Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
C |
4: 144,344,572 (GRCm39) |
I116T |
probably damaging |
Het |
Aatk |
G |
T |
11: 119,903,003 (GRCm39) |
F407L |
probably damaging |
Het |
Abca8a |
A |
T |
11: 109,917,681 (GRCm39) |
L1586Q |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,388,289 (GRCm39) |
|
probably null |
Het |
Ap5m1 |
A |
G |
14: 49,318,552 (GRCm39) |
D420G |
probably damaging |
Het |
Bcl6 |
A |
T |
16: 23,791,382 (GRCm39) |
L324* |
probably null |
Het |
Bicc1 |
A |
G |
10: 70,785,955 (GRCm39) |
S396P |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 36,929,679 (GRCm39) |
|
probably null |
Het |
Ccdc83 |
G |
A |
7: 89,908,722 (GRCm39) |
S4L |
probably damaging |
Het |
Cdkal1 |
T |
A |
13: 29,538,741 (GRCm39) |
M473L |
probably benign |
Het |
Cep85 |
T |
C |
4: 133,881,178 (GRCm39) |
H363R |
probably damaging |
Het |
Cfap61 |
G |
A |
2: 145,878,736 (GRCm39) |
|
probably null |
Het |
Cfap65 |
T |
C |
1: 74,943,184 (GRCm39) |
I1614V |
probably damaging |
Het |
Cluh |
T |
A |
11: 74,557,947 (GRCm39) |
F1062I |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,508,369 (GRCm39) |
T1294S |
possibly damaging |
Het |
Cops8 |
A |
C |
1: 90,534,341 (GRCm39) |
N94T |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,042,641 (GRCm39) |
D2364G |
possibly damaging |
Het |
Cyb5d1 |
T |
C |
11: 69,285,871 (GRCm39) |
D55G |
probably benign |
Het |
Cyp2c29 |
A |
T |
19: 39,275,676 (GRCm39) |
I39F |
probably benign |
Het |
Cyp2j8 |
T |
C |
4: 96,332,862 (GRCm39) |
S495G |
probably benign |
Het |
Dhx30 |
A |
G |
9: 109,916,703 (GRCm39) |
L575P |
probably damaging |
Het |
Dnah7a |
C |
T |
1: 53,560,333 (GRCm39) |
V2113I |
probably benign |
Het |
Dusp3 |
T |
C |
11: 101,865,631 (GRCm39) |
N95D |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fer1l4 |
T |
G |
2: 155,873,684 (GRCm39) |
Y1207S |
probably damaging |
Het |
Gdf6 |
A |
G |
4: 9,844,770 (GRCm39) |
H98R |
probably damaging |
Het |
Ggnbp2 |
T |
C |
11: 84,727,439 (GRCm39) |
N63S |
possibly damaging |
Het |
Ggt7 |
A |
G |
2: 155,337,639 (GRCm39) |
S504P |
probably damaging |
Het |
Gtf2h5 |
G |
A |
17: 6,134,853 (GRCm39) |
E48K |
probably benign |
Het |
Hivep3 |
T |
G |
4: 119,591,235 (GRCm39) |
V81G |
possibly damaging |
Het |
Igsf21 |
A |
G |
4: 139,755,425 (GRCm39) |
M410T |
probably damaging |
Het |
Insrr |
T |
C |
3: 87,716,725 (GRCm39) |
L651P |
probably damaging |
Het |
Iqcb1 |
A |
T |
16: 36,663,824 (GRCm39) |
|
probably null |
Het |
Klhdc7a |
G |
A |
4: 139,692,764 (GRCm39) |
R728C |
probably benign |
Het |
Lars2 |
T |
C |
9: 123,247,845 (GRCm39) |
L334P |
probably damaging |
Het |
Mast3 |
T |
C |
8: 71,233,607 (GRCm39) |
E994G |
probably damaging |
Het |
Mertk |
T |
A |
2: 128,643,392 (GRCm39) |
N930K |
probably benign |
Het |
Mettl21a |
A |
T |
1: 64,655,442 (GRCm39) |
V46E |
probably damaging |
Het |
Nedd4 |
T |
A |
9: 72,643,989 (GRCm39) |
C614S |
probably damaging |
Het |
Or13a19 |
T |
C |
7: 139,903,484 (GRCm39) |
S291P |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,348,895 (GRCm39) |
Y258* |
probably null |
Het |
Or5k1 |
G |
T |
16: 58,617,987 (GRCm39) |
A74D |
possibly damaging |
Het |
Pard3b |
C |
T |
1: 62,518,842 (GRCm39) |
R976* |
probably null |
