Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
T |
1: 11,484,814 (GRCm39) |
R8* |
probably null |
Het |
Acacb |
A |
T |
5: 114,333,346 (GRCm39) |
H490L |
probably damaging |
Het |
Ace |
C |
A |
11: 105,875,932 (GRCm39) |
H417N |
probably damaging |
Het |
Adamtsl3 |
A |
G |
7: 82,099,298 (GRCm39) |
N151D |
possibly damaging |
Het |
Agap1 |
A |
G |
1: 89,591,452 (GRCm39) |
N114S |
probably damaging |
Het |
Arap3 |
A |
T |
18: 38,117,298 (GRCm39) |
V926D |
probably damaging |
Het |
Arhgap12 |
A |
T |
18: 6,112,340 (GRCm39) |
I8N |
probably benign |
Het |
Arhgef17 |
A |
T |
7: 100,578,711 (GRCm39) |
F746I |
probably damaging |
Het |
Atp6v0a1 |
T |
C |
11: 100,929,612 (GRCm39) |
S471P |
possibly damaging |
Het |
Ccdc88c |
C |
A |
12: 100,879,733 (GRCm39) |
R1789L |
probably damaging |
Het |
Cckar |
A |
T |
5: 53,857,215 (GRCm39) |
N327K |
probably benign |
Het |
Cfap65 |
T |
C |
1: 74,956,334 (GRCm39) |
T1082A |
probably damaging |
Het |
Clcn7 |
T |
A |
17: 25,378,672 (GRCm39) |
I719N |
probably damaging |
Het |
Col27a1 |
C |
G |
4: 63,246,868 (GRCm39) |
|
probably benign |
Het |
Cspp1 |
C |
T |
1: 10,196,663 (GRCm39) |
T179I |
probably damaging |
Het |
Dnah1 |
C |
T |
14: 31,024,249 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,132,279 (GRCm39) |
V1141A |
probably benign |
Het |
Dusp4 |
A |
G |
8: 35,285,633 (GRCm39) |
Y298C |
probably damaging |
Het |
Efhc1 |
C |
A |
1: 21,037,625 (GRCm39) |
Y267* |
probably null |
Het |
Eif2s1 |
T |
A |
12: 78,913,295 (GRCm39) |
|
probably null |
Het |
Epo |
A |
G |
5: 137,481,417 (GRCm39) |
V169A |
possibly damaging |
Het |
Esr1 |
A |
T |
10: 4,951,380 (GRCm39) |
Y586F |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,178,609 (GRCm39) |
T1484A |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,187,007 (GRCm39) |
T1280A |
possibly damaging |
Het |
Gm5828 |
T |
C |
1: 16,839,485 (GRCm39) |
|
noncoding transcript |
Het |
Idh3b |
T |
C |
2: 130,123,430 (GRCm39) |
I187V |
possibly damaging |
Het |
Kif13a |
A |
C |
13: 46,947,398 (GRCm39) |
V862G |
probably benign |
Het |
Kndc1 |
A |
G |
7: 139,510,669 (GRCm39) |
D1327G |
probably damaging |
Het |
Mfsd9 |
T |
A |
1: 40,812,958 (GRCm39) |
R452S |
probably benign |
Het |
Myh15 |
C |
T |
16: 48,952,566 (GRCm39) |
R879C |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,319,437 (GRCm39) |
R260G |
possibly damaging |
Het |
Npat |
T |
G |
9: 53,481,472 (GRCm39) |
L1060R |
probably damaging |
Het |
Or2aj4 |
T |
A |
16: 19,385,156 (GRCm39) |
H159L |
probably benign |
Het |
Or4c126 |
A |
T |
2: 89,824,297 (GRCm39) |
T187S |
possibly damaging |
Het |
Or4c15 |
A |
T |
2: 88,759,731 (GRCm39) |
D309E |
probably benign |
Het |
Or52n2b |
A |
C |
7: 104,566,015 (GRCm39) |
F163V |
probably benign |
Het |
Or6f2 |
T |
C |
7: 139,756,561 (GRCm39) |
V176A |
probably benign |
Het |
Pld5 |
T |
C |
1: 175,803,192 (GRCm39) |
T296A |
possibly damaging |
Het |
Polq |
C |
T |
16: 36,880,626 (GRCm39) |
A651V |
probably damaging |
Het |
Polr3a |
G |
A |
14: 24,520,692 (GRCm39) |
P607S |
probably damaging |
Het |
Ranbp9 |
G |
A |
13: 43,566,015 (GRCm39) |
R424C |
probably damaging |
Het |
Rsl1 |
G |
A |
13: 67,325,229 (GRCm39) |
|
probably benign |
Het |
Sema4c |
A |
G |
1: 36,589,885 (GRCm39) |
S490P |
probably damaging |
Het |
Setd3 |
A |
T |
12: 108,079,603 (GRCm39) |
L300Q |
possibly damaging |
Het |
Slc15a3 |
T |
C |
