Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
G |
A |
9: 57,165,805 (GRCm39) |
R190* |
probably null |
Het |
Aldh7a1 |
A |
T |
18: 56,660,060 (GRCm39) |
S529T |
probably benign |
Het |
Carmil2 |
T |
G |
8: 106,415,130 (GRCm39) |
Y214* |
probably null |
Het |
Ccdc136 |
A |
G |
6: 29,406,109 (GRCm39) |
I152V |
probably damaging |
Het |
Ccdc88c |
T |
C |
12: 100,932,676 (GRCm39) |
D285G |
possibly damaging |
Het |
Clec4a3 |
T |
A |
6: 122,946,328 (GRCm39) |
F191I |
probably damaging |
Het |
Dlg5 |
A |
T |
14: 24,206,547 (GRCm39) |
S1222T |
|
Het |
Dnaaf9 |
T |
A |
2: 130,579,300 (GRCm39) |
R777* |
probably null |
Het |
Dnah14 |
T |
G |
1: 181,508,321 (GRCm39) |
L1833W |
probably damaging |
Het |
Dsg2 |
T |
C |
18: 20,725,535 (GRCm39) |
W549R |
probably damaging |
Het |
Ezh2 |
A |
T |
6: 47,510,713 (GRCm39) |
V632E |
possibly damaging |
Het |
Fam83a |
G |
A |
15: 57,873,313 (GRCm39) |
V381M |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,706,882 (GRCm39) |
|
probably null |
Het |
Fmo2 |
T |
C |
1: 162,704,398 (GRCm39) |
T503A |
probably benign |
Het |
Foxo1 |
T |
C |
3: 52,252,703 (GRCm39) |
F289L |
probably damaging |
Het |
Gckr |
A |
G |
5: 31,456,903 (GRCm39) |
E96G |
probably damaging |
Het |
Gm18596 |
G |
A |
10: 77,578,162 (GRCm39) |
A104V |
unknown |
Het |
Gm21680 |
A |
T |
5: 26,176,347 (GRCm39) |
N83K |
probably damaging |
Het |
Gnb5 |
T |
C |
9: 75,252,236 (GRCm39) |
V393A |
possibly damaging |
Het |
Gtsf2 |
T |
C |
15: 103,352,783 (GRCm39) |
I79V |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,105,055 (GRCm39) |
I1040V |
probably benign |
Het |
Kif2b |
C |
T |
11: 91,468,023 (GRCm39) |
E87K |
probably benign |
Het |
Klk1b8 |
G |
A |
7: 43,604,206 (GRCm39) |
G225S |
probably damaging |
Het |
L3mbtl3 |
A |
T |
10: 26,220,084 (GRCm39) |
C94S |
unknown |
Het |
Man2c1 |
T |
G |
9: 57,048,456 (GRCm39) |
Y872* |
probably null |
Het |
Mical3 |
T |
A |
6: 120,984,325 (GRCm39) |
M832L |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,216,334 (GRCm39) |
D41G |
probably benign |
Het |
Nedd1 |
T |
A |
10: 92,558,258 (GRCm39) |
|
probably benign |
Het |
Nefh |
TTTGGCCTCAGCTGGTGACTTGGGCTCAGCTGGAGACTTGGCCTCACCTGGTGACTTG |
TTTGGCCTCACCTGGTGACTTG |
11: 4,890,530 (GRCm39) |
|
probably benign |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Notch3 |
C |
T |
17: 32,372,792 (GRCm39) |
R593Q |
probably benign |
Het |
Nxpe3 |
T |
G |
16: 55,669,997 (GRCm39) |
E369D |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,977,695 (GRCm39) |
T1802S |
possibly damaging |
Het |
Or1e33 |
A |
T |
11: 73,738,406 (GRCm39) |
F182I |
probably benign |
Het |
Or2a7 |
T |
C |
6: 43,151,669 (GRCm39) |
F250L |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,585,107 (GRCm39) |
H171L |
probably benign |
Het |
Or9s14 |
A |
G |
1: 92,536,438 (GRCm39) |
N293S |
probably damaging |
Het |
Oscar |
A |
C |
7: 3,614,747 (GRCm39) |
V75G |
probably benign |
Het |
Pcdhb17 |
G |
A |
18: 37,620,372 (GRCm39) |
A721T |
probably benign |
Het |
Pcnx2 |
T |
C |
8: 126,614,659 (GRCm39) |
Y264C |
probably benign |
Het |
Pear1 |
G |
T |
3: 87,661,890 (GRCm39) |
A495D |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Plekhf1 |
C |
A |
7: 37,920,998 (GRCm39) |
R190L |
probably damaging |
Het |
Plppr5 |
T |
C |
3: 117,369,532 (GRCm39) |
V63A |
probably benign |
Het |
Pyroxd1 |
T |
A |
6: 142,300,437 (GRCm39) |
F189Y |
probably damaging |
Het |
Rab13 |
C |
T |
3: 90,128,120 (GRCm39) |
|
probably benign |
Het |
Rptor |
C |
T |
11: 119,782,036 (GRCm39) |
T1121I |
probably benign |
Het |
Scgb2b7 |
T |
C |
7: 31,404,602 (GRCm39) |
S33G |
probably benign |
Het |
Slc25a36 |
A |
G |
9: 96,982,126 (GRCm39) |
|
probably null |
Het |
Smc1b |
A |
T |
15: 84,991,273 (GRCm39) |
|
probably null |
Het |
Smtn |
T |
A |
11: 3,479,477 (GRCm39) |
H530L |
possibly damaging |
Het |
Srrt |
C |
T |
5: 137,297,070 (GRCm39) |
C411Y |
probably benign |
Het |
Stag1 |
C |
A |
9: 100,587,298 (GRCm39) |
P7Q |
possibly damaging |
Het |
Tarm1 |
G |
A |
7: 3,537,719 (GRCm39) |
T248I |
possibly damaging |
Het |
Tektl1 |
T |
C |
10: 78,588,258 (GRCm39) |
Y184C |
probably damaging |
Het |
Trim6 |
C |
T |
7: 103,881,655 (GRCm39) |
A328V |
probably benign |
Het |
Vmn1r189 |
T |
C |
13: 22,286,811 (GRCm39) |
I9V |
probably benign |
Het |
Vmn2r93 |
A |
G |
17: 18,546,500 (GRCm39) |
T791A |
