmental pigmentation disrupted
|
| un-named t31307 |
|
| retinaldehyde binding protein 1a |
-
pigmentation decreased intensity
|
| coatomer protein complex, subunit beta 2 |
-
developmental pigmentation disrupted
|
| wanda |
|
| ATPase, H+ transporting, lysosomal, V1 subunit H |
|
| un-named t30761 |
|
| un-named t31182 |
|
| transcription factor AP-2 alpha |
|
| lysyl oxidase |
|
| coatomer protein complex, subunit beta 1 |
-
developmental pigmentation disrupted
|
| basonuclin 2 |
|
| un-named t31418 |
|
| un-named t31306 |
|
| vacuolar protein sorting protein 18 |
|
| ATPase, Cu++ transporting, alpha polypeptide |
-
pigmentation disrupted
-
pigmentation abolished
-
pigmentation normal
|
| endothelin receptor B |
|
| duchamp |
|
| v-erb-b2 erythroblastic leukemia viral oncogene homolog 3b |
-
pigmentation disrupted
-
pigmentation abnormal
-
pigmentation normal
|
| tumor protein p53 |
|
| forkhead box D3 |
|
| un-named t30824 |
|
| colony stimulating factor 1 receptor |
|
| oberon |
|
| mind bomb |
|
| growth differentiation factor 6a |
|
| huntingtin |
-
pigment accumulation delayed
|
| Kallmann syndrome 1a sequence |
-
developmental pigmentation normal
|
| iroquois homeobox protein 1, a |
|
| end zone |
|
| un-named t30981 |
|
| adaptor-related protein complex 1, sigma 1 subunit |
-
pigmentation decreased occurrence
|
| histone deacetylase 1 |
|
| potassium inwardly-rectifying channel, subfamily J, member 13 |
|
| un-named t31482 |
|
| ATPase, H+ transporting, lysosomal, V1 subunit E isoform 1 |
|
| dali |
|
| un-named t30954 |
|
| kit receptor a |
|
| retinaldehyde binding protein 1b |
-
pigmentation decreased intensity
|
| ATPase, H+ transporting, V0 subunit D isoform 1 |
-
pigmentation abolished
-
pigmentation normal
|
| un-named t30763 |
|
| vacuolar protein sorting 39 homolog (S. cerevisiae) |
|
| microphthalmia-associated transcription factor a |
-
developmental pigmentation disrupted
-
pigmentation disrupted
|
| SRY-box containing gene 10 |
|
| eukaryotic translation initiation factor 3, subunit E, a |
|
| Rtf1, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) |
|
| un-named t30818 |
|
| seurat |
|
| paired box gene 7a |
-
developmental pigmentation disrupted
|
| ATPase, H+ transporting, lysosomal, V0 subunit c |
|
| un-named t30760 |
|
| albino |
|
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