Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agl |
T |
C |
3: 116,544,060 (GRCm39) |
T1416A |
probably damaging |
Het |
Atp7b |
A |
G |
8: 22,518,494 (GRCm39) |
S103P |
probably damaging |
Het |
Ces1h |
A |
C |
8: 94,078,654 (GRCm39) |
*563G |
probably null |
Het |
Cfap157 |
G |
T |
2: 32,669,086 (GRCm39) |
A339E |
probably benign |
Het |
Crebbp |
C |
T |
16: 3,937,670 (GRCm39) |
A698T |
possibly damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,785,324 (GRCm39) |
H231R |
possibly damaging |
Het |
Ddx31 |
A |
T |
2: 28,765,750 (GRCm39) |
T483S |
probably damaging |
Het |
Defa25 |
A |
T |
8: 21,575,201 (GRCm39) |
D60V |
possibly damaging |
Het |
Dnah5 |
G |
A |
15: 28,403,633 (GRCm39) |
A3453T |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,115,743 (GRCm39) |
F1500I |
probably damaging |
Het |
Eprs1 |
C |
T |
1: 185,146,621 (GRCm39) |
A1217V |
probably damaging |
Het |
Ermp1 |
T |
C |
19: 29,604,335 (GRCm39) |
Y481C |
probably benign |
Het |
Fmn2 |
T |
A |
1: 174,420,670 (GRCm39) |
N635K |
unknown |
Het |
Fras1 |
A |
G |
5: 96,883,061 (GRCm39) |
D2531G |
probably damaging |
Het |
Frat1 |
C |
T |
19: 41,819,264 (GRCm39) |
Q220* |
probably null |
Het |
Gcc2 |
T |
A |
10: 58,123,103 (GRCm39) |
|
probably null |
Het |
Gm3285 |
T |
C |
10: 77,698,447 (GRCm39) |
|
probably benign |
Het |
Gm9857 |
T |
C |
3: 108,847,379 (GRCm39) |
|
probably benign |
Het |
Hells |
T |
A |
19: 38,919,948 (GRCm39) |
L33I |
probably benign |
Het |
Ift81 |
T |
A |
5: 122,748,229 (GRCm39) |
R54* |
probably null |
Het |
Ints12 |
G |
A |
3: 132,802,639 (GRCm39) |
R41Q |
possibly damaging |
Het |
Katnal2 |
C |
T |
18: 77,067,733 (GRCm39) |
E403K |
probably benign |
Het |
Kcnk1 |
A |
G |
8: 126,722,199 (GRCm39) |
M1V |
probably null |
Het |
Kdm5a |
A |
G |
6: 120,389,422 (GRCm39) |
T950A |
probably benign |
Het |
Kdr |
G |
A |
5: 76,113,549 (GRCm39) |
A773V |
probably damaging |
Het |
Lats1 |
G |
C |
10: 7,573,271 (GRCm39) |
M118I |
possibly damaging |
Het |
Mug1 |
A |
G |
6: 121,817,200 (GRCm39) |
I90V |
probably benign |
Het |
Nid2 |
A |
G |
14: 19,852,484 (GRCm39) |
D1064G |
probably benign |
Het |
Nkx2-4 |
A |
T |
2: 146,926,187 (GRCm39) |
I225N |
possibly damaging |
Het |
Nlrp4e |
A |
G |
7: 23,020,740 (GRCm39) |
D409G |
probably benign |
Het |
Ogfod2 |
G |
C |
5: 124,252,866 (GRCm39) |
R292P |
possibly damaging |
Het |
Oprk1 |
C |
T |
1: 5,672,507 (GRCm39) |
P215S |
probably damaging |
Het |
Or5d36 |
A |
T |
2: 87,901,053 (GRCm39) |
F224L |
probably benign |
Het |
Or6c35 |
T |
A |
10: 129,169,033 (GRCm39) |
C94* |
probably null |
Het |
Or7g27 |
T |
A |
9: 19,249,925 (GRCm39) |
H56Q |
possibly damaging |
Het |
Or8g21 |
T |
C |
9: 38,906,210 (GRCm39) |
I174V |
possibly damaging |
Het |
Pcdhb16 |
A |
G |
18: 37,612,225 (GRCm39) |
K395R |
possibly damaging |
Het |
Ptprg |
C |
A |
14: 11,962,714 (GRCm38) |
P171T |
probably damaging |
Het |
Pycard |
T |
C |
7: 127,592,741 (GRCm39) |
T29A |
probably benign |
Het |
Rap1gap2 |
G |
A |
11: 74,298,754 (GRCm39) |
A452V |
probably benign |
Het |
Rasgrf1 |
C |
G |
9: 89,892,516 (GRCm39) |
T1072S |
probably benign |
Het |
Rc3h2 |
G |
A |
2: 37,272,956 (GRCm39) |
R707* |
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Senp7 |
T |
C |
16: 55,993,618 (GRCm39) |
I767T |
probably damaging |
Het |
Setd7 |
A |
G |
3: 51,450,183 (GRCm39) |
V81A |
probably benign |
Het |
Shisal2a |
A |
G |
4: 108,225,224 (GRCm39) |
S113P |
probably benign |
Het |
Shkbp1 |
A |
G |
7: 27,041,800 (GRCm39) |
S685P |
probably benign |
Het |
Snrnp200 |
A |
G |
2: 127,068,372 (GRCm39) |
E904G |
probably damaging |
Het |
Spata22 |
T |
A |
11: 73,245,526 (GRCm39) |
|
probably null |
Het |
Spata31e2 |
T |
A |
1: 26,721,659 (GRCm39) |
N1174Y |
probably damaging |
Het |
Tas2r138 |
G |
T |
6: 40,589,733 (GRCm39) |
T171K |
possibly damaging |
Het |
Tor1aip1 |
T |
C |
1: 155,893,999 (GRCm39) |
D77G |
possibly damaging |
Het |
Vav3 |
A |
T |
3: 109,434,732 (GRCm39) |
H421L |
probably benign |
Het |
Vmn1r43 |
A |
G |
6: 89,846,841 (GRCm39) |
L215P |
probably damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,742,785 (GRCm39) |
S386R |
probably benign |
Het |
Xpa |
T |
A |
4: 46,183,089 (GRCm39) |
R233S |
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 |
|
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 |
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 |
|
|