Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,247,653 (GRCm39) |
F2467I |
probably benign |
Het |
Acod1 |
A |
G |
14: 103,286,765 (GRCm39) |
T23A |
probably benign |
Het |
Adam2 |
T |
A |
14: 66,291,361 (GRCm39) |
K306* |
probably null |
Het |
Adcy10 |
A |
C |
1: 165,337,841 (GRCm39) |
I152L |
probably damaging |
Het |
Amigo1 |
T |
C |
3: 108,094,546 (GRCm39) |
L15P |
probably benign |
Het |
Aqp2 |
A |
G |
15: 99,480,005 (GRCm39) |
N156S |
probably benign |
Het |
AU041133 |
A |
G |
10: 81,987,105 (GRCm39) |
K253E |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 135,998,797 (GRCm39) |
T231A |
possibly damaging |
Het |
Carf |
A |
T |
1: 60,148,553 (GRCm39) |
N83I |
probably damaging |
Het |
Ccdc121rt1 |
T |
C |
1: 181,338,532 (GRCm39) |
K140R |
probably benign |
Het |
Cdc42bpb |
C |
T |
12: 111,271,527 (GRCm39) |
V1111M |
possibly damaging |
Het |
Cep78 |
A |
G |
19: 15,946,561 (GRCm39) |
S424P |
probably benign |
Het |
Cfap74 |
G |
A |
4: 155,549,507 (GRCm39) |
V123M |
unknown |
Het |
Crot |
T |
A |
5: 9,026,051 (GRCm39) |
N312I |
probably damaging |
Het |
Cyp2c69 |
C |
A |
19: 39,869,610 (GRCm39) |
M136I |
possibly damaging |
Het |
Cyp4f39 |
A |
G |
17: 32,710,803 (GRCm39) |
D454G |
probably damaging |
Het |
Dnaja4 |
A |
T |
9: 54,621,569 (GRCm39) |
H298L |
possibly damaging |
Het |
Eif2ak4 |
C |
T |
2: 118,287,638 (GRCm39) |
T1081M |
probably damaging |
Het |
Eif3j2 |
T |
C |
18: 43,610,574 (GRCm39) |
K80E |
probably damaging |
Het |
Elp4 |
T |
A |
2: 105,622,647 (GRCm39) |
I351F |
probably damaging |
Het |
Fbxw26 |
C |
G |
9: 109,554,012 (GRCm39) |
G209A |
possibly damaging |
Het |
Fsip2 |
T |
A |
2: 82,822,651 (GRCm39) |
V6128D |
possibly damaging |
Het |
Gm2042 |
A |
G |
12: 87,924,719 (GRCm39) |
E60G |
probably benign |
Het |
Gm26566 |
G |
T |
4: 88,640,542 (GRCm39) |
R111L |
unknown |
Het |
Gm3138 |
C |
A |
14: 15,632,269 (GRCm39) |
H147Q |
probably damaging |
Het |
Gucy1b1 |
T |
A |
3: 81,940,581 (GRCm39) |
N615I |
unknown |
Het |
Ighv14-1 |
A |
T |
12: 113,895,981 (GRCm39) |
F8I |
not run |
Het |
Kcnh8 |
C |
T |
17: 53,263,744 (GRCm39) |
T747I |
probably benign |
Het |
Kctd1 |
T |
A |
18: 15,195,469 (GRCm39) |
S385C |
possibly damaging |
Het |
Lmo7 |
T |
A |
14: 102,133,971 (GRCm39) |
M672K |
probably damaging |
Het |
Lrrc69 |
T |
A |
4: 14,775,027 (GRCm39) |
K80N |
probably damaging |
Het |
Map2k5 |
C |
T |
9: 63,265,304 (GRCm39) |
D75N |
probably damaging |
Het |
Matr3 |
T |
C |
18: 35,695,537 (GRCm39) |
V4A |
unknown |
Het |
Megf10 |
T |
C |
18: 57,322,661 (GRCm39) |
C69R |
probably damaging |
Het |
Mettl1 |
A |
G |
10: 126,881,152 (GRCm39) |
E221G |
probably benign |
Het |
Mkrn3 |
C |
A |
7: 62,069,415 (GRCm39) |
R125S |
probably benign |
Het |
Mlh3 |
A |
T |
12: 85,282,430 (GRCm39) |
L1401Q |
probably benign |
Het |
Nacad |
T |
C |
11: 6,548,412 (GRCm39) |
I1412V |
probably benign |
Het |
Nkain4 |
A |
T |
2: 180,596,362 (GRCm39) |
|
probably null |
Het |
Notch2 |
T |
A |
3: 98,044,633 (GRCm39) |
C1518* |
probably null |
Het |
Npw |
A |
G |
17: 24,877,065 (GRCm39) |
V112A |
probably benign |
Het |
Or10a5 |
A |
T |
7: 106,636,307 (GRCm39) |
H315L |
probably benign |
Het |
Or2v1 |
T |
A |
11: 49,025,706 (GRCm39) |
M229K |
possibly damaging |
Het |
Pdzd2 |
T |
C |
15: 12,373,059 (GRCm39) |
T2359A |
probably benign |
Het |
Pdzd2 |
T |
A |
15: 12,458,231 (GRCm39) |
K37* |
probably null |
Het |
Phkb |
T |
G |
8: 86,569,636 (GRCm39) |
|
probably benign |
Het |
Pou2af2 |
T |
C |
9: 51,202,956 (GRCm39) |
D66G |
probably damaging |
Het |
Prrc2b |
C |
A |
2: 32,104,318 (GRCm39) |
Y1265* |
probably null |
Het |
Rab31 |
T |
A |
17: 66,024,548 (GRCm39) |
M44L |
probably benign |
Het |
Rap1gds1 |
C |
T |
3: 138,663,228 (GRCm39) |
G373R |
probably damaging |
Het |
Rapgef2 |
T |
C |
3: 78,976,525 (GRCm39) |
D1279G |
probably benign |
Het |
Rbm46 |
T |
C |
3: 82,749,840 (GRCm39) |
D468G |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,692,197 (GRCm39) |
E1059G |
probably damaging |
Het |
Sez6l2 |
T |
C |
7: 126,552,897 (GRCm39) |
L221P |
probably damaging |
Het |
Slit3 |
T |
A |
11: 35,490,245 (GRCm39) |
V361E |
probably damaging |
Het |
Soat1 |
G |
A |
1: 156,261,808 (GRCm39) |
S400F |