Het |
Pcdhb16 |
A |
G |
18: 37,612,020 (GRCm39) |
T327A |
probably benign |
Het |
Pira12 |
A |
T |
7: 3,900,488 (GRCm39) |
N87K |
probably benign |
Het |
Ppp1r37 |
C |
A |
7: 19,266,371 (GRCm39) |
R465L |
probably null |
Het |
Ppp3ca |
C |
A |
3: 136,503,685 (GRCm39) |
T86K |
probably damaging |
Het |
Ralgapa2 |
G |
A |
2: 146,263,599 (GRCm39) |
T706I |
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,327,254 (GRCm39) |
L1747P |
possibly damaging |
Het |
Slc11a1 |
T |
A |
1: 74,419,824 (GRCm39) |
F166I |
probably damaging |
Het |
Slc25a18 |
G |
A |
6: 120,770,518 (GRCm39) |
|
probably null |
Het |
Stt3a |
A |
G |
9: 36,660,847 (GRCm39) |
|
probably null |
Het |
Supt16 |
G |
A |
14: 52,409,601 (GRCm39) |
R770* |
probably null |
Het |
Syde2 |
A |
G |
3: 145,707,713 (GRCm39) |
I551V |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,631,872 (GRCm39) |
N876K |
probably benign |
Het |
Tecta |
T |
C |
9: 42,303,326 (GRCm39) |
D102G |
probably damaging |
Het |
Tmc7 |
A |
T |
7: 118,152,039 (GRCm39) |
I294N |
possibly damaging |
Het |
Tmem174 |
T |
C |
13: 98,773,767 (GRCm39) |
Y21C |
probably damaging |
Het |
Tomm40l |
A |
T |
1: 171,049,550 (GRCm39) |
L13* |
probably null |
Het |
Trim30c |
A |
G |
7: 104,032,474 (GRCm39) |
V284A |
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,652 (GRCm39) |
S206L |
probably benign |
Het |
Uggt2 |
A |
T |
14: 119,312,749 (GRCm39) |
N353K |
probably damaging |
Het |
Vps13d |
C |
T |
4: 144,904,890 (GRCm39) |
V79M |
probably damaging |
Het |
Wfdc18 |
C |
T |
11: 83,600,739 (GRCm39) |
R45* |
probably null |
Het |
|
Other mutations in Flg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Flg2
|
APN |
3 |
93,109,416 (GRCm39) |
nonsense |
probably null |
|
IGL00092:Flg2
|
APN |
3 |
93,127,162 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00985:Flg2
|
APN |
3 |
93,110,585 (GRCm39) |
missense |
unknown |
|
IGL01077:Flg2
|
APN |
3 |
93,127,513 (GRCm39) |
missense |
unknown |
|
IGL01093:Flg2
|
APN |
3 |
93,109,678 (GRCm39) |
missense |
unknown |
|
IGL01120:Flg2
|
APN |
3 |
93,108,475 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01473:Flg2
|
APN |
3 |
93,110,327 (GRCm39) |
missense |
unknown |
|
IGL01584:Flg2
|
APN |
3 |
93,122,777 (GRCm39) |
missense |
unknown |
|
IGL01584:Flg2
|
APN |
3 |
93,120,773 (GRCm39) |
missense |
unknown |
|
IGL01686:Flg2
|
APN |
3 |
93,109,591 (GRCm39) |
missense |
unknown |
|
IGL02207:Flg2
|
APN |
3 |
93,127,435 (GRCm39) |
missense |
unknown |
|
IGL02294:Flg2
|
APN |
3 |
93,111,053 (GRCm39) |
missense |
unknown |
|
IGL02418:Flg2
|
APN |
3 |
93,108,361 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02581:Flg2
|
APN |
3 |
93,127,199 (GRCm39) |
missense |
unknown |
|
IGL02719:Flg2
|
APN |
3 |
93,127,438 (GRCm39) |
nonsense |
probably null |
|
IGL02795:Flg2
|
APN |
3 |
93,110,920 (GRCm39) |
missense |
unknown |
|
IGL02893:Flg2
|
APN |
3 |
93,110,920 (GRCm39) |
missense |
unknown |
|
IGL02958:Flg2
|
APN |
3 |
93,110,920 (GRCm39) |
missense |
unknown |
|
IGL03060:Flg2
|
APN |
3 |
93,110,920 (GRCm39) |
missense |
unknown |
|
IGL03088:Flg2
|
APN |
3 |
93,110,498 (GRCm39) |
missense |
unknown |
|
IGL03165:Flg2
|
APN |
3 |
93,121,918 (GRCm39) |
missense |
unknown |
|
IGL03342:Flg2
