Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcl9l |
A |
G |
9: 44,420,496 (GRCm39) |
N1264D |
probably benign |
Het |
Bmyc |
A |
G |
2: 25,597,082 (GRCm39) |
K49E |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Ceacam2 |
A |
G |
7: 25,230,166 (GRCm39) |
S147P |
probably benign |
Het |
Cep152 |
G |
T |
2: 125,444,856 (GRCm39) |
|
probably null |
Het |
Cnbd1 |
G |
T |
4: 18,894,993 (GRCm39) |
P250T |
possibly damaging |
Het |
Col6a4 |
A |
G |
9: 105,940,304 (GRCm39) |
C1209R |
possibly damaging |
Het |
Coro1c |
T |
C |
5: 113,990,334 (GRCm39) |
T116A |
probably benign |
Het |
Ddx46 |
A |
G |
13: 55,825,416 (GRCm39) |
|
probably benign |
Het |
Dnaaf5 |
T |
C |
5: 139,137,268 (GRCm39) |
I207T |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,794,758 (GRCm39) |
D139G |
probably benign |
Het |
Fbxw22 |
A |
T |
9: 109,231,087 (GRCm39) |
I121N |
possibly damaging |
Het |
Fcmr |
T |
C |
1: 130,802,872 (GRCm39) |
S162P |
probably benign |
Het |
Gadl1 |
A |
G |
9: 115,766,225 (GRCm39) |
|
probably benign |
Het |
Gm10717 |
A |
T |
9: 3,026,287 (GRCm39) |
Y195F |
probably damaging |
Het |
Gne |
T |
C |
4: 44,037,306 (GRCm39) |
N692D |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,902,489 (GRCm39) |
T1397A |
possibly damaging |
Het |
Lama3 |
C |
A |
18: 12,601,371 (GRCm39) |
A1016E |
probably damaging |
Het |
Lhfpl2 |
A |
G |
13: 94,328,419 (GRCm39) |
D160G |
probably benign |
Het |
Lmtk2 |
T |
A |
5: 144,112,769 (GRCm39) |
V1163E |
probably benign |
Het |
Lrrtm2 |
G |
T |
18: 35,345,868 (GRCm39) |
S478* |
probably null |
Het |
Nfatc2ip |
T |
C |
7: 125,989,736 (GRCm39) |
|
probably null |
Het |
Nlrp12 |
A |
G |
7: 3,282,574 (GRCm39) |
I775T |
probably benign |
Het |
Npr1 |
A |
G |
3: 90,372,165 (GRCm39) |
F216L |
probably benign |
Het |
Or4m1 |
A |
T |
14: 50,557,617 (GRCm39) |
L225H |
probably damaging |
Het |
Or5ac24 |
T |
A |
16: 59,165,387 (GRCm39) |
N226Y |
probably benign |
Het |
Or5b99 |
G |
T |
19: 12,976,929 (GRCm39) |
S193I |
possibly damaging |
Het |
Pkd1l1 |
C |
A |
11: 8,783,800 (GRCm39) |
G2052C |
probably damaging |
Het |
Ppp1r16b |
A |
G |
2: 158,588,451 (GRCm39) |
N112S |
possibly damaging |
Het |
Prr11 |
A |
G |
11: 86,994,141 (GRCm39) |
|
probably benign |
Het |
Scap |
A |
G |
9: 110,210,724 (GRCm39) |
|
probably benign |
Het |
Sirt1 |
C |
T |
10: 63,171,608 (GRCm39) |
R191Q |
probably damaging |
Het |
Slc38a6 |
A |
C |
12: 73,397,320 (GRCm39) |
S321R |
possibly damaging |
Het |
Sp140 |
T |
C |
1: 85,570,940 (GRCm39) |
V460A |
probably benign |
Het |
Spdye4c |
A |
T |
2: 128,434,586 (GRCm39) |
K54N |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,030,860 (GRCm39) |
N947K |
probably benign |
Het |
Srgap1 |
A |
G |
10: 121,621,598 (GRCm39) |
V965A |
possibly damaging |
Het |
Tmem209 |
A |
C |
6: 30,508,659 (GRCm39) |
|
probably null |
Het |
Trim37 |
A |
T |
11: 87,092,230 (GRCm39) |
K123* |
probably null |
Het |
Trio |
T |
C |
15: 27,744,244 (GRCm39) |
T2563A |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,289,717 (GRCm39) |
S734T |
possibly damaging |
Het |
Vars2 |
A |
G |
17: 35,975,513 (GRCm39) |
|
probably benign |
Het |
Xrn1 |
G |
A |
9: 95,859,858 (GRCm39) |
E417K |
probably benign |
Het |
Yeats2 |
T |
A |
16: 20,011,970 (GRCm39) |
V515E |
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 |
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 |
R2199:Gli2
|
UTSW |
1 |
118,765,378 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
|