Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
A |
10: 79,838,973 (GRCm39) |
L689Q |
|
Het |
Abcc2 |
G |
A |
19: 43,793,391 (GRCm39) |
V348M |
probably benign |
Het |
Abhd5 |
T |
C |
9: 122,196,992 (GRCm39) |
S60P |
probably benign |
Het |
Adamts10 |
C |
A |
17: 33,756,330 (GRCm39) |
H324Q |
probably benign |
Het |
Akap1 |
A |
G |
11: 88,723,165 (GRCm39) |
L823P |
probably damaging |
Het |
Aoc1 |
G |
A |
6: 48,885,522 (GRCm39) |
V676I |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,893,241 (GRCm39) |
|
probably benign |
Het |
Arl4d |
A |
C |
11: 101,557,620 (GRCm39) |
S49R |
possibly damaging |
Het |
Atr |
A |
G |
9: 95,747,851 (GRCm39) |
I378V |
probably benign |
Het |
Bicd1 |
G |
A |
6: 149,385,674 (GRCm39) |
V136I |
probably benign |
Het |
Brd1 |
A |
T |
15: 88,585,374 (GRCm39) |
L820H |
possibly damaging |
Het |
Cfap70 |
T |
C |
14: 20,497,590 (GRCm39) |
T55A |
probably benign |
Het |
Cog7 |
G |
T |
7: 121,570,561 (GRCm39) |
N182K |
probably damaging |
Het |
Col4a4 |
T |
A |
1: 82,431,752 (GRCm39) |
T1511S |
unknown |
Het |
Cr2 |
A |
T |
1: 194,840,977 (GRCm39) |
Y438* |
probably null |
Het |
Ctnnbl1 |
T |
A |
2: 157,648,623 (GRCm39) |
V198E |
probably damaging |
Het |
Fam117b |
C |
T |
1: 60,018,456 (GRCm39) |
Q58* |
probably null |
Het |
Fam171a2 |
A |
G |
11: 102,330,519 (GRCm39) |
Y288H |
probably damaging |
Het |
Fam186a |
A |
T |
15: 99,840,472 (GRCm39) |
I1924K |
possibly damaging |
Het |
Fancd2 |
A |
G |
6: 113,532,180 (GRCm39) |
I498V |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,909,421 (GRCm39) |
I2194F |
probably benign |
Het |
Gbp9 |
T |
C |
5: 105,231,695 (GRCm39) |
Y297C |
|
Het |
Gck |
T |
G |
11: 5,854,377 (GRCm39) |
N283H |
possibly damaging |
Het |
Gm13941 |
A |
T |
2: 110,935,146 (GRCm39) |
L28Q |
unknown |
Het |
Gpr155 |
A |
G |
2: 73,204,109 (GRCm39) |
I235T |
possibly damaging |
Het |
Junb |
A |
C |
8: 85,704,052 (GRCm39) |
L336R |
probably damaging |
Het |
Krt14 |
A |
T |
11: 100,095,904 (GRCm39) |
M218K |
probably benign |
Het |
Leprotl1 |
A |
G |
8: 34,604,967 (GRCm39) |
V102A |
probably benign |
Het |
Lrrc8d |
T |
C |
5: 105,961,908 (GRCm39) |
F773L |
probably damaging |
Het |
Mad2l1bp |
G |
A |
17: 46,458,958 (GRCm39) |
R191C |
probably damaging |
Het |
Man1c1 |
C |
T |
4: 134,311,705 (GRCm39) |
V274M |
possibly damaging |
Het |
Mtor |
C |
A |
4: 148,637,198 (GRCm39) |
P2466T |
probably benign |
Het |
Mycbpap |
C |
A |
11: 94,398,032 (GRCm39) |
|
probably benign |
Het |
Myef2l |
G |
A |
3: 10,153,593 (GRCm39) |
V121M |
probably damaging |
Het |
Myo18b |
T |
C |
5: 112,975,862 (GRCm39) |
E1329G |
probably damaging |
Het |
Nipbl |
A |
T |
15: 8,380,340 (GRCm39) |
D817E |
probably benign |
Het |
Nthl1 |
C |
T |
17: 24,853,753 (GRCm39) |
Q133* |
probably null |
Het |
Nup133 |
A |
G |
8: 124,660,155 (GRCm39) |
M381T |
probably benign |
Het |
Or13c7 |
T |
C |
4: 43,854,602 (GRCm39) |
C98R |
probably damaging |
Het |
Or2j3 |
T |
C |
