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. 2010 Oct;186(2):493–503. doi: 10.1534/genetics.110.120105

TABLE 2.

Genome location of mutations detected in the Mut2, 3, and 4 lines

Amino acid change Distribution of sequence reads
Chromosome SGD Position HP tract Strain Gene Mutation A G T C Indel
1 139,349–139,358 10 4 del 1 11 8
2 275,549–275,557 9 2 del 3 3
2 92,271–92,279 9 3 del 1 10 8
2 92,271–92,279 9 2 del 3 0
2 423,462–423,469 8 3 ins 8 16
2 662,560–662,569 10 4 YBR219C fs; 103–106 del 6 5
2 653,035–653,045 11 4 del 13 9
3 212,451–212,457 7C 3 YCR048W/ARE1 fs; 176–178 del 15 11
3 275,289 NA 4 YCR091W/KIN82 297; V to I G to A 12 15
4 512,796 NA 2 A to T 8 7
4 814,336 NA 2 G to A 10 6
4 929,182–929,193 12 3 del 1 5 4
4 963,768 NA 3 YDR252W/BTT1 120: G to V T to G 12 18
4 231,908–231,914 7 4 del 12 12
4 1,386,657–1,386,664 8 4 del 17 11
4 470,576–470,584 9 4 del 19 12
4 832,716–832,726 11 4 del 15 7
4 50,592–50,603 12 4 del 10 9
1,054,759 NA 4 A to T 9 11
5 305,972 NA 2 C to A 5 5
5 479,369 NA 2 YER155C/BEM2 1159; S to C T to A 8 3
5 225,319–225,327 9 3 Del 9 7
5 403,576 NA 3 YER122C/GLO3 258; A to E G to T 8 14
5 34,325–34,333 9 4 del 11 7
5 402,832–402,843 12 4 del 13 7
6 223,108–223,118 11 3 del 10 7
6 114,200–114,210 11 4 del 6 7
6 88,832 NA 4 YFL024C/EPL1 504; D to E G to T 15 13
6 225,229 NA 4 YFR034C/PHO4 240; R to G G to C 9 8
7 194,092–194,098 7 3 YGL163C/RAD54 fs; 771–773 del 13 13
7 878,690–878,701 12 3 del 6 4
7 653,363–653,369 7 4 del 14 10
7 882,549–882,558 10 4 del 10 6
7 20,017–20,027 11 4 del 10 5
7 678,172–678,182 11 4 del 11 9
8 150,380–150,386 7 3 del 11 1 12
8 472,612–472,624 13 3 del 10 8
8 288,299 NA 3 YHR092C/HXT4 172; K to K C to T 5 6 1
8 370,253 NA 3 YHR132W-A/IGO2 46: Y to F A to T 15 12 1 1
9 270,327 NA 2 YIL046W/MET30 560; A to S G to T 5 4
9 375,856 NA 3 YIR010W/DSN1 143; M to I G to A 7 10
9 199,995 NA 4 YIL087C/AIM19 41; T to I G to A 12 18
10 445,012–445,020 9 3 del 10 6
10 131,051–131,059 9 4 del 11 15
10 469,684–469,694 11 4 del 19 6
11 162,688–162,695 8 4 del 9 1 7
11 403,466 NA 4 YKL018C-A 19; S to S C to T 13 13
12 405,712–405,719 8 2 YLR131C/ACE2 fs; 369–371 del 4 3
12 32,320-32,330 11 3 del 9 5
12 964,065 NA 3 YLR420W/URA4 95: R to H G to A 11 12
12 1,009,007 NA 3 YLR436C/ECM30 746; I to V T to C 12 12
12 363,531-363,537 7 4 YLR106C/MDN1 fs; 68–70 del 11 13
12 201,846-201,856 11 4 del 14 9
12 1,047,741 NA 4 YLR454W/FMP27 1249: D to G A to G 10 12 1
13 763,010-763,016 7 2 SNR86 (small nucleolar RNA) ins 5 5
13 241,855-241,867 13 3 del 12 6
13 311,843 NA 3 C to T 15 25
13 139,705-139,709 5 4 YML067C/ERV41 fs; 138–139 del 15 13
13 816,457-816,463 7 4 YMR275C/BUL1 fs; 706–708 del 11 9
14 761,792 NA 2 YNR069C/BSC5 267; V to V C to T 8 6 1
14 222,733 NA 3 YNL225C/CMN67 580; V to M C to T 1 17 10
14 435,595-435,601 7 4 YNL101W/AVT4 fs; 199–201 del 9 10
14 481,123-481,129 7 4 del 15 8
14 685,574-685,582 9 4 del 12 1 9
14 575,616-575,626 11 4 del 12 8
14 400,002 NA 4 YNL121C/TOM70 180; G to STOP C to A 15 15
14 734,521 NA 4 YNR058W/BIO3 77; L to L A to G 11 10
15 854,146-854,153 8 2 del 4 5
15 874,052-874,057 6 3 YOR296W fs; 1284–1286 del 10 7
15 767,667-767,673 7 3 YOR228C fs; 36–38 del 10 7
15 822,829-822,835 7 3 YOR267C/HRK1 fs; 678–680 del 11 8
16 146,421-146,427 7 2 YPL216W fs; 868–870 del 7 5
16 22,677 NA 4 C to T 20 14
16 131,583 NA 4 YPL222W/FMP40 475; A to T G to A 11 15 1
16 509,632 NA 4 YPL022W/RAD1 980; A to S G to T 19 18 1
16 570,131 NA 4 YPR007C/REC8 415; S to M G to A 11 11

The type of mutation [base substitution, single-nt insertion (ins), single-nt deletion (del)] is shown, as well as the length of the HP tract that contains an indel. The specific Mut line (2, 3, or 4) is indicated under “strain.” All HP tracts were poly(A) or poly(T) except for the mutation in chromosome 3 at 212,451–212,457, which involved a poly(C) tract. For mutations that occurred within an open reading frame, both the gene name and predicted amino acid changes (fs, frameshift) are provided. NA, not applicable. Coordinates are presented as shown in the SGD (http://www.yeastgenome.org/). The number and distribution of the sequence reads are presented for each mutation. The frameshift mutation in YLR106C/MDN1 conferred a recessive lethal phenotype (data not shown).