19: 10,834,595 (GRCm39) |
I492T |
possibly damaging |
Het |
Stag1 |
T |
C |
9: 100,762,953 (GRCm39) |
|
probably benign |
Het |
Tgm4 |
A |
G |
9: 122,880,481 (GRCm39) |
Y294C |
probably damaging |
Het |
Tm9sf1 |
A |
G |
14: 55,878,757 (GRCm39) |
S212P |
probably benign |
Het |
Tmcc1 |
A |
G |
6: 116,110,826 (GRCm39) |
S156P |
probably damaging |
Het |
Vmn1r184 |
A |
C |
7: 25,966,670 (GRCm39) |
M139L |
probably benign |
Het |
Vmn1r209 |
A |
C |
13: 22,990,652 (GRCm39) |
F13V |
possibly damaging |
Het |
Xkr5 |
T |
C |
8: 18,984,141 (GRCm39) |
E467G |
probably benign |
Het |
Zdbf2 |
C |
T |
1: 63,348,131 (GRCm39) |
S2170L |
possibly damaging |
Het |
Zfp277 |
G |
T |
12: 40,379,609 (GRCm39) |
|
probably null |
Het |
Zfp62 |
T |
C |
11: 49,106,596 (GRCm39) |
I229T |
probably damaging |
Het |
Zfp810 |
A |
G |
9: 22,190,324 (GRCm39) |
S195P |
possibly damaging |
Het |
Zfp94 |
G |
A |
7: 24,010,927 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Bdp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Bdp1
|
APN |
13 |
100,235,018 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00096:Bdp1
|
APN |
13 |
100,197,373 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL00160:Bdp1
|
APN |
13 |
100,197,706 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00924:Bdp1
|
APN |
13 |
100,234,087 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01337:Bdp1
|
APN |
13 |
100,192,700 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01344:Bdp1
|
APN |
13 |
100,214,588 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01347:Bdp1
|
APN |
13 |
100,206,711 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01620:Bdp1
|
APN |
13 |
100,220,713 (GRCm39) |
splice site |
probably benign |
|
IGL01871:Bdp1
|
APN |
13 |
100,202,561 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02008:Bdp1
|
APN |
13 |
100,160,335 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02112:Bdp1
|
APN |
13 |
100,174,308 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02214:Bdp1
|
APN |
13 |
100,178,043 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02236:Bdp1
|
APN |
13 |
100,197,399 (GRCm39) |
missense |
probably benign |
|
IGL02307:Bdp1
|
APN |
13 |
100,229,946 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02364:Bdp1
|
APN |
13 |
100,191,816 (GRCm39) |
splice site |
probably benign |
|
IGL02415:Bdp1
|
APN |
13 |
100,225,916 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02601:Bdp1
|
APN |
13 |
100,235,022 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02605:Bdp1
|
APN |
13 |
100,214,623 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02664:Bdp1
|
APN |
13 |
100,188,047 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02738:Bdp1
|
APN |
13 |
100,187,861 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02754:Bdp1
|
APN |
13 |
100,197,481 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02967:Bdp1
|
APN |
13 |
100,178,778 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02974:Bdp1
|
APN |
13 |
100,191,800 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03156:Bdp1
|
APN |
13 |
100,197,544 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03166:Bdp1
|
APN |
13 |
100,172,308 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03232:Bdp1
|
APN |
13 |
100,187,989 (GRCm39) |
missense |
probably damaging |
1.00 |
D3080:Bdp1
|
UTSW |
13 |
100,160,129 (GRCm39) |
missense |
probably benign |
