Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadm |
G |
A |
3: 153,644,273 (GRCm39) |
T70M |
probably benign |
Het |
Adamtsl3 |
G |
A |
7: 82,223,650 (GRCm39) |
A218T |
possibly damaging |
Het |
Ahnak2 |
T |
C |
12: 112,741,642 (GRCm39) |
D810G |
probably damaging |
Het |
Ak7 |
T |
A |
12: 105,707,341 (GRCm39) |
L315* |
probably null |
Het |
Apoa5 |
T |
C |
9: 46,181,887 (GRCm39) |
F321S |
possibly damaging |
Het |
Baiap2l1 |
G |
C |
5: 144,212,768 (GRCm39) |
P416A |
probably damaging |
Het |
Bco1 |
A |
G |
8: 117,835,432 (GRCm39) |
I128V |
possibly damaging |
Het |
Bpifb2 |
T |
C |
2: 153,717,905 (GRCm39) |
|
probably benign |
Het |
Cdt1 |
G |
A |
8: 123,294,832 (GRCm39) |
R13H |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,789,880 (GRCm39) |
V723A |
probably benign |
Het |
Chl1 |
T |
A |
6: 103,685,675 (GRCm39) |
W849R |
probably damaging |
Het |
Cpne9 |
A |
G |
6: 113,267,192 (GRCm39) |
D169G |
probably damaging |
Het |
Cyp2d22 |
A |
G |
15: 82,256,772 (GRCm39) |
V334A |
probably damaging |
Het |
Cyp4f39 |
C |
A |
17: 32,689,807 (GRCm39) |
N84K |
probably benign |
Het |
Cyp4f40 |
T |
A |
17: 32,888,796 (GRCm39) |
F192I |
probably damaging |
Het |
Disp3 |
T |
C |
4: 148,342,554 (GRCm39) |
D632G |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,352,416 (GRCm39) |
R2523Q |
probably damaging |
Het |
Echs1 |
G |
T |
7: 139,692,426 (GRCm39) |
T107K |
probably benign |
Het |
Ehmt2 |
C |
T |
17: 35,118,067 (GRCm39) |
R40* |
probably null |
Het |
Ergic1 |
G |
A |
17: 26,843,580 (GRCm39) |
V17I |
probably damaging |
Het |
Fank1 |
G |
T |
7: 133,478,569 (GRCm39) |
C210F |
probably damaging |
Het |
Fbxo15 |
T |
G |
18: 84,978,194 (GRCm39) |
M136R |
probably damaging |
Het |
Ggcx |
C |
A |
6: 72,401,017 (GRCm39) |
P240H |
probably damaging |
Het |
Gpr179 |
T |
C |
11: 97,227,608 (GRCm39) |
R1516G |
probably benign |
Het |
Gprin3 |
G |
A |
6: 59,330,931 (GRCm39) |
Q459* |
probably null |
Het |
Hadha |
C |
A |
5: 30,350,252 (GRCm39) |
V99F |
possibly damaging |
Het |
Hirip3 |
A |
G |
7: 126,463,034 (GRCm39) |
D330G |
possibly damaging |
Het |
Irx2 |
T |
C |
13: 72,779,714 (GRCm39) |
W333R |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,841,271 (GRCm39) |
T10A |
probably benign |
Het |
Kcnd2 |
T |
C |
6: 21,723,211 (GRCm39) |
I467T |
probably benign |
Het |
Klc3 |
A |
T |
7: 19,130,932 (GRCm39) |
I215N |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,504,337 (GRCm39) |
V3657A |
probably benign |
Het |
Lin28b |
A |
T |
10: 45,345,164 (GRCm39) |
L54* |
probably null |
Het |
Mgll |
T |
C |
6: 88,702,743 (GRCm39) |
V14A |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,234,408 (GRCm39) |
N976S |
probably benign |
Het |
Myh8 |
C |
A |
11: 67,196,788 (GRCm39) |
