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Table 2 Positions of potential QTL detected for BUN and MBUN

From: Using mid-infrared spectroscopy to increase GWAS power to detect QTL associated with blood urea nitrogen

Chr Pos (bp) Trait pBUN pMBUN Annotation Genes Start (bp) End (bp) N
2 47,485,307 MBUN 6.5 × 10–1 9.4 × 10–7 Intron EPC2 47,485,307 47,485,307 1
3 18,190,277 MBUN 3.1 × 10–2 6.3 × 10–7 Upstream CRCT1 18,190,277 18,190,277 1
3 55,238,179 MBUN 1.2 × 10–3 3.5 × 10–7 Intergenic PKN2-ENSBTAG00000051499 55,238,179 55,257,795 33
9 97,711,991 MBUN 3.0 × 10–2 8.4 × 10–7 Intron PRKN 97,711,991 97,711,991 1
11 99,897,676 MBUN 4.1 × 10–1 2.7 × 10–7 Intron ENSBTAG00000054738 99,897,676 99,916,846 6
11 103,271,858 MBUN 7.7 × 10–1 7.7 × 10–11 Synonymous GLT6D1 101,401,373 103,606,366 382
11 105,110,370 MBUN 8.0 × 10–1 6.8 × 10–7 Intron RXRA 105,110,370 105,110,370 1
12 84,682,464 MBUN 2.8 × 10–1 6.0 × 10–7 Intergenic IRS2-RF00001 84,682,431 84,699,022 3
13 15,837,206 BUN 4.8 × 10–7 6.6 × 10–2 Intergenic ENSBTAG00000048047-GATA3 15,835,519 15,839,775 5
14 631,698 MBUN 1.5 × 10–1 8.6 × 10–14 Upstream BOP1 512,818 1,278,273 209
X 31,752,695 MBUN 2.7 × 10–2 9.0 × 10–7 Intergenic ENSBTAG00000018311-IDS 31,752,695 31,752,695 1
X 100,768,475 MBUN 4.2 × 10–1 2.7 × 10–7 Intergenic MAOA-PPP1R2C 100,768,475 100,768,475 1
X 107,587,617 MBUN 3.1 × 10–1 8.7 × 10–7 Intergenic MAGEB16-ENSBTAG00000040406 107,587,617 107,587,617 1
  1. BUN, blood urea nitrogen; MBUN, BUN predicted using mid-infrared spectroscopy; chr, chromosome; pos, position of the most significant variant associated with the QTL; trait, trait for which the QTL is significant; bp, base pair according to the ARS-UCD1.2 annotation; pBUN, p-value in the GWAS for BUN; pMBUN, p-value in the GWAS for MBUN; annotation, annotation of the most significant variant; gene, gene in which the most significant region was located or, if the most significant variant was intergenic, the genes between which the most significant variant was located, start, start of the QTL interval; end, end of the QTL interval; N, number of variants with p ≤ 10–6 in the QTL interval