0.02 |
R0115:Bdp1
|
UTSW |
13 |
100,177,962 (GRCm39) |
missense |
probably benign |
0.28 |
R0481:Bdp1
|
UTSW |
13 |
100,177,962 (GRCm39) |
missense |
probably benign |
0.28 |
R0619:Bdp1
|
UTSW |
13 |
100,174,366 (GRCm39) |
missense |
probably benign |
0.00 |
R0730:Bdp1
|
UTSW |
13 |
100,195,459 (GRCm39) |
splice site |
probably benign |
|
R0744:Bdp1
|
UTSW |
13 |
100,172,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0833:Bdp1
|
UTSW |
13 |
100,172,333 (GRCm39) |
missense |
probably benign |
0.01 |
R1307:Bdp1
|
UTSW |
13 |
100,186,271 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1325:Bdp1
|
UTSW |
13 |
100,235,516 (GRCm39) |
missense |
probably damaging |
0.97 |
R1346:Bdp1
|
UTSW |
13 |
100,215,263 (GRCm39) |
nonsense |
probably null |
|
R1670:Bdp1
|
UTSW |
13 |
100,163,941 (GRCm39) |
critical splice donor site |
probably null |
|
R1836:Bdp1
|
UTSW |
13 |
100,171,653 (GRCm39) |
missense |
probably benign |
|
R1869:Bdp1
|
UTSW |
13 |
100,178,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1920:Bdp1
|
UTSW |
13 |
100,235,097 (GRCm39) |
missense |
probably benign |
0.30 |
R1944:Bdp1
|
UTSW |
13 |
100,210,889 (GRCm39) |
splice site |
probably null |
|
R2030:Bdp1
|
UTSW |
13 |
100,197,697 (GRCm39) |
missense |
probably benign |
0.00 |
R2069:Bdp1
|
UTSW |
13 |
100,187,496 (GRCm39) |
missense |
probably benign |
0.00 |
R2180:Bdp1
|
UTSW |
13 |
100,197,913 (GRCm39) |
small insertion |
probably benign |
|
R2263:Bdp1
|
UTSW |
13 |
100,202,545 (GRCm39) |
missense |
probably damaging |
0.96 |
R2277:Bdp1
|
UTSW |
13 |
100,197,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R2277:Bdp1
|
UTSW |
13 |
100,197,838 (GRCm39) |
missense |
probably benign |
0.05 |
R2278:Bdp1
|
UTSW |
13 |
100,197,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Bdp1
|
UTSW |
13 |
100,197,838 (GRCm39) |
missense |
probably benign |
0.05 |
R2336:Bdp1
|
UTSW |
13 |
100,189,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R2380:Bdp1
|
UTSW |
13 |
100,196,878 (GRCm39) |
missense |
probably benign |
0.08 |
R3154:Bdp1
|
UTSW |
13 |
100,186,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R4212:Bdp1
|
UTSW |
13 |
100,196,093 (GRCm39) |
missense |
probably benign |
|
R4322:Bdp1
|
UTSW |
13 |
100,228,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R4414:Bdp1
|
UTSW |
13 |
100,167,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4415:Bdp1
|
UTSW |
13 |
100,167,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4764:Bdp1
|
UTSW |
13 |
100,192,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R4766:Bdp1
|
UTSW |
13 |
100,186,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R4888:Bdp1
|
UTSW |
13 |
100,187,627 (GRCm39) |
missense |
probably benign |
0.26 |
R4914:Bdp1
|
UTSW |
13 |
100,192,844 (GRCm39) |
missense |
probably benign |
0.28 |
R4917:Bdp1
|
UTSW |
13 |
100,191,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Bdp1
|
UTSW |
13 |
100,191,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5170:Bdp1
|
UTSW |
13 |
100,167,302 (GRCm39) |
nonsense |
probably null |
|
R5266:Bdp1
|
UTSW |
13 |
100,204,043 (GRCm39) |
missense |
probably benign |
0.33 |
R5312:Bdp1
|
UTSW |
13 |
100,234,109 (GRCm39) |
splice site |
probably null |
|
R5420:Bdp1
|
UTSW |
13 |
100,202,551 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5486:Bdp1
|
UTSW |
13 |
100,235,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Bdp1
