Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,224,702 (GRCm39) |
S472P |
probably benign |
Het |
Armh3 |
A |
G |
19: 45,920,788 (GRCm39) |
|
probably null |
Het |
Arsi |
T |
C |
18: 61,049,737 (GRCm39) |
Y207H |
probably damaging |
Het |
Atp2b4 |
C |
T |
1: 133,654,271 (GRCm39) |
R778Q |
probably benign |
Het |
Car12 |
C |
A |
9: 66,654,913 (GRCm39) |
Y114* |
probably null |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col4a1 |
A |
G |
8: 11,362,586 (GRCm39) |
|
probably benign |
Het |
Cryl1 |
G |
T |
14: 57,523,865 (GRCm39) |
Y232* |
probably null |
Het |
Dnah11 |
T |
A |
12: 117,843,760 (GRCm39) |
M4362L |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,930,374 (GRCm39) |
T3324A |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,892,809 (GRCm39) |
N798S |
probably damaging |
Het |
Dok4 |
A |
T |
8: 95,593,140 (GRCm39) |
C182S |
probably damaging |
Het |
Ehbp1 |
A |
T |
11: 22,045,462 (GRCm39) |
N737K |
probably benign |
Het |
Eif2b4 |
T |
C |
5: 31,349,918 (GRCm39) |
|
probably benign |
Het |
Elp1 |
A |
G |
4: 56,755,298 (GRCm39) |
|
probably null |
Het |
Fat4 |
T |
C |
3: 38,943,138 (GRCm39) |
V677A |
possibly damaging |
Het |
Fbn2 |
A |
G |
18: 58,228,248 (GRCm39) |
|
probably benign |
Het |
Fbxl3 |
G |
T |
14: 103,320,648 (GRCm39) |
Y314* |
probably null |
Het |
Fgf12 |
T |
A |
16: 28,008,363 (GRCm39) |
K84* |
probably null |
Het |
Flt3 |
G |
A |
5: 147,284,873 (GRCm39) |
P748L |
probably benign |
Het |
Folh1 |
C |
T |
7: 86,368,973 (GRCm39) |
S685N |
probably benign |
Het |
Gpr65 |
A |
T |
12: 98,241,494 (GRCm39) |
N49I |
probably damaging |
Het |
Hdac7 |
A |
G |
15: 97,708,732 (GRCm39) |
|
probably null |
Het |
Heatr5a |
A |
T |
12: 51,962,933 (GRCm39) |
V989E |
probably damaging |
Het |
Kif12 |
A |
G |
4: 63,087,758 (GRCm39) |
S242P |
probably benign |
Het |
Ltbp3 |
G |
A |
19: 5,804,050 (GRCm39) |
R854Q |
probably benign |
Het |
Mia3 |
A |
G |
1: 183,115,647 (GRCm39) |
Y295H |
probably benign |
Het |
Nell1 |
C |
T |
7: 50,210,569 (GRCm39) |
T494I |
possibly damaging |
Het |
Nmur2 |
A |
T |
11: 55,920,387 (GRCm39) |
V286E |
probably damaging |
Het |
Or1ad6 |
G |
A |
11: 50,860,696 (GRCm39) |
V284I |
possibly damaging |
Het |
Or1e1 |
T |
A |
11: 73,245,131 (GRCm39) |
L184Q |
possibly damaging |
Het |
Or51t4 |
T |
C |
7: 102,598,464 (GRCm39) |
F254S |
probably damaging |
Het |
Pcdh1 |
A |
T |
18: 38,331,710 (GRCm39) |
L431H |
probably benign |
Het |
Pramel31 |
A |
G |
4: 144,090,111 (GRCm39) |
I384V |
probably benign |
Het |
Prex1 |
A |
T |
2: 166,430,988 (GRCm39) |
|
probably benign |
Het |
Prim1 |
T |
A |
10: 127,851,132 (GRCm39) |
D5E |
probably benign |
Het |
Rubcnl |
A |
T |
14: 75,278,260 (GRCm39) |
N348I |
possibly damaging |
Het |
Shisa9 |
G |
T |
16: 11,802,631 (GRCm39) |
A63S |
possibly damaging |
Het |
Shpk |
G |
A |
11: 73,097,319 (GRCm39) |
|
probably benign |
Het |
Slx4ip |
T |
C |
2: 136,885,935 (GRCm39) |
I85T |
probably damaging |
Het |
Sptbn4 |
T |
A |
7: 27,133,782 (GRCm39) |
D77V |
probably damaging |
Het |
Strn3 |
A |
T |
12: 51,690,006 (GRCm39) |
|
probably null |
Het |
Synrg |
T |
C |
11: 83,867,978 (GRCm39) |
M61T |
possibly damaging |
Het |
Tekt4 |
T |
A |
17: 25,695,485 (GRCm39) |
S439R |
possibly damaging |
Het |
Ticam1 |
A |
T |
17: 56,578,888 (GRCm39) |
V69E |
possibly damaging |
Het |
Trpv1 |
C |
T |
11: 73,132,508 (GRCm39) |
A374V |
probably damaging |
Het |
Ubqln3 |
A |
T |
7: 103,790,842 (GRCm39) |
L416* |
probably null |
Het |
Uqcrfs1 |
G |
A |
13: 30,725,090 (GRCm39) |
S150L |
probably benign |
Het |
Utp15 |
T |
C |
13: 98,394,433 (GRCm39) |
N153S |
probably benign |
Het |
Vmn2r63 |
G |
T |
7: 42,578,031 (GRCm39) |
T169N |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,646,327 (GRCm39) |
V1477E |
probably benign |
Het |
Wdr87-ps |
T |
C |
7: 29,231,987 (GRCm39) |
|
noncoding transcript |
Het |
Xpo1 |
T |
A |
11: 23,234,634 (GRCm39) |
|
probably null |
Het |
Xpo5 |
A |
G |
17: 46,541,269 (GRCm39) |
I769V |
probably benign |
Het |
Zc3h14 |
A |
T |
12: 98,724,773 (GRCm39) |
H252L |
probably benign |
Het |
Zfp410 |
G |
T |
12: 84,369,794 (GRCm39) |
|
probably null |
Het |
Zfp521 |
T |
C |
18: 13,979,297 (GRCm39) |
E372G |
possibly damaging |
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 |
|
R1644:Bdp1
|
UTSW |
13 |
100,197,448 (GRCm39) |
missense |
probably benign |
0.03 |
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 |
|
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 |
|