Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam8 |
G |
A |
7: 139,567,591 (GRCm39) |
T384I |
probably benign |
Het |
Astn1 |
T |
C |
1: 158,424,886 (GRCm39) |
F691L |
probably benign |
Het |
Azgp1 |
A |
G |
5: 137,985,869 (GRCm39) |
E164G |
probably damaging |
Het |
Cactin |
T |
C |
10: 81,161,699 (GRCm39) |
Y744H |
possibly damaging |
Het |
Clstn1 |
T |
A |
4: 149,698,594 (GRCm39) |
I60N |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,948,001 (GRCm39) |
C240* |
probably null |
Het |
Col6a5 |
T |
C |
9: 105,805,720 (GRCm39) |
D1062G |
unknown |
Het |
Csmd2 |
T |
C |
4: 128,313,346 (GRCm39) |
L1341P |
|
Het |
Cyp51 |
A |
T |
5: 4,150,173 (GRCm39) |
F183L |
probably damaging |
Het |
Dbnl |
T |
A |
11: 5,741,779 (GRCm39) |
|
probably null |
Het |
Ddx60 |
G |
A |
8: 62,430,924 (GRCm39) |
V820I |
possibly damaging |
Het |
Dnaaf9 |
A |
T |
2: 130,633,923 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
A |
12: 117,867,003 (GRCm39) |
D4046V |
possibly damaging |
Het |
Dnah6 |
G |
A |
6: 73,112,450 (GRCm39) |
|
probably null |
Het |
Dnttip1 |
A |
G |
2: 164,589,472 (GRCm39) |
Y89C |
probably benign |
Het |
Efr3a |
T |
A |
15: 65,696,527 (GRCm39) |
V144E |
probably damaging |
Het |
Epha8 |
T |
C |
4: 136,659,050 (GRCm39) |
Q868R |
possibly damaging |
Het |
Ercc5 |
G |
T |
1: 44,214,998 (GRCm39) |
|
probably null |
Het |
Fam118a |
A |
G |
15: 84,929,834 (GRCm39) |
S21G |
probably damaging |
Het |
Fam171b |
T |
C |
2: 83,683,849 (GRCm39) |
I122T |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,941,690 (GRCm39) |
S194R |
probably damaging |
Het |
Fcho2 |
T |
A |
13: 98,932,871 (GRCm39) |
T44S |
possibly damaging |
Het |
Gm21698 |
C |
A |
5: 26,189,256 (GRCm39) |
L232F |
probably benign |
Het |
Gpr149 |
T |
A |
3: 62,502,356 (GRCm39) |
D500V |
probably benign |
Het |
Gpx8 |
T |
A |
13: 113,182,035 (GRCm39) |
T133S |
probably benign |
Het |
Hdlbp |
A |
T |
1: 93,351,092 (GRCm39) |
I542N |
probably damaging |
Het |
Hid1 |
G |
A |
11: 115,246,187 (GRCm39) |
S361F |
probably damaging |
Het |
Igdcc4 |
C |
A |
9: 65,041,801 (GRCm39) |
A1076E |
probably benign |
Het |
Il4ra |
A |
G |
7: 125,164,845 (GRCm39) |
K7E |
probably benign |
Het |
Inka2 |
T |
C |
3: 105,623,730 (GRCm39) |
C35R |
probably damaging |
Het |
Itga9 |
G |
T |
9: 118,706,294 (GRCm39) |
|
probably null |
Het |
Kif5c |
T |
C |
2: 49,591,095 (GRCm39) |
S316P |
probably damaging |
Het |
Kmt5c |
A |
T |
7: 4,749,158 (GRCm39) |
T264S |
probably damaging |
Het |
Litafd |
A |
G |
16: 8,501,681 (GRCm39) |
H61R |
|
Het |
Lrrc18 |
A |
G |
14: 32,731,052 (GRCm39) |
N197S |
probably benign |
Het |
Mcoln1 |
C |
A |
8: 3,558,356 (GRCm39) |
D203E |
probably benign |
Het |
Mitf |
T |
C |
6: 97,990,671 (GRCm39) |
V358A |
probably damaging |
Het |
Mki67 |
A |
T |
7: 135,294,816 (GRCm39) |
L3161Q |
possibly damaging |
Het |
Mmp20 |
T |
A |
