Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
T |
A |
2: 103,535,463 (GRCm39) |
D543E |
probably benign |
Het |
Acad9 |
A |
C |
3: 36,144,274 (GRCm39) |
N583T |
possibly damaging |
Het |
Arhgap5 |
G |
A |
12: 52,563,643 (GRCm39) |
V205M |
probably damaging |
Het |
Arid1b |
G |
A |
17: 5,392,674 (GRCm39) |
R2068Q |
probably damaging |
Het |
Bex3 |
T |
C |
X: 135,172,218 (GRCm39) |
F60S |
probably damaging |
Het |
Casd1 |
C |
T |
6: 4,619,833 (GRCm39) |
P193S |
possibly damaging |
Het |
Ceacam11 |
A |
T |
7: 17,712,435 (GRCm39) |
I295F |
possibly damaging |
Het |
Ceacam3 |
T |
A |
7: 16,885,782 (GRCm39) |
N128K |
probably benign |
Het |
Cyp1a2 |
C |
T |
9: 57,587,176 (GRCm39) |
E372K |
probably damaging |
Het |
Ddb1 |
T |
G |
19: 10,583,071 (GRCm39) |
M1R |
probably null |
Het |
Ecel1 |
T |
C |
1: 87,080,915 (GRCm39) |
D329G |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,175,017 (GRCm39) |
N1899D |
probably benign |
Het |
Gm20507 |
A |
T |
17: 33,863,727 (GRCm39) |
|
probably benign |
Het |
Gml |
T |
G |
15: 74,685,688 (GRCm39) |
Y99S |
probably damaging |
Het |
Gpr119 |
G |
T |
X: 47,762,125 (GRCm39) |
|
probably benign |
Het |
Hcn1 |
T |
C |
13: 117,793,458 (GRCm39) |
Y237H |
unknown |
Het |
Hook2 |
G |
A |
8: 85,721,560 (GRCm39) |
V273I |
probably benign |
Het |
Il12rb2 |
T |
C |
6: 67,338,849 (GRCm39) |
|
probably benign |
Het |
Kdm2a |
A |
G |
19: 4,369,279 (GRCm39) |
F1112S |
probably benign |
Het |
Lpl |
A |
T |
8: 69,345,277 (GRCm39) |
K94* |
probably null |
Het |
Lrrc8a |
T |
A |
2: 30,145,822 (GRCm39) |
L212Q |
probably damaging |
Het |
Me2 |
A |
T |
18: 73,903,887 (GRCm39) |
|
probably benign |
Het |
Mmp11 |
A |
T |
10: 75,762,655 (GRCm39) |
M266K |
probably benign |
Het |
Mprip |
T |
A |
11: 59,622,399 (GRCm39) |
V162E |
possibly damaging |
Het |
Nsf |
C |
T |
11: 103,752,711 (GRCm39) |
|
probably benign |
Het |
Or56b2 |
T |
C |
7: 104,337,588 (GRCm39) |
V122A |
probably benign |
Het |
Pcif1 |
T |
A |
2: 164,727,708 (GRCm39) |
L167H |
probably damaging |
Het |
Reps1 |
T |
C |
10: 17,969,643 (GRCm39) |
S249P |
probably damaging |
Het |
Sdf4 |
T |
A |
4: 156,093,763 (GRCm39) |
M299K |
probably benign |
Het |
Slc30a7 |
A |
G |
3: 115,747,759 (GRCm39) |
V344A |
possibly damaging |
Het |
Svep1 |
G |
A |
4: 58,146,569 (GRCm39) |
P358S |
probably damaging |
Het |
Syt9 |
G |
T |
7: 107,024,356 (GRCm39) |
R83L |
probably damaging |
Het |
Tbc1d15 |
T |
C |
10: 115,038,435 (GRCm39) |
I593V |
probably benign |
Het |
Trio |
T |
A |
15: 27,749,867 (GRCm39) |
N1134I |
probably damaging |
Het |
Trpv3 |
A |
G |
11: 73,187,544 (GRCm39) |
|
probably benign |
Het |
Ugp2 |
T |
A |
11: 21,273,273 (GRCm39) |
I449L |
possibly damaging |
Het |
Usp24 |
C |
A |
4: 106,294,041 (GRCm39) |
H2595N |
probably benign |
Het |
Vat1l |
A |
G |
8: 115,096,629 (GRCm39) |
N370S |
possibly damaging |
Het |
Wwc1 |
C |
A |
11: 35,758,103 (GRCm39) |
D748Y |
probably damaging |
Het |
Zfyve9 |
G |
A |
4: 108,538,261 (GRCm39) |
H1002Y |
probably damaging |
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 |
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 |
R7228:Gli3
|
UTSW |
13 |
15,899,087 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|