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Table 2 Mutations identified by TILLING.

From: TILLING is an effective reverse genetics technique for Caenorhabditis elegans

Gene

Strain

Allele

Change

Effect

C05C10.5

CN556

vc21

C112T

P23S

C05C10.5

CN1688

vc40

G178A

G45R

C05C10.5

CN1746

vc41

G230A

Non-coding

mel-32 C05D11.11

CN843

vc11

G361A

V106I

mel-32 C05D11.11

CN1181

vc68

C1339T

Q416*

mel-32 C05D11.11

CN1621

vc69

G289A

G82R

mel-32 C05D11.11

CN1665

vc70

G373A

D110N

mel-32 C05D11.11

CN1738

vc71

G384A

K113=

mel-32 C05D11.11

CN1805

vc72

G972A

K293=

mel-32 C05D11.11

CN1856

vc73

G373A

D110N

mus-81 C43E11.2

CN1162

vc42

C1830T

L368F

mus-81 C43E11.2

CN1162

vc43

G1231A

Non-coding

mus-81 C43E11.2

CN1211

vc44

A955T

Non-coding

mus-81 C43E11.2

CN1456

vc45

G972A

Non-coding

mus-81 C43E11.2

CN1604

vc46

G1897A

G390E

mus-81 C43E11.2

CN1766

vc47

C1687T

T320I

mus-81 C43E11.2

CN568

vc48

G1313A

D214N

xpf-1 C47D12.8

CN665

vc18

C602T

L183F

xpf-1 C47D12.8

CN720

vc19

G930A

R292H

xpf-1 C47D12.8

CN1286

vc62

G1036A

R278Q

xpf-1 C47D12.8

CN1475

vc63

G446A

E100K

xpf-1 C47D12.8

CN1574

vc64

C101T

Non-coding

xpf-1 C47D12.8

CN1574

vc65

G818T

S205=

xpf-1 C47D12.8

CN1751

vc66

C902T

V233=

xpf-1 C47D12.8

CN1798

vc67

G942A

D247N

F25H2.13

CN838

vc10

A1200T

I277F

F25H2.13

CN1245

vc52

G1206A

E279K

F25H2.13

CN1326

vc53

G421A

Non-coding

F25H2.13

CN1742

vc54

G285A

E95=

F25H2.13

CN1812

vc55

G399A

Non-coding

F25H2.13

CN1838

vc56

G1167A

A266T

F25H2.13

CN579

vc7

C649T

Non-coding

F25H2.13

CN579

vc8

C1165T

S265F

F25H2.13

CN48

vc9

G1242A

E291K

htp-3 F57C9.5

CN646

vc1

G2224A

E616K

htp-3 F57C9.5

CN823

vc13

G1785A

E469=

htp-3 F57C9.5

CN727

vc2

G2029A

E551K

htp-3 F57C9.5

CN1362

vc23

C2048T

P557L

htp-3 F57C9.5

CN1369

vc24

G1905A

S509=

htp-3 F57C9.5

CN1425

vc25

G2181A

Q601=

htp-3 F57C9.5

CN1630

vc26

G2230A

V618I

htp-3 F57C9.5

CN1723

vc27

C1245T

P306L

htp-3 F57C9.5

CN1735

vc28

C2331T

Y651=

htp-3 F57C9.5

CN825

vc3

G1333A

R335=

M03C11.2

CN1246

vc57

G4804A

E680K

M03C11.2

CN1479

vc58

G5097A

G725D

M03C11.2

CN1543

vc59

C4755T

I663=

M03C11.2

CN1643

vc60

C4739T

P658L

M03C11.2

CN1712

vc61

C5740T

H782Y

Cki-2 T05A6.2

CN843

vc20

C413T

T123I

Cki-2 T05A6.2

CN1157

vc31

G869A

Non-coding

Cki-2 T05A6.2

CN1231

vc32

C338T

T98I

Cki-2 T05A6.2

CN1254

vc33

G214A

G57R

Cki-2 T05A6.2

CN1309

vc34

G524A

E146K

Cki-2 T05A6.2

CN1364

vc35

G876A

Non-coding

Cki-2 T05A6.2

CN1575

vc36

G370A

V109M

Cki-2 T05A6.2

CN1643

vc37

C170T

S42F

Cki-2 T05A6.2

CN1672

vc38

G148A

E35K

Cki-2 T05A6.2

CN1787

vc39

G76A

Splice Junction

mdf-2 Y69A2AR.30

CN711

vc15

G243A

D65N

mdf-2 Y69A2AR.30

CN902

vc17

C1083T

Non-coding

mdf-2 Y69A2AR.30

CN1613

vc49

C838T

Non-coding

mdf-2 Y69A2AR.30

CN1703

vc50

C838T

Non-coding

mdf-2 Y69A2AR.30

CN1865

vc51

C520T

Non-coding

mdf-2 Y69A2AR.30

CN1114

vc74

G76A

Non-coding

htp-2 Y73B6BL.2

CN750

vc14

C507T

A139V

htp-2 Y73B6BL.2

CN50

vc22

C756T

T222I

htp-2 Y73B6BL.2

CN1271

vc29

C712T

S207=

htp-2 Y73B6BL.2

CN1540

vc30

G345A

R85Q

htp-2 Y73B6BL.2

CN574

vc5

G49A

D17N

htp-2 Y73B6BL.2

CN901

vc6

G878A

G263R

  1. One letter nucleotide and amino acid codes follow IUPAC-IUB nomenclature. The first letter in the Nucleotide Change column indicates the wildtype nucleotide at this site, followed by the position of the mutation from the start codon in the genomic DNA and then the mutant nucleotide. The first letter in the Effect column indicates the wildtype amino acid at this site, followed by the position of the mutation within the predicted protein sequence and then mutated amino acid. An equal sign after the amino acid position means no change in the amino acid encoded by that codon, and an asterisk indicates a stop codon. Mutations in introns and intergenic regions are designated "Non-coding".