| QTL Map Information |
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| Chromosome: | 3 |
| QTL Peak Location: | n/a |
| QTL Span: | n/a
79.5-79.5 (Mbp) |
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Upper, "Suggestive": | n/a |
| Upper, "Significant": | n/a |
| Peak: | |
| Lower, "Significant": | n/a |
| Lower, "Suggestive": | n/a |
| Marker type: | SNP |
| Analysis type: | Association |
| Model tested: | - |
| Test base: | - |
| Threshold significance level: | - |
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P_values | <0.05 | | Dominance effect: | n/a |
| Additive effect: | n/a |
| Associated Gene: | KIT (KIT proto-oncogene receptor tyrosine kinase) |
| Cis/Trans acting type: |  |
| Links:
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| Extended information: |
|---|
| (none) |
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| QTL Experiment in Brief |
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| Animals: | The animal was a New Zealand Standardbred filly with a sabino-like white spotting pattern. |
| Breeds associated:
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| Design: | The KIT gene was investigated as a cause of the white spotting pattern. |
| Analysis: | The filly was genotyped for all known white patterning variants in the KIT gene, and KIT coding sequence was analyzed to identify novel variants. |
| Software: | |
| Notes: | |
| Links: | Edit |
| Reference |
|---|
| Authors: | Esdaile E, Till B, Kallenberg A, Fremeux M, Bickel L, Bellone RR |
| Affiliation: | Veterinary Genetics Laboratory, School of Veterinary Medicine, University of California-Davis, Davis, California, USA |
| Title: | A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse |
| Journal: | Animal Genetics, 2022, 53(4): 534-537 |
| Links: |
PubMed | Abstract | List all data
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