Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700031F05Rik |
G |
T |
X: 101,904,515 (GRCm39) |
N132K |
possibly damaging |
Het |
2010315B03Rik |
T |
A |
9: 124,056,228 (GRCm39) |
Y232F |
probably benign |
Het |
Acadl |
A |
T |
1: 66,870,602 (GRCm39) |
S428R |
probably benign |
Het |
Adamts10 |
A |
G |
17: 33,764,529 (GRCm39) |
D683G |
probably damaging |
Het |
Angptl4 |
G |
A |
17: 34,000,273 (GRCm39) |
P32S |
probably benign |
Het |
Apob |
A |
G |
12: 8,062,759 (GRCm39) |
N134S |
probably benign |
Het |
Atr |
G |
A |
9: 95,753,250 (GRCm39) |
|
probably null |
Het |
B4galnt1 |
G |
A |
10: 127,003,705 (GRCm39) |
V223M |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
C1galt1c1 |
A |
T |
X: 37,720,349 (GRCm39) |
S216T |
probably benign |
Het |
C2cd3 |
A |
C |
7: 100,021,657 (GRCm39) |
|
probably benign |
Het |
Clca4b |
A |
C |
3: 144,634,286 (GRCm39) |
H102Q |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,039,473 (GRCm39) |
I557T |
probably damaging |
Het |
Col26a1 |
G |
A |
5: 136,876,404 (GRCm39) |
S72F |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 15,982,511 (GRCm39) |
I2719V |
possibly damaging |
Het |
Cul9 |
C |
T |
17: 46,849,943 (GRCm39) |
W502* |
probably null |
Het |
Dazl |
A |
T |
17: 50,595,183 (GRCm39) |
F84I |
probably damaging |
Het |
Dcaf1 |
G |
T |
9: 106,724,006 (GRCm39) |
R478L |
probably benign |
Het |
Dock5 |
T |
G |
14: 68,080,228 (GRCm39) |
I198L |
probably benign |
Het |
Dock9 |
A |
T |
14: 121,823,658 (GRCm39) |
L1428H |
probably damaging |
Het |
Dync1li1 |
T |
A |
9: 114,538,237 (GRCm39) |
V198E |
probably damaging |
Het |
Egf |
A |
T |
3: 129,513,925 (GRCm39) |
C429S |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,781,696 (GRCm39) |
E7G |
probably null |
Het |
Ercc4 |
G |
T |
16: 12,965,438 (GRCm39) |
R690L |
probably damaging |
Het |
Erich5 |
T |
C |
15: 34,471,112 (GRCm39) |
C114R |
possibly damaging |
Het |
Etv1 |
T |
C |
12: 38,915,685 (GRCm39) |
S428P |
possibly damaging |
Het |
Fbxo31 |
G |
T |
8: 122,286,755 (GRCm39) |
F174L |
probably benign |
Het |
Fbxo33 |
T |
A |
12: 59,251,217 (GRCm39) |
I433L |
probably benign |
Het |
Fez2 |
A |
T |
17: 78,720,357 (GRCm39) |
V99E |
probably damaging |
Het |
Gabarapl2 |
A |
C |
8: 112,669,185 (GRCm39) |
K48Q |
probably damaging |
Het |
Gfi1b |
T |
A |
2: 28,500,149 (GRCm39) |
H294L |
probably damaging |
Het |
Gk2 |
A |
G |
5: 97,604,056 (GRCm39) |
S261P |
probably damaging |
Het |
Gpr158 |
T |
C |
2: 21,831,864 (GRCm39) |
I988T |
probably benign |
Het |
Grk3 |
G |
C |
5: 113,077,586 (GRCm39) |
H394D |
probably benign |
Het |
Grm6 |
A |
G |
11: 50,748,033 (GRCm39) |
E381G |
probably benign |
Het |
Gtf3c1 |
A |
T |
7: 125,258,266 (GRCm39) |
M1268K |
possibly damaging |
Het |
Hikeshi |
A |
T |
7: 89,572,854 (GRCm39) |
I113N |
probably damaging |
Het |
Hmg20b |
T |
A |
10: 81,184,416 (GRCm39) |
Q129L |
probably damaging |
Het |
Hunk |
C |
A |
16: 90,272,791 (GRCm39) |
T365K |
probably damaging |
Het |
Ints15 |
A |
T |
5: 143,293,740 (GRCm39) |
W246R |
probably damaging |
Het |
Kdm5a |
T |
G |
6: 120,351,938 (GRCm39) |
V176G |
possibly damaging |
Het |
Kif2a |
T |
A |
13: 107,098,693 (GRCm39) |
E691V |
probably damaging |
Het |
Ly6e |
T |
C |
15: 74,830,510 (GRCm39) |
|
probably null |
Het |
Map1b |
G |
T |
13: 99,568,977 (GRCm39) |
P1248Q |
unknown |
Het |
Mettl25 |
A |
G |
10: 105,662,416 (GRCm39) |
S185P |
probably damaging |
Het |
Mfap3l |
T |
A |
8: 61,124,184 (GRCm39) |
V142D |
probably damaging |
Het |
Mip |
T |
A |
10: 128,062,922 (GRCm39) |
H122Q |
probably benign |
Het |
Mkx |
G |
A |
18: 6,992,040 (GRCm39) |
T280I |
probably benign |
Het |
Msi1 |
A |
T |
5: 115,589,514 (GRCm39) |
|
probably null |
