Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210017I01Rik |
A |
G |
3: 92,512,382 (GRCm39) |
I59T |
unknown |
Het |
Aspm |
C |
T |
1: 139,406,389 (GRCm39) |
Q1759* |
probably null |
Het |
Atn1 |
A |
T |
6: 124,724,861 (GRCm39) |
I124K |
unknown |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Ccdc88c |
C |
T |
12: 100,911,198 (GRCm39) |
V879M |
probably benign |
Het |
Cd300c |
A |
G |
11: 114,850,609 (GRCm39) |
C65R |
possibly damaging |
Het |
Cd69 |
A |
T |
6: 129,247,005 (GRCm39) |
S112T |
possibly damaging |
Het |
Cdh19 |
T |
C |
1: 110,821,137 (GRCm39) |
T534A |
probably benign |
Het |
Cdk5rap2 |
T |
A |
4: 70,210,145 (GRCm39) |
D701V |
probably damaging |
Het |
D130052B06Rik |
A |
G |
11: 33,573,874 (GRCm39) |
H157R |
possibly damaging |
Het |
Dpf1 |
T |
A |
7: 29,011,052 (GRCm39) |
F150L |
probably benign |
Het |
Dsg1c |
T |
C |
18: 20,416,166 (GRCm39) |
L689P |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,381,861 (GRCm39) |
M538I |
probably benign |
Het |
E4f1 |
T |
A |
17: 24,663,299 (GRCm39) |
I669F |
probably damaging |
Het |
Gm7138 |
T |
C |
10: 77,612,589 (GRCm39) |
T64A |
unknown |
Het |
Gnai2 |
A |
C |
9: 107,492,972 (GRCm39) |
D310E |
|
Het |
Iqca1 |
A |
G |
1: 89,998,272 (GRCm39) |
V567A |
possibly damaging |
Het |
Iqgap1 |
A |
T |
7: 80,409,587 (GRCm39) |
N249K |
probably benign |
Het |
Lamc1 |
A |
G |
1: 153,110,396 (GRCm39) |
V1093A |
possibly damaging |
Het |
Mfap3 |
A |
G |
11: 57,420,582 (GRCm39) |
K188E |
probably damaging |
Het |
N4bp2 |
T |
A |
5: 65,951,888 (GRCm39) |
V431D |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,795,445 (GRCm39) |
T792A |
probably benign |
Het |
Ntn4 |
A |
G |
10: 93,581,603 (GRCm39) |
H592R |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,362,317 (GRCm39) |
C202R |
probably benign |
Het |
Or10j2 |
T |
C |
1: 173,098,561 (GRCm39) |
I273T |
probably benign |
Het |
Or2a7 |
A |
G |
6: 43,151,435 (GRCm39) |
K172E |
probably benign |
Het |
Or5p55 |
T |
C |
7: 107,567,395 (GRCm39) |
S264P |
probably benign |
Het |
Or5p72 |
A |
G |
7: 108,022,140 (GRCm39) |
M121V |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,009 (GRCm39) |
D70G |
probably benign |
Het |
Or8g24 |
A |
T |
9: 38,989,906 (GRCm39) |
M45K |
probably damaging |
Het |
Parpbp |
G |
A |
10: 87,960,802 (GRCm39) |
T228I |
probably damaging |
Het |
Pcdhgb8 |
G |
A |
18: 37,896,756 (GRCm39) |
V609M |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,100,830 (GRCm39) |
N543S |
probably damaging |
Het |
Puf60 |
A |
G |
15: 75,944,388 (GRCm39) |
|
probably benign |
Het |
Rbm6 |
A |
T |
9: 107,730,095 (GRCm39) |
D184E |
probably damaging |
Het |
Rnase9 |
A |
C |
14: 51,276,436 (GRCm39) |
S181A |
probably benign |
Het |
Rnpc3 |
T |
A |
3: 113,410,480 (GRCm39) |
R270S |
probably damaging |
Het |
Rundc1 |
T |
C |
11: 101,322,374 (GRCm39) |
|
probably null |
Het |
Ryr1 |
T |
C |
7: 28,751,440 (GRCm39) |
S3715G |
possibly damaging |
Het |
Scn3a |
A |
T |
2: 65,299,386 (GRCm39) |
D1373E |
possibly damaging |
Het |
Serpina3k |
T |
G |
12: 104,306,861 (GRCm39) |
I31S |
probably benign |
Het |
Sipa1l2 |
A |
G |
8: 126,196,599 (GRCm39) |
F712L |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,138,875 (GRCm39) |
V529A |
probably damaging |
Het |
Tdrd3 |
A |
G |
14: 87,696,239 (GRCm39) |
N58S |
probably benign |
Het |
Tmc2 |
C |
T |
2: 130,076,724 (GRCm39) |
T350I |
possibly damaging |
Het |
Tpst2 |
T |
C |
5: 112,455,544 (GRCm39) |
