Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
ACCAGCCC |
ACC |
14: 118,615,270 |
|
probably null |
Het |
Abhd14b |
T |
C |
9: 106,451,620 |
Y147H |
probably damaging |
Het |
Adam26b |
C |
A |
8: 43,521,695 |
R90L |
probably benign |
Het |
Agt |
A |
T |
8: 124,564,550 |
M6K |
probably benign |
Het |
Akr1c14 |
T |
C |
13: 4,059,644 |
S5P |
probably benign |
Het |
Cabp5 |
A |
G |
7: 13,400,733 |
D31G |
probably benign |
Het |
Cacna1h |
T |
A |
17: 25,385,805 |
D1178V |
probably damaging |
Het |
Ccdc88a |
A |
T |
11: 29,482,381 |
E1199D |
probably damaging |
Het |
Cd244 |
A |
T |
1: 171,577,305 |
I242F |
probably benign |
Het |
Clpb |
G |
T |
7: 101,722,717 |
R220L |
probably damaging |
Het |
Cltc |
C |
T |
11: 86,719,493 |
R638H |
probably damaging |
Het |
Cnr1 |
A |
T |
4: 33,944,892 |
M427L |
probably benign |
Het |
Ctnnbl1 |
C |
T |
2: 157,737,470 |
|
probably benign |
Het |
Epb41l2 |
A |
T |
10: 25,493,573 |
T597S |
probably benign |
Het |
Epb41l3 |
T |
C |
17: 69,238,426 |
Y163H |
probably damaging |
Het |
Fam129b |
A |
G |
2: 32,919,832 |
T314A |
possibly damaging |
Het |
Fgg |
A |
G |
3: 83,013,126 |
|
probably null |
Het |
Gm37240 |
A |
T |
3: 84,509,925 |
D162E |
possibly damaging |
Het |
Gm44511 |
T |
A |
6: 128,820,277 |
T83S |
probably benign |
Het |
Gm6685 |
T |
A |
11: 28,339,252 |
Y188F |
probably benign |
Het |
Gprin2 |
A |
T |
14: 34,195,613 |
C67S |
probably benign |
Het |
Grk6 |
A |
G |
13: 55,451,007 |
D140G |
probably benign |
Het |
Hps3 |
T |
C |
3: 20,018,808 |
|
probably null |
Het |
Hspb7 |
T |
C |
4: 141,424,024 |
V159A |
possibly damaging |
Het |
Ibsp |
A |
G |
5: 104,306,005 |
N70D |
probably benign |
Het |
Ibsp |
A |
G |
5: 104,310,184 |
N196D |
probably damaging |
Het |
Igfn1 |
A |
T |
1: 135,982,405 |
F147Y |
possibly damaging |
Het |
Iqca |
T |
G |
1: 90,077,810 |
D492A |
possibly damaging |
Het |
Klhl42 |
T |
C |
6: 147,091,860 |
L110P |
possibly damaging |
Het |
Krt12 |
C |
T |
11: 99,418,026 |
R395Q |
probably damaging |
Het |
Lig4 |
A |
T |
8: 9,973,629 |
H50Q |
possibly damaging |
Het |
Mttp |
A |
C |
3: 138,103,112 |
L730R |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,660,507 |
I239L |
unknown |
Het |
Myo15 |
T |
C |
11: 60,509,149 |
F1723L |
|
Het |
Nin |
T |
C |
12: 70,043,230 |
D1137G |
|
Het |
Nsf |
C |
T |
11: 103,928,839 |
V35M |
probably damaging |
Het |
Numa1 |
T |
A |
7: 101,999,000 |
I646K |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,804,504 |
N477S |
probably damaging |
Het |
Olfr59 |
T |
A |
11: 74,288,763 |
V39E |
probably damaging |
Het |
P4ha3 |
A |
G |
7: 100,285,717 |
D62G |
probably damaging |
Het |
Palb2 |
G |
T |
7: 122,128,415 |
D77E |
probably benign |
Het |
Pcmtd2 |
T |
C |
2: 181,851,701 |
V233A |
probably benign |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,218,068 |
|
probably benign |
Het |
Pgr |
C |
T |
9: 8,946,855 |
T699I |
possibly damaging |
Het |
Pknox2 |
C |
A |
9: 36,895,306 |
|
probably null |
Het |
Ppp2r3d |
T |
C |
9: 124,439,087 |
H110R |
|
Het |
Psmd11 |
T |
A |
11: 80,434,582 |
|
probably benign |
Het |
Pyroxd2 |
T |
C |
19: 42,747,562 |
N59S |
probably benign |
Het |
Qser1 |
A |
T |
2: 104,758,576 |
D1662E |
possibly damaging |
Het |
Rasip1 |
A |
G |
7: 45,628,815 |
Y180C |
probably damaging |
Het |
Rbl1 |
T |
C |
2: 157,191,980 |
S393G |
probably benign |
Het |
Rtn4r |
C |
T |
16: 18,151,289 |
P194S |
probably benign |
Het |
Ryr1 |
C |
T |
7: 29,098,785 |
G944D |
probably damaging |
Het |
Scamp3 |
A |
G |
3: 89,177,991 |
D23G |
probably damaging |
Het |
Secisbp2l |
CTGGG |
C |
2: 125,771,545 |
|
probably benign |
Het |
Shcbp1 |
A |
G |
8: 4,739,232 |
I529T |
probably damaging |
Het |
Slc5a10 |
T |
A |
11: 61,673,647 |
D502V |
probably damaging |
Het |
Smad5 |
T |
C |
13: 56,733,042 |
I323T |
possibly damaging |
Het |
Spred1 |
T |
C |
2: 117,177,449 |
S279P |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,944,827 |
V949D |
possibly damaging |
Het |
Stxbp3 |
A |
G |
3: 108,800,828 |
S386P |
probably benign |
Het |
Syt14 |
A |
G |
1: 192,984,324 |
S91P |
unknown |
Het |
Thpo |
C |
T |
16: 20,725,651 |
A211T |
probably benign |
Het |
Tns1 |
T |
A |
1: 73,953,371 |
D716V |
probably damaging |
Het |
Trbv26 |
A |
G |
6: 41,227,547 |
Y8C |
probably benign |
Het |
Tshr |
A |
G |
12: 91,538,270 |
I661V |
probably damaging |
Het |
Uvrag |
G |
A |
7: 98,979,721 |
P380S |
probably damaging |
Het |
Vkorc1 |
G |
T |
7: 127,894,524 |
Y88* |
probably null |
Het |
Vmn1r63 |
C |
T |
7: 5,803,370 |
V88M |
probably damaging |
Het |
Wdsub1 |
A |
G |
2: 59,878,419 |
Y37H |
probably damaging |
Het |
Zap70 |
A |
G |
1: 36,770,902 |
D31G |
probably benign |
Het |
Zc3h12d |
G |
A |
10: 7,867,626 |
A387T |
probably benign |
Het |
Zfp438 |
C |
T |
18: 5,213,377 |
R527H |
possibly damaging |
Het |
|