Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,546,642 (GRCm39) |
S320T |
probably benign |
Het |
Alg8 |
T |
A |
7: 97,036,006 (GRCm39) |
|
probably benign |
Het |
Anp32b |
G |
A |
4: 46,469,930 (GRCm39) |
E202K |
unknown |
Het |
Apcdd1 |
A |
G |
18: 63,069,973 (GRCm39) |
|
probably null |
Het |
Apobec2 |
A |
G |
17: 48,730,444 (GRCm39) |
V74A |
possibly damaging |
Het |
Arid3c |
A |
T |
4: 41,729,959 (GRCm39) |
C79S |
probably benign |
Het |
Atp1a2 |
A |
T |
1: 172,118,994 (GRCm39) |
|
probably benign |
Het |
B2m |
A |
T |
2: 121,981,471 (GRCm39) |
N62I |
probably damaging |
Het |
Borcs5 |
T |
C |
6: 134,663,086 (GRCm39) |
|
probably null |
Het |
Ccn1 |
A |
G |
3: 145,355,075 (GRCm39) |
L60P |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,714,674 (GRCm39) |
K127E |
probably damaging |
Het |
Cep170 |
T |
C |
1: 176,563,433 (GRCm39) |
H726R |
possibly damaging |
Het |
Col5a2 |
A |
C |
1: 45,466,219 (GRCm39) |
S190A |
probably benign |
Het |
Cryba4 |
T |
C |
5: 112,398,990 (GRCm39) |
D5G |
probably damaging |
Het |
Cyp2a5 |
T |
G |
7: 26,535,299 (GRCm39) |
V87G |
probably damaging |
Het |
Dcaf8 |
A |
G |
1: 172,013,965 (GRCm39) |
|
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,404,500 (GRCm39) |
S2681P |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,327 (GRCm39) |
S673P |
probably damaging |
Het |
Deptor |
T |
A |
15: 55,044,428 (GRCm39) |
I198N |
probably damaging |
Het |
Ebf2 |
T |
C |
14: 67,628,007 (GRCm39) |
I334T |
possibly damaging |
Het |
F5 |
A |
G |
1: 164,020,134 (GRCm39) |
R870G |
probably benign |
Het |
Gm11938 |
T |
A |
11: 99,494,119 (GRCm39) |
|
probably null |
Het |
Gm6370 |
A |
G |
5: 146,430,708 (GRCm39) |
T298A |
probably benign |
Het |
H60b |
C |
A |
10: 22,159,441 (GRCm39) |
|
probably benign |
Het |
Hsbp1 |
A |
G |
8: 120,071,324 (GRCm39) |
T4A |
possibly damaging |
Het |
Hsd3b3 |
A |
T |
3: 98,649,524 (GRCm39) |
D266E |
possibly damaging |
Het |
Ift172 |
T |
C |
5: 31,440,426 (GRCm39) |
Y287C |
probably damaging |
Het |
Il20rb |
T |
A |
9: 100,368,371 (GRCm39) |
Q4L |
probably benign |
Het |
Krt5 |
T |
C |
15: 101,617,470 (GRCm39) |
D421G |
probably damaging |
Het |
Lonp1 |
G |
C |
17: 56,927,263 (GRCm39) |
A330G |
probably benign |
Het |
Me3 |
A |
G |
7: 89,445,871 (GRCm39) |
D196G |
probably damaging |
Het |
Mfsd12 |
T |
A |
10: 81,199,461 (GRCm39) |
V451E |
probably null |
Het |
Mib1 |
A |
G |
18: 10,794,503 (GRCm39) |
N663S |
possibly damaging |
Het |
Mtus2 |
A |
T |
5: 148,015,244 (GRCm39) |
N679I |
probably benign |
Het |
Myt1 |
A |
G |
2: 181,438,915 (GRCm39) |
T146A |
probably benign |
Het |
Neb |
T |
A |
2: 52,160,281 (GRCm39) |
H2244L |
probably damaging |
Het |
Or51l4 |
T |
C |
7: 103,404,376 (GRCm39) |
T139A |
probably damaging |
Het |
Or5b21 |
A |
C |
19: 12,839,663 (GRCm39) |
I175L |
probably benign |
Het |
Or5p81 |
C |
T |
7: 108,267,289 (GRCm39) |
T222I |
probably benign |
Het |
Pabpc4 |
A |
G |
4: 123,185,524 (GRCm39) |
|
probably null |
Het |
Padi1 |
C |
A |
4: 140,552,266 (GRCm39) |
V393L |
probably damaging |
Het |
Pax2 |
A |
T |
19: 44,806,905 (GRCm39) |
D300V |
probably damaging |
Het |
Pcgf2 |
T |
C |
11: 97,581,078 (GRCm39) |
E71G |
probably damaging |
Het |
Pi4kb |
A |
G |
3: 94,906,172 (GRCm39) |
Q573R |
possibly damaging |
Het |
Pitpna |
T |
A |
11: 75,511,153 (GRCm39) |
M242K |
possibly damaging |
Het |
Pkd1 |
A |
G |
17: 24,793,014 (GRCm39) |
E1567G |
possibly damaging |
Het |
Plcb2 |
A |
T |
2: 118,545,210 (GRCm39) |
S630R |
probably damaging |
Het |
Prrt2 |
A |
T |
7: 126,618,937 (GRCm39) |
V176D |
probably benign |
Het |
Prss1l |
A |
C |
6: 41,373,084 (GRCm39) |
N119H |
probably damaging |
Het |
Prss42 |
T |
C |
9: 110,628,490 (GRCm39) |
|
probably null |
Het |
Rhoq |
A |
G |
17: 87,304,459 (GRCm39) |
R197G |
probably benign |
Het |
Rin2 |
A |
T |
2: 145,702,299 (GRCm39) |
T332S |
probably benign |
Het |
Rnps1-ps |
C |
T |
6: 7,982,605 (GRCm39) |
|
noncoding transcript |
Het |
Rp1 |
A |
T |
1: 4,418,060 (GRCm39) |
N1017K |
possibly damaging |
Het |
Setbp1 |
T |
A |
18: 78,900,700 (GRCm39) |
Y989F |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,420,065 (GRCm39) |
G191D |
probably damaging |
Het |
Slc35f5 |
G |
A |
1: 125,517,693 (GRCm39) |
R497Q |
probably damaging |
Het |
Slf1 |
T |
C |
13: 77,198,090 (GRCm39) |
K728R |
probably benign |
Het |
Tiparp |
T |
G |
3: 65,454,946 (GRCm39) |
S364A |
probably benign |
Het |
Tph1 |
G |
A |
7: 46,296,969 (GRCm39) |
Q409* |
probably null |
Het |
Trp73 |
A |
T |
4: 154,145,049 (GRCm39) |
I526N |
possibly damaging |
Het |
Ttc9c |
G |
A |
19: 8,793,332 (GRCm39) |
R103* |
probably null |
Het |
Vmn2r75 |
T |
A |
7: 85,797,702 (GRCm39) |
I704F |
probably benign |
Het |
Wdr76 |
A |
G |
2: 121,348,216 (GRCm39) |
R63G |
probably damaging |
Het |
Zc3h3 |
T |
A |
15: 75,648,928 (GRCm39) |
S735C |
probably damaging |
Het |
Zfp383 |
G |
A |
7: 29,611,615 (GRCm39) |
V32M |
probably damaging |
Het |
Zfp810 |
T |
A |
9: 22,190,392 (GRCm39) |
Y172F |
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 |
|
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 |
|
|