Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
G |
A |
9: 50,651,973 (GRCm39) |
T85M |
probably damaging |
Het |
Actn1 |
A |
G |
12: 80,219,731 (GRCm39) |
|
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,870,570 (GRCm39) |
S603T |
probably damaging |
Het |
Ahcy |
T |
C |
2: 154,910,851 (GRCm39) |
Y39C |
probably benign |
Het |
Ankmy2 |
T |
C |
12: 36,236,941 (GRCm39) |
|
probably null |
Het |
Anxa13 |
A |
T |
15: 58,220,655 (GRCm39) |
|
noncoding transcript |
Het |
Aoc1 |
T |
C |
6: 48,882,720 (GRCm39) |
S221P |
possibly damaging |
Het |
Arhgef10 |
C |
A |
8: 15,041,211 (GRCm39) |
A770D |
possibly damaging |
Het |
Arhgef19 |
A |
G |
4: 140,982,065 (GRCm39) |
D707G |
probably benign |
Het |
Arhgef3 |
G |
A |
14: 27,123,692 (GRCm39) |
R444H |
probably damaging |
Het |
Asphd1 |
T |
C |
7: 126,548,271 (GRCm39) |
I11V |
probably benign |
Het |
Atp2b1 |
A |
G |
10: 98,830,537 (GRCm39) |
M333V |
probably benign |
Het |
BC051665 |
T |
C |
13: 60,932,841 (GRCm39) |
Y40C |
probably damaging |
Het |
Ccdc87 |
T |
A |
19: 4,890,341 (GRCm39) |
S278T |
probably benign |
Het |
Ccn3 |
T |
A |
15: 54,612,648 (GRCm39) |
M219K |
possibly damaging |
Het |
Cdcp3 |
T |
A |
7: 130,846,560 (GRCm39) |
Y777* |
probably null |
Het |
Chaf1b |
G |
A |
16: 93,698,118 (GRCm39) |
G463D |
possibly damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,100 (GRCm39) |
T219A |
possibly damaging |
Het |
Clcnkb |
T |
G |
4: 141,134,406 (GRCm39) |
T584P |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,755,866 (GRCm39) |
S161P |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,777 (GRCm39) |
E1437G |
possibly damaging |
Het |
Col13a1 |
A |
T |
10: 61,702,205 (GRCm39) |
|
probably null |
Het |
Col3a1 |
T |
C |
1: 45,385,128 (GRCm39) |
S82P |
possibly damaging |
Het |
Cpeb3 |
A |
T |
19: 37,116,482 (GRCm39) |
M383K |
probably benign |
Het |
Cr2 |
T |
A |
1: 194,845,622 (GRCm39) |
H111L |
probably damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,375,974 (GRCm39) |
S1522G |
possibly damaging |
Het |
Cul3 |
T |
C |
1: 80,260,506 (GRCm39) |
D281G |
possibly damaging |
Het |
Cyp2c70 |
T |
G |
19: 40,172,426 (GRCm39) |
K72T |
probably benign |
Het |
Cyp39a1 |
A |
T |
17: 43,991,020 (GRCm39) |
I110F |
probably damaging |
Het |
Cyp46a1 |
T |
A |
12: 108,318,198 (GRCm39) |
M203K |
probably null |
Het |
Cyp8b1 |
A |
T |
9: 121,744,024 (GRCm39) |
V436D |
possibly damaging |
Het |
Ddx17 |
T |
C |
15: 79,422,766 (GRCm39) |
D324G |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,567,041 (GRCm39) |
N1274S |
probably damaging |
Het |
Dscaml1 |
G |
A |
9: 45,632,631 (GRCm39) |
V1166I |
probably benign |
Het |
Dsp |
T |
C |
13: 38,379,714 (GRCm39) |
V1554A |
probably damaging |
Het |
Efr3a |
T |
A |
15: 65,726,641 (GRCm39) |
|
probably null |
Het |
Egfem1 |
A |
T |
3: 29,702,420 (GRCm39) |
N223I |
probably benign |
Het |
Egr2 |
T |
C |
10: 67,375,805 (GRCm39) |
S147P |
probably damaging |
Het |
Elmo3 |
A |
G |
8: 106,034,933 (GRCm39) |
T408A |
probably benign |
Het |
Flnb |
A |
G |
14: 7,883,908 (GRCm38) |
D378G |
probably damaging |
Het |
Foxj2 |
T |
A |
6: 122,810,220 (GRCm39) |
M193K |
probably benign |
Het |
Gm6327 |
A |
G |
16: 12,578,020 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,130,335 (GRCm39) |
H21R |
probably benign |
Het |
Gpr107 |
A |
G |
2: 31,057,037 (GRCm39) |
D43G |
probably damaging |
Het |
Grin2c |
G |
A |
11: 115,146,900 (GRCm39) |
P432S |
possibly damaging |
Het |
H2-M10.1 |
A |
G |
17: 36,636,625 (GRCm39) |
F60L |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,439,941 (GRCm39) |
D1147G |
possibly damaging |
Het |
Idua |
G |
T |
5: 108,828,455 (GRCm39) |
A223S |
probably benign |
Het |
Ifi206 |
T |
C |
1: 173,314,419 (GRCm39) |
Q7R |