|
APN |
3 |
93,108,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03352:Flg2
|
APN |
3 |
93,109,801 (GRCm39) |
missense |
unknown |
|
IGL02796:Flg2
|
UTSW |
3 |
93,110,920 (GRCm39) |
missense |
unknown |
|
IGL02837:Flg2
|
UTSW |
3 |
93,109,044 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4618001:Flg2
|
UTSW |
3 |
93,111,088 (GRCm39) |
missense |
unknown |
|
R0087:Flg2
|
UTSW |
3 |
93,109,738 (GRCm39) |
missense |
unknown |
|
R0233:Flg2
|
UTSW |
3 |
93,109,104 (GRCm39) |
nonsense |
probably null |
|
R0233:Flg2
|
UTSW |
3 |
93,109,104 (GRCm39) |
nonsense |
probably null |
|
R0315:Flg2
|
UTSW |
3 |
93,122,029 (GRCm39) |
missense |
unknown |
|
R0390:Flg2
|
UTSW |
3 |
93,107,662 (GRCm39) |
splice site |
probably benign |
|
R0462:Flg2
|
UTSW |
3 |
93,108,744 (GRCm39) |
missense |
probably benign |
0.18 |
R0553:Flg2
|
UTSW |
3 |
93,110,891 (GRCm39) |
missense |
unknown |
|
R0828:Flg2
|
UTSW |
3 |
93,110,639 (GRCm39) |
missense |
unknown |
|
R1006:Flg2
|
UTSW |
3 |
93,108,514 (GRCm39) |
missense |
probably benign |
0.41 |
R1444:Flg2
|
UTSW |
3 |
93,109,620 (GRCm39) |
missense |
unknown |
|
R1497:Flg2
|
UTSW |
3 |
93,127,076 (GRCm39) |
missense |
unknown |
|
R1518:Flg2
|
UTSW |
3 |
93,110,445 (GRCm39) |
missense |
unknown |
|
R1737:Flg2
|
UTSW |
3 |
93,110,928 (GRCm39) |
missense |
unknown |
|
R1780:Flg2
|
UTSW |
3 |
93,110,306 (GRCm39) |
missense |
unknown |
|
R1797:Flg2
|
UTSW |
3 |
93,108,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Flg2
|
UTSW |
3 |
93,109,538 (GRCm39) |
missense |
unknown |
|
R2168:Flg2
|
UTSW |
3 |
93,109,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2292:Flg2
|
UTSW |
3 |
93,127,984 (GRCm39) |
missense |
unknown |
|
R2327:Flg2
|
UTSW |
3 |
93,110,913 (GRCm39) |
nonsense |
probably null |
|
R2512:Flg2
|
UTSW |
3 |
93,109,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Flg2
|
UTSW |
3 |
93,122,195 (GRCm39) |
missense |
unknown |
|
R3277:Flg2
|
UTSW |
3 |
93,122,195 (GRCm39) |
missense |
unknown |
|
R3522:Flg2
|
UTSW |
3 |
93,127,334 (GRCm39) |
missense |
unknown |
|
R3779:Flg2
|
UTSW |
3 |
93,109,730 (GRCm39) |
missense |
unknown |
|
R3926:Flg2
|
UTSW |
3 |
93,110,522 (GRCm39) |
missense |
unknown |
|
R4082:Flg2
|
UTSW |
3 |
93,110,828 (GRCm39) |
missense |
unknown |
|
R4407:Flg2
|
UTSW |
3 |
93,122,176 (GRCm39) |
missense |
unknown |
|
R5152:Flg2
|
UTSW |
3 |
93,122,284 (GRCm39) |
missense |
unknown |
|
R5253:Flg2
|
UTSW |
3 |
93,108,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Flg2
|
UTSW |
3 |
93,127,873 (GRCm39) |
missense |
unknown |
|
R5464:Flg2
|
UTSW |
3 |
93,109,277 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5539:Flg2
|
UTSW |
3 |
93,127,753 (GRCm39) |
missense |
unknown |
|
R5622:Flg2
|
UTSW |
3 |
93,109,871 (GRCm39) |
missense |
unknown |
|
R5788:Flg2
|
UTSW |
3 |
93,108,296 (GRCm39) |
missense |
probably benign |
0.41 |
R5792:Flg2
|
UTSW |
3 |
93,110,804 (GRCm39) |
missense |
unknown |
|
R5831:Flg2
|
UTSW |
3 |
93,107,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Flg2
|
UTSW |
3 |
93,110,756 (GRCm39) |
missense |
unknown |
|
R6041:Flg2
|
UTSW |
3 |
93,127,668 (GRCm39) |
missense |
probably benign |
0.01 |
R6189:Flg2
|
UTSW |
3 |
93,127,381 (GRCm39) |
missense |
unknown |
