Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
C |
17: 24,554,598 (GRCm39) |
I119V |
probably benign |
Het |
Arfgap2 |
T |
A |
2: 91,096,037 (GRCm39) |
|
probably null |
Het |
Ccm2 |
T |
C |
11: 6,540,790 (GRCm39) |
V216A |
probably damaging |
Het |
Ctdspl2 |
T |
C |
2: 121,817,510 (GRCm39) |
|
probably null |
Het |
Dmxl2 |
T |
C |
9: 54,283,527 (GRCm39) |
T2769A |
probably benign |
Het |
Dnah3 |
C |
T |
7: 119,550,792 (GRCm39) |
V3165M |
possibly damaging |
Het |
Dnajc1 |
A |
C |
2: 18,313,710 (GRCm39) |
F137C |
probably damaging |
Het |
Gnrhr |
T |
C |
5: 86,345,677 (GRCm39) |
N3S |
probably benign |
Het |
Grhl1 |
G |
T |
12: 24,662,169 (GRCm39) |
R536L |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,475,033 (GRCm39) |
|
probably null |
Het |
Il20 |
T |
A |
1: 130,838,476 (GRCm39) |
I74L |
probably benign |
Het |
Ints11 |
A |
G |
4: 155,959,738 (GRCm39) |
K115R |
probably benign |
Het |
Irx4 |
A |
T |
13: 73,413,720 (GRCm39) |
E63D |
probably benign |
Het |
Itch |
A |
C |
2: 155,044,141 (GRCm39) |
Q482P |
probably benign |
Het |
Kctd8 |
C |
A |
5: 69,498,588 (GRCm39) |
M19I |
probably benign |
Het |
Klhl31 |
T |
C |
9: 77,557,383 (GRCm39) |
L33P |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,382,709 (GRCm39) |
C3691S |
probably damaging |
Het |
Lrrc39 |
A |
G |
3: 116,364,610 (GRCm39) |
D167G |
probably damaging |
Het |
Lrrd1 |
A |
T |
5: 3,916,478 (GRCm39) |
I832L |
possibly damaging |
Het |
Lrriq1 |
A |
G |
10: 102,904,774 (GRCm39) |
V1620A |
probably damaging |
Het |
Ltbr |
T |
C |
6: 125,289,024 (GRCm39) |
K213E |
probably benign |
Het |
Megf8 |
T |
A |
7: 25,039,039 (GRCm39) |
D883E |
possibly damaging |
Het |
Nherf2 |
T |
C |
17: 24,859,570 (GRCm39) |
E174G |
probably null |
Het |
Nmt1 |
T |
A |
11: 102,954,682 (GRCm39) |
S405T |
probably damaging |
Het |
Nsd3 |
G |
T |
8: 26,156,073 (GRCm39) |
V547F |
probably damaging |
Het |
Or4c110 |
A |
G |
2: 88,831,894 (GRCm39) |
V246A |
probably damaging |
Het |
Or7g16 |
C |
A |
9: 18,727,219 (GRCm39) |
V124F |
probably damaging |
Het |
Otud7a |
A |
G |
7: 63,407,404 (GRCm39) |
K569R |
possibly damaging |
Het |
Otud7b |
A |
G |
3: 96,063,089 (GRCm39) |
Y776C |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,006,341 (GRCm39) |
I73T |
probably damaging |
Het |
Rnf213 |
A |
T |
11: 119,350,835 (GRCm39) |
H3890L |
probably benign |
Het |
Sall3 |
T |
C |
18: 81,015,085 (GRCm39) |
T948A |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,307,393 (GRCm39) |
I198V |
probably benign |
Het |
Smg7 |
C |
A |
1: 152,730,079 (GRCm39) |
D405Y |
probably damaging |
Het |
Synpo2l |
A |
G |
14: 20,711,987 (GRCm39) |
L211S |
probably benign |
Het |
Thsd7b |
A |
G |
1: 130,145,895 (GRCm39) |
Y1601C |
probably benign |
Het |
Traf4 |
T |
C |
11: 78,050,806 (GRCm39) |
Y450C |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,131,077 (GRCm39) |
K239E |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,585,150 (GRCm39) |
G20302S |
probably damaging |
Het |
Ube2o |
A |
G |
11: 116,435,571 (GRCm39) |
S406P |
probably benign |
Het |
Xrn2 |
C |
T |
2: 146,866,670 (GRCm39) |
A80V |
probably damaging |
Het |
Zfp616 |
C |
T |
11: 73,975,456 (GRCm39) |
T575I |
possibly damaging |
Het |
|
Other mutations in Gli2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01410:Gli2
|
APN |
1 |
118,764,621 (GRCm39) |
missense |
probably benign |
|
IGL01686:Gli2
|
APN |
1 |
118,776,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01925:Gli2
|
APN |
1 |
118,781,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Gli2
|
APN |
1 |
118,764,465 (GRCm39) |
missense |
probably benign |
|