A1807E |
possibly damaging |
Het |
Nalcn |
G |
A |
14: 123,647,155 (GRCm39) |
P573S |
probably damaging |
Het |
Ncam2 |
C |
T |
16: 81,231,766 (GRCm39) |
R77* |
probably null |
Het |
Neb |
T |
C |
2: 52,168,827 (GRCm39) |
S1903G |
probably benign |
Het |
Nfe2 |
T |
A |
15: 103,157,556 (GRCm39) |
D145V |
probably damaging |
Het |
Or52a20 |
T |
A |
7: 103,366,687 (GRCm39) |
Y295* |
probably null |
Het |
Padi1 |
A |
T |
4: 140,542,164 (GRCm39) |
V586D |
probably damaging |
Het |
Pcdh12 |
T |
C |
18: 38,416,192 (GRCm39) |
D311G |
probably damaging |
Het |
Pcdha11 |
A |
T |
18: 37,145,439 (GRCm39) |
H510L |
probably damaging |
Het |
Plcb1 |
C |
A |
2: 135,102,486 (GRCm39) |
P221H |
probably benign |
Het |
Plekhg2 |
A |
T |
7: 28,069,856 (GRCm39) |
V58E |
probably damaging |
Het |
Pparg |
A |
C |
6: 115,467,032 (GRCm39) |
Q435P |
probably damaging |
Het |
Ppp1r36 |
A |
G |
12: 76,484,892 (GRCm39) |
T282A |
possibly damaging |
Het |
Prcd |
T |
C |
11: 116,559,110 (GRCm39) |
|
probably benign |
Het |
Pygo1 |
A |
T |
9: 72,852,266 (GRCm39) |
H151L |
possibly damaging |
Het |
Rnmt |
A |
G |
18: 68,446,773 (GRCm39) |
Y266C |
probably benign |
Het |
Rxrb |
T |
C |
17: 34,255,411 (GRCm39) |
V246A |
probably damaging |
Het |
Sart1 |
A |
G |
19: 5,433,704 (GRCm39) |
S378P |
probably damaging |
Het |
Sema4d |
T |
C |
13: 51,865,390 (GRCm39) |
N318S |
possibly damaging |
Het |
Sis |
C |
T |
3: 72,798,754 (GRCm39) |
V1765I |
probably benign |
Het |
Slc17a6 |
A |
T |
7: 51,276,598 (GRCm39) |
K116* |
probably null |
Het |
Smc6 |
T |
A |
12: 11,341,540 (GRCm39) |
H519Q |
probably benign |
Het |
Sowahc |
T |
A |
10: 59,058,785 (GRCm39) |
M307K |
probably benign |
Het |
Sptbn1 |
A |
G |
11: 30,087,560 (GRCm39) |
Y960H |
probably damaging |
Het |
Tmem270 |
A |
C |
5: 134,931,636 (GRCm39) |
V102G |
probably benign |
Het |
Tmprss11d |
A |
G |
5: 86,486,729 (GRCm39) |
F54L |
probably benign |
Het |
Top1 |
T |
A |
2: 160,544,695 (GRCm39) |
Y270* |
probably null |
Het |
Ttf2 |
A |
G |
3: 100,866,558 (GRCm39) |
S525P |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,777,241 (GRCm39) |
M1387K |
possibly damaging |
Het |
Upk3bl |
A |
T |
5: 136,088,954 (GRCm39) |
R156W |
probably damaging |
Het |
Usp34 |
G |
T |
11: 23,299,198 (GRCm39) |
R290L |
probably benign |
Het |
Vwf |
T |
C |
6: 125,620,005 (GRCm39) |
V1561A |
|
Het |
Zan |
A |
G |
5: 137,420,155 (GRCm39) |
I2834T |
unknown |
Het |
Zfp105 |
A |
G |
9: 122,755,454 (GRCm39) |
Y90C |
probably benign |
Het |
Zfp804a |
T |
C |
2: 82,089,339 (GRCm39) |
V1056A |
probably damaging |
Het |
Zfp956 |
A |
T |
6: 47,930,455 (GRCm39) |
|
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 |
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 |
|