Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,851,478 (GRCm39) |
M819V |
probably benign |
Het |
Abca5 |
T |
A |
11: 110,168,248 (GRCm39) |
T1461S |
possibly damaging |
Het |
Actl6b |
C |
T |
5: 137,562,766 (GRCm39) |
R161C |
probably damaging |
Het |
Aoc3 |
C |
G |
11: 101,221,914 (GRCm39) |
P50R |
possibly damaging |
Het |
Atr |
G |
A |
9: 95,797,050 (GRCm39) |
A1698T |
probably benign |
Het |
Caml |
T |
A |
13: 55,779,670 (GRCm39) |
S248T |
possibly damaging |
Het |
Cdh11 |
C |
T |
8: 103,384,879 (GRCm39) |
G399S |
possibly damaging |
Het |
Chrna10 |
G |
T |
7: 101,761,416 (GRCm39) |
L392I |
probably benign |
Het |
Clip2 |
C |
T |
5: 134,533,616 (GRCm39) |
R487Q |
probably benign |
Het |
Copg1 |
A |
G |
6: 87,879,225 (GRCm39) |
I424V |
probably damaging |
Het |
Cwh43 |
A |
T |
5: 73,565,629 (GRCm39) |
N65Y |
possibly damaging |
Het |
Defb1 |
A |
G |
8: 22,284,486 (GRCm39) |
Y35C |
probably damaging |
Het |
Disp2 |
T |
C |
2: 118,620,627 (GRCm39) |
V453A |
probably benign |
Het |
Dpp9 |
A |
G |
17: 56,494,458 (GRCm39) |
Y834H |
probably damaging |
Het |
Emsy |
A |
G |
7: 98,262,285 (GRCm39) |
I598T |
possibly damaging |
Het |
Entpd2 |
C |
T |
2: 25,288,153 (GRCm39) |
R126C |
probably damaging |
Het |
Fbxl17 |
A |
T |
17: 63,806,426 (GRCm39) |
M196K |
probably benign |
Het |
Gcc1 |
T |
C |
6: 28,420,544 (GRCm39) |
R258G |
probably damaging |
Het |
Gga2 |
A |
T |
7: 121,606,494 (GRCm39) |
M157K |
possibly damaging |
Het |
Gna11 |
T |
C |
10: 81,370,918 (GRCm39) |
N106S |
probably benign |
Het |
Gtf3c1 |
A |
C |
7: 125,262,199 (GRCm39) |
S1116A |
possibly damaging |
Het |
Gucy2d |
C |
A |
7: 98,099,064 (GRCm39) |
D294E |
probably damaging |
Het |
Igkv12-46 |
G |
T |
6: 69,741,967 (GRCm39) |
P4T |
possibly damaging |
Het |
Iqcf5 |
A |
T |
9: 106,393,168 (GRCm39) |
I142L |
probably damaging |
Het |
Klhdc9 |
A |
G |
1: 171,187,357 (GRCm39) |
S214P |
probably damaging |
Het |
Kmt2e |
T |
C |
5: 23,683,617 (GRCm39) |
Y292H |
probably damaging |
Het |
Lgr6 |
A |
G |
1: 134,915,245 (GRCm39) |
L778P |
probably damaging |
Het |
Lrrk2 |
A |
G |
15: 91,618,228 (GRCm39) |
N909S |
probably benign |
Het |
Ly75 |
A |
G |
2: 60,154,184 (GRCm39) |
S1088P |
probably damaging |
Het |
Mei1 |
G |
A |
15: 81,966,098 (GRCm39) |
G240D |
|
Het |
Miox |
A |
T |
15: 89,218,703 (GRCm39) |
|
probably benign |
Het |
Myo1e |
A |
G |
9: 70,223,924 (GRCm39) |
Y128C |
probably damaging |
Het |
Necab2 |
T |
C |
8: 120,189,403 (GRCm39) |
V191A |
possibly damaging |
Het |
Nlrp9a |
T |
A |
7: 26,256,915 (GRCm39) |
Y178N |
probably damaging |
Het |
Nr4a3 |
A |
G |
4: 48,051,353 (GRCm39) |
T36A |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,105,402 (GRCm39) |
T1517A |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or4a27 |
T |
C |
2: 88,559,142 (GRCm39) |
K267R |
probably damaging |
Het |
Or4g17 |
T |
G |
2: 111,210,239 (GRCm39) |
I298R |
probably damaging |
Het |
Or4p23 |
T |
C |
2: 88,576,872 (GRCm39) |
Y120C |
probably damaging |
Het |
Or51h7 |
C |
T |
7: 102,591,259 (GRCm39) |
C175Y |
probably damaging |
Het |
Pcnx2 |
A |
T |
8: 126,487,592 (GRCm39) |
S1804T |
probably damaging |
Het |
Pdcd11 |
T |
A |
19: 47,082,191 (GRCm39) |
V35D |
possibly damaging |
Het |
Pde10a |
C |
A |
17: 9,170,370 (GRCm39) |
T347K |
probably damaging |
Het |
Rcc1l |
A |
G |
5: 134,182,977 (GRCm39) |
Y432H |
probably benign |
Het |
Rgs22 |
A |
T |
15: 36,040,856 (GRCm39) |
V1001E |
probably benign |
Het |
Ripor3 |
T |
A |
2: 167,831,646 (GRCm39) |
D385V |
probably damaging |
Het |
Rrbp1 |
T |
C |
2: 143,831,178 (GRCm39) |
K330E |
probably damaging |
Het |
Ryr3 |
T |
G |
2: 112,664,074 (GRCm39) |
D1759A |
probably benign |
Het |
Scube3 |
A |
G |
17: 28,371,414 (GRCm39) |
D43G |
probably benign |
Het |
Sec24b |
A |
G |
3: 129,790,422 (GRCm39) |
I701T |
probably damaging |
Het |
Setd5 |
G |
T |
6: 113,128,366 (GRCm39) |
V1440L |
probably benign |
Het |
Sik3 |
A |
G |
9: 46,106,142 (GRCm39) |
K337E |
possibly damaging |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc1a6 |
T |
A |
10: 78,648,698 (GRCm39) |
M473K |
probably benign |
Het |
Spag16 |
A |
G |
1: 69,962,842 (GRCm39) |
R330G |
probably benign |
Het |
Spag6 |
C |
A |
2: 18,704,047 (GRCm39) |
Q32K |
probably benign |
Het |
Sspo |
G |
A |
6: 48,432,707 (GRCm39) |
G861D |
probably damaging |
Het |
Togaram2 |
T |
A |
17: 72,024,365 (GRCm39) |
S850T |
probably damaging |
Het |
Trbv15 |
A |
T |
6: 41,118,550 (GRCm39) |
E102V |
possibly damaging |
Het |
Trim43b |
G |
T |
9: 88,973,395 (GRCm39) |
H113N |
probably benign |
Het |
Ttn |
T |
C |
2: 76,599,152 (GRCm39) |
I19286V |
probably benign |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Tubb6 |
A |
G |
18: 67,534,671 (GRCm39) |
H190R |
probably benign |
Het |
Vmn1r214 |
T |
C |
13: 23,219,007 (GRCm39) |
V167A |
probably benign |
Het |
Vwf |
C |
A |
6: 125,568,670 (GRCm39) |
L398I |
possibly damaging |
Het |
Zfp9 |
G |
T |
6: 118,443,851 (GRCm39) |
A58E |
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 |
R7240:Trpm2
|
UTSW |
10 |
77,771,710 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|