17: 38,615,654 (GRCm39) |
T233A |
probably benign |
Het |
Or51t4 |
T |
C |
7: 102,598,527 (GRCm39) |
I285T |
possibly damaging |
Het |
Or7e175 |
T |
C |
9: 20,048,633 (GRCm39) |
Y74H |
probably damaging |
Het |
Or7g20 |
T |
C |
9: 18,946,773 (GRCm39) |
M118T |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Pmpcb |
A |
T |
5: 21,961,608 (GRCm39) |
I422F |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,380,589 (GRCm39) |
H97Q |
possibly damaging |
Het |
Psat1 |
A |
G |
19: 15,898,332 (GRCm39) |
L30P |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,472,820 (GRCm39) |
D774G |
probably damaging |
Het |
Rag1 |
C |
T |
2: 101,475,137 (GRCm39) |
A2T |
probably benign |
Het |
Rccd1 |
G |
T |
7: 79,970,728 (GRCm39) |
F17L |
probably damaging |
Het |
Rhobtb1 |
T |
A |
10: 69,106,579 (GRCm39) |
D443E |
probably damaging |
Het |
Rnf13 |
A |
G |
3: 57,709,866 (GRCm39) |
|
probably null |
Het |
Ryr2 |
A |
G |
13: 11,587,185 (GRCm39) |
S4699P |
possibly damaging |
Het |
Scart1 |
A |
G |
7: 139,808,277 (GRCm39) |
T754A |
probably benign |
Het |
Sdc3 |
T |
C |
4: 130,546,352 (GRCm39) |
V237A |
probably benign |
Het |
Serinc5 |
T |
A |
13: 92,797,514 (GRCm39) |
|
probably benign |
Het |
Sertad4 |
A |
G |
1: 192,528,973 (GRCm39) |
I281T |
probably benign |
Het |
Shroom1 |
T |
C |
11: 53,354,490 (GRCm39) |
S137P |
probably damaging |
Het |
Slurp1 |
C |
T |
15: 74,599,450 (GRCm39) |
G20D |
probably damaging |
Het |
Sncb |
T |
A |
13: 54,910,512 (GRCm39) |
N75Y |
probably damaging |
Het |
Spag8 |
C |
T |
4: 43,653,231 (GRCm39) |
G77S |
unknown |
Het |
Spink14 |
A |
T |
18: 44,164,059 (GRCm39) |
I76F |
probably damaging |
Het |
Srfbp1 |
A |
T |
18: 52,623,102 (GRCm39) |
E372D |
possibly damaging |
Het |
Synpo |
A |
T |
18: 60,735,599 (GRCm39) |
N782K |
probably damaging |
Het |
Syt7 |
T |
C |
19: 10,421,373 (GRCm39) |
M519T |
probably damaging |
Het |
Tlr5 |
C |
T |
1: 182,802,160 (GRCm39) |
P488L |
probably benign |
Het |
Tmod3 |
A |
T |
9: 75,412,202 (GRCm39) |
I315N |
probably damaging |
Het |
Ttc12 |
T |
C |
9: 49,364,757 (GRCm39) |
M340V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,710,959 (GRCm39) |
I8392F |
unknown |
Het |
Ttn |
A |
G |
2: 76,769,232 (GRCm39) |
V2822A |
unknown |
Het |
Ube3b |
C |
T |
5: 114,542,837 (GRCm39) |
|
probably benign |
Het |
Ubr4 |
C |
A |
4: 139,145,785 (GRCm39) |
N238K |
|
Het |
Vmn2r12 |
T |
C |
5: 109,233,885 (GRCm39) |
T776A |
probably damaging |
Het |
Vps50 |
G |
A |
6: 3,588,091 (GRCm39) |
|
probably benign |
Het |
Vwa3a |
A |
G |
7: 120,366,470 (GRCm39) |
D165G |
|
Het |
Wdr17 |
T |
A |
8: 55,114,605 (GRCm39) |
H644L |
probably damaging |
Het |
Zfp628 |
T |
C |
7: 4,924,202 (GRCm39) |
V808A |
probably benign |
Het |
Zscan21 |
T |
A |
5: 138,123,937 (GRCm39) |
D205E |
probably damaging |
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 |
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 |
|
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 |
|
|