Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
T |
C |
15: 59,888,179 (GRCm39) |
D87G |
probably benign |
Het |
Acap1 |
C |
T |
11: 69,786,112 (GRCm39) |
R18Q |
probably damaging |
Het |
Atp1a1 |
A |
C |
3: 101,499,179 (GRCm39) |
V140G |
probably damaging |
Het |
Bmpr1b |
G |
A |
3: 141,576,498 (GRCm39) |
P112S |
possibly damaging |
Het |
Chst8 |
T |
A |
7: 34,374,759 (GRCm39) |
N360I |
possibly damaging |
Het |
Cldn23 |
A |
T |
8: 36,293,359 (GRCm39) |
V43E |
possibly damaging |
Het |
Clta |
T |
C |
4: 44,030,232 (GRCm39) |
F168S |
probably damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,755,926 (GRCm39) |
I463V |
probably benign |
Het |
E2f2 |
A |
G |
4: 135,920,323 (GRCm39) |
D436G |
probably damaging |
Het |
Fbxo24 |
T |
G |
5: 137,622,611 (GRCm39) |
T52P |
probably damaging |
Het |
Gria4 |
G |
A |
9: 4,793,878 (GRCm39) |
A60V |
probably damaging |
Het |
Hexa |
A |
G |
9: 59,464,586 (GRCm39) |
T159A |
probably benign |
Het |
Inf2 |
T |
A |
12: 112,568,048 (GRCm39) |
V200E |
probably damaging |
Het |
Kif20b |
T |
A |
19: 34,913,044 (GRCm39) |
V319E |
probably damaging |
Het |
Klhl10 |
A |
G |
11: 100,336,577 (GRCm39) |
D188G |
probably benign |
Het |
Mobp |
G |
A |
9: 119,996,980 (GRCm39) |
R37H |
probably damaging |
Het |
Mybpc2 |
T |
A |
7: 44,153,204 (GRCm39) |
D1086V |
probably damaging |
Het |
Nadk |
A |
C |
4: 155,663,860 (GRCm39) |
|
probably benign |
Het |
Or7g33 |
T |
A |
9: 19,448,749 (GRCm39) |
H159L |
probably benign |
Het |
Per1 |
A |
G |
11: 68,995,125 (GRCm39) |
E619G |
probably damaging |
Het |
Rab3gap1 |
G |
A |
1: 127,796,652 (GRCm39) |
|
probably benign |
Het |
Rimkla |
A |
G |
4: 119,325,344 (GRCm39) |
L355P |
probably damaging |
Het |
Rnf139 |
A |
G |
15: 58,771,880 (GRCm39) |
D635G |
possibly damaging |
Het |
Sall1 |
T |
A |
8: 89,757,003 (GRCm39) |
N1034Y |
probably damaging |
Het |
Serpinb13 |
A |
T |
1: 106,926,688 (GRCm39) |
Q228L |
probably damaging |
Het |
Sin3b |
G |
T |
8: 73,480,208 (GRCm39) |
M903I |
possibly damaging |
Het |
Slco1a5 |
A |
T |
6: 142,200,172 (GRCm39) |
M204K |
probably benign |
Het |
Smo |
A |
G |
6: 29,754,707 (GRCm39) |
D259G |
possibly damaging |
Het |
Spata31g1 |
A |
C |
4: 42,972,685 (GRCm39) |
K673Q |
possibly damaging |
Het |
Sult2a4 |
T |
C |
7: 13,723,469 (GRCm39) |
I15M |
probably benign |
Het |
Ttn |
T |
A |
2: 76,772,785 (GRCm39) |
|
probably null |
Het |
Wdtc1 |
C |
A |
4: 133,033,271 (GRCm39) |
D176Y |
probably damaging |
Het |
|
Other mutations in Grm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01371:Grm1
|
APN |
10 |
10,595,783 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02156:Grm1
|
APN |
10 |
10,595,720 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02476:Grm1
|
APN |
10 |
10,565,197 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02498:Grm1
|
APN |
10 |
10,595,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02621:Grm1
|
APN |
10 |
10,564,755 (GRCm39) |
nonsense |
probably null |
|
IGL03192:Grm1
|
APN |
10 |
10,955,660 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03342:Grm1
|
APN |
10 |
10,955,715 (GRCm39) |
missense |
probably benign |
0.08 |
dewey
|
UTSW |
10 |
10,595,339 (GRCm39) |
missense |
probably damaging |
1.00 |
Dingus
|
UTSW |
10 |
10,595,711 (GRCm39) |
missense |
probably benign |
0.06 |
donald
|
UTSW |
10 |
10,617,252 (GRCm39) |
nonsense |
probably null |
|
jim
|
UTSW |
10 |
10,595,549 (GRCm39) |
missense |
probably damaging |
1.00 |
lightness
|
UTSW |
10 |
10,955,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02796:Grm1
|
UTSW |
10 |
10,565,411 (GRCm39) |
missense |
probably benign |
|
R0294:Grm1
|
UTSW |
10 |
10,956,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Grm1
|
UTSW |
10 |
10,594,953 (GRCm39) |
splice site |
probably benign |
|
R0554:Grm1
|
UTSW |
10 |
10,595,667 (GRCm39) |
missense |
probably benign |
0.01 |
R1184:Grm1
|
UTSW |
10 |
10,595,778 (GRCm39) |
missense |
probably benign |
0.40 |
R1319:Grm1
|
UTSW |
10 |
10,565,142 (GRCm39) |
missense |
probably benign |
0.05 |
R1403:Grm1
|
UTSW |
10 |
10,955,879 (GRCm39) |
missense |
probably benign |
0.00 |
R1403:Grm1
|
UTSW |
10 |
10,955,879 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Grm1
|
UTSW |
10 |
10,595,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Grm1
|
UTSW |
10 |
10,595,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Grm1
|
UTSW |
10 |
10,565,450 (GRCm39) |
missense |
probably benign |
0.04 |
R1589:Grm1
|
UTSW |
10 |
10,595,711 (GRCm39) |
missense |
