Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730013G03Rik |
A |
T |
1: 192,515,691 (GRCm39) |
|
noncoding transcript |
Het |
Abcb10 |
G |
A |
8: 124,681,166 (GRCm39) |
H677Y |
probably benign |
Het |
Ager |
T |
C |
17: 34,819,094 (GRCm39) |
V314A |
probably damaging |
Het |
Asxl3 |
A |
G |
18: 22,586,683 (GRCm39) |
M158V |
possibly damaging |
Het |
Atp1a2 |
G |
A |
1: 172,107,298 (GRCm39) |
Q741* |
probably null |
Het |
Atp1a2 |
A |
T |
1: 172,107,285 (GRCm39) |
M745K |
probably damaging |
Het |
Begain |
A |
G |
12: 108,999,656 (GRCm39) |
S577P |
probably benign |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Camk2b |
A |
G |
11: 5,926,872 (GRCm39) |
L497P |
possibly damaging |
Het |
Cand2 |
T |
A |
6: 115,780,773 (GRCm39) |
I1219N |
probably damaging |
Het |
Cckbr |
T |
A |
7: 105,083,255 (GRCm39) |
Y153N |
probably damaging |
Het |
Cep250 |
T |
G |
2: 155,833,514 (GRCm39) |
V1812G |
probably benign |
Het |
Cyp2c39 |
A |
T |
19: 39,556,643 (GRCm39) |
|
probably benign |
Het |
Ddx43 |
T |
A |
9: 78,324,001 (GRCm39) |
M444K |
probably damaging |
Het |
Dnm1 |
A |
T |
2: 32,213,462 (GRCm39) |
M506K |
probably benign |
Het |
Fcgbpl1 |
T |
C |
7: 27,854,060 (GRCm39) |
Y1675H |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,808,174 (GRCm39) |
T1498A |
probably benign |
Het |
Gcn1 |
A |
T |
5: 115,751,826 (GRCm39) |
Q2067L |
possibly damaging |
Het |
Get4 |
G |
T |
5: 139,249,384 (GRCm39) |
|
probably null |
Het |
Gm6370 |
G |
A |
5: 146,430,453 (GRCm39) |
A213T |
possibly damaging |
Het |
Gpr135 |
T |
C |
12: 72,117,047 (GRCm39) |
Y240C |
probably damaging |
Het |
Gstm5 |
T |
A |
3: 107,805,347 (GRCm39) |
L145Q |
probably damaging |
Het |
Hoxb3 |
T |
C |
11: 96,236,986 (GRCm39) |
Y355H |
probably damaging |
Het |
Hsf2 |
A |
C |
10: 57,372,370 (GRCm39) |
K108Q |
probably damaging |
Het |
Kdm3a |
T |
C |
6: 71,577,718 (GRCm39) |
N694S |
probably benign |
Het |
Lrpap1 |
G |
A |
5: 35,253,411 (GRCm39) |
|
probably benign |
Het |
Mapk8ip3 |
T |
C |
17: 25,118,532 (GRCm39) |
T1162A |
probably damaging |
Het |
Mettl14 |
T |
C |
3: 123,168,540 (GRCm39) |
|
probably benign |
Het |
Mrgprx1 |
T |
C |
7: 47,671,477 (GRCm39) |
Y90C |
probably benign |
Het |
Mybpc3 |
A |
T |
2: 90,951,368 (GRCm39) |
|
probably null |
Het |
Nup88 |
C |
T |
11: 70,860,518 (GRCm39) |
G87D |
probably benign |
Het |
Or5w20 |
A |
G |
2: 87,727,317 (GRCm39) |
Y258C |
possibly damaging |
Het |
Or7d9 |
A |
T |
9: 20,197,756 (GRCm39) |
T254S |
probably benign |
Het |
Or9i1 |
C |
T |
19: 13,839,187 (GRCm39) |
T10M |
probably damaging |
Het |
Pan2 |
G |
A |
10: 128,156,221 (GRCm39) |
E1133K |
probably benign |
Het |
Pcsk2 |
T |
C |
2: 143,635,045 (GRCm39) |
S307P |
probably damaging |
Het |
Pdgfa |
C |
T |
5: 138,971,950 (GRCm39) |
V150I |
probably damaging |
Het |
Phf12 |
T |
C |
11: 77,875,022 (GRCm39) |
C83R |
probably damaging |
Het |
Pla2g2c |
A |
G |
4: 138,463,319 (GRCm39) |
Y71C |
probably damaging |
Het |
Pou2f2 |
T |
A |
7: 24,797,107 (GRCm39) |
Q218L |
probably damaging |
Het |
Prl8a9 |
C |
T |
13: 27,743,353 (GRCm39) |
V151I |
possibly damaging |
Het |
Prop1 |
T |
C |
11: 50,842,911 (GRCm39) |
D92G |
probably damaging |
Het |
Rnf13 |
A |
G |
3: 57,703,644 (GRCm39) |
Y116C |
probably damaging |
Het |
Ro60 |
A |
G |
1: 143,637,013 (GRCm39) |
C400R |
possibly damaging |
Het |
Scrib |
T |
A |
15: 75,936,885 (GRCm39) |
K383* |
probably null |
Het |
Slc44a5 |
T |
C |
3: 153,944,796 (GRCm39) |
Y138H |
possibly damaging |
Het |
Stra6 |
G |
A |
9: 58,047,752 (GRCm39) |
V108M |
probably benign |
Het |
Tspan10 |
G |
T |
11: 120,337,198 (GRCm39) |
A323S |
probably benign |
Het |
Ttc22 |
T |
A |
4: 106,495,687 (GRCm39) |
V347D |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 87,983,780 (GRCm39) |
L193F |
probably benign |
Het |
Vps13d |
G |
T |
4: 144,894,716 (GRCm39) |
H457N |
probably benign |
Het |
Vrtn |
A |
G |
12: 84,695,607 (GRCm39) |
Y119C |
probably damaging |
Het |
Xpnpep3 |
T |
C |
15: 81,311,657 (GRCm39) |
F121S |
probably damaging |
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 |
|
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 |
IGL02447:Duox2
|
APN |
2 |
122,127,949 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|