|
UTSW |
13 |
100,228,794 (GRCm39) |
missense |
probably benign |
0.08 |
R5913:Bdp1
|
UTSW |
13 |
100,187,612 (GRCm39) |
missense |
probably benign |
0.41 |
R6018:Bdp1
|
UTSW |
13 |
100,174,732 (GRCm39) |
missense |
probably benign |
0.00 |
R6037:Bdp1
|
UTSW |
13 |
100,163,957 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6037:Bdp1
|
UTSW |
13 |
100,163,957 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6700:Bdp1
|
UTSW |
13 |
100,162,036 (GRCm39) |
missense |
probably benign |
0.00 |
R6969:Bdp1
|
UTSW |
13 |
100,211,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R6972:Bdp1
|
UTSW |
13 |
100,174,269 (GRCm39) |
missense |
probably null |
1.00 |
R6996:Bdp1
|
UTSW |
13 |
100,180,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Bdp1
|
UTSW |
13 |
100,215,215 (GRCm39) |
missense |
probably benign |
0.03 |
R7060:Bdp1
|
UTSW |
13 |
100,196,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Bdp1
|
UTSW |
13 |
100,206,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Bdp1
|
UTSW |
13 |
100,197,659 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7175:Bdp1
|
UTSW |
13 |
100,186,478 (GRCm39) |
missense |
probably damaging |
0.97 |
R7177:Bdp1
|
UTSW |
13 |
100,186,478 (GRCm39) |
missense |
probably damaging |
0.97 |
R7327:Bdp1
|
UTSW |
13 |
100,178,040 (GRCm39) |
missense |
probably damaging |
0.97 |
R7512:Bdp1
|
UTSW |
13 |
100,187,457 (GRCm39) |
missense |
probably benign |
0.03 |
R7562:Bdp1
|
UTSW |
13 |
100,162,049 (GRCm39) |
missense |
probably benign |
0.04 |
R7583:Bdp1
|
UTSW |
13 |
100,186,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Bdp1
|
UTSW |
13 |
100,191,759 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7842:Bdp1
|
UTSW |
13 |
100,235,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Bdp1
|
UTSW |
13 |
100,228,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Bdp1
|
UTSW |
13 |
100,177,944 (GRCm39) |
missense |
probably benign |
0.37 |
R7975:Bdp1
|
UTSW |
13 |
100,156,884 (GRCm39) |
missense |
probably benign |
0.01 |
R7999:Bdp1
|
UTSW |
13 |
100,195,404 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8126:Bdp1
|
UTSW |
13 |
100,192,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8340:Bdp1
|
UTSW |
13 |
100,202,476 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8414:Bdp1
|
UTSW |
13 |
100,200,985 (GRCm39) |
missense |
probably benign |
0.03 |
R8468:Bdp1
|
UTSW |
13 |
100,197,076 (GRCm39) |
missense |
probably benign |
0.04 |
R8688:Bdp1
|
UTSW |
13 |
100,240,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Bdp1
|
UTSW |
13 |
100,186,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Bdp1
|
UTSW |
13 |
100,197,407 (GRCm39) |
nonsense |
probably null |
|
R8987:Bdp1
|
UTSW |
13 |
100,204,021 (GRCm39) |
missense |
probably benign |
0.01 |
R9157:Bdp1
|
UTSW |
13 |
100,186,436 (GRCm39) |
missense |
probably benign |
0.40 |
R9437:Bdp1
|
UTSW |
13 |
100,162,158 (GRCm39) |
missense |
probably benign |
0.31 |
R9612:Bdp1
|
UTSW |
13 |
100,214,370 (GRCm39) |
missense |
probably benign |
0.18 |
R9679:Bdp1
|
UTSW |
13 |
100,180,285 (GRCm39) |
missense |
probably damaging |
0.98 |
RF003:Bdp1
|
UTSW |
13 |
100,196,958 (GRCm39) |
missense |
probably benign |
0.31 |
RF003:Bdp1
|
UTSW |
13 |
100,196,957 (GRCm39) |
missense |
probably benign |
0.31 |
Z1177:Bdp1
|
UTSW |
13 |
100,197,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|