Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts19 |
T |
A |
18: 59,060,369 (GRCm39) |
V454E |
probably damaging |
Het |
Atp7b |
G |
T |
8: 22,484,786 (GRCm39) |
Q1424K |
probably damaging |
Het |
Bicra |
T |
C |
7: 15,727,066 (GRCm39) |
D30G |
possibly damaging |
Het |
Cdhr2 |
A |
G |
13: 54,865,701 (GRCm39) |
D233G |
probably null |
Het |
Clint1 |
C |
T |
11: 45,784,883 (GRCm39) |
T294M |
probably damaging |
Het |
Cntnap5c |
C |
T |
17: 58,445,694 (GRCm39) |
T578I |
probably benign |
Het |
Col12a1 |
G |
T |
9: 79,588,797 (GRCm39) |
T1106N |
probably damaging |
Het |
Csta3 |
A |
G |
16: 36,030,847 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,896,430 (GRCm39) |
Y3598C |
probably damaging |
Het |
Dnaja3 |
A |
G |
16: 4,512,300 (GRCm39) |
T235A |
probably benign |
Het |
Eif2s1 |
T |
C |
12: 78,926,790 (GRCm39) |
I180T |
probably damaging |
Het |
Ergic1 |
C |
A |
17: 26,848,601 (GRCm39) |
P108Q |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,161,085 (GRCm39) |
D3215V |
probably damaging |
Het |
Galnt17 |
A |
T |
5: 131,335,371 (GRCm39) |
I23N |
probably benign |
Het |
Gpr20 |
C |
T |
15: 73,568,275 (GRCm39) |
R38Q |
probably benign |
Het |
H2-T5 |
T |
C |
17: 36,476,299 (GRCm39) |
I350V |
probably benign |
Het |
Hmbs |
A |
G |
9: 44,252,510 (GRCm39) |
|
probably null |
Het |
Hunk |
T |
C |
16: 90,272,829 (GRCm39) |
Y302H |
probably damaging |
Het |
Mybph |
A |
T |
1: 134,125,188 (GRCm39) |
I239F |
probably damaging |
Het |
Ncoa3 |
G |
A |
2: 165,899,120 (GRCm39) |
A821T |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,335,474 (GRCm39) |
I979V |
possibly damaging |
Het |
Or5w14 |
T |
C |
2: 87,541,353 (GRCm39) |
E299G |
probably benign |
Het |
Or7h8 |
A |
T |
9: 20,124,377 (GRCm39) |
H244L |
probably damaging |
Het |
Pdilt |
G |
A |
7: 119,118,890 (GRCm39) |
T53M |
probably benign |
Het |
Pdlim1 |
T |
C |
19: 40,211,505 (GRCm39) |
T263A |
probably benign |
Het |
Pik3cg |
A |
T |
12: 32,244,820 (GRCm39) |
M878K |
possibly damaging |
Het |
Plod1 |
T |
C |
4: 148,010,614 (GRCm39) |
K279R |
probably benign |
Het |
Plxna4 |
T |
C |
6: 32,142,052 (GRCm39) |
T1602A |
possibly damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,335,847 (GRCm39) |
|
probably null |
Het |
Rnls |
G |
A |
19: 33,145,783 (GRCm39) |
T112I |
probably benign |
Het |
Ropn1 |
G |
A |
16: 34,497,647 (GRCm39) |
V180I |
probably benign |
Het |
Rptor |
T |
C |
11: 119,737,741 (GRCm39) |
Y605H |
possibly damaging |
Het |
Sidt2 |
T |
C |
9: 45,858,299 (GRCm39) |
Y80C |
probably benign |
Het |
Slit1 |
A |
T |
19: 41,590,119 (GRCm39) |
V1389E |
possibly damaging |
Het |
Spz1 |
G |
A |
13: 92,712,393 (GRCm39) |
P28S |
probably benign |
Het |
Sult1c2 |
T |
A |
17: 54,269,458 (GRCm39) |
M257L |
probably benign |
Het |
Tent2 |
C |
T |
13: 93,312,041 (GRCm39) |
V220I |
probably benign |
Het |
Tm2d3 |
T |
C |
7: 65,348,917 (GRCm39) |
|
probably null |
Het |
Uqcr10 |
T |
C |
11: 4,654,153 (GRCm39) |
|
probably null |
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 |
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 |
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 |
|
|