Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
T |
17: 46,624,730 (GRCm39) |
L198H |
probably damaging |
Het |
Anks1 |
C |
T |
17: 28,214,993 (GRCm39) |
T480I |
probably damaging |
Het |
Arhgef18 |
G |
A |
8: 3,503,165 (GRCm39) |
R857Q |
probably damaging |
Het |
B230208B08Rik |
A |
G |
4: 78,132,297 (GRCm39) |
|
noncoding transcript |
Het |
B9d2 |
T |
A |
7: 25,382,724 (GRCm39) |
W33R |
probably damaging |
Het |
Bcl2a1c |
A |
G |
9: 114,159,572 (GRCm39) |
T117A |
probably benign |
Het |
Btbd8 |
T |
G |
5: 107,655,460 (GRCm39) |
D574E |
probably damaging |
Het |
Cabin1 |
A |
G |
10: 75,557,366 (GRCm39) |
S1091P |
probably damaging |
Het |
Clip3 |
C |
A |
7: 29,996,298 (GRCm39) |
D64E |
probably damaging |
Het |
Col6a5 |
C |
G |
9: 105,740,000 (GRCm39) |
D2540H |
possibly damaging |
Het |
Commd5 |
A |
T |
15: 76,785,136 (GRCm39) |
M178L |
probably benign |
Het |
Crtc3 |
T |
A |
7: 80,245,542 (GRCm39) |
H361L |
possibly damaging |
Het |
Dip2b |
T |
A |
15: 100,049,065 (GRCm39) |
L153Q |
possibly damaging |
Het |
Eif2s1 |
T |
A |
12: 78,926,817 (GRCm39) |
V189D |
probably damaging |
Het |
Etl4 |
C |
T |
2: 20,748,718 (GRCm39) |
A483V |
probably damaging |
Het |
Foxo3 |
T |
C |
10: 42,072,583 (GRCm39) |
I645V |
probably benign |
Het |
Gm4841 |
A |
G |
18: 60,403,506 (GRCm39) |
S196P |
possibly damaging |
Het |
Hip1 |
A |
G |
5: 135,453,717 (GRCm39) |
|
probably null |
Het |
Il36rn |
G |
T |
2: 24,167,502 (GRCm39) |
|
probably benign |
Het |
Ints2 |
A |
G |
11: 86,106,371 (GRCm39) |
|
probably null |
Het |
Khnyn |
A |
G |
14: 56,124,523 (GRCm39) |
D259G |
probably benign |
Het |
Lyst |
T |
A |
13: 13,871,346 (GRCm39) |
Y2694* |
probably null |
Het |
Map4k2 |
T |
C |
19: 6,401,346 (GRCm39) |
|
probably benign |
Het |
Marchf10 |
C |
T |
11: 105,281,065 (GRCm39) |
V407I |
probably benign |
Het |
Mast4 |
C |
A |
13: 102,874,764 (GRCm39) |
V1367F |
probably damaging |
Het |
Mthfd1l |
T |
C |
10: 4,039,392 (GRCm39) |
F801S |
probably damaging |
Het |
Nhsl3 |
A |
G |
4: 129,115,941 (GRCm39) |
S908P |
probably damaging |
Het |
Notch2 |
T |
C |
3: 98,031,239 (GRCm39) |
|
probably benign |
Het |
Nr2e1 |
T |
C |
10: 42,448,765 (GRCm39) |
S158G |
probably benign |
Het |
Nup214 |
A |
G |
2: 31,881,353 (GRCm39) |
I404V |
probably benign |
Het |
Or13n4 |
T |
C |
7: 106,423,404 (GRCm39) |
T110A |
probably benign |
Het |
Pik3c2g |
G |
A |
6: 139,714,436 (GRCm39) |
R196H |
|
Het |
Pik3r3 |
A |
T |
4: 116,129,955 (GRCm39) |
D213V |
probably benign |
Het |
Pip5k1b |
A |
T |
19: 24,374,501 (GRCm39) |
S27T |
possibly damaging |
Het |
Pkp1 |
G |
A |
1: 135,846,621 (GRCm39) |
Q44* |
probably null |
Het |
Pnma8b |
C |
T |
7: 16,680,968 (GRCm39) |
R651C |
unknown |
Het |
Pnpt1 |
T |
A |
11: 29,080,887 (GRCm39) |
S44T |
probably benign |
Het |
Polb |
A |
T |
8: 23,132,319 (GRCm39) |
|
probably null |
Het |
Pom121l2 |
A |
G |
13: 22,165,984 (GRCm39) |
N85S |
probably damaging |
Het |
Prim1 |
A |
G |
10: 127,853,893 (GRCm39) |
K104E |
probably damaging |
Het |
Prl8a1 |
T |
A |
13: 27,758,040 (GRCm39) |
Y223F |
probably benign |
Het |
Rbak |
T |
G |
5: 143,159,391 (GRCm39) |
H554P |
probably damaging |
Het |
Serpina3c |
T |
C |
12: 104,117,970 (GRCm39) |
R123G |
probably benign |
Het |
Sh3bp4 |
T |
G |
1: 89,073,605 (GRCm39) |
S818A |
probably damaging |
Het |
Sh3rf3 |
C |
G |
10: 58,885,270 (GRCm39) |
H384Q |
probably benign |
Het |
Slc9a8 |
C |
T |
2: 167,293,090 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
C |
7: 27,103,678 (GRCm39) |
E1181G |
probably benign |
Het |
Taf2 |
G |
A |
15: 54,935,402 (GRCm39) |
|
probably benign |
Het |
Taf7l2 |
A |
T |
10: 115,949,133 (GRCm39) |
I131N |
probably benign |
Het |
Tbc1d9 |
A |
T |
8: 83,976,174 (GRCm39) |
M578L |
probably benign |
