Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox5 |
A |
T |
6: 116,404,098 (GRCm39) |
|
probably null |
Het |
Aoc1l1 |
A |
T |
6: 48,952,305 (GRCm39) |
I77F |
probably damaging |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
Cep135 |
T |
C |
5: 76,769,210 (GRCm39) |
|
probably null |
Het |
Cfap206 |
T |
A |
4: 34,716,310 (GRCm39) |
H385L |
possibly damaging |
Het |
Dach2 |
T |
C |
X: 112,729,664 (GRCm39) |
I417T |
possibly damaging |
Het |
Dcaf8l |
A |
T |
X: 88,448,327 (GRCm39) |
Y601N |
probably benign |
Het |
Dhx32 |
T |
C |
7: 133,327,085 (GRCm39) |
Y332C |
probably damaging |
Het |
Dlx1 |
T |
A |
2: 71,362,740 (GRCm39) |
W216R |
probably damaging |
Het |
Dna2 |
G |
A |
10: 62,784,981 (GRCm39) |
A33T |
possibly damaging |
Het |
Dyrk1a |
G |
A |
16: 94,469,660 (GRCm39) |
|
probably benign |
Het |
Fam227b |
T |
C |
2: 125,966,006 (GRCm39) |
T140A |
probably benign |
Het |
Fem1b |
T |
C |
9: 62,703,836 (GRCm39) |
I475V |
probably benign |
Het |
Fign |
T |
A |
2: 63,809,044 (GRCm39) |
Q742L |
possibly damaging |
Het |
Hip1r |
A |
G |
5: 124,138,204 (GRCm39) |
D766G |
probably benign |
Het |
Hsd17b12 |
C |
T |
2: 93,864,303 (GRCm39) |
R268Q |
probably benign |
Het |
Htt |
T |
C |
5: 34,961,875 (GRCm39) |
S287P |
probably benign |
Het |
Icam5 |
A |
G |
9: 20,947,954 (GRCm39) |
I617M |
probably benign |
Het |
Ifi27l2b |
T |
C |
12: 103,417,594 (GRCm39) |
T198A |
unknown |
Het |
Ip6k3 |
T |
C |
17: 27,376,516 (GRCm39) |
Y65C |
probably damaging |
Het |
Kif15 |
A |
C |
9: 122,817,026 (GRCm39) |
Q542P |
probably damaging |
Het |
Kit |
C |
T |
5: 75,808,488 (GRCm39) |
A744V |
probably null |
Het |
Kit |
G |
T |
5: 75,808,487 (GRCm39) |
A744S |
probably benign |
Het |
Lonp1 |
A |
G |
17: 56,933,488 (GRCm39) |
I129T |
possibly damaging |
Het |
Ltbp4 |
C |
T |
7: 27,027,203 (GRCm39) |
R389Q |
possibly damaging |
Het |
Map3k21 |
A |
T |
8: 126,668,593 (GRCm39) |
K726N |
probably benign |
Het |
Mcpt8 |
A |
T |
14: 56,321,398 (GRCm39) |
I22K |
probably damaging |
Het |
Npb |
G |
A |
11: 120,499,728 (GRCm39) |
V103I |
possibly damaging |
Het |
Or13a22 |
T |
C |
7: 140,072,764 (GRCm39) |
M71T |
probably benign |
Het |
Or2y3 |
G |
A |
17: 38,392,903 (GRCm39) |
|
probably null |
Het |
Plin2 |
G |
T |
4: 86,575,381 (GRCm39) |
Y389* |
probably null |
Het |
Pnpla6 |
G |
T |
8: 3,584,670 (GRCm39) |
G763C |
probably null |
Het |
Pnpla7 |
A |
G |
2: 24,932,150 (GRCm39) |
D935G |
probably damaging |
Het |
Prr29 |
A |
G |
11: 106,265,711 (GRCm39) |
S10G |
probably benign |
Het |
Pthlh |
A |
T |
6: 147,164,789 (GRCm39) |
V27E |
probably damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Serpina12 |
G |
A |
12: 104,004,242 (GRCm39) |
T130I |
probably benign |
Het |
Slc6a18 |
A |
G |
13: 73,825,921 (GRCm39) |
F43S |
probably damaging |
Het |
Stx6 |
C |
T |
1: 155,034,654 (GRCm39) |
P6S |
probably damaging |
Het |
Togaram1 |
G |
T |
12: 65,013,118 (GRCm39) |
R123L |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Trim9 |
C |
T |
12: 70,295,167 (GRCm39) |
G648R |
probably damaging |
Het |
Trpm6 |
C |
G |
19: 18,831,795 (GRCm39) |
H1553Q |
probably benign |
Het |
Vav3 |
G |
A |
3: 109,535,484 (GRCm39) |
|
probably null |
Het |
Zfp574 |
G |
T |
7: 24,781,026 (GRCm39) |
A683S |
possibly damaging |
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 |
|
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 |
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 |
|