Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
A |
13: 77,451,529 (GRCm39) |
M871K |
probably benign |
Het |
5530400C23Rik |
A |
C |
6: 133,271,256 (GRCm39) |
E100A |
possibly damaging |
Het |
Aatf |
A |
T |
11: 84,402,338 (GRCm39) |
I116N |
probably benign |
Het |
Abcb11 |
G |
T |
2: 69,087,754 (GRCm39) |
|
probably benign |
Het |
Adarb2 |
G |
T |
13: 8,802,680 (GRCm39) |
A652S |
probably benign |
Het |
Adgb |
C |
T |
10: 10,281,028 (GRCm39) |
|
probably null |
Het |
Ankrd34a |
C |
T |
3: 96,504,791 (GRCm39) |
|
probably benign |
Het |
Ano2 |
A |
G |
6: 125,840,513 (GRCm39) |
I395V |
probably benign |
Het |
Cadm2 |
C |
A |
16: 66,581,696 (GRCm39) |
R203L |
probably damaging |
Het |
Ccr2 |
T |
C |
9: 123,906,448 (GRCm39) |
F243L |
probably benign |
Het |
Ccr4 |
A |
G |
9: 114,321,918 (GRCm39) |
V49A |
probably damaging |
Het |
Cemip2 |
G |
A |
19: 21,803,465 (GRCm39) |
G833R |
probably damaging |
Het |
Corin |
T |
C |
5: 72,592,695 (GRCm39) |
D234G |
probably benign |
Het |
Drd5 |
G |
T |
5: 38,477,433 (GRCm39) |
R142I |
probably benign |
Het |
Dsg1b |
A |
G |
18: 20,529,056 (GRCm39) |
D264G |
probably damaging |
Het |
Ezh2 |
T |
C |
6: 47,553,534 (GRCm39) |
K61R |
probably damaging |
Het |
Frmd4b |
T |
A |
6: 97,269,370 (GRCm39) |
T981S |
probably benign |
Het |
Gcg |
T |
A |
2: 62,305,325 (GRCm39) |
K180N |
probably damaging |
Het |
Gm10840 |
G |
A |
11: 106,051,742 (GRCm39) |
E23K |
unknown |
Het |
Gm2696 |
T |
G |
10: 77,651,037 (GRCm39) |
C174W |
unknown |
Het |
Hepacam |
T |
A |
9: 37,293,030 (GRCm39) |
V207E |
probably damaging |
Het |
Igf1r |
T |
A |
7: 67,864,745 (GRCm39) |
M1181K |
probably damaging |
Het |
Lmo2 |
T |
C |
2: 103,806,384 (GRCm39) |
S96P |
possibly damaging |
Het |
Marf1 |
T |
A |
16: 13,935,168 (GRCm39) |
E1533D |
probably benign |
Het |
Megf9 |
A |
G |
4: 70,353,511 (GRCm39) |
C432R |
probably damaging |
Het |
Mpp2 |
A |
G |
11: 101,954,040 (GRCm39) |
Y236H |
probably damaging |
Het |
Neb |
T |
C |
2: 52,172,613 (GRCm39) |
I1565V |
probably damaging |
Het |
Or2y1f |
A |
G |
11: 49,183,993 (GRCm39) |
|
probably benign |
Het |
Or56b2j |
A |
T |
7: 104,353,067 (GRCm39) |
I98F |
probably damaging |
Het |
Or5ac21 |
T |
A |
16: 59,123,973 (GRCm39) |
F152L |
probably benign |
Het |
Or5b3 |
A |
G |
19: 13,388,092 (GRCm39) |
D53G |
probably benign |
Het |
Or5g24-ps1 |
T |
A |
2: 85,464,221 (GRCm39) |
Y149* |
probably null |
Het |
Or6f1 |
C |
T |
7: 85,970,437 (GRCm39) |
C241Y |
probably damaging |
Het |
Or9k2b |
T |
C |
10: 130,016,086 (GRCm39) |
Y221C |
probably damaging |
Het |
Patj |
T |
A |
4: 98,394,067 (GRCm39) |
|
probably benign |
Het |
Pknox1 |
A |
T |
17: 31,809,624 (GRCm39) |
Q76L |
possibly damaging |
Het |
Plekhg1 |
C |
A |
10: 3,907,777 (GRCm39) |
T953K |
|
Het |
Plekhn1 |
C |
A |
4: 156,316,682 (GRCm39) |
R333L |
probably damaging |
Het |
Plk5 |
T |
A |
10: 80,194,610 (GRCm39) |
V111D |
probably benign |
Het |
Polr1b |
A |
G |
2: 128,954,597 (GRCm39) |
I398M |
possibly damaging |
Het |
Ranbp3 |
T |
C |
17: 57,009,826 (GRCm39) |
V137A |
probably benign |
Het |
Rc3h1 |
T |
A |
1: 160,757,744 (GRCm39) |
F21I |
probably damaging |
Het |
Rgs8 |
T |
C |
1: 153,547,537 (GRCm39) |
S56P |
probably damaging |
Het |
Rhpn1 |
G |
A |
15: 75,585,425 (GRCm39) |
V593M |
probably damaging |
Het |
Sdad1 |
A |
G |
5: 92,437,784 (GRCm39) |
S589P |
probably benign |
Het |
Skp1 |
A |
G |
11: 52,136,843 (GRCm39) |
K163R |
probably damaging |
Het |
Slf2 |
A |
G |
19: 44,962,063 (GRCm39) |
Y1080C |
probably damaging |
Het |
Tcf4 |
C |
T |
18: 69,654,572 (GRCm39) |
|
probably benign |
Het |
Tmem144 |
C |
T |
3: 79,732,655 (GRCm39) |
V208M |
probably damaging |
Het |
Tomm34 |
A |
T |
2: 163,902,884 (GRCm39) |
L142Q |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,176,120 (GRCm39) |
V2316D |
unknown |
Het |
Yme1l1 |
T |
A |
2: 23,052,543 (GRCm39) |
S66T |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,243,885 (GRCm39) |
S739P |
probably damaging |
Het |
Zscan25 |
T |
A |
5: 145,224,157 (GRCm39) |
V209E |
possibly damaging |
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 |
R8925:Grin2b
|
UTSW |
6 |
135,749,339 (GRCm39) |
missense |
probably damaging |
0.97 |
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 |
|
|