Het |
Mtcl2 |
T |
C |
2: 156,862,426 (GRCm39) |
E1501G |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,416,377 (GRCm39) |
M3108V |
probably benign |
Het |
Mybl1 |
A |
G |
1: 9,742,511 (GRCm39) |
S625P |
probably damaging |
Het |
Myo7b |
C |
A |
18: 32,127,422 (GRCm39) |
V627F |
probably benign |
Het |
Ndst3 |
A |
T |
3: 123,465,684 (GRCm39) |
I96N |
probably damaging |
Het |
Nrp1 |
A |
T |
8: 129,184,425 (GRCm39) |
T357S |
probably benign |
Het |
Obscn |
G |
T |
11: 59,015,396 (GRCm39) |
Y1050* |
probably null |
Het |
Or2ak7 |
A |
G |
11: 58,575,556 (GRCm39) |
N286D |
probably damaging |
Het |
Or2d4 |
A |
T |
7: 106,543,547 (GRCm39) |
N220K |
probably benign |
Het |
Or2y1c |
A |
C |
11: 49,361,451 (GRCm39) |
I158L |
probably benign |
Het |
Or4c107 |
T |
A |
2: 88,789,556 (GRCm39) |
F249I |
probably damaging |
Het |
Or5d47 |
A |
T |
2: 87,804,142 (GRCm39) |
I289K |
probably benign |
Het |
Or5i1 |
T |
C |
2: 87,613,565 (GRCm39) |
V227A |
possibly damaging |
Het |
Otof |
T |
C |
5: 30,540,914 (GRCm39) |
E875G |
possibly damaging |
Het |
Pick1 |
A |
T |
15: 79,133,137 (GRCm39) |
D399V |
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,665,744 (GRCm39) |
S22T |
probably benign |
Het |
Pnpla2 |
A |
G |
7: 141,038,574 (GRCm39) |
E276G |
possibly damaging |
Het |
Pomk |
A |
T |
8: 26,473,633 (GRCm39) |
S107T |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,765 (GRCm39) |
D283E |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,030,962 (GRCm39) |
D1462G |
probably damaging |
Het |
Rnf112 |
T |
A |
11: 61,342,936 (GRCm39) |
E230V |
probably damaging |
Het |
Rock1 |
T |
C |
18: 10,112,391 (GRCm39) |
T455A |
probably benign |
Het |
Rtp4 |
A |
T |
16: 23,428,790 (GRCm39) |
M18L |
probably benign |
Het |
Scaf11 |
A |
T |
15: 96,317,981 (GRCm39) |
|
probably null |
Het |
Schip1 |
T |
C |
3: 67,972,297 (GRCm39) |
V8A |
probably benign |
Het |
Sec31b |
T |
C |
19: 44,515,060 (GRCm39) |
H351R |
probably benign |
Het |
Sh3bp5l |
A |
G |
11: 58,237,177 (GRCm39) |
D378G |
probably benign |
Het |
Sowahb |
T |
C |
5: 93,190,715 (GRCm39) |
D668G |
probably damaging |
Het |
Spam1 |
A |
G |
6: 24,800,586 (GRCm39) |
T442A |
probably benign |
Het |
Syt14 |
T |
A |
1: 192,615,633 (GRCm39) |
Y451F |
probably damaging |
Het |
Tafa5 |
T |
G |
15: 87,604,783 (GRCm39) |
S115A |
probably damaging |
Het |
Tdh |
A |
G |
14: 63,731,205 (GRCm39) |
L323P |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,193,843 (GRCm39) |
M197K |
probably benign |
Het |
Thbs1 |
G |
A |
2: 117,948,810 (GRCm39) |
A489T |
probably benign |
Het |
Tnfaip1 |
C |
T |
11: 78,420,008 (GRCm39) |
R88Q |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,973,612 (GRCm39) |
M252V |
probably benign |
Het |
Trdn |
G |
T |
10: 33,071,977 (GRCm39) |
E215* |
probably null |
Het |
Trim55 |
T |
C |
3: 19,725,286 (GRCm39) |
F268L |
probably benign |
Het |
Trmt112 |
T |
A |
19: 6,887,816 (GRCm39) |
V55E |
possibly damaging |
Het |
Tube1 |
A |
G |
10: 39,018,363 (GRCm39) |
M147V |
possibly damaging |
Het |
Ubn1 |
A |
G |
16: 4,895,851 (GRCm39) |
T966A |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,708,394 (GRCm39) |
I2651V |
probably benign |
Het |
Vmn1r172 |
G |
A |
7: 23,359,919 (GRCm39) |
R268H |
probably benign |
Het |
Vmn1r231 |
T |
A |
17: 21,110,571 (GRCm39) |
I115F |
probably damaging |
Het |
Vmn1r237 |
A |
G |
17: 21,534,400 (GRCm39) |
K41R |
probably benign |
Het |
Vmn2r58 |
A |
T |
7: 41,509,935 (GRCm39) |
N547K |
probably damaging |
Het |
Vmn2r74 |
T |
C |
7: 85,606,782 (GRCm39) |
D188G |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,415,079 (GRCm39) |
K367R |
probably damaging |
Het |
Washc4 |
T |
A |
10: 83,410,407 (GRCm39) |