probably benign |
Het |
Itgad |
T |
A |
7: 127,802,406 (GRCm39) |
V986E |
probably damaging |
Het |
Itsn2 |
G |
A |
12: 4,700,044 (GRCm39) |
R670H |
probably benign |
Het |
Kdm4a |
T |
C |
4: 117,996,146 (GRCm39) |
E961G |
possibly damaging |
Het |
Klra5 |
T |
A |
6: 129,883,585 (GRCm39) |
I91L |
probably damaging |
Het |
Kntc1 |
A |
G |
5: 123,910,176 (GRCm39) |
T525A |
probably damaging |
Het |
Lct |
A |
G |
1: 128,221,932 (GRCm39) |
F1536L |
probably benign |
Het |
Lmod1 |
T |
A |
1: 135,291,671 (GRCm39) |
D175E |
probably benign |
Het |
Lonrf1 |
A |
C |
8: 36,701,126 (GRCm39) |
D361E |
probably benign |
Het |
Lrrc19 |
T |
C |
4: 94,526,666 (GRCm39) |
Y297C |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,873,431 (GRCm39) |
E1787G |
possibly damaging |
Het |
Mpp2 |
G |
A |
11: 101,951,374 (GRCm39) |
A452V |
probably benign |
Het |
Msh2 |
T |
C |
17: 88,026,080 (GRCm39) |
V686A |
possibly damaging |
Het |
Mthfd1 |
C |
T |
12: 76,317,193 (GRCm39) |
Q15* |
probably null |
Het |
Mtnr1b |
A |
T |
9: 15,774,438 (GRCm39) |
I207N |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,855,480 (GRCm39) |
T1207A |
probably benign |
Het |
Nin |
A |
T |
12: 70,085,524 (GRCm39) |
V1569D |
probably damaging |
Het |
Nrcam |
T |
A |
12: 44,584,147 (GRCm39) |
|
probably benign |
Het |
Nsd1 |
T |
A |
13: 55,394,782 (GRCm39) |
H897Q |
probably damaging |
Het |
Or10g9 |
A |
G |
9: 39,912,490 (GRCm39) |
F11S |
probably benign |
Het |
Or12d2 |
A |
T |
17: 37,624,371 (GRCm39) |
N301K |
probably benign |
Het |
Or2w2 |
T |
A |
13: 21,758,480 (GRCm39) |
I49F |
possibly damaging |
Het |
Or7d10 |
G |
T |
9: 19,832,208 (GRCm39) |
K234N |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,588,320 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
G |
A |
19: 5,735,375 (GRCm39) |
R484* |
probably null |
Het |
Pdxk |
A |
G |
10: 78,283,814 (GRCm39) |
Y127H |
probably damaging |
Het |
Phf20 |
T |
A |
2: 156,129,754 (GRCm39) |
V442E |
probably benign |
Het |
Phlpp1 |
G |
A |
1: 106,320,519 (GRCm39) |
D1505N |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,417,664 (GRCm39) |
T2496A |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,406,869 (GRCm39) |
T2369A |
probably benign |
Het |
Plod2 |
T |
A |
9: 92,485,120 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
A |
2: 24,905,263 (GRCm39) |
M617K |
possibly damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prkch |
T |
A |
12: 73,696,131 (GRCm39) |
|
probably null |
Het |
Prr12 |
G |
A |
7: 44,678,224 (GRCm39) |
H1974Y |
unknown |
Het |
Prr16 |
A |
G |
18: 51,436,042 (GRCm39) |
I174V |
probably benign |
Het |
Prss45 |
A |
T |
9: 110,667,497 (GRCm39) |
T39S |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,445,515 (GRCm39) |
D161E |
probably damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,113 (GRCm39) |
D345G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,288,119 (GRCm39) |
|
probably benign |
Het |
Rasgrp3 |
A |
G |
17: 75,807,729 (GRCm39) |
H262R |
possibly damaging |
Het |
Rnf213 |
T |
A |
11: 119,327,437 (GRCm39) |
I1809N |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,761,616 (GRCm39) |
L3177P |
probably damaging |
Het |
Scyl2 |
C |
A |
10: 89,486,818 (GRCm39) |
R230L |
probably damaging |
Het |
Sfxn2 |
T |
C |
19: 46,570,915 (GRCm39) |
|
probably benign |
Het |
Slc18b1 |
T |
C |
10: 23,674,639 (GRCm39) |
|
probably benign |
Het |
Spata31d1d |
T |
C |
13: 59,876,005 (GRCm39) |
H510R |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,872,780 (GRCm39) |
N1109K |
probably damaging |
Het |
Styxl2 |
C |
T |
1: 165,927,024 (GRCm39) |
V863M |
possibly damaging |
Het |
Sult3a2 |
A |
G |
10: 33,657,973 (GRCm39) |
S47P |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,682,028 (GRCm39) |