IGL02202:Gli2
|
APN |
1 |
118,764,596 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02255:Gli2
|
APN |
1 |
118,772,079 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02437:Gli2
|
APN |
1 |
118,763,733 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02615:Gli2
|
APN |
1 |
118,772,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02817:Gli2
|
APN |
1 |
118,764,101 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03294:Gli2
|
APN |
1 |
118,765,166 (GRCm39) |
missense |
probably benign |
|
fairyfly
|
UTSW |
1 |
118,768,220 (GRCm39) |
missense |
possibly damaging |
0.93 |
flea
|
UTSW |
1 |
118,763,655 (GRCm39) |
missense |
probably damaging |
0.99 |
patu_digua
|
UTSW |
1 |
118,765,236 (GRCm39) |
missense |
probably damaging |
1.00 |
BB006:Gli2
|
UTSW |
1 |
118,769,772 (GRCm39) |
missense |
possibly damaging |
0.88 |
BB016:Gli2
|
UTSW |
1 |
118,769,772 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0055:Gli2
|
UTSW |
1 |
118,818,138 (GRCm39) |
intron |
probably benign |
|
R0055:Gli2
|
UTSW |
1 |
118,818,138 (GRCm39) |
intron |
probably benign |
|
R0164:Gli2
|
UTSW |
1 |
118,818,013 (GRCm39) |
intron |
probably benign |
|
R0233:Gli2
|
UTSW |
1 |
118,763,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R0233:Gli2
|
UTSW |
1 |
118,763,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R0308:Gli2
|
UTSW |
1 |
118,769,792 (GRCm39) |
missense |
probably benign |
0.00 |
R0418:Gli2
|
UTSW |
1 |
118,768,220 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0558:Gli2
|
UTSW |
1 |
118,765,379 (GRCm39) |
missense |
probably benign |
0.01 |
R0600:Gli2
|
UTSW |
1 |
118,768,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Gli2
|
UTSW |
1 |
118,769,648 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0690:Gli2
|
UTSW |
1 |
118,772,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R0942:Gli2
|
UTSW |
1 |
118,765,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Gli2
|
UTSW |
1 |
118,782,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1104:Gli2
|
UTSW |
1 |
118,781,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R1141:Gli2
|
UTSW |
1 |
118,765,667 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1344:Gli2
|
UTSW |
1 |
118,769,666 (GRCm39) |
missense |
probably damaging |
0.98 |
R1418:Gli2
|
UTSW |
1 |
118,769,666 (GRCm39) |
missense |
probably damaging |
0.98 |
R1565:Gli2
|
UTSW |
1 |
118,769,660 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1605:Gli2
|
UTSW |
1 |
118,782,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Gli2
|
UTSW |
1 |
118,764,254 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1728:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1729:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1730:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1739:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1762:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1783:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1785:Gli2
|
UTSW |
1 |
118,929,774 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Gli2
|
UTSW |
1 |
118,795,817 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1874:Gli2
|
UTSW |
1 |
118,929,779 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1969:Gli2
|
UTSW |
1 |
118,765,430 (GRCm39) |
missense |
probably benign |
0.00 |
R2377:Gli2
|
UTSW |
1 |
118,764,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2883:Gli2
|
UTSW |
1 |
118,795,874 (GRCm39) |
missense |
probably damaging |
0.97 |
R2924:Gli2
|
UTSW |
1 |
118,764,089 (GRCm39) |
missense |
probably benign |
0.00 |
R4363:Gli2
|
UTSW |
1 |
118,781,100 (GRCm39) |
missense |