|
R6214:Flg2
|
UTSW |
3 |
93,109,166 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6215:Flg2
|
UTSW |
3 |
93,109,166 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6239:Flg2
|
UTSW |
3 |
93,108,579 (GRCm39) |
missense |
probably benign |
0.36 |
R6288:Flg2
|
UTSW |
3 |
93,111,092 (GRCm39) |
missense |
unknown |
|
R6413:Flg2
|
UTSW |
3 |
93,127,683 (GRCm39) |
missense |
unknown |
|
R6457:Flg2
|
UTSW |
3 |
93,127,789 (GRCm39) |
missense |
unknown |
|
R6468:Flg2
|
UTSW |
3 |
93,121,728 (GRCm39) |
missense |
unknown |
|
R6667:Flg2
|
UTSW |
3 |
93,109,068 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6930:Flg2
|
UTSW |
3 |
93,108,642 (GRCm39) |
nonsense |
probably null |
|
R6996:Flg2
|
UTSW |
3 |
93,110,256 (GRCm39) |
missense |
unknown |
|
R6996:Flg2
|
UTSW |
3 |
93,109,977 (GRCm39) |
missense |
unknown |
|
R7100:Flg2
|
UTSW |
3 |
93,111,018 (GRCm39) |
missense |
unknown |
|
R7133:Flg2
|
UTSW |
3 |
93,127,069 (GRCm39) |
missense |
unknown |
|
R7180:Flg2
|
UTSW |
3 |
93,110,140 (GRCm39) |
missense |
unknown |
|
R7325:Flg2
|
UTSW |
3 |
93,110,679 (GRCm39) |
missense |
unknown |
|
R7349:Flg2
|
UTSW |
3 |
93,127,513 (GRCm39) |
missense |
unknown |
|
R7531:Flg2
|
UTSW |
3 |
93,108,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R7571:Flg2
|
UTSW |
3 |
93,127,303 (GRCm39) |
nonsense |
probably null |
|
R7684:Flg2
|
UTSW |
3 |
93,126,956 (GRCm39) |
missense |
unknown |
|
R7810:Flg2
|
UTSW |
3 |
93,107,548 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7853:Flg2
|
UTSW |
3 |
93,128,054 (GRCm39) |
missense |
unknown |
|
R8031:Flg2
|
UTSW |
3 |
93,127,521 (GRCm39) |
missense |
unknown |
|
R8078:Flg2
|
UTSW |
3 |
93,107,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R8142:Flg2
|
UTSW |
3 |
93,122,782 (GRCm39) |
nonsense |
probably null |
|
R8156:Flg2
|
UTSW |
3 |
93,127,390 (GRCm39) |
missense |
unknown |
|
R8172:Flg2
|
UTSW |
3 |
93,108,468 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8204:Flg2
|
UTSW |
3 |
93,110,074 (GRCm39) |
missense |
unknown |
|
R8262:Flg2
|
UTSW |
3 |
93,127,517 (GRCm39) |
missense |
unknown |
|
R8269:Flg2
|
UTSW |
3 |
93,109,187 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8290:Flg2
|
UTSW |
3 |
93,110,069 (GRCm39) |
missense |
unknown |
|
R8444:Flg2
|
UTSW |
3 |
93,107,585 (GRCm39) |
missense |
probably damaging |
0.97 |
R8670:Flg2
|
UTSW |
3 |
93,108,791 (GRCm39) |
missense |
probably damaging |
0.97 |
R8755:Flg2
|
UTSW |
3 |
93,108,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R9039:Flg2
|
UTSW |
3 |
93,110,899 (GRCm39) |
missense |
unknown |
|
R9116:Flg2
|
UTSW |
3 |
93,109,591 (GRCm39) |
missense |
unknown |
|
R9214:Flg2
|
UTSW |
3 |
93,110,884 (GRCm39) |
missense |
unknown |
|
R9231:Flg2
|
UTSW |
3 |
93,109,508 (GRCm39) |
missense |
unknown |
|
R9553:Flg2
|
UTSW |
3 |
93,121,901 (GRCm39) |
missense |
unknown |
|
R9607:Flg2
|
UTSW |
3 |
93,108,719 (GRCm39) |
missense |
probably damaging |
0.98 |
R9735:Flg2
|
UTSW |
3 |
93,127,669 (GRCm39) |
missense |
unknown |
|
R9752:Flg2
|
UTSW |
3 |
93,108,467 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Flg2
|
UTSW |
3 |
93,110,045 (GRCm39) |
missense |
unknown |
|
Z1177:Flg2
|
UTSW |
3 |
93,109,727 (GRCm39) |
missense |
unknown |
|
|