probably damaging |
Het |
Spp1 |
T |
C |
5: 104,588,311 (GRCm39) |
S238P |
probably damaging |
Het |
Tdpoz8 |
T |
A |
3: 92,980,993 (GRCm39) |
C4S |
possibly damaging |
Het |
Tfap2c |
T |
C |
2: 172,393,492 (GRCm39) |
S136P |
probably benign |
Het |
Tgfbr2 |
T |
C |
9: 115,939,011 (GRCm39) |
E297G |
probably damaging |
Het |
Trim2 |
T |
C |
3: 84,099,488 (GRCm39) |
D228G |
probably benign |
Het |
Wdr82 |
C |
A |
9: 106,053,871 (GRCm39) |
A74E |
probably benign |
Het |
Zfp451 |
T |
C |
1: 33,842,475 (GRCm39) |
T136A |
unknown |
Het |
|
Other mutations in Gli3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Gli3
|
APN |
13 |
15,818,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00471:Gli3
|
APN |
13 |
15,898,354 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00484:Gli3
|
APN |
13 |
15,818,977 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00588:Gli3
|
APN |
13 |
15,818,977 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01161:Gli3
|
APN |
13 |
15,722,983 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01633:Gli3
|
APN |
13 |
15,823,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01799:Gli3
|
APN |
13 |
15,900,746 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01861:Gli3
|
APN |
13 |
15,899,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02063:Gli3
|
APN |
13 |
15,900,957 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02112:Gli3
|
APN |
13 |
15,837,099 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02255:Gli3
|
APN |
13 |
15,823,304 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02270:Gli3
|
APN |
13 |
15,901,371 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02336:Gli3
|
APN |
13 |
15,894,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02346:Gli3
|
APN |
13 |
15,898,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02744:Gli3
|
APN |
13 |
15,788,471 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02877:Gli3
|
APN |
13 |
15,899,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02975:Gli3
|
APN |
13 |
15,899,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03018:Gli3
|
APN |
13 |
15,834,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03378:Gli3
|
APN |
13 |
15,819,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03406:Gli3
|
APN |
13 |
15,823,166 (GRCm39) |
missense |
probably damaging |
1.00 |
Capone
|
UTSW |
13 |
15,889,619 (GRCm39) |
missense |
probably damaging |
1.00 |
Carpals
|
UTSW |
13 |
15,888,235 (GRCm39) |
critical splice donor site |
probably null |
|
Ness
|
UTSW |
13 |
15,898,140 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4737:Gli3
|
UTSW |
13 |
15,818,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Gli3
|
UTSW |
13 |
15,899,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R0329:Gli3
|
UTSW |
13 |
15,898,143 (GRCm39) |
missense |
probably damaging |
0.98 |
R0330:Gli3
|
UTSW |
13 |
15,898,143 (GRCm39) |
missense |
probably damaging |
0.98 |
R0360:Gli3
|
UTSW |
13 |
15,899,349 (GRCm39) |
missense |
probably benign |
0.32 |
R0364:Gli3
|
UTSW |
13 |
15,899,349 (GRCm39) |
missense |
probably benign |
0.32 |
R0469:Gli3
|
UTSW |
13 |
15,899,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Gli3
|
UTSW |
13 |
15,836,991 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0639:Gli3
|
UTSW |
13 |
15,899,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R1072:Gli3
|
UTSW |
13 |
15,888,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1257:Gli3
|
UTSW |
13 |
15,900,581 (GRCm39) |
nonsense |
probably null |
|
R1270:Gli3
|
UTSW |
13 |
15,898,329 (GRCm39) |
missense |
probably benign |
0.02 |
R1424:Gli3
|
UTSW |
13 |
15,900,899 (GRCm39) |
missense |
probably benign |
0.00 |
R1481:Gli3
|
UTSW |
13 |
15,788,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R1596:Gli3
|
UTSW |
13 |
15,900,056 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1628:Gli3
|
UTSW |
13 |
15,900,897 (GRCm39) |
missense |
probably benign |
0.00 |
R1721:Gli3
|
UTSW |
13 |
15,900,882 (GRCm39) |
missense |
probably benign |
0.27 |
R1797:Gli3
|
UTSW |
13 |
15,888,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R1813:Gli3
|
UTSW |
13 |
15,823,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R1819:Gli3
