Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,727,713 (GRCm39) |
W309* |
probably null |
Het |
Aox1 |
G |
A |
1: 58,124,620 (GRCm39) |
V954I |
probably benign |
Het |
Asnsd1 |
A |
C |
1: 53,387,187 (GRCm39) |
|
probably null |
Het |
Aste1 |
A |
G |
9: 105,274,056 (GRCm39) |
K38E |
probably damaging |
Het |
Catsperg1 |
A |
G |
7: 28,899,664 (GRCm39) |
V339A |
probably damaging |
Het |
Ccdc13 |
A |
G |
9: 121,627,975 (GRCm39) |
|
probably benign |
Het |
Cd79b |
C |
A |
11: 106,203,267 (GRCm39) |
|
probably null |
Het |
Cemip2 |
C |
A |
19: 21,789,751 (GRCm39) |
N650K |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,247,380 (GRCm39) |
L981P |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,029,761 (GRCm39) |
F132L |
probably damaging |
Het |
Dhx9 |
G |
A |
1: 153,348,209 (GRCm39) |
P336S |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,303,945 (GRCm39) |
K1320E |
probably damaging |
Het |
Dmbt1 |
G |
T |
7: 130,668,463 (GRCm39) |
C573F |
possibly damaging |
Het |
Dmtn |
A |
G |
14: 70,850,776 (GRCm39) |
I205T |
probably benign |
Het |
Efnb3 |
C |
A |
11: 69,447,591 (GRCm39) |
V181L |
probably benign |
Het |
Gabbr1 |
A |
G |
17: 37,380,257 (GRCm39) |
D604G |
probably damaging |
Het |
Glis2 |
T |
A |
16: 4,428,197 (GRCm39) |
L83* |
probably null |
Het |
Gm10719 |
T |
A |
9: 3,019,040 (GRCm39) |
|
probably null |
Homo |
Hipk3 |
T |
C |
2: 104,264,086 (GRCm39) |
D804G |
probably damaging |
Het |
Kcnd1 |
G |
C |
X: 7,690,148 (GRCm39) |
A23P |
probably damaging |
Homo |
Kcnj13 |
A |
G |
1: 87,314,256 (GRCm39) |
V322A |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,688,426 (GRCm39) |
L617P |
probably damaging |
Het |
Npc1 |
ACAGCAGCAGCAGCAGCAG |
ACAGCAGCAGCAGCAG |
18: 12,369,249 (GRCm39) |
|
probably benign |
Het |
Or8b3b |
A |
G |
9: 38,584,510 (GRCm39) |
S90P |
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,172,183 (GRCm39) |
V326I |
probably benign |
Het |
Pcsk7 |
A |
C |
9: 45,821,674 (GRCm39) |
N156T |
possibly damaging |
Het |
Pde4d |
C |
T |
13: 110,085,967 (GRCm39) |
S515L |
probably damaging |
Het |
Peg10 |
GC |
GCCCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Ppp2r5a |
T |
A |
1: 191,094,447 (GRCm39) |
Q191L |
probably benign |
Het |
Prom2 |
A |
G |
2: 127,381,695 (GRCm39) |
|
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Sart3 |
C |
T |
5: 113,881,267 (GRCm39) |
A938T |
probably benign |
Het |
Scn3a |
T |
C |
2: 65,325,380 (GRCm39) |
I1046V |
probably benign |
Het |
Sh3glb2 |
T |
C |
2: 30,235,805 (GRCm39) |
E313G |
possibly damaging |
Het |
Slc13a1 |
A |
T |
6: 24,090,795 (GRCm39) |
Y541* |
probably null |
Het |
Smtnl2 |
G |
A |
11: 72,292,225 (GRCm39) |
A274V |
probably damaging |
Het |
Spata31h1 |
T |
A |
10: 82,126,946 (GRCm39) |
K2021N |
probably benign |
Het |
Speer1d |
C |
T |
5: 11,307,197 (GRCm39) |
T25I |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,525,724 (GRCm39) |
V27A |
possibly damaging |
Het |
Tmem116 |
C |
T |
5: 121,629,171 (GRCm39) |
T188M |
probably benign |
Het |
Trim21 |
A |
G |
7: 102,208,646 (GRCm39) |
S358P |
probably damaging |
Het |
Ttc21a |
A |
G |
9: 119,795,838 (GRCm39) |
Y1224C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,710,552 (GRCm39) |
|
probably benign |
Het |
Vmn2r99 |
A |
G |
17: 19,602,820 (GRCm39) |
Q525R |
probably benign |
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 |
R2220:Flg2
|
UTSW |
3 |
93,109,492 (GRCm39) |
missense |
unknown |
|
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 |
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 |
|
|