C28R |
probably benign |
Het |
Trbv21 |
A |
T |
6: 41,179,892 (GRCm39) |
K69N |
probably benign |
Het |
Ttn |
A |
G |
2: 76,679,334 (GRCm39) |
V10796A |
unknown |
Het |
Ush2a |
A |
G |
1: 188,643,858 (GRCm39) |
T4407A |
possibly damaging |
Het |
Vmn2r95 |
A |
G |
17: 18,672,225 (GRCm39) |
H726R |
probably benign |
Het |
Zfp777 |
A |
G |
6: 48,021,383 (GRCm39) |
S80P |
probably benign |
Het |
|
Other mutations in Trpm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00730:Trpm2
|
APN |
10 |
77,778,749 (GRCm39) |
splice site |
probably null |
|
IGL00773:Trpm2
|
APN |
10 |
77,785,048 (GRCm39) |
nonsense |
probably null |
|
IGL00962:Trpm2
|
APN |
10 |
77,779,750 (GRCm39) |
splice site |
probably benign |
|
IGL01093:Trpm2
|
APN |
10 |
77,768,114 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01124:Trpm2
|
APN |
10 |
77,781,659 (GRCm39) |
splice site |
probably benign |
|
IGL01301:Trpm2
|
APN |
10 |
77,759,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02094:Trpm2
|
APN |
10 |
77,778,830 (GRCm39) |
nonsense |
probably null |
|
IGL02175:Trpm2
|
APN |
10 |
77,773,741 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02653:Trpm2
|
APN |
10 |
77,748,503 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02667:Trpm2
|
APN |
10 |
77,771,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02668:Trpm2
|
APN |
10 |
77,771,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Trpm2
|
APN |
10 |
77,754,820 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02951:Trpm2
|
APN |
10 |
77,765,112 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03188:Trpm2
|
APN |
10 |
77,754,743 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03242:Trpm2
|
APN |
10 |
77,753,568 (GRCm39) |
missense |
probably benign |
|
IGL03405:Trpm2
|
APN |
10 |
77,801,906 (GRCm39) |
splice site |
probably benign |
|
Fugit
|
UTSW |
10 |
77,774,202 (GRCm39) |
missense |
probably damaging |
1.00 |
scusate
|
UTSW |
10 |
77,802,828 (GRCm39) |
nonsense |
probably null |
|
temporal
|
UTSW |
10 |
77,761,516 (GRCm39) |
missense |
probably benign |
0.30 |
ANU18:Trpm2
|
UTSW |
10 |
77,759,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R0147:Trpm2
|
UTSW |
10 |
77,761,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Trpm2
|
UTSW |
10 |
77,761,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Trpm2
|
UTSW |
10 |
77,779,824 (GRCm39) |
splice site |
probably benign |
|
R0332:Trpm2
|
UTSW |
10 |
77,783,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Trpm2
|
UTSW |
10 |
77,759,350 (GRCm39) |
missense |
probably damaging |
0.99 |
R0847:Trpm2
|
UTSW |
10 |
77,765,122 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1183:Trpm2
|
UTSW |
10 |
77,759,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Trpm2
|
UTSW |
10 |
77,801,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R1510:Trpm2
|
UTSW |
10 |
77,802,828 (GRCm39) |
nonsense |
probably null |
|
R1518:Trpm2
|
UTSW |
10 |
77,778,839 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1564:Trpm2
|
UTSW |
10 |
77,778,833 (GRCm39) |
missense |
probably benign |
0.14 |
R1593:Trpm2
|
UTSW |
10 |
77,778,910 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1617:Trpm2
|
UTSW |
10 |
77,771,709 (GRCm39) |
splice site |
probably null |
|
R1673:Trpm2
|
UTSW |
10 |
77,778,778 (GRCm39) |
missense |
probably benign |
|
R1912:Trpm2
|
UTSW |
10 |
77,781,710 (GRCm39) |
missense |
probably benign |
0.10 |
R1932:Trpm2
|
UTSW |
10 |