|
UTSW |
13 |
15,900,377 (GRCm39) |
nonsense |
probably null |
|
R1988:Gli3
|
UTSW |
13 |
15,900,965 (GRCm39) |
missense |
probably benign |
|
R2132:Gli3
|
UTSW |
13 |
15,900,134 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2352:Gli3
|
UTSW |
13 |
15,836,977 (GRCm39) |
missense |
probably benign |
0.02 |
R3085:Gli3
|
UTSW |
13 |
15,835,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Gli3
|
UTSW |
13 |
15,900,567 (GRCm39) |
missense |
probably benign |
0.28 |
R3277:Gli3
|
UTSW |
13 |
15,900,567 (GRCm39) |
missense |
probably benign |
0.28 |
R4162:Gli3
|
UTSW |
13 |
15,899,700 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4497:Gli3
|
UTSW |
13 |
15,898,156 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4526:Gli3
|
UTSW |
13 |
15,888,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Gli3
|
UTSW |
13 |
15,899,049 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5327:Gli3
|
UTSW |
13 |
15,723,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R5395:Gli3
|
UTSW |
13 |
15,889,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5494:Gli3
|
UTSW |
13 |
15,900,567 (GRCm39) |
missense |
probably benign |
0.28 |
R5609:Gli3
|
UTSW |
13 |
15,723,038 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5718:Gli3
|
UTSW |
13 |
15,652,750 (GRCm39) |
critical splice donor site |
probably null |
|
R5810:Gli3
|
UTSW |
13 |
15,818,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R5896:Gli3
|
UTSW |
13 |
15,900,765 (GRCm39) |
missense |
probably benign |
0.00 |
R5930:Gli3
|
UTSW |
13 |
15,723,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Gli3
|
UTSW |
13 |
15,900,747 (GRCm39) |
nonsense |
probably null |
|
R5985:Gli3
|
UTSW |
13 |
15,898,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6224:Gli3
|
UTSW |
13 |
15,899,730 (GRCm39) |
missense |
probably benign |
|
R6278:Gli3
|
UTSW |
13 |
15,899,698 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6330:Gli3
|
UTSW |
13 |
15,899,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Gli3
|
UTSW |
13 |
15,898,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6523:Gli3
|
UTSW |
13 |
15,888,235 (GRCm39) |
critical splice donor site |
probably null |
|
R7072:Gli3
|
UTSW |
13 |
15,900,280 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7085:Gli3
|
UTSW |
13 |
15,889,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7327:Gli3
|
UTSW |
13 |
15,900,144 (GRCm39) |
missense |
probably benign |
0.02 |
R7451:Gli3
|
UTSW |
13 |
15,900,876 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7974:Gli3
|
UTSW |
13 |
15,900,841 (GRCm39) |
missense |
probably benign |
0.00 |
R8167:Gli3
|
UTSW |
13 |
15,900,228 (GRCm39) |
missense |
probably benign |
0.00 |
R8170:Gli3
|
UTSW |
13 |
15,894,793 (GRCm39) |
missense |
probably benign |
|
R8199:Gli3
|
UTSW |
13 |
15,900,576 (GRCm39) |
missense |
probably benign |
0.08 |
R8247:Gli3
|
UTSW |
13 |
15,901,360 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8332:Gli3
|
UTSW |
13 |
15,888,133 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8347:Gli3
|
UTSW |
13 |
15,898,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Gli3
|
UTSW |
13 |
15,834,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Gli3
|
UTSW |
13 |
15,889,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Gli3
|
UTSW |
13 |
15,901,116 (GRCm39) |
missense |
probably benign |
0.01 |
R9099:Gli3
|
UTSW |
13 |
15,901,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Gli3
|
UTSW |
13 |
15,899,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R9317:Gli3
|
UTSW |
13 |
15,889,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Gli3
|
UTSW |
13 |
15,900,296 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9546:Gli3
|
UTSW |
13 |
15,788,443 (GRCm39) |
missense |
probably benign |
0.00 |
R9571:Gli3
|
UTSW |
13 |
15,900,858 (GRCm39) |
missense |
probably benign |
0.00 |
R9621:Gli3
|
UTSW |
13 |
15,901,253 (GRCm39) |
missense |
probably benign |
0.01 |
R9704:Gli3
|
UTSW |
13 |
15,898,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9787:Gli3
|
UTSW |
13 |
15,900,386 (GRCm39) |
missense |
probably damaging |
0.96 |
RF010:Gli3
|
UTSW |
13 |
15,900,954 (GRCm39) |
missense |
probably damaging |
1.00 |
|