M665K |
possibly damaging |
Het |
Wbp11 |
T |
A |
6: 136,798,189 (GRCm39) |
Y236F |
probably benign |
Het |
Wbp4 |
T |
A |
14: 79,709,801 (GRCm39) |
I145F |
possibly damaging |
Het |
Wwc2 |
C |
A |
8: 48,373,636 (GRCm39) |
D77Y |
probably damaging |
Het |
Zpld2 |
G |
A |
4: 133,929,459 (GRCm39) |
A282V |
probably benign |
Het |
|
Other mutations in Crocc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Crocc2
|
APN |
1 |
93,144,766 (GRCm39) |
nonsense |
probably null |
|
Popper
|
UTSW |
1 |
93,111,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0396:Crocc2
|
UTSW |
1 |
93,151,936 (GRCm39) |
splice site |
probably benign |
|
R1382:Crocc2
|
UTSW |
1 |
93,144,815 (GRCm39) |
critical splice donor site |
probably null |
|
R4608:Crocc2
|
UTSW |
1 |
93,096,516 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4609:Crocc2
|
UTSW |
1 |
93,096,516 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4619:Crocc2
|
UTSW |
1 |
93,141,372 (GRCm39) |
missense |
probably benign |
|
R4647:Crocc2
|
UTSW |
1 |
93,096,516 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4648:Crocc2
|
UTSW |
1 |
93,096,516 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4767:Crocc2
|
UTSW |
1 |
93,130,578 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4811:Crocc2
|
UTSW |
1 |
93,133,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R5046:Crocc2
|
UTSW |
1 |
93,133,624 (GRCm39) |
missense |
probably damaging |
0.96 |
R5389:Crocc2
|
UTSW |
1 |
93,143,363 (GRCm39) |
missense |
probably benign |
0.03 |
R5632:Crocc2
|
UTSW |
1 |
93,145,575 (GRCm39) |
missense |
probably damaging |
0.98 |
R5887:Crocc2
|
UTSW |
1 |
93,121,838 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6128:Crocc2
|
UTSW |
1 |
93,122,123 (GRCm39) |
missense |
probably benign |
0.28 |
R6142:Crocc2
|
UTSW |
1 |
93,118,201 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6258:Crocc2
|
UTSW |
1 |
93,141,360 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6260:Crocc2
|
UTSW |
1 |
93,141,360 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6288:Crocc2
|
UTSW |
1 |
93,122,227 (GRCm39) |
missense |
probably benign |
0.07 |
R6312:Crocc2
|
UTSW |
1 |
93,143,432 (GRCm39) |
nonsense |
probably null |
|
R6335:Crocc2
|
UTSW |
1 |
93,130,560 (GRCm39) |
missense |
probably benign |
0.02 |
R6339:Crocc2
|
UTSW |
1 |
93,141,754 (GRCm39) |
missense |
probably benign |
0.23 |
R6371:Crocc2
|
UTSW |
1 |
93,143,353 (GRCm39) |
missense |
probably benign |
0.10 |
R6439:Crocc2
|
UTSW |
1 |
93,111,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6442:Crocc2
|
UTSW |
1 |
93,112,775 (GRCm39) |
missense |
probably benign |
0.38 |
R6545:Crocc2
|
UTSW |
1 |
93,140,659 (GRCm39) |
missense |
probably benign |
0.45 |
R6619:Crocc2
|
UTSW |
1 |
93,118,223 (GRCm39) |
missense |
probably benign |
0.09 |
R6898:Crocc2
|
UTSW |
1 |
93,143,304 (GRCm39) |
missense |
probably benign |
0.06 |
R7170:Crocc2
|
UTSW |
1 |
93,121,704 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7378:Crocc2
|
UTSW |
1 |
93,121,809 (GRCm39) |
missense |
probably damaging |
0.98 |
R7395:Crocc2
|
UTSW |
1 |
93,143,829 (GRCm39) |
nonsense |
probably null |
|
R7461:Crocc2
|
UTSW |
1 |
93,122,311 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7613:Crocc2
|
UTSW |
1 |
93,122,311 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7831:Crocc2
|
UTSW |
1 |
93,143,195 (GRCm39) |
missense |
probably benign |
0.17 |
R7915:Crocc2
|
UTSW |
1 |
93,141,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Crocc2
|
UTSW |
1 |
93,130,578 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8171:Crocc2
|
UTSW |
1 |
93,116,723 (GRCm39) |
critical splice donor site |
probably null |
|
R8193:Crocc2
|
UTSW |
1 |
