Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447F04Rik |
T |
C |
X: 65,347,274 (GRCm39) |
E91G |
unknown |
Het |
Acot1 |
A |
G |
12: 84,064,113 (GRCm39) |
Q407R |
probably benign |
Het |
Adcy10 |
T |
A |
1: 165,398,297 (GRCm39) |
Y1465N |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,440,702 (GRCm39) |
I249F |
probably damaging |
Het |
Arhgap10 |
T |
C |
8: 77,977,594 (GRCm39) |
N721S |
probably damaging |
Het |
Arrdc4 |
T |
G |
7: 68,391,619 (GRCm39) |
E216A |
probably damaging |
Het |
Axin1 |
T |
C |
17: 26,392,637 (GRCm39) |
V306A |
probably benign |
Het |
Cct3 |
T |
C |
3: 88,210,173 (GRCm39) |
|
probably null |
Het |
Cfap58 |
G |
A |
19: 47,963,119 (GRCm39) |
|
probably null |
Het |
Chd9 |
T |
C |
8: 91,699,859 (GRCm39) |
S49P |
possibly damaging |
Het |
Clcn2 |
C |
A |
16: 20,529,178 (GRCm39) |
|
probably null |
Het |
Col26a1 |
T |
C |
5: 136,783,047 (GRCm39) |
N286D |
probably benign |
Het |
Cpt1b |
T |
A |
15: 89,308,596 (GRCm39) |
I111F |
possibly damaging |
Het |
Cyp4f16 |
T |
A |
17: 32,756,061 (GRCm39) |
I30N |
probably damaging |
Het |
Ddc |
T |
G |
11: 11,830,587 (GRCm39) |
D19A |
possibly damaging |
Het |
Depdc1a |
T |
A |
3: 159,222,537 (GRCm39) |
|
probably null |
Het |
Evc2 |
T |
A |
5: 37,574,828 (GRCm39) |
C1028S |
possibly damaging |
Het |
Fam228a |
T |
C |
12: 4,781,457 (GRCm39) |
E134G |
probably damaging |
Het |
Fasl |
T |
C |
1: 161,615,523 (GRCm39) |
E111G |
probably benign |
Het |
Fbxw10 |
A |
G |
11: 62,767,564 (GRCm39) |
N800S |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,910,524 (GRCm39) |
S3318P |
probably damaging |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gad1 |
T |
A |
2: 70,409,545 (GRCm39) |
M212K |
probably damaging |
Het |
Gm17455 |
T |
G |
10: 60,238,752 (GRCm39) |
S6A |
probably benign |
Het |
Grm5 |
T |
C |
7: 87,779,997 (GRCm39) |
S1146P |
probably damaging |
Het |
Gsn |
T |
C |
2: 35,194,651 (GRCm39) |
L649P |
probably damaging |
Het |
H2-DMb1 |
A |
G |
17: 34,374,685 (GRCm39) |
T112A |
probably benign |
Het |
Hcn3 |
T |
A |
3: 89,060,201 (GRCm39) |
I148F |
probably damaging |
Het |
Hdac10 |
T |
C |
15: 89,009,961 (GRCm39) |
|
probably null |
Het |
Hk3 |
C |
A |
13: 55,156,518 (GRCm39) |
D619Y |
probably damaging |
Het |
Ifi44 |
T |
A |
3: 151,451,134 (GRCm39) |
R272S |
possibly damaging |
Het |
Il1rap |
A |
C |
16: 26,517,625 (GRCm39) |
D275A |
probably damaging |
Het |
Irag2 |
A |
G |
6: 145,113,710 (GRCm39) |
R293G |
possibly damaging |
Het |
Itgam |
A |
T |
7: 127,707,152 (GRCm39) |
N660I |
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,332,793 (GRCm39) |
M1853T |
probably benign |
Het |
Lrrc8c |
A |
C |
5: 105,754,965 (GRCm39) |
K247Q |
probably damaging |
Het |
Map3k21 |
T |
C |
8: 126,668,858 (GRCm39) |
S815P |
probably benign |
Het |
Mast4 |
A |
G |
13: 102,888,068 (GRCm39) |
S1114P |
probably damaging |
Het |
Myh8 |
C |
T |
11: 67,194,591 (GRCm39) |
Q1601* |
probably null |
Het |
Nhlrc2 |
A |
G |
19: 56,558,959 (GRCm39) |
D148G |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,081,385 (GRCm39) |
S1196T |
probably benign |
Het |
Nsmaf |
C |
T |
4: 6,424,874 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,890,449 (GRCm39) |
D7361G |
unknown |
Het |
Or2t35 |
T |
C |
14: 14,407,777 (GRCm38) |
V183A |
probably damaging |
Het |
Or52ad1 |
C |
A |
7: 102,996,085 (GRCm39) |
A17S |
probably benign |
Het |
Or5bw2 |
C |
T |
7: 6,573,359 (GRCm39) |
A123V |
probably damaging |
Het |
Pank3 |
T |
G |
11: 35,668,536 (GRCm39) |
M175R |
probably benign |
Het |
Papolg |
A |
G |
11: 23,829,868 (GRCm39) |
|
probably null |
Het |
Pcdhb21 |
G |
A |
18: 37,647,566 (GRCm39) |
D232N |
probably damaging |
Het |
Pcdhb22 |
T |
C |
18: 37,651,925 (GRCm39) |
F131S |
probably damaging |
Het |
Pik3r6 |
G |
A |
11: 68,419,608 (GRCm39) |
A140T |
possibly damaging |
Het |
Pinlyp |
T |
C |
7: 24,241,947 (GRCm39) |
T87A |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,178,724 (GRCm39) |
S873P |
probably damaging |
Het |
Pld5 |
T |
A |
1: 176,102,295 (GRCm39) |
Y49F |
probably benign |
Het |
Polq |
T |
C |
16: 36,855,252 (GRCm39) |
V449A |
probably damaging |
Het |
Prkca |
A |
G |
11: 107,869,106 (GRCm39) |
V69A |
probably benign |
Het |
Ptk6 |
A |
G |
2: 180,844,075 (GRCm39) |
S75P |
possibly damaging |
Het |
Ptprq |
G |
A |
10: 107,418,391 (GRCm39) |
Q1662* |
probably null |
Het |
Ptprt |
C |
A |
2: 161,395,742 (GRCm39) |
A1144S |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,116,133 (GRCm39) |
W684R |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,735,500 (GRCm39) |