probably benign |
0.00 |
R4430:Gli2
|
UTSW |
1 |
118,764,974 (GRCm39) |
missense |
probably benign |
|
R4463:Gli2
|
UTSW |
1 |
118,763,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Gli2
|
UTSW |
1 |
118,769,798 (GRCm39) |
missense |
probably benign |
|
R4613:Gli2
|
UTSW |
1 |
118,765,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R4674:Gli2
|
UTSW |
1 |
118,763,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Gli2
|
UTSW |
1 |
118,768,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Gli2
|
UTSW |
1 |
118,910,318 (GRCm39) |
intron |
probably benign |
|
R4936:Gli2
|
UTSW |
1 |
118,763,870 (GRCm39) |
missense |
probably benign |
|
R5137:Gli2
|
UTSW |
1 |
118,783,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Gli2
|
UTSW |
1 |
118,763,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Gli2
|
UTSW |
1 |
118,772,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Gli2
|
UTSW |
1 |
118,764,485 (GRCm39) |
missense |
probably benign |
0.27 |
R5661:Gli2
|
UTSW |
1 |
118,781,032 (GRCm39) |
nonsense |
probably null |
|
R6005:Gli2
|
UTSW |
1 |
118,769,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R6012:Gli2
|
UTSW |
1 |
118,765,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R6341:Gli2
|
UTSW |
1 |
118,763,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6357:Gli2
|
UTSW |
1 |
118,769,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6425:Gli2
|
UTSW |
1 |
118,763,624 (GRCm39) |
nonsense |
probably null |
|
R6513:Gli2
|
UTSW |
1 |
118,783,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:Gli2
|
UTSW |
1 |
118,769,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Gli2
|
UTSW |
1 |
118,772,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Gli2
|
UTSW |
1 |
118,764,264 (GRCm39) |
missense |
probably benign |
|
R7378:Gli2
|
UTSW |
1 |
118,776,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7420:Gli2
|
UTSW |
1 |
118,763,669 (GRCm39) |
missense |
probably benign |
0.00 |
R7489:Gli2
|
UTSW |
1 |
118,765,905 (GRCm39) |
missense |
probably benign |
0.00 |
R7498:Gli2
|
UTSW |
1 |
118,763,565 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7929:Gli2
|
UTSW |
1 |
118,769,772 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8032:Gli2
|
UTSW |
1 |
118,763,900 (GRCm39) |
missense |
probably damaging |
0.98 |
R8150:Gli2
|
UTSW |
1 |
118,763,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R8233:Gli2
|
UTSW |
1 |
118,772,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8282:Gli2
|
UTSW |
1 |
118,765,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Gli2
|
UTSW |
1 |
118,795,842 (GRCm39) |
intron |
probably benign |
|
R8686:Gli2
|
UTSW |
1 |
118,764,417 (GRCm39) |
missense |
probably benign |
|
R8698:Gli2
|
UTSW |
1 |
118,769,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Gli2
|
UTSW |
1 |
118,764,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:Gli2
|
UTSW |
1 |
118,763,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Gli2
|
UTSW |
1 |
118,783,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R9214:Gli2
|
UTSW |
1 |
118,795,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Gli2
|
UTSW |
1 |
118,764,021 (GRCm39) |
missense |
probably benign |
0.00 |
R9295:Gli2
|
UTSW |
1 |
118,764,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Gli2
|
UTSW |
1 |
118,765,885 (GRCm39) |
missense |
probably benign |
0.04 |
R9496:Gli2
|
UTSW |
1 |
118,764,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9757:Gli2
|
UTSW |
1 |
118,773,652 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Gli2
|
UTSW |
1 |
118,765,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|