Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430069I07Rik |
T |
A |
15: 34,355,778 (GRCm39) |
I261N |
probably benign |
Het |
Bace1 |
T |
A |
9: 45,770,199 (GRCm39) |
|
probably null |
Het |
Caprin2 |
G |
T |
6: 148,779,352 (GRCm39) |
Q152K |
probably benign |
Het |
Cdh16 |
C |
T |
8: 105,345,917 (GRCm39) |
D285N |
probably benign |
Het |
Cnnm2 |
G |
A |
19: 46,866,473 (GRCm39) |
A874T |
possibly damaging |
Het |
Dhx38 |
A |
T |
8: 110,285,722 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
A |
C |
7: 105,362,940 (GRCm39) |
E3834A |
possibly damaging |
Het |
Erc2 |
A |
C |
14: 27,733,680 (GRCm39) |
S585R |
probably damaging |
Het |
Gpr161 |
T |
C |
1: 165,138,077 (GRCm39) |
L204P |
probably damaging |
Het |
Hp |
A |
G |
8: 110,302,339 (GRCm39) |
V203A |
probably damaging |
Het |
Krtap6-5 |
A |
T |
16: 88,844,677 (GRCm39) |
C19S |
unknown |
Het |
Lce1i |
A |
T |
3: 92,685,033 (GRCm39) |
S48T |
unknown |
Het |
Lrp2 |
A |
T |
2: 69,261,496 (GRCm39) |
S4482T |
probably damaging |
Het |
Mpdz |
A |
T |
4: 81,337,285 (GRCm39) |
|
probably benign |
Het |
Or1q1 |
T |
C |
2: 36,886,915 (GRCm39) |
F31S |
probably damaging |
Het |
Or4c100 |
T |
A |
2: 88,356,498 (GRCm39) |
Y190* |
probably null |
Het |
Or8k18 |
T |
A |
2: 86,085,363 (GRCm39) |
I225L |
possibly damaging |
Het |
Papola |
G |
T |
12: 105,775,692 (GRCm39) |
|
probably null |
Het |
Prss23 |
T |
C |
7: 89,159,352 (GRCm39) |
D239G |
probably damaging |
Het |
Setd2 |
A |
G |
9: 110,382,220 (GRCm39) |
T83A |
unknown |
Het |
Sh3pxd2b |
T |
G |
11: 32,331,443 (GRCm39) |
L56V |
probably damaging |
Het |
Ski |
A |
G |
4: 155,245,329 (GRCm39) |
S300P |
probably benign |
Het |
Srebf2 |
T |
C |
15: 82,053,989 (GRCm39) |
S17P |
probably damaging |
Het |
Svs5 |
C |
A |
2: 164,175,260 (GRCm39) |
H37Q |
probably benign |
Het |
Tbx21 |
A |
G |
11: 97,005,567 (GRCm39) |
S133P |
probably benign |
Het |
Tgfbr3 |
G |
T |
5: 107,257,568 (GRCm39) |
S830R |
probably damaging |
Het |
Thsd1 |
A |
T |
8: 22,733,794 (GRCm39) |
K280N |
probably benign |
Het |
Tnfrsf13c |
T |
A |
15: 82,108,513 (GRCm39) |
M1L |
probably benign |
Het |
Ttll7 |
T |
C |
3: 146,615,408 (GRCm39) |
F291L |
probably benign |
Het |
Ttn |
A |
G |
2: 76,599,907 (GRCm39) |
V10762A |
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 |
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 |
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 |
|