77,776,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Trpm2
|
UTSW |
10 |
77,783,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Trpm2
|
UTSW |
10 |
77,761,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Trpm2
|
UTSW |
10 |
77,768,013 (GRCm39) |
missense |
probably benign |
0.01 |
R2201:Trpm2
|
UTSW |
10 |
77,756,305 (GRCm39) |
nonsense |
probably null |
|
R2217:Trpm2
|
UTSW |
10 |
77,777,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R2312:Trpm2
|
UTSW |
10 |
77,754,798 (GRCm39) |
missense |
probably benign |
0.04 |
R2339:Trpm2
|
UTSW |
10 |
77,750,640 (GRCm39) |
splice site |
probably benign |
|
R2395:Trpm2
|
UTSW |
10 |
77,783,714 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2396:Trpm2
|
UTSW |
10 |
77,766,471 (GRCm39) |
missense |
probably benign |
0.14 |
R2405:Trpm2
|
UTSW |
10 |
77,770,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Trpm2
|
UTSW |
10 |
77,777,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R3001:Trpm2
|
UTSW |
10 |
77,766,368 (GRCm39) |
critical splice donor site |
probably null |
|
R3002:Trpm2
|
UTSW |
10 |
77,766,368 (GRCm39) |
critical splice donor site |
probably null |
|
R3125:Trpm2
|
UTSW |
10 |
77,747,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Trpm2
|
UTSW |
10 |
77,768,136 (GRCm39) |
missense |
probably benign |
0.03 |
R3777:Trpm2
|
UTSW |
10 |
77,771,824 (GRCm39) |
missense |
probably benign |
0.13 |
R3778:Trpm2
|
UTSW |
10 |
77,771,824 (GRCm39) |
missense |
probably benign |
0.13 |
R4272:Trpm2
|
UTSW |
10 |
77,769,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4384:Trpm2
|
UTSW |
10 |
77,753,559 (GRCm39) |
missense |
probably benign |
0.44 |
R4395:Trpm2
|
UTSW |
10 |
77,765,053 (GRCm39) |
missense |
probably benign |
0.01 |
R4423:Trpm2
|
UTSW |
10 |
77,770,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4452:Trpm2
|
UTSW |
10 |
77,759,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Trpm2
|
UTSW |
10 |
77,781,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R4662:Trpm2
|
UTSW |
10 |
77,773,972 (GRCm39) |
missense |
probably benign |
0.05 |
R4825:Trpm2
|
UTSW |
10 |
77,777,007 (GRCm39) |
missense |
probably damaging |
0.98 |
R4906:Trpm2
|
UTSW |
10 |
77,768,023 (GRCm39) |
nonsense |
probably null |
|
R4943:Trpm2
|
UTSW |
10 |
77,801,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Trpm2
|
UTSW |
10 |
77,753,626 (GRCm39) |
missense |
probably benign |
0.34 |
R5046:Trpm2
|
UTSW |
10 |
77,801,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Trpm2
|
UTSW |
10 |
77,759,355 (GRCm39) |
missense |
probably benign |
0.06 |
R5523:Trpm2
|
UTSW |
10 |
77,771,795 (GRCm39) |
missense |
probably benign |
0.04 |
R5562:Trpm2
|
UTSW |
10 |
77,795,773 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5623:Trpm2
|
UTSW |
10 |
77,767,973 (GRCm39) |
missense |
probably damaging |
0.96 |
R5628:Trpm2
|
UTSW |
10 |
77,748,470 (GRCm39) |
missense |
probably benign |
0.00 |
R5633:Trpm2
|
UTSW |
10 |
77,774,187 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5817:Trpm2
|
UTSW |
10 |
77,801,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5989:Trpm2
|
UTSW |
10 |
77,795,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6018:Trpm2
|
UTSW |
10 |
77,753,547 (GRCm39) |
missense |
probably benign |
0.00 |
R6075:Trpm2
|
UTSW |
10 |
77,770,877 (GRCm39) |
critical splice donor site |
probably null |
|
R6092:Trpm2
|
UTSW |
10 |
77,761,516 (GRCm39) |
missense |
probably benign |
