Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
A |
C |
2: 152,282,744 (GRCm39) |
N200H |
probably damaging |
Het |
Abca17 |
T |
A |
17: 24,547,720 (GRCm39) |
D218V |
probably damaging |
Het |
Ap1b1 |
T |
C |
11: 4,973,135 (GRCm39) |
V326A |
possibly damaging |
Het |
Chrna3 |
C |
T |
9: 54,923,334 (GRCm39) |
C158Y |
probably damaging |
Het |
Cnnm3 |
T |
A |
1: 36,560,303 (GRCm39) |
S608T |
probably damaging |
Het |
Cnot1 |
T |
C |
8: 96,470,906 (GRCm39) |
E1314G |
possibly damaging |
Het |
Cobll1 |
A |
T |
2: 64,937,394 (GRCm39) |
M406K |
probably benign |
Het |
Cyp2d34 |
T |
C |
15: 82,501,767 (GRCm39) |
K248E |
probably benign |
Het |
Dcdc2a |
A |
C |
13: 25,286,340 (GRCm39) |
I125L |
probably benign |
Het |
Dgat1 |
G |
A |
15: 76,386,721 (GRCm39) |
L439F |
probably benign |
Het |
Disc1 |
T |
A |
8: 125,862,043 (GRCm39) |
S472T |
probably damaging |
Het |
Dnajb3 |
C |
A |
1: 88,132,773 (GRCm39) |
V210F |
probably benign |
Het |
Fancd2 |
A |
G |
6: 113,570,230 (GRCm39) |
S1394G |
possibly damaging |
Het |
Fasn |
A |
T |
11: 120,698,765 (GRCm39) |
L2475Q |
probably damaging |
Het |
Fn1 |
A |
T |
1: 71,632,242 (GRCm39) |
C2335S |
probably damaging |
Het |
Gpld1 |
T |
C |
13: 25,127,603 (GRCm39) |
S2P |
unknown |
Het |
Gpld1 |
G |
T |
13: 25,140,146 (GRCm39) |
|
probably null |
Het |
Gsc2 |
G |
A |
16: 17,732,364 (GRCm39) |
R137W |
probably damaging |
Het |
Gsdme |
T |
C |
6: 50,228,343 (GRCm39) |
R42G |
probably damaging |
Het |
Gtf3c5 |
T |
C |
2: 28,469,548 (GRCm39) |
T119A |
probably damaging |
Het |
Hs6st3 |
T |
C |
14: 120,106,389 (GRCm39) |
S266P |
probably damaging |
Het |
Htr2a |
T |
C |
14: 74,943,262 (GRCm39) |
F281L |
probably benign |
Het |
Hus1b |
T |
C |
13: 31,131,236 (GRCm39) |
K141R |
probably benign |
Het |
Ireb2 |
T |
C |
9: 54,793,230 (GRCm39) |
|
probably null |
Het |
Klhdc7a |
T |
A |
4: 139,693,024 (GRCm39) |
Y641F |
probably benign |
Het |
Kri1 |
T |
C |
9: 21,193,190 (GRCm39) |
E57G |
possibly damaging |
Het |
Map4 |
A |
G |
9: 109,828,860 (GRCm39) |
T82A |
probably benign |
Het |
Mthfr |
T |
G |
4: 148,136,061 (GRCm39) |
M353R |
probably benign |
Het |
Mtus2 |
A |
G |
5: 148,240,083 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
T |
A |
7: 141,346,473 (GRCm39) |
|
probably null |
Het |
Myo15a |
T |
A |
11: 60,370,186 (GRCm39) |
|
probably null |
Het |
Nynrin |
A |
T |
14: 56,101,044 (GRCm39) |
Q278L |
possibly damaging |
Het |
Pced1b |
T |
G |
15: 97,282,423 (GRCm39) |
|
probably null |
Het |
Penk |
T |
C |
4: 4,134,152 (GRCm39) |
D165G |
probably damaging |
Het |
Pfkm |
T |
A |
15: 98,016,090 (GRCm39) |
V90D |
probably damaging |
Het |
Pgk2 |
T |
A |
17: 40,519,134 (GRCm39) |
D98V |
probably damaging |
Het |
Psg28 |
C |
A |
7: 18,160,348 (GRCm39) |
A283S |
possibly damaging |
Het |
Rgl3 |
A |
G |
9: 21,892,070 (GRCm39) |
L338P |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,465 (GRCm39) |
I149N |
probably damaging |
Het |
Ros1 |
T |
C |
10: 51,927,077 (GRCm39) |
H2181R |
probably benign |
Het |
Slc38a11 |
C |
T |
2: 65,160,679 (GRCm39) |
C305Y |
probably damaging |
Het |
Speg |
T |
A |
1: 75,378,186 (GRCm39) |
V798E |
probably damaging |
Het |
Spesp1 |
G |
A |
9: 62,189,376 (GRCm39) |
|
probably benign |
Het |
Styk1 |
A |
T |
6: 131,286,975 (GRCm39) |
Y84* |
probably null |
Het |
Syt2 |
T |
C |
1: 134,669,599 (GRCm39) |
L80P |
possibly damaging |
Het |
Tra2a |
C |
T |
6: 49,222,446 (GRCm39) |
|
probably benign |
Het |
Trim10 |
T |
A |
17: 37,182,580 (GRCm39) |
C149S |
probably damaging |
Het |
Vmn2r38 |
T |
C |
7: 9,097,689 (GRCm39) |
T135A |
probably benign |
Het |
Wipf1 |
A |
G |
2: 73,267,834 (GRCm39) |
V188A |
possibly damaging |
Het |
Yipf2 |
G |
A |
9: 21,501,197 (GRCm39) |
A67V |
probably benign |
Het |
Zfp759 |
A |
G |
13: 67,286,719 (GRCm39) |
E96G |
probably benign |
Het |
Zic3 |
G |
A |
X: 57,076,838 (GRCm39) |
V100M |
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 |
|
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 |
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 |
|