Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,548,801 (GRCm39) |
V1316A |
possibly damaging |
Het |
Ada |
T |
G |
2: 163,572,236 (GRCm39) |
K254N |
probably benign |
Het |
Adamts17 |
A |
G |
7: 66,490,037 (GRCm39) |
R40G |
probably benign |
Het |
Akr1d1 |
C |
T |
6: 37,507,178 (GRCm39) |
|
probably benign |
Het |
Aldh1l1 |
T |
A |
6: 90,536,215 (GRCm39) |
|
probably benign |
Het |
Bbox1 |
T |
A |
2: 110,095,831 (GRCm39) |
I378F |
probably benign |
Het |
BC028528 |
T |
C |
3: 95,796,212 (GRCm39) |
N50S |
probably damaging |
Het |
Casp8ap2 |
T |
A |
4: 32,641,294 (GRCm39) |
S783T |
possibly damaging |
Het |
Cmpk2 |
C |
T |
12: 26,527,177 (GRCm39) |
R389W |
probably damaging |
Het |
Cplx1 |
C |
T |
5: 108,696,393 (GRCm39) |
|
probably null |
Het |
Crim1 |
T |
C |
17: 78,651,863 (GRCm39) |
L529P |
probably benign |
Het |
Ctps1 |
A |
G |
4: 120,411,183 (GRCm39) |
S278P |
probably benign |
Het |
Defb21 |
C |
A |
2: 152,416,821 (GRCm39) |
|
probably benign |
Het |
Ecm1 |
T |
A |
3: 95,643,376 (GRCm39) |
N308I |
probably benign |
Het |
Flg2 |
T |
C |
3: 93,109,591 (GRCm39) |
S540P |
unknown |
Het |
Gabrp |
G |
T |
11: 33,502,826 (GRCm39) |
S346* |
probably null |
Het |
Gli2 |
C |
A |
1: 118,776,165 (GRCm39) |
C419F |
probably damaging |
Het |
Hormad1 |
T |
G |
3: 95,485,580 (GRCm39) |
M256R |
probably benign |
Het |
Itsn2 |
T |
G |
12: 4,686,693 (GRCm39) |
|
probably benign |
Het |
Klhl38 |
A |
T |
15: 58,186,707 (GRCm39) |
D7E |
probably benign |
Het |
Map3k1 |
G |
A |
13: 111,891,196 (GRCm39) |
T1248I |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,309,542 (GRCm39) |
V303E |
probably benign |
Het |
Mterf4 |
A |
T |
1: 93,232,443 (GRCm39) |
L136* |
probably null |
Het |
Mtmr14 |
A |
G |
6: 113,217,391 (GRCm39) |
D61G |
possibly damaging |
Het |
Nf2 |
A |
T |
11: 4,768,613 (GRCm39) |
D85E |
probably benign |
Het |
Nmnat2 |
G |
T |
1: 152,952,743 (GRCm39) |
|
probably benign |
Het |
Olfm3 |
T |
A |
3: 114,916,497 (GRCm39) |
D476E |
probably benign |
Het |
Or14c45 |
T |
C |
7: 86,175,986 (GRCm39) |
V7A |
probably benign |
Het |
Or8b53 |
T |
A |
9: 38,667,550 (GRCm39) |
C189S |
probably damaging |
Het |
Pdia6 |
T |
C |
12: 17,333,958 (GRCm39) |
|
probably benign |
Het |
Prrg1 |
G |
A |
X: 77,527,388 (GRCm39) |
A47V |
probably damaging |
Het |
Rgs22 |
A |
T |
15: 36,103,981 (GRCm39) |
I160K |
probably benign |
Het |
Sardh |
T |
C |
2: 27,079,625 (GRCm39) |
Y889C |
probably damaging |
Het |
Syne2 |
C |
A |
12: 75,956,110 (GRCm39) |
D605E |
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 |
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 |
R1572:Grid2
|
UTSW |
6 |
64,406,678 (GRCm39) |
nonsense |
probably null |
|
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 |
|
|