Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
C |
T |
6: 91,911,591 (GRCm39) |
T613I |
probably benign |
Het |
Ankrd12 |
C |
T |
17: 66,292,355 (GRCm39) |
R1026K |
probably benign |
Het |
Apol7b |
T |
C |
15: 77,307,674 (GRCm39) |
T274A |
probably benign |
Het |
Arid4a |
A |
T |
12: 71,109,916 (GRCm39) |
R86* |
probably null |
Het |
Asnsd1 |
C |
T |
1: 53,387,417 (GRCm39) |
G70D |
probably damaging |
Het |
Atg4c |
T |
A |
4: 99,116,797 (GRCm39) |
V313D |
possibly damaging |
Het |
Atp13a5 |
A |
C |
16: 29,085,715 (GRCm39) |
C885G |
probably damaging |
Het |
Bpifb9a |
A |
T |
2: 154,104,183 (GRCm39) |
I209F |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,990,742 (GRCm39) |
D1670G |
probably damaging |
Het |
Cct8 |
T |
A |
16: 87,288,210 (GRCm39) |
I121F |
probably benign |
Het |
Cd209a |
T |
G |
8: 3,794,151 (GRCm39) |
D217A |
probably damaging |
Het |
Cdk19 |
C |
T |
10: 40,353,954 (GRCm39) |
S456L |
possibly damaging |
Het |
Chd9 |
C |
T |
8: 91,721,208 (GRCm39) |
H999Y |
unknown |
Het |
Col5a1 |
G |
A |
2: 27,841,395 (GRCm39) |
V339M |
unknown |
Het |
Cr2 |
G |
A |
1: 194,851,648 (GRCm39) |
R115* |
probably null |
Het |
Cyb561 |
A |
T |
11: 105,828,470 (GRCm39) |
F62I |
probably damaging |
Het |
Cyp2c38 |
A |
T |
19: 39,393,187 (GRCm39) |
N293K |
possibly damaging |
Het |
Cyp2c69 |
A |
T |
19: 39,848,342 (GRCm39) |
D293E |
probably damaging |
Het |
Dcbld2 |
T |
A |
16: 58,244,932 (GRCm39) |
C69S |
possibly damaging |
Het |
Dcdc2a |
T |
C |
13: 25,303,356 (GRCm39) |
S296P |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,027,024 (GRCm39) |
I2044K |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,347,098 (GRCm39) |
D2527G |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,126,413 (GRCm39) |
T1305A |
probably benign |
Het |
Dnajc9 |
A |
G |
14: 20,438,712 (GRCm39) |
V47A |
probably benign |
Het |
Dnmt3b |
A |
G |
2: 153,518,619 (GRCm39) |
Y594C |
probably damaging |
Het |
Dph7 |
A |
G |
2: 24,855,642 (GRCm39) |
D147G |
probably damaging |
Het |
Drap1 |
T |
C |
19: 5,473,380 (GRCm39) |
H164R |
possibly damaging |
Het |
Dsg3 |
T |
A |
18: 20,660,837 (GRCm39) |
V392E |
possibly damaging |
Het |
Dxo |
A |
G |
17: 35,056,616 (GRCm39) |
D81G |
probably benign |
Het |
E230025N22Rik |
G |
T |
18: 36,828,645 (GRCm39) |
T11K |
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,354,801 (GRCm39) |
V533A |
possibly damaging |
Het |
Etv3 |
T |
A |
3: 87,443,338 (GRCm39) |
C307* |
probably null |
Het |
Fam114a1 |
T |
A |
5: 65,187,402 (GRCm39) |
|
probably null |
Het |
Fam3c |
T |
A |
6: 22,326,404 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
G |
T |
2: 125,239,772 (GRCm39) |
T305K |
probably benign |
Het |
Ggt1 |
A |
T |
10: 75,421,428 (GRCm39) |
I484F |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,993,237 (GRCm39) |
D536G |
probably damaging |
Het |
Gpx4 |
T |
C |
10: 79,890,875 (GRCm39) |
I189T |
probably damaging |
Het |
Gsr |
T |
A |
8: 34,159,193 (GRCm39) |
C85S |
probably damaging |
Het |
Gsta5 |
A |
T |
9: 78,211,751 (GRCm39) |
D171V |
possibly damaging |
Het |
Havcr1 |
T |
A |
11: 46,661,369 (GRCm39) |
|
probably null |
Het |
Heatr4 |
T |
C |
12: 84,026,418 (GRCm39) |
T280A |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,313,923 (GRCm39) |
E3532D |
probably benign |
Het |
Hnrnpc |
T |
C |
14: 52,312,556 (GRCm39) |
N308S |
possibly damaging |
Het |
Ighv8-9 |
A |
G |
12: 115,432,358 (GRCm39) |
V13A |
probably benign |
Het |
Itgb2l |
A |
T |
16: 96,227,439 (GRCm39) |
F535I |
probably benign |
Het |
Kdm5a |
T |
G |
6: 120,404,803 (GRCm39) |
D1348E |
probably damaging |
Het |
Kndc1 |
CT |
C |
7: 139,503,691 (GRCm39) |
|
probably null |
Het |
Ky |
A |
G |
9: 102,419,528 (GRCm39) |
I512V |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,119,021 (GRCm39) |
F866Y |
possibly damaging |
Het |
Lbx1 |
C |
A |
19: 45,223,687 (GRCm39) |
|
probably benign |
Het |
Magel2 |
A |
G |
7: 62,028,658 (GRCm39) |
T521A |
possibly damaging |
Het |
Mgam |
A |
T |
