Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
T |
A |
4: 144,401,269 (GRCm39) |
I72F |
probably benign |
Het |
Abhd18 |
T |
A |
3: 40,888,208 (GRCm39) |
F351I |
probably benign |
Het |
Agfg1 |
T |
A |
1: 82,859,944 (GRCm39) |
|
probably benign |
Het |
Antxr2 |
C |
T |
5: 98,178,267 (GRCm39) |
V48I |
possibly damaging |
Het |
Bcl9l |
T |
C |
9: 44,418,631 (GRCm39) |
M823T |
probably benign |
Het |
Card11 |
G |
A |
5: 140,892,679 (GRCm39) |
H129Y |
possibly damaging |
Het |
Ccr1 |
A |
T |
9: 123,763,753 (GRCm39) |
V259E |
probably benign |
Het |
Cdk13 |
G |
T |
13: 17,947,001 (GRCm39) |
P586T |
probably benign |
Het |
Cep295 |
C |
T |
9: 15,243,807 (GRCm39) |
V1502I |
probably damaging |
Het |
Csnk1g3 |
T |
C |
18: 54,028,942 (GRCm39) |
S32P |
probably benign |
Het |
Dpysl4 |
G |
A |
7: 138,678,516 (GRCm39) |
R492Q |
probably damaging |
Het |
Gm7361 |
T |
C |
5: 26,462,853 (GRCm39) |
S32P |
probably benign |
Het |
Grip1 |
T |
A |
10: 119,855,976 (GRCm39) |
V234E |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,404,610 (GRCm39) |
I4477L |
possibly damaging |
Het |
Il18r1 |
G |
A |
1: 40,537,497 (GRCm39) |
|
probably null |
Het |
Itpkb |
A |
G |
1: 180,248,919 (GRCm39) |
|
probably benign |
Het |
Jag2 |
T |
C |
12: 112,876,232 (GRCm39) |
Y799C |
probably damaging |
Het |
Jak2 |
A |
G |
19: 29,277,014 (GRCm39) |
K857R |
probably damaging |
Het |
Kbtbd12 |
A |
T |
6: 88,595,676 (GRCm39) |
S51R |
probably damaging |
Het |
Kcnc2 |
T |
G |
10: 112,291,851 (GRCm39) |
D346E |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 191,907,224 (GRCm39) |
M92K |
possibly damaging |
Het |
Kcnk1 |
A |
G |
8: 126,751,819 (GRCm39) |
I142V |
probably damaging |
Het |
Lsm11 |
T |
C |
11: 45,828,191 (GRCm39) |
N196D |
probably damaging |
Het |
Mpeg1 |
G |
T |
19: 12,440,156 (GRCm39) |
C538F |
probably damaging |
Het |
Nrap |
G |
A |
19: 56,333,951 (GRCm39) |
Q969* |
probably null |
Het |
Nt5el |
A |
T |
13: 105,236,967 (GRCm39) |
S73C |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,204,511 (GRCm39) |
|
probably null |
Het |
Pdcd5 |
A |
G |
7: 35,342,110 (GRCm39) |
V166A |
possibly damaging |
Het |
Plcb2 |
A |
T |
2: 118,543,636 (GRCm39) |
I745N |
probably damaging |
Het |
Ptprt |
T |
C |
2: 162,120,027 (GRCm39) |
T147A |
probably benign |
Het |
Rbp3 |
A |
T |
14: 33,676,460 (GRCm39) |
D136V |
probably damaging |
Het |
Ripor3 |
G |
T |
2: 167,834,750 (GRCm39) |
T247N |
probably damaging |
Het |
Sgcd |
A |
C |
11: 46,870,082 (GRCm39) |
|
probably benign |
Het |
Slc26a6 |
T |
C |
9: 108,734,251 (GRCm39) |
Y211H |
probably benign |
Het |
Slc37a3 |
T |
A |
6: 39,314,129 (GRCm39) |
E494D |
probably benign |
Het |
Smc5 |
T |
C |
19: 23,234,856 (GRCm39) |
E326G |
probably benign |
Het |
Tctn2 |
T |
C |
5: 124,753,316 (GRCm39) |
|
noncoding transcript |
Het |
Tk2 |
T |
A |
8: 104,967,770 (GRCm39) |
N93I |
probably damaging |
Het |
Tmed6 |
A |
G |
8: 107,792,240 (GRCm39) |
F2L |
possibly damaging |
Het |
Tox3 |
A |
G |
8: 90,984,781 (GRCm39) |
|
probably benign |
Het |
Tspan9 |
T |
C |
6: 127,941,401 (GRCm39) |
Y237C |
probably benign |
Het |
Ubqlnl |
A |
G |
7: 103,797,856 (GRCm39) |
L547P |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,189,223 (GRCm39) |
D1421G |
probably damaging |
Het |
Unc80 |
T |
A |
1: 66,542,703 (GRCm39) |
I319K |
possibly damaging |
Het |
Vac14 |
A |
G |
8: 111,380,260 (GRCm39) |
D441G |
probably benign |
Het |
Vamp8 |
C |
T |
6: 72,365,316 (GRCm39) |
V5M |
probably damaging |
Het |
Yeats2 |
T |
A |
16: 20,012,429 (GRCm39) |
H560Q |
probably benign |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
Zfp773 |
G |
T |
7: 7,139,655 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Duox2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00474:Duox2
|
APN |
2 |
122,114,056 (GRCm39) |
missense |
probably benign |
|