probably benign |
0.06 |
R1615:Grm1
|
UTSW |
10 |
10,617,252 (GRCm39) |
nonsense |
probably null |
|
R1720:Grm1
|
UTSW |
10 |
10,622,538 (GRCm39) |
splice site |
probably null |
|
R1738:Grm1
|
UTSW |
10 |
10,812,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Grm1
|
UTSW |
10 |
10,955,610 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1774:Grm1
|
UTSW |
10 |
10,955,610 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2041:Grm1
|
UTSW |
10 |
10,622,347 (GRCm39) |
missense |
probably damaging |
0.98 |
R2092:Grm1
|
UTSW |
10 |
10,564,969 (GRCm39) |
missense |
probably benign |
0.00 |
R2198:Grm1
|
UTSW |
10 |
10,658,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2297:Grm1
|
UTSW |
10 |
10,956,158 (GRCm39) |
missense |
probably benign |
0.03 |
R2333:Grm1
|
UTSW |
10 |
10,595,363 (GRCm39) |
missense |
probably benign |
0.31 |
R2333:Grm1
|
UTSW |
10 |
10,595,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R2914:Grm1
|
UTSW |
10 |
10,955,601 (GRCm39) |
missense |
probably benign |
0.07 |
R3105:Grm1
|
UTSW |
10 |
10,955,601 (GRCm39) |
missense |
probably benign |
0.07 |
R3106:Grm1
|
UTSW |
10 |
10,955,601 (GRCm39) |
missense |
probably benign |
0.07 |
R3705:Grm1
|
UTSW |
10 |
10,658,473 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3931:Grm1
|
UTSW |
10 |
10,595,622 (GRCm39) |
missense |
probably benign |
0.44 |
R4810:Grm1
|
UTSW |
10 |
10,658,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4892:Grm1
|
UTSW |
10 |
10,595,331 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4938:Grm1
|
UTSW |
10 |
10,812,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Grm1
|
UTSW |
10 |
10,658,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Grm1
|
UTSW |
10 |
10,595,409 (GRCm39) |
nonsense |
probably null |
|
R5152:Grm1
|
UTSW |
10 |
10,955,619 (GRCm39) |
missense |
probably benign |
0.13 |
R5283:Grm1
|
UTSW |
10 |
10,608,936 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5317:Grm1
|
UTSW |
10 |
10,622,443 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5374:Grm1
|
UTSW |
10 |
10,956,186 (GRCm39) |
missense |
probably benign |
0.14 |
R5428:Grm1
|
UTSW |
10 |
10,595,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Grm1
|
UTSW |
10 |
10,622,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Grm1
|
UTSW |
10 |
10,955,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5896:Grm1
|
UTSW |
10 |
10,956,294 (GRCm39) |
utr 5 prime |
probably benign |
|
R5899:Grm1
|
UTSW |
10 |
10,565,092 (GRCm39) |
missense |
probably benign |
|
R6032:Grm1
|
UTSW |
10 |
10,595,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Grm1
|
UTSW |
10 |
10,595,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Grm1
|
UTSW |
10 |
10,622,075 (GRCm39) |
intron |
probably benign |
|
R6144:Grm1
|
UTSW |
10 |
10,955,640 (GRCm39) |
missense |
probably benign |
0.08 |
R6208:Grm1
|
UTSW |
10 |
10,595,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6976:Grm1
|
UTSW |
10 |
10,564,924 (GRCm39) |
missense |
probably benign |
0.00 |
R7027:Grm1
|
UTSW |
10 |
10,595,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7079:Grm1
|
UTSW |
10 |
10,955,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7286:Grm1
|
UTSW |
10 |
10,565,440 (GRCm39) |
missense |
probably benign |
0.19 |
R7352:Grm1
|
UTSW |
10 |
10,595,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Grm1
|
UTSW |
10 |
10,622,403 (GRCm39) |
missense |
probably benign |
0.06 |
R7838:Grm1
|
UTSW |
10 |
10,956,096 (GRCm39) |
missense |
probably benign |
0.02 |
R8108:Grm1
|
UTSW |
10 |
10,595,876 (GRCm39) |
missense |
probably benign |
0.01 |
R8379:Grm1
|
UTSW |
10 |
10,564,879 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8498:Grm1
|
UTSW |
10 |
10,955,605 (GRCm39) |
nonsense |
probably null |
|
R8712:Grm1
|
UTSW |
10 |
10,565,296 (GRCm39) |
missense |
probably benign |
0.34 |
R8856:Grm1
|
UTSW |
10 |
10,595,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Grm1
|
UTSW |
10 |
10,595,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Grm1
|
UTSW |
10 |
10,565,056 (GRCm39) |
nonsense |
probably null |
|
R9477:Grm1
|
UTSW |
10 |
10,595,405 (GRCm39) |
missense |
probably benign |
0.15 |
R9674:Grm1
|
UTSW |
10 |
10,609,028 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9685:Grm1
|
UTSW |
10 |
10,564,775 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9777:Grm1
|
UTSW |
10 |
10,573,826 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0002:Grm1
|
UTSW |
10 |
10,812,257 (GRCm39) |
missense |
probably damaging |
1.00 |
|