probably damaging |
Het |
Vsig10l |
A |
G |
7: 43,116,020 (GRCm39) |
T454A |
probably benign |
Het |
|
Other mutations in Grin2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00494:Grin2b
|
APN |
6 |
135,713,329 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00835:Grin2b
|
APN |
6 |
135,710,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Grin2b
|
APN |
6 |
135,713,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Grin2b
|
APN |
6 |
136,021,263 (GRCm39) |
missense |
probably null |
0.99 |
IGL01719:Grin2b
|
APN |
6 |
135,710,379 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01907:Grin2b
|
APN |
6 |
135,710,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Grin2b
|
APN |
6 |
135,709,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02309:Grin2b
|
APN |
6 |
135,713,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Grin2b
|
APN |
6 |
135,716,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02409:Grin2b
|
APN |
6 |
136,020,906 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02527:Grin2b
|
APN |
6 |
135,900,389 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Grin2b
|
APN |
6 |
135,756,367 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02570:Grin2b
|
APN |
6 |
135,899,996 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02702:Grin2b
|
APN |
6 |
135,716,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03001:Grin2b
|
APN |
6 |
135,716,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03274:Grin2b
|
APN |
6 |
135,757,253 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0055:Grin2b
|
UTSW |
6 |
135,900,201 (GRCm39) |
missense |
probably benign |
|
R0055:Grin2b
|
UTSW |
6 |
135,900,201 (GRCm39) |
missense |
probably benign |
|
R0164:Grin2b
|
UTSW |
6 |
135,755,646 (GRCm39) |
splice site |
probably benign |
|
R0194:Grin2b
|
UTSW |
6 |
135,756,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Grin2b
|
UTSW |
6 |
135,710,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Grin2b
|
UTSW |
6 |
135,820,193 (GRCm39) |
missense |
probably benign |
0.04 |
R1928:Grin2b
|
UTSW |
6 |
136,021,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Grin2b
|
UTSW |
6 |
135,709,730 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1996:Grin2b
|
UTSW |
6 |
136,021,209 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2002:Grin2b
|
UTSW |
6 |
135,710,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Grin2b
|
UTSW |
6 |
135,710,894 (GRCm39) |
missense |
probably benign |
0.12 |
R2103:Grin2b
|
UTSW |
6 |
135,757,138 (GRCm39) |
missense |
probably benign |
0.02 |
R2127:Grin2b
|
UTSW |
6 |
135,755,698 (GRCm39) |
missense |
probably benign |
0.03 |
R2495:Grin2b
|
UTSW |
6 |
135,710,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Grin2b
|
UTSW |
6 |
135,710,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R2847:Grin2b
|
UTSW |
6 |
135,717,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R2866:Grin2b
|
UTSW |
6 |
135,710,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Grin2b
|
UTSW |
6 |
135,710,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Grin2b
|
UTSW |
6 |
135,710,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R3196:Grin2b
|
UTSW |
6 |
135,709,453 (GRCm39) |
small deletion |
probably benign |
|
R3418:Grin2b
|
UTSW |
6 |
135,820,108 (GRCm39) |
missense |
probably benign |
0.02 |
R3808:Grin2b
|
UTSW |
6 |
135,900,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R4028:Grin2b
|
UTSW |
6 |
135,713,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Grin2b
|
UTSW |
6 |
135,755,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Grin2b
|
UTSW |
6 |
135,710,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R4677:Grin2b
|
UTSW |
6 |
135,751,870 (GRCm39) |
missense |
probably benign |
0.13 |
R4744:Grin2b
|
UTSW |
6 |
135,755,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Grin2b
|
UTSW |
6 |
135,710,405 (GRCm39) |
missense |
probably benign |
0.01 |
R5051:Grin2b
|
UTSW |
6 |
135,756,393 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5105:Grin2b
|
UTSW |
6 |
135,709,439 (GRCm39) |
missense |
probably benign |
0.03 |
R5125:Grin2b
|
UTSW |
6 |
135,900,297 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5146:Grin2b
|
UTSW |
6 |
135,756,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Grin2b
|
UTSW |
6 |
135,710,916 (GRCm39) |
missense |