N2518S |
possibly damaging |
Het |
Tex21 |
G |
T |
12: 76,253,665 (GRCm39) |
P416Q |
probably benign |
Het |
Tex38 |
T |
C |
4: 115,637,503 (GRCm39) |
N100S |
probably benign |
Het |
Thsd4 |
A |
C |
9: 60,301,836 (GRCm39) |
|
probably benign |
Het |
Ticrr |
T |
C |
7: 79,331,572 (GRCm39) |
V723A |
probably damaging |
Het |
Tmprss15 |
A |
G |
16: 78,887,717 (GRCm39) |
V30A |
probably benign |
Het |
Uba3 |
A |
G |
6: 97,162,298 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,765,800 (GRCm39) |
|
probably benign |
Het |
Uchl4 |
A |
T |
9: 64,143,013 (GRCm39) |
I165L |
probably benign |
Het |
Vmn2r112 |
A |
T |
17: 22,822,125 (GRCm39) |
T268S |
possibly damaging |
Het |
Wfdc3 |
T |
C |
2: 164,586,114 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
T |
A |
6: 47,869,801 (GRCm39) |
L282Q |
probably damaging |
Het |
Zfp422 |
A |
T |
6: 116,603,745 (GRCm39) |
C85S |
probably damaging |
Het |
Zfp790 |
A |
T |
7: 29,527,564 (GRCm39) |
Q83L |
probably benign |
Het |
|
Other mutations in Grid2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Grid2
|
APN |
6 |
64,322,573 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00596:Grid2
|
APN |
6 |
64,510,688 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01686:Grid2
|
APN |
6 |
64,297,180 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01712:Grid2
|
APN |
6 |
64,642,899 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02064:Grid2
|
APN |
6 |
64,040,919 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02216:Grid2
|
APN |
6 |
64,322,650 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02563:Grid2
|
APN |
6 |
64,322,857 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02685:Grid2
|
APN |
6 |
64,322,800 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03129:Grid2
|
APN |
6 |
64,040,888 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03324:Grid2
|
APN |
6 |
64,406,806 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03395:Grid2
|
APN |
6 |
63,886,053 (GRCm39) |
missense |
possibly damaging |
0.94 |
crawler
|
UTSW |
6 |
64,406,678 (GRCm39) |
nonsense |
probably null |
|
swagger
|
UTSW |
6 |
64,372,263 (GRCm39) |
synonymous |
probably benign |
|
R0133:Grid2
|
UTSW |
6 |
64,297,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0147:Grid2
|
UTSW |
6 |
64,510,571 (GRCm39) |
missense |
probably benign |
|
R0193:Grid2
|
UTSW |
6 |
64,040,937 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0370:Grid2
|
UTSW |
6 |
64,322,718 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0399:Grid2
|
UTSW |
6 |
64,643,036 (GRCm39) |
missense |
probably benign |
0.33 |
R0600:Grid2
|
UTSW |
6 |
63,480,419 (GRCm39) |
missense |
probably benign |
0.38 |
R0717:Grid2
|
UTSW |
6 |
64,643,259 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1524:Grid2
|
UTSW |
6 |
64,406,738 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1555:Grid2
|
UTSW |
6 |
64,406,668 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1762:Grid2
|
UTSW |
6 |
64,510,638 (GRCm39) |
missense |
probably damaging |
0.98 |
R1944:Grid2
|
UTSW |
6 |
63,886,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1961:Grid2
|
UTSW |
6 |
63,885,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Grid2
|
UTSW |
6 |
63,885,902 (GRCm39) |
nonsense |
probably null |
|
R2138:Grid2
|
UTSW |
6 |
64,322,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R3500:Grid2
|
UTSW |
6 |
63,480,383 (GRCm39) |
missense |
probably damaging |
0.97 |
R3547:Grid2
|
UTSW |
6 |
64,297,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R3845:Grid2
|
UTSW |
6 |
64,322,826 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4124:Grid2
|
UTSW |
6 |
63,480,417 (GRCm39) |
missense |
probably benign |
0.41 |
R4273:Grid2
|
UTSW |
6 |