Het |
Tinagl1 |
G |
T |
4: 130,066,763 (GRCm39) |
Y111* |
probably null |
Het |
Tor2a |
T |
C |
2: 32,651,697 (GRCm39) |
L304P |
probably damaging |
Het |
Trp53bp1 |
A |
G |
2: 121,067,304 (GRCm39) |
V474A |
probably benign |
Het |
Trrap |
C |
A |
5: 144,723,518 (GRCm39) |
A325E |
probably damaging |
Het |
Ube4a |
A |
G |
9: 44,859,322 (GRCm39) |
|
probably null |
Het |
Use1 |
G |
C |
8: 71,822,257 (GRCm39) |
K239N |
probably damaging |
Het |
Vps9d1 |
G |
T |
8: 123,973,563 (GRCm39) |
Q407K |
probably benign |
Het |
Zfp36l1 |
A |
T |
12: 80,156,449 (GRCm39) |
S311T |
possibly damaging |
Het |
Zfp729b |
T |
C |
13: 67,739,374 (GRCm39) |
K964E |
probably benign |
Het |
Zfp974 |
T |
A |
7: 27,610,382 (GRCm39) |
M448L |
probably benign |
Het |
Zfyve28 |
A |
T |
5: 34,374,214 (GRCm39) |
V600E |
possibly damaging |
Het |
|
Other mutations in Mrgprb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03069:Mrgprb3
|
APN |
7 |
48,293,198 (GRCm39) |
missense |
possibly damaging |
0.71 |
Reserve
|
UTSW |
7 |
48,293,447 (GRCm39) |
missense |
probably benign |
0.02 |
starker
|
UTSW |
7 |
48,293,116 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03052:Mrgprb3
|
UTSW |
7 |
48,293,341 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0446:Mrgprb3
|
UTSW |
7 |
48,292,984 (GRCm39) |
missense |
probably benign |
0.42 |
R0546:Mrgprb3
|
UTSW |
7 |
48,293,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Mrgprb3
|
UTSW |
7 |
48,292,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Mrgprb3
|
UTSW |
7 |
48,292,771 (GRCm39) |
missense |
probably benign |
0.01 |
R2044:Mrgprb3
|
UTSW |
7 |
48,293,482 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2230:Mrgprb3
|
UTSW |
7 |
48,292,770 (GRCm39) |
missense |
probably benign |
0.05 |
R2232:Mrgprb3
|
UTSW |
7 |
48,292,770 (GRCm39) |
missense |
probably benign |
0.05 |
R2240:Mrgprb3
|
UTSW |
7 |
48,293,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R3001:Mrgprb3
|
UTSW |
7 |
48,293,232 (GRCm39) |
missense |
probably benign |
|
R3002:Mrgprb3
|
UTSW |
7 |
48,293,232 (GRCm39) |
missense |
probably benign |
|
R4717:Mrgprb3
|
UTSW |
7 |
48,293,000 (GRCm39) |
missense |
probably benign |
0.01 |
R4805:Mrgprb3
|
UTSW |
7 |
48,293,054 (GRCm39) |
missense |
probably benign |
0.01 |
R5083:Mrgprb3
|
UTSW |
7 |
48,292,762 (GRCm39) |
missense |
probably benign |
0.01 |
R5311:Mrgprb3
|
UTSW |
7 |
48,293,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Mrgprb3
|
UTSW |
7 |
48,292,682 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5331:Mrgprb3
|
UTSW |
7 |
48,292,682 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5615:Mrgprb3
|
UTSW |
7 |
48,293,234 (GRCm39) |
missense |
probably benign |
0.01 |
R5621:Mrgprb3
|
UTSW |
7 |
48,293,116 (GRCm39) |
missense |
probably benign |
0.28 |
R5697:Mrgprb3
|
UTSW |
7 |
48,292,673 (GRCm39) |
missense |
probably damaging |
0.96 |
R5725:Mrgprb3
|
UTSW |
7 |
48,293,548 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R5758:Mrgprb3
|
UTSW |
7 |
48,293,067 (GRCm39) |
missense |
probably benign |
0.01 |
R5807:Mrgprb3
|
UTSW |
7 |
48,293,110 (GRCm39) |
missense |
probably benign |
0.02 |
R6902:Mrgprb3
|
UTSW |
7 |
48,293,447 (GRCm39) |
missense |
probably benign |
0.02 |
R7037:Mrgprb3
|
UTSW |
7 |
48,292,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R7288:Mrgprb3
|
UTSW |
7 |
48,293,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Mrgprb3
|
UTSW |
7 |
48,292,862 (GRCm39) |
missense |
probably benign |
0.01 |
R8246:Mrgprb3
|
UTSW |
7 |
48,293,268 (GRCm39) |
missense |
probably benign |
0.02 |
R8292:Mrgprb3
|
UTSW |
7 |
48,293,255 (GRCm39) |
missense |
probably benign |
0.01 |
R8972:Mrgprb3
|
UTSW |
7 |
48,293,422 (GRCm39) |
missense |
possibly damaging |
0.95 |
|