probably damaging |
0.99 |
R5349:Grin2b
|
UTSW |
6 |
136,021,281 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5426:Grin2b
|
UTSW |
6 |
135,709,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R5438:Grin2b
|
UTSW |
6 |
135,713,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5439:Grin2b
|
UTSW |
6 |
135,713,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Grin2b
|
UTSW |
6 |
135,713,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Grin2b
|
UTSW |
6 |
135,710,721 (GRCm39) |
missense |
probably benign |
0.00 |
R5603:Grin2b
|
UTSW |
6 |
135,900,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5657:Grin2b
|
UTSW |
6 |
135,710,085 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5788:Grin2b
|
UTSW |
6 |
135,717,962 (GRCm39) |
missense |
probably benign |
0.24 |
R5941:Grin2b
|
UTSW |
6 |
135,713,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R6057:Grin2b
|
UTSW |
6 |
135,710,942 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6137:Grin2b
|
UTSW |
6 |
135,900,456 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6216:Grin2b
|
UTSW |
6 |
135,749,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R6309:Grin2b
|
UTSW |
6 |
135,710,025 (GRCm39) |
missense |
probably benign |
0.00 |
R6316:Grin2b
|
UTSW |
6 |
135,757,277 (GRCm39) |
missense |
probably benign |
0.00 |
R6419:Grin2b
|
UTSW |
6 |
135,717,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R6551:Grin2b
|
UTSW |
6 |
135,710,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R6612:Grin2b
|
UTSW |
6 |
135,717,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Grin2b
|
UTSW |
6 |
135,709,549 (GRCm39) |
missense |
probably benign |
|
R6647:Grin2b
|
UTSW |
6 |
135,710,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Grin2b
|
UTSW |
6 |
135,751,826 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6976:Grin2b
|
UTSW |
6 |
135,757,198 (GRCm39) |
missense |
probably benign |
|
R7033:Grin2b
|
UTSW |
6 |
135,900,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Grin2b
|
UTSW |
6 |
135,757,304 (GRCm39) |
missense |
probably damaging |
0.97 |
R7144:Grin2b
|
UTSW |
6 |
135,710,474 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7190:Grin2b
|
UTSW |
6 |
135,709,946 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7238:Grin2b
|
UTSW |
6 |
135,757,249 (GRCm39) |
missense |
probably damaging |
0.97 |
R7453:Grin2b
|
UTSW |
6 |
135,717,947 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7553:Grin2b
|
UTSW |
6 |
135,749,394 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7585:Grin2b
|
UTSW |
6 |
135,756,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R7615:Grin2b
|
UTSW |
6 |
135,900,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7632:Grin2b
|
UTSW |
6 |
135,709,553 (GRCm39) |
missense |
probably benign |
0.02 |
R7779:Grin2b
|
UTSW |
6 |
135,755,792 (GRCm39) |
nonsense |
probably null |
|
R8058:Grin2b
|
UTSW |
6 |
135,710,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8084:Grin2b
|
UTSW |
6 |
135,710,486 (GRCm39) |
missense |
probably benign |
0.03 |
R8145:Grin2b
|
UTSW |
6 |
135,709,497 (GRCm39) |
missense |
probably benign |
0.01 |
R8308:Grin2b
|
UTSW |
6 |
135,900,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R8357:Grin2b
|
UTSW |
6 |
135,709,197 (GRCm39) |
missense |
probably benign |
0.00 |
R8379:Grin2b
|
UTSW |
6 |
135,899,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Grin2b
|
UTSW |
6 |
135,710,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R8457:Grin2b
|
UTSW |
6 |
135,709,197 (GRCm39) |
missense |
probably benign |
0.00 |
R8746:Grin2b
|
UTSW |
6 |
135,899,985 (GRCm39) |
missense |
probably benign |
0.02 |
R8927:Grin2b
|
UTSW |
6 |
135,749,339 (GRCm39) |
missense |
probably damaging |
0.97 |
R8963:Grin2b
|
UTSW |
6 |
136,021,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Grin2b
|
UTSW |
6 |
135,709,509 (GRCm39) |
frame shift |
probably null |
|
R9076:Grin2b
|
UTSW |
6 |
135,709,509 (GRCm39) |
frame shift |
probably null |
|
R9172:Grin2b
|
UTSW |
6 |
135,756,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9520:Grin2b
|
UTSW |
6 |
135,710,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R9740:Grin2b
|
UTSW |
6 |
135,899,868 (GRCm39) |
critical splice donor site |
probably null |
|
RF001:Grin2b
|
UTSW |
6 |
136,021,238 (GRCm39) |
missense |
probably benign |
|
|