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. 2005 Jan;169(1):243–257. doi: 10.1534/genetics.104.032870

TABLE 6.

Genotype-to-transcript-level associations*

Phenotype Marker Frequency of “fit” allele Marker typea Adjusted r2b Other associationsc
Acp26Aa Acp33s1559** 0.91 GAT(pref.):GAC(un.) 0.05 None
CG8137 CG8137s2957** 0.50 GGA(un.):GGT(un.) 0.08 29, 33 (−): 36 (+)
Acp29AB CG17331s2065**** 0.70 AAC(pref.):AAT(un.) 0.15 P1 (+)
CG31872 None NA NA NA NA
Acp32CD None NA NA NA NA
Acp33A Acp29s2633*** 0.95 Downstream 0.10 32, 8137 (+)
CG17331 CG17331s486*** 0.33 Upstream 0.08 53 (+)
Acp36DE CG8137s2957** 0.50 GGA(un.):GGT(un.) 0.07 29, 33 (−): FecO, 8137 (+)
Acp36s2084** 0.52 CUA(un.):GUC(un.) 0.09 None
Acp36Indel2623**** 0.47 LLREAQQK pos. 253 0.12 None
PEBs1155*** 0.44 Upstream 0.11 None
Acp53Ea Acp26s2193*** 0.29 AGC(pref.):AGT(un.) 0.11 26, 33, 36, 31872 (+)
Acp26s2201** 0.28 ATA(I):AGC(S) 0.07 P2 (−)
PEBII Acp53s1760** 0.91 ACC(pref.):ACT(un.) 0.10 None
Acp53s1766** 0.70 CGT(un.):CGC(pref.) 0.08 26, 29, 33, 31872 (+)
*

Comparisonwise P < 0.05,

**

P < 0.01,

***

P ≤ 0.001,

****

Experimentwise P < 0.05. NA, not applicable.

a

High-fitness codon shown on the left with its amino acid for nonsynonymous changes or usage; preferred (pref.) and unpreferred (un.) for synonymous changes indicated in parentheses.

b

Calculated using a simple linear regression considering only the individually significant marker (see text).

c

“Other associations” indicates other phenotypes that were associated with that marker. Significant associations are underlined. Antagonistic associations indicated by (−) and protagonistic associations indicated by (+). Markers associated with both phenotype and expression were considered protagonistic if the same allele produced higher fitness and higher transcript abundance. Genes are listed excluding the “CG” or “Acp” prefix.