IGL00790:Duox2
|
APN |
2 |
122,122,781 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01346:Duox2
|
APN |
2 |
122,117,683 (GRCm39) |
splice site |
probably benign |
|
IGL01607:Duox2
|
APN |
2 |
122,122,800 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01798:Duox2
|
APN |
2 |
122,112,389 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Duox2
|
APN |
2 |
122,121,190 (GRCm39) |
missense |
probably benign |
|
IGL02219:Duox2
|
APN |
2 |
122,125,145 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02227:Duox2
|
APN |
2 |
122,115,634 (GRCm39) |
splice site |
probably benign |
|
IGL02276:Duox2
|
APN |
2 |
122,124,566 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02806:Duox2
|
APN |
2 |
122,115,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03091:Duox2
|
APN |
2 |
122,119,955 (GRCm39) |
missense |
probably benign |
0.03 |
Bedazzled
|
UTSW |
2 |
122,117,602 (GRCm39) |
missense |
possibly damaging |
0.76 |
Birthday
|
UTSW |
2 |
122,112,352 (GRCm39) |
missense |
probably benign |
|
gregorian
|
UTSW |
2 |
122,119,826 (GRCm39) |
nonsense |
probably null |
|
julian
|
UTSW |
2 |
122,119,813 (GRCm39) |
missense |
probably benign |
0.08 |
mayan
|
UTSW |
2 |
122,115,064 (GRCm39) |
missense |
probably benign |
0.00 |
minor
|
UTSW |
2 |
122,111,977 (GRCm39) |
missense |
probably damaging |
1.00 |
oaf
|
UTSW |
2 |
122,125,657 (GRCm39) |
missense |
probably damaging |
0.98 |
paltry
|
UTSW |
2 |
122,113,541 (GRCm39) |
critical splice donor site |
probably null |
|
promethius
|
UTSW |
2 |
122,126,862 (GRCm39) |
missense |
probably benign |
|
Recruit
|
UTSW |
2 |
122,114,378 (GRCm39) |
missense |
possibly damaging |
0.83 |
schlemiel
|
UTSW |
2 |
122,120,044 (GRCm39) |
missense |
probably null |
0.89 |
stumblebum
|
UTSW |
2 |
122,115,148 (GRCm39) |
missense |
probably damaging |
1.00 |
Two-bit
|
UTSW |
2 |
122,111,483 (GRCm39) |
missense |
probably benign |
0.42 |
R0049:Duox2
|
UTSW |
2 |
122,127,167 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0244:Duox2
|
UTSW |
2 |
122,122,341 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Duox2
|
UTSW |
2 |
122,122,785 (GRCm39) |
missense |
probably benign |
0.10 |
R0378:Duox2
|
UTSW |
2 |
122,115,064 (GRCm39) |
missense |
probably benign |
0.00 |
R0383:Duox2
|
UTSW |
2 |
122,122,291 (GRCm39) |
critical splice donor site |
probably null |
|
R0442:Duox2
|
UTSW |
2 |
122,119,813 (GRCm39) |
missense |
probably benign |
0.08 |
R0524:Duox2
|
UTSW |
2 |
122,112,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0560:Duox2
|
UTSW |
2 |
122,122,035 (GRCm39) |
missense |
probably benign |
0.04 |
R0562:Duox2
|
UTSW |
2 |
122,120,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Duox2
|
UTSW |
2 |
122,123,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Duox2
|
UTSW |
2 |
122,115,249 (GRCm39) |
missense |
probably benign |
0.01 |
R0963:Duox2
|
UTSW |
2 |
122,117,653 (GRCm39) |
missense |
probably benign |
0.03 |
R1254:Duox2
|
UTSW |
2 |
122,113,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Duox2
|
UTSW |
2 |
122,112,232 (GRCm39) |
missense |
probably benign |
0.20 |
R1473:Duox2
|
UTSW |
2 |
122,117,602 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1489:Duox2
|
UTSW |
2 |
122,123,877 (GRCm39) |
missense |
probably benign |
|
R1738:Duox2
|
UTSW |
2 |
122,123,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Duox2
|
UTSW |
2 |
122,117,532 (GRCm39) |
missense |
probably benign |
0.00 |
R1809:Duox2
|
UTSW |
2 |
122,114,378 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1843:Duox2
|
UTSW |
2 |
122,122,739 (GRCm39) |
critical splice donor site |
probably null |
|
R1903:Duox2
|
UTSW |
2 |
122,125,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Duox2
|
UTSW |
2 |
122,127,853 (GRCm39) |
splice site |
probably null |
|
R2069:Duox2
|
UTSW |
2 |
122,117,589 (GRCm39) |
missense |