0.30 |
R6309:Trpm2
|
UTSW |
10 |
77,774,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:Trpm2
|
UTSW |
10 |
77,768,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6568:Trpm2
|
UTSW |
10 |
77,773,660 (GRCm39) |
missense |
probably benign |
0.01 |
R6579:Trpm2
|
UTSW |
10 |
77,773,660 (GRCm39) |
missense |
probably benign |
0.01 |
R6640:Trpm2
|
UTSW |
10 |
77,773,660 (GRCm39) |
missense |
probably benign |
0.01 |
R6642:Trpm2
|
UTSW |
10 |
77,773,660 (GRCm39) |
missense |
probably benign |
0.01 |
R6798:Trpm2
|
UTSW |
10 |
77,750,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R6999:Trpm2
|
UTSW |
10 |
77,771,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Trpm2
|
UTSW |
10 |
77,748,426 (GRCm39) |
missense |
probably benign |
|
R7036:Trpm2
|
UTSW |
10 |
77,748,426 (GRCm39) |
missense |
probably benign |
|
R7113:Trpm2
|
UTSW |
10 |
77,783,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R7171:Trpm2
|
UTSW |
10 |
77,759,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Trpm2
|
UTSW |
10 |
77,759,389 (GRCm39) |
missense |
probably benign |
0.00 |
R7379:Trpm2
|
UTSW |
10 |
77,750,568 (GRCm39) |
missense |
probably benign |
|
R7527:Trpm2
|
UTSW |
10 |
77,801,894 (GRCm39) |
missense |
probably benign |
0.01 |
R7571:Trpm2
|
UTSW |
10 |
77,773,784 (GRCm39) |
missense |
probably benign |
0.21 |
R7600:Trpm2
|
UTSW |
10 |
77,773,885 (GRCm39) |
missense |
probably benign |
0.02 |
R7727:Trpm2
|
UTSW |
10 |
77,761,623 (GRCm39) |
missense |
probably benign |
0.34 |
R7771:Trpm2
|
UTSW |
10 |
77,768,013 (GRCm39) |
missense |
probably benign |
0.01 |
R7844:Trpm2
|
UTSW |
10 |
77,759,340 (GRCm39) |
missense |
probably benign |
0.00 |
R8158:Trpm2
|
UTSW |
10 |
77,783,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R8225:Trpm2
|
UTSW |
10 |
77,783,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R8226:Trpm2
|
UTSW |
10 |
77,783,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R8239:Trpm2
|
UTSW |
10 |
77,771,836 (GRCm39) |
missense |
probably benign |
0.06 |
R8275:Trpm2
|
UTSW |
10 |
77,801,859 (GRCm39) |
nonsense |
probably null |
|
R8340:Trpm2
|
UTSW |
10 |
77,759,458 (GRCm39) |
nonsense |
probably null |
|
R8354:Trpm2
|
UTSW |
10 |
77,769,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Trpm2
|
UTSW |
10 |
77,747,236 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8445:Trpm2
|
UTSW |
10 |
77,746,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Trpm2
|
UTSW |
10 |
77,768,128 (GRCm39) |
missense |
probably benign |
0.00 |
R9144:Trpm2
|
UTSW |
10 |
77,765,122 (GRCm39) |
missense |
probably benign |
0.01 |
R9286:Trpm2
|
UTSW |
10 |
77,777,014 (GRCm39) |
missense |
probably benign |
0.06 |
R9319:Trpm2
|
UTSW |
10 |
77,785,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Trpm2
|
UTSW |
10 |
77,778,776 (GRCm39) |
nonsense |
probably null |
|
R9381:Trpm2
|
UTSW |
10 |
77,747,191 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9457:Trpm2
|
UTSW |
10 |
77,747,226 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9477:Trpm2
|
UTSW |
10 |
77,747,224 (GRCm39) |
missense |
probably benign |
0.12 |
R9547:Trpm2
|
UTSW |
10 |
77,748,467 (GRCm39) |
missense |
probably benign |
0.33 |
R9660:Trpm2
|
UTSW |
10 |
77,766,389 (GRCm39) |
missense |
probably benign |
0.00 |
R9663:Trpm2
|
UTSW |
10 |
77,756,320 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Trpm2
|
UTSW |
10 |
77,773,702 (GRCm39) |
missense |
possibly damaging |
0.94 |
|