9: 7,644,076 (GRCm39) |
F255I |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,566,946 (GRCm39) |
T1858A |
unknown |
Het |
Mug1 |
G |
A |
6: 121,828,424 (GRCm39) |
V279I |
probably benign |
Het |
Or6c68 |
T |
C |
10: 129,157,665 (GRCm39) |
Y58H |
probably damaging |
Het |
Otulin |
G |
T |
15: 27,630,580 (GRCm39) |
A39E |
probably benign |
Het |
Pcdh17 |
A |
T |
14: 84,685,924 (GRCm39) |
D797V |
possibly damaging |
Het |
Pdlim5 |
G |
A |
3: 142,018,154 (GRCm39) |
S147L |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Ppp2r1a |
T |
G |
17: 21,182,003 (GRCm39) |
|
probably null |
Het |
Ranbp6 |
T |
C |
19: 29,789,813 (GRCm39) |
I180V |
probably benign |
Het |
Rbm27 |
G |
T |
18: 42,465,921 (GRCm39) |
R869L |
probably damaging |
Het |
Rtn4r |
A |
G |
16: 17,969,349 (GRCm39) |
D259G |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,611,369 (GRCm39) |
E2271G |
probably damaging |
Het |
Sbk1 |
A |
G |
7: 125,891,208 (GRCm39) |
Y214C |
probably damaging |
Het |
Scg3 |
C |
T |
9: 75,551,149 (GRCm39) |
E459K |
probably damaging |
Het |
Scin |
T |
G |
12: 40,126,999 (GRCm39) |
E449D |
probably damaging |
Het |
Sel1l3 |
T |
C |
5: 53,297,166 (GRCm39) |
K760R |
probably benign |
Het |
Sh3pxd2a |
A |
G |
19: 47,308,753 (GRCm39) |
L145S |
possibly damaging |
Het |
Sh3yl1 |
A |
G |
12: 30,991,995 (GRCm39) |
D188G |
probably benign |
Het |
Slc38a1 |
A |
T |
15: 96,521,921 (GRCm39) |
L13Q |
possibly damaging |
Het |
Smyd4 |
T |
C |
11: 75,240,613 (GRCm39) |
I36T |
possibly damaging |
Het |
Spata31f1a |
A |
G |
4: 42,850,765 (GRCm39) |
S464P |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,790,056 (GRCm39) |
L570* |
probably null |
Het |
Tg |
G |
T |
15: 66,577,128 (GRCm39) |
A1484S |
probably benign |
Het |
Tm7sf2 |
A |
T |
19: 6,118,942 (GRCm39) |
N677K |
probably damaging |
Het |
Tmem235 |
T |
G |
11: 117,751,717 (GRCm39) |
L47R |
probably damaging |
Het |
Tmem87a |
A |
G |
2: 120,210,198 (GRCm39) |
S252P |
probably damaging |
Het |
Unc13b |
A |
G |
4: 43,217,075 (GRCm39) |
D458G |
probably benign |
Het |
Wfdc1 |
A |
G |
8: 120,406,770 (GRCm39) |
|
probably null |
Het |
Wnt16 |
A |
G |
6: 22,297,989 (GRCm39) |
Y285C |
probably damaging |
Het |
Wwc2 |
A |
T |
8: 48,309,270 (GRCm39) |
N837K |
unknown |
Het |
Xdh |
A |
G |
17: 74,229,467 (GRCm39) |
F329L |
probably benign |
Het |
Yaf2 |
G |
T |
15: 93,183,466 (GRCm39) |
H115N |
probably benign |
Het |
Zbtb16 |
G |
T |
9: 48,744,272 (GRCm39) |
N13K |
probably damaging |
Het |
Zfhx3 |
A |
T |
8: 109,677,695 (GRCm39) |
D2915V |
probably damaging |
Het |
Zfp236 |
A |
T |
18: 82,627,507 (GRCm39) |
V1564E |
possibly damaging |
Het |
Zfp407 |
G |
T |
18: 84,579,381 (GRCm39) |
H577Q |
not run |
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 |
|
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 |
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 |
|