probably benign |
0.01 |
R2073:Duox2
|
UTSW |
2 |
122,125,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Duox2
|
UTSW |
2 |
122,125,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Duox2
|
UTSW |
2 |
122,125,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Duox2
|
UTSW |
2 |
122,111,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R3123:Duox2
|
UTSW |
2 |
122,111,554 (GRCm39) |
splice site |
probably benign |
|
R3907:Duox2
|
UTSW |
2 |
122,113,541 (GRCm39) |
critical splice donor site |
probably null |
|
R4572:Duox2
|
UTSW |
2 |
122,112,207 (GRCm39) |
missense |
probably benign |
0.00 |
R4614:Duox2
|
UTSW |
2 |
122,120,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4675:Duox2
|
UTSW |
2 |
122,111,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Duox2
|
UTSW |
2 |
122,115,397 (GRCm39) |
missense |
probably benign |
0.01 |
R4817:Duox2
|
UTSW |
2 |
122,126,996 (GRCm39) |
missense |
probably damaging |
0.98 |
R4931:Duox2
|
UTSW |
2 |
122,127,236 (GRCm39) |
missense |
probably benign |
0.01 |
R5138:Duox2
|
UTSW |
2 |
122,128,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Duox2
|
UTSW |
2 |
122,125,617 (GRCm39) |
missense |
probably benign |
|
R5344:Duox2
|
UTSW |
2 |
122,112,352 (GRCm39) |
missense |
probably benign |
|
R5385:Duox2
|
UTSW |
2 |
122,125,617 (GRCm39) |
missense |
probably benign |
|
R5386:Duox2
|
UTSW |
2 |
122,125,617 (GRCm39) |
missense |
probably benign |
|
R5493:Duox2
|
UTSW |
2 |
122,111,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R5632:Duox2
|
UTSW |
2 |
122,111,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5742:Duox2
|
UTSW |
2 |
122,115,402 (GRCm39) |
missense |
probably benign |
0.00 |
R6228:Duox2
|
UTSW |
2 |
122,117,674 (GRCm39) |
missense |
probably benign |
0.38 |
R6380:Duox2
|
UTSW |
2 |
122,111,483 (GRCm39) |
missense |
probably benign |
0.42 |
R6398:Duox2
|
UTSW |
2 |
122,126,851 (GRCm39) |
missense |
probably benign |
0.06 |
R6409:Duox2
|
UTSW |
2 |
122,115,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:Duox2
|
UTSW |
2 |
122,125,095 (GRCm39) |
missense |
probably benign |
0.29 |
R6596:Duox2
|
UTSW |
2 |
122,115,819 (GRCm39) |
missense |
probably benign |
|
R6719:Duox2
|
UTSW |
2 |
122,114,867 (GRCm39) |
splice site |
probably null |
|
R6981:Duox2
|
UTSW |
2 |
122,121,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7036:Duox2
|
UTSW |
2 |
122,110,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:Duox2
|
UTSW |
2 |
122,119,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Duox2
|
UTSW |
2 |
122,120,033 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7127:Duox2
|
UTSW |
2 |
122,122,430 (GRCm39) |
missense |
probably benign |
0.02 |
R7259:Duox2
|
UTSW |
2 |
122,125,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R7698:Duox2
|
UTSW |
2 |
122,111,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Duox2
|
UTSW |
2 |
122,113,948 (GRCm39) |
missense |
probably benign |
0.00 |
R8103:Duox2
|
UTSW |
2 |
122,117,535 (GRCm39) |
missense |
probably benign |
|
R8231:Duox2
|
UTSW |
2 |
122,120,044 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8439:Duox2
|
UTSW |
2 |
122,128,636 (GRCm39) |
missense |
probably benign |
|
R8712:Duox2
|
UTSW |
2 |
122,119,826 (GRCm39) |
nonsense |
probably null |
|
R8887:Duox2
|
UTSW |
2 |
122,120,044 (GRCm39) |
missense |
probably null |
0.89 |
R8909:Duox2
|
UTSW |
2 |
122,126,862 (GRCm39) |
missense |
probably benign |
|
R9022:Duox2
|
UTSW |
2 |
122,110,919 (GRCm39) |
makesense |
probably null |
|
R9350:Duox2
|
UTSW |
2 |
122,115,729 (GRCm39) |
nonsense |
probably null |
|
R9727:Duox2
|
UTSW |
2 |
122,116,998 (GRCm39) |
nonsense |
probably null |
|
Z1176:Duox2
|
UTSW |
2 |
122,126,988 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Duox2
|
UTSW |
2 |
122,123,933 (GRCm39) |
missense |
probably damaging |
0.98 |
|