63,886,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Grid2
|
UTSW |
6 |
64,297,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Grid2
|
UTSW |
6 |
64,642,899 (GRCm39) |
missense |
probably benign |
0.27 |
R4721:Grid2
|
UTSW |
6 |
64,643,185 (GRCm39) |
missense |
probably benign |
0.33 |
R4755:Grid2
|
UTSW |
6 |
63,885,972 (GRCm39) |
missense |
probably benign |
0.04 |
R4869:Grid2
|
UTSW |
6 |
64,406,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5083:Grid2
|
UTSW |
6 |
64,297,136 (GRCm39) |
nonsense |
probably null |
|
R5091:Grid2
|
UTSW |
6 |
64,053,862 (GRCm39) |
missense |
probably benign |
0.07 |
R5117:Grid2
|
UTSW |
6 |
63,233,917 (GRCm39) |
missense |
probably benign |
0.15 |
R5128:Grid2
|
UTSW |
6 |
64,642,982 (GRCm39) |
missense |
probably benign |
0.01 |
R5386:Grid2
|
UTSW |
6 |
63,908,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R5404:Grid2
|
UTSW |
6 |
63,907,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R5534:Grid2
|
UTSW |
6 |
63,480,345 (GRCm39) |
missense |
probably benign |
|
R5626:Grid2
|
UTSW |
6 |
64,053,929 (GRCm39) |
critical splice donor site |
probably null |
|
R5699:Grid2
|
UTSW |
6 |
63,885,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5700:Grid2
|
UTSW |
6 |
64,071,416 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5876:Grid2
|
UTSW |
6 |
64,640,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R6446:Grid2
|
UTSW |
6 |
64,322,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R6694:Grid2
|
UTSW |
6 |
63,908,031 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6697:Grid2
|
UTSW |
6 |
63,908,031 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6699:Grid2
|
UTSW |
6 |
63,908,031 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6767:Grid2
|
UTSW |
6 |
63,907,999 (GRCm39) |
missense |
probably benign |
0.01 |
R6895:Grid2
|
UTSW |
6 |
64,372,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6999:Grid2
|
UTSW |
6 |
64,053,893 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7053:Grid2
|
UTSW |
6 |
64,677,402 (GRCm39) |
missense |
unknown |
|
R7126:Grid2
|
UTSW |
6 |
64,053,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R7432:Grid2
|
UTSW |
6 |
64,252,854 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7553:Grid2
|
UTSW |
6 |
64,053,925 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7619:Grid2
|
UTSW |
6 |
63,908,085 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7997:Grid2
|
UTSW |
6 |
64,297,120 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8112:Grid2
|
UTSW |
6 |
63,885,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R8296:Grid2
|
UTSW |
6 |
63,233,929 (GRCm39) |
critical splice donor site |
probably null |
|
R8320:Grid2
|
UTSW |
6 |
63,233,917 (GRCm39) |
missense |
probably benign |
0.15 |
R8467:Grid2
|
UTSW |
6 |
64,510,635 (GRCm39) |
missense |
probably benign |
0.01 |
R8691:Grid2
|
UTSW |
6 |
63,480,321 (GRCm39) |
missense |
probably damaging |
0.97 |
R8890:Grid2
|
UTSW |
6 |
63,233,923 (GRCm39) |
missense |
probably benign |
|
R8965:Grid2
|
UTSW |
6 |
64,296,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Grid2
|
UTSW |
6 |
64,643,139 (GRCm39) |
missense |
probably benign |
0.14 |
R9220:Grid2
|
UTSW |
6 |
63,885,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Grid2
|
UTSW |
6 |
64,677,506 (GRCm39) |
missense |
unknown |
|
R9653:Grid2
|
UTSW |
6 |
63,907,968 (GRCm39) |
missense |
possibly damaging |
0.75 |
Z1176:Grid2
|
UTSW |
6 |
64,640,212 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Grid2
|
UTSW |
6 |
63,885,863 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1177:Grid2
|
UTSW |
6 |
64,322,841 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Grid2
|
UTSW |
6 |
64,322,840 (GRCm39) |
nonsense |
probably null |
|
|