Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
C |
T |
16: 20,367,430 (GRCm39) |
T3I |
probably benign |
Het |
Ahi1 |
T |
A |
10: 20,862,976 (GRCm39) |
V717E |
probably damaging |
Het |
Anapc4 |
A |
G |
5: 53,002,672 (GRCm39) |
T238A |
probably damaging |
Het |
Arhgap27 |
A |
T |
11: 103,251,367 (GRCm39) |
C120* |
probably null |
Het |
Bdp1 |
A |
T |
13: 100,178,040 (GRCm39) |
V1943D |
probably damaging |
Het |
Cdc14b |
A |
G |
13: 64,373,461 (GRCm39) |
V141A |
probably damaging |
Het |
Cfap46 |
G |
T |
7: 139,215,062 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
C |
A |
9: 71,633,165 (GRCm39) |
R62L |
possibly damaging |
Het |
Chaf1a |
A |
G |
17: 56,369,573 (GRCm39) |
S522G |
probably benign |
Het |
Cox19 |
A |
G |
5: 139,328,402 (GRCm39) |
F37S |
probably damaging |
Het |
Csmd1 |
G |
A |
8: 16,108,721 (GRCm39) |
S1894L |
probably damaging |
Het |
Cyp4a12a |
A |
T |
4: 115,184,756 (GRCm39) |
R346W |
probably damaging |
Het |
Dip2a |
A |
C |
10: 76,108,396 (GRCm39) |
C1315G |
probably benign |
Het |
Dmxl2 |
A |
C |
9: 54,308,869 (GRCm39) |
W1961G |
probably damaging |
Het |
Dst |
T |
C |
1: 34,240,486 (GRCm39) |
L1945P |
probably damaging |
Het |
Efr3a |
A |
G |
15: 65,691,627 (GRCm39) |
S92G |
probably damaging |
Het |
Ep300 |
C |
T |
15: 81,511,515 (GRCm39) |
T865I |
unknown |
Het |
Ercc6 |
A |
G |
14: 32,248,361 (GRCm39) |
E304G |
probably benign |
Het |
Filip1l |
A |
C |
16: 57,391,300 (GRCm39) |
E629D |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,938,992 (GRCm39) |
T30I |
possibly damaging |
Het |
Glb1 |
T |
C |
9: 114,246,126 (GRCm39) |
F59S |
probably benign |
Het |
Gpatch2l |
A |
G |
12: 86,303,646 (GRCm39) |
T223A |
probably damaging |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,479,565 (GRCm39) |
M4633K |
probably benign |
Het |
Hoxc8 |
T |
A |
15: 102,899,542 (GRCm39) |
Y111N |
probably damaging |
Het |
Ifi207 |
A |
G |
1: 173,556,581 (GRCm39) |
L726P |
probably benign |
Het |
Iqcn |
T |
A |
8: 71,169,453 (GRCm39) |
M1181K |
possibly damaging |
Het |
Iqgap2 |
T |
A |
13: 95,772,163 (GRCm39) |
M1339L |
probably benign |
Het |
Kif21b |
A |
G |
1: 136,087,387 (GRCm39) |
Q901R |
possibly damaging |
Het |
Krtap4-8 |
C |
A |
11: 99,671,234 (GRCm39) |
C79F |
unknown |
Het |
Ldb3 |
T |
C |
14: 34,293,759 (GRCm39) |
N155S |
probably damaging |
Het |
Mad2l1 |
T |
A |
6: 66,516,794 (GRCm39) |
V162E |
probably benign |
Het |
Map7 |
T |
A |
10: 20,109,208 (GRCm39) |
V87E |
unknown |
Het |
Mndal |
A |
T |
1: 173,703,185 (GRCm39) |
D73E |
unknown |
Het |
Msantd1 |
T |
C |
5: 35,075,039 (GRCm39) |
S34P |
probably damaging |
Het |
Myh14 |
T |
C |
7: 44,260,977 (GRCm39) |
Q1838R |
possibly damaging |
Het |
Myh15 |
G |
T |
16: 48,993,369 (GRCm39) |
R1668L |
possibly damaging |
Het |
Ncoa7 |
A |
G |
10: 30,565,796 (GRCm39) |
M666T |
probably damaging |
Het |
Nol6 |
A |
T |
4: 41,116,686 (GRCm39) |
L944Q |
probably benign |
Het |
Or5h27 |
A |
T |
16: 59,006,376 (GRCm39) |
F157I |
unknown |
Het |
Orc1 |
A |
G |
4: 108,445,911 (GRCm39) |
T10A |
probably benign |
Het |
Pcp4l1 |
G |
A |
1: 171,002,034 (GRCm39) |
A42V |
possibly damaging |
Het |
Pglyrp2 |
C |
T |
17: 32,634,893 (GRCm39) |
A490T |
probably benign |
Het |
Pirb |
A |
T |
7: 3,720,187 (GRCm39) |
C395* |
probably null |
Het |
Ppp1r11 |
T |
C |
17: 37,261,900 (GRCm39) |
R12G |
possibly damaging |
Het |
Prlr |
A |
G |
15: 10,346,524 (GRCm39) |
D290G |
probably benign |
Het |
Ptpn21 |
G |
T |
12: 98,646,360 (GRCm39) |
R1033S |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,570,660 (GRCm39) |
L1220P |
possibly damaging |
Het |
Rufy3 |
G |
A |
5: 88,790,811 (GRCm39) |
R504H |
probably damaging |
Het |
Scgb2b21 |
C |
T |
7: 33,219,330 (GRCm39) |
V25I |
probably benign |
Het |
Sh3bgrl2 |
T |
C |
9: 83,430,542 (GRCm39) |
S11P |
possibly damaging |
Het |
Slain2 |
A |
T |
5: 73,132,002 (GRCm39) |
T498S |
probably benign |
Het |
Slc12a4 |
C |
T |
8: 106,682,347 (GRCm39) |
G121S |
probably damaging |
Het |
Slc30a9 |
A |
T |
5: 67,499,462 (GRCm39) |
I307F |
probably damaging |
Het |
Snap91 |
C |
T |
9: 86,655,598 (GRCm39) |
G800R |
unknown |
Het |
Tnc |
G |
T |
4: 63,882,999 (GRCm39) |
|
probably null |
Het |
Trav21-dv12 |
T |
C |
14: 54,113,514 (GRCm39) |
|
probably benign |
Het |
Txk |
A |
T |
5: 72,873,226 (GRCm39) |
I228N |
probably damaging |
Het |
Vac14 |
T |
C |
8: 111,438,252 (GRCm39) |
Y622H |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdr35 |
T |
G |
12: 9,037,312 (GRCm39) |
M306R |
probably benign |
Het |
Zan |
A |
T |
5: 137,463,494 (GRCm39) |
S562T |
probably benign |
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 |
R7228:Gli3
|
UTSW |
13 |
15,899,087 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|