6: 40,723,367 (GRCm39) |
I491L |
probably benign |
Het |
Mitd1 |
T |
C |
1: 37,929,273 (GRCm39) |
E40G |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 44,981,985 (GRCm39) |
T218A |
probably benign |
Het |
Mrpl42 |
A |
G |
10: 95,316,827 (GRCm39) |
S77P |
probably benign |
Het |
Mup5 |
C |
T |
4: 61,752,911 (GRCm39) |
W37* |
probably null |
Het |
Myh14 |
T |
C |
7: 44,281,850 (GRCm39) |
I803V |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,107,153 (GRCm39) |
T744S |
|
Het |
Ndufv3 |
A |
G |
17: 31,746,596 (GRCm39) |
D162G |
probably damaging |
Het |
Nostrin |
A |
G |
2: 69,006,150 (GRCm39) |
E278G |
probably damaging |
Het |
Nrxn1 |
T |
G |
17: 90,469,807 (GRCm39) |
E1288A |
probably benign |
Het |
Or4c11c |
A |
G |
2: 88,661,472 (GRCm39) |
N4D |
possibly damaging |
Het |
Or51b6b |
C |
A |
7: 103,310,088 (GRCm39) |
R123L |
probably damaging |
Het |
Or52h1 |
T |
A |
7: 103,828,955 (GRCm39) |
Y220F |
probably damaging |
Het |
Or8g55 |
A |
T |
9: 39,784,751 (GRCm39) |
Y60F |
possibly damaging |
Het |
Patj |
T |
A |
4: 98,312,737 (GRCm39) |
|
probably null |
Het |
Pcm1 |
T |
G |
8: 41,720,381 (GRCm39) |
I314R |
possibly damaging |
Het |
Pcsk6 |
A |
G |
7: 65,683,646 (GRCm39) |
T754A |
probably benign |
Het |
Pde2a |
A |
T |
7: 101,152,041 (GRCm39) |
N326I |
probably benign |
Het |
Plekhg4 |
T |
C |
8: 106,105,316 (GRCm39) |
S594P |
possibly damaging |
Het |
Plekhm3 |
T |
C |
1: 64,977,065 (GRCm39) |
D135G |
probably damaging |
Het |
Plin4 |
A |
T |
17: 56,413,776 (GRCm39) |
M283K |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 44,990,172 (GRCm39) |
|
probably null |
Het |
Prdm9 |
T |
C |
17: 15,775,914 (GRCm39) |
N179S |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,471,449 (GRCm39) |
S908G |
probably damaging |
Het |
Psg22 |
C |
A |
7: 18,456,660 (GRCm39) |
S181Y |
possibly damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rp1l1 |
T |
A |
14: 64,269,023 (GRCm39) |
C1536* |
probably null |
Het |
Rpp25l |
T |
C |
4: 41,712,529 (GRCm39) |
H82R |
probably damaging |
Het |
Rps3a1 |
T |
A |
3: 86,046,396 (GRCm39) |
M172L |
probably benign |
Het |
Rtbdn |
T |
C |
8: 85,679,556 (GRCm39) |
L110P |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,778,010 (GRCm39) |
Q2169L |
probably damaging |
Het |
Scn4a |
A |
T |
11: 106,211,299 (GRCm39) |
C1573S |
possibly damaging |
Het |
Sec16b |
A |
T |
1: 157,358,965 (GRCm39) |
|
probably null |
Het |
Serpina1a |
A |
T |
12: 103,820,096 (GRCm39) |
D383E |
possibly damaging |
Het |
Sh3gl3 |
T |
C |
7: 81,934,285 (GRCm39) |
M262T |
probably benign |
Het |
Sos2 |
G |
A |
12: 69,637,654 (GRCm39) |
T1052M |
probably damaging |
Het |
Spag16 |
G |
A |
1: 70,036,000 (GRCm39) |
V343I |
probably benign |
Het |
Spocd1 |
T |
G |
4: 129,823,957 (GRCm39) |
D251E |
|
Het |
Stc2 |
G |
T |
11: 31,317,798 (GRCm39) |
N74K |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,623,621 (GRCm39) |
Y2110H |
probably damaging |
Het |
Thbs3 |
C |
T |
3: 89,126,359 (GRCm39) |
Q227* |
probably null |
Het |
Tmem92 |
A |
C |
11: 94,669,816 (GRCm39) |
I105R |
probably benign |
Het |
Tmod1 |
T |
A |
4: 46,083,632 (GRCm39) |
N20K |
probably benign |
Het |
Tns1 |
T |
C |
1: 73,992,638 (GRCm39) |
D53G |
probably damaging |
Het |
Tspan33 |
T |
A |
6: 29,717,337 (GRCm39) |
L246Q |
probably damaging |
Het |
Ttc16 |
A |
G |
2: 32,658,980 (GRCm39) |
L392P |
probably damaging |
Het |
Uggt1 |
T |
A |
1: 36,224,919 (GRCm39) |
T572S |
probably benign |
Het |
Usp17la |
A |
T |
7: 104,509,604 (GRCm39) |
T70S |
probably damaging |
Het |
Usp31 |
C |
T |
7: 121,274,186 (GRCm39) |
R370H |
probably damaging |
Het |
Wdr83 |
C |
T |
8: 85,806,463 (GRCm39) |
V112M |
probably damaging |
Het |
Zbtb25 |
T |
A |
12: 76,416,366 (GRCm39) |
|
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,583,267 (GRCm39) |
N638K |
possibly damaging |
Het |
Zfp747l1 |
T |
A |
7: 126,984,455 (GRCm39) |
S216C |
probably benign |
Het |
Zfp820 |
T |
C |
17: 22,037,994 (GRCm39) |
T445A |
probably benign |
Het |
|