QTL Map Information |
Chromosome: | 21 |
QTL Peak Location: | n/a |
QTL Span: | n/a 0.2-0.2 (Mbp) |
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Upper, "Suggestive": | n/a |
Upper, "Significant": | n/a |
Peak: | rs1148949845 |
Lower, "Significant": | n/a |
Lower, "Suggestive": | n/a |
Marker type: | SNP |
Analysis type: | Association |
Model tested: | n/a |
Test base: | n/a |
Threshold significance level: | Significant |
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P_values | <0.01 | Dominance effect: | n/a |
Additive effect: | n/a |
Associated Gene: | n/a |
Cis/Trans acting type: |  |
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Extended information: |
(none) |
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QTL Experiment in Brief |
Animals: | Animals were NAD/EDM affected and control Quarter Horses. |
Breeds associated:
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Design: | Animals were subjected to whole-genome sequencing, and association analysis was performed for equine neuroaxonal dystrophy/degenerative myeloencephalopathy. |
Analysis: | A case-control study was used. Genetic variants were identified in 28 candidate genes and subsequently used in a follow-up study in a validation population. |
Software: | SAMtools, GATK HaplotypeCaller, PLINK |
Notes: | |
Links: | Edit |
Reference |
Authors: | Ma Y, Peng S, Donnelly CG, Ghosh S, Miller AD, Woolard K, Finno CJ |
Affiliation: | Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, California 95616, USA |
Title: | Genetic polymorphisms in vitamin E transport genes as determinants for risk of equine neuroaxonal dystrophy |
Journal: | Journal of veterinary internal medicine, 2024, 38(1):417-423 |
Links: |
PubMed | Abstract | List all data
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Additional Information |
Comments: | Whole-genome sequencing |

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