M4093L |
probably damaging |
Het |
Scnn1a |
C |
T |
6: 125,299,189 (GRCm39) |
L90F |
probably damaging |
Het |
Slc25a19 |
G |
T |
11: 115,508,423 (GRCm39) |
Y188* |
probably null |
Het |
Slc31a1 |
C |
T |
4: 62,303,866 (GRCm39) |
|
probably benign |
Het |
Slc5a11 |
C |
G |
7: 122,864,458 (GRCm39) |
S351R |
possibly damaging |
Het |
Slc6a17 |
A |
G |
3: 107,384,183 (GRCm39) |
L387P |
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,364 (GRCm39) |
L781H |
probably damaging |
Het |
Spam1 |
T |
A |
6: 24,797,837 (GRCm39) |
L331Q |
probably damaging |
Het |
Spata32 |
A |
G |
11: 103,100,125 (GRCm39) |
W127R |
probably damaging |
Het |
Spring1 |
A |
G |
5: 118,393,886 (GRCm39) |
E88G |
possibly damaging |
Het |
Spta1 |
T |
G |
1: 174,041,508 (GRCm39) |
I1324S |
probably damaging |
Het |
St6galnac4 |
A |
G |
2: 32,484,330 (GRCm39) |
Y176C |
probably damaging |
Het |
Stk10 |
A |
G |
11: 32,546,724 (GRCm39) |
E327G |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,954,646 (GRCm39) |
Y912F |
possibly damaging |
Het |
Tchp |
G |
A |
5: 114,858,243 (GRCm39) |
E459K |
probably benign |
Het |
Terf2 |
C |
T |
8: 107,822,842 (GRCm39) |
W100* |
probably null |
Het |
Thoc2l |
T |
G |
5: 104,666,077 (GRCm39) |
S200A |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,634 (GRCm39) |
N26S |
probably damaging |
Het |
Tln1 |
C |
A |
4: 43,553,504 (GRCm39) |
R297L |
probably benign |
Het |
Tmeff2 |
C |
A |
1: 50,967,234 (GRCm39) |
T43N |
possibly damaging |
Het |
Tmx1 |
C |
T |
12: 70,499,947 (GRCm39) |
A2V |
possibly damaging |
Het |
Tnks1bp1 |
T |
A |
2: 84,902,481 (GRCm39) |
L1053Q |
probably damaging |
Het |
Trmt10b |
A |
T |
4: 45,304,286 (GRCm39) |
K107N |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,955,972 (GRCm39) |
|
probably null |
Het |
Trrap |
A |
G |
5: 144,783,287 (GRCm39) |
K3371R |
probably damaging |
Het |
Usp19 |
T |
C |
9: 108,371,439 (GRCm39) |
|
probably null |
Het |
Usp28 |
C |
A |
9: 48,950,401 (GRCm39) |
D615E |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,657,931 (GRCm39) |
D43G |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,997 (GRCm39) |
K78Q |
possibly damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,151,327 (GRCm39) |
M96V |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,079,023 (GRCm39) |
E273G |
probably damaging |
Het |
Xpc |
C |
T |
6: 91,468,208 (GRCm39) |
A860T |
probably benign |
Het |
Zscan21 |
T |
C |
5: 138,131,865 (GRCm39) |
I463T |
possibly damaging |
Het |
|
Other mutations in Tuba3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02159:Tuba3b
|
APN |
6 |
145,565,392 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03027:Tuba3b
|
APN |
6 |
145,565,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Tuba3b
|
APN |
6 |
145,565,450 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0086:Tuba3b
|
UTSW |
6 |
145,566,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Tuba3b
|
UTSW |
6 |
145,565,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R1376:Tuba3b
|
UTSW |
6 |
145,564,500 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1376:Tuba3b
|
UTSW |
6 |
145,564,500 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1476:Tuba3b
|
UTSW |
6 |
145,564,179 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2137:Tuba3b
|
UTSW |
6 |
145,564,559 (GRCm39) |
missense |
probably benign |
|
R4993:Tuba3b
|
UTSW |
6 |
145,566,999 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5796:Tuba3b
|
UTSW |
6 |
145,565,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5945:Tuba3b
|
UTSW |
6 |
145,565,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R6045:Tuba3b
|
UTSW |
6 |
145,566,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768:Tuba3b
|
UTSW |
6 |
145,564,455 (GRCm39) |
splice site |
probably null |
|
R7055:Tuba3b
|
UTSW |
6 |
145,566,935 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7815:Tuba3b
|
UTSW |
6 |
145,566,847 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8997:Tuba3b
|
UTSW |
6 |
145,566,954 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9006:Tuba3b
|
UTSW |
6 |
145,565,564 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9026:Tuba3b
|
UTSW |
6 |
145,563,996 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9786:Tuba3b
|
UTSW |
6 |
145,564,482 (GRCm39) |
missense |
probably benign |
0.19 |
X0023:Tuba3b
|
UTSW |
6 |
145,566,900 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tuba3b
|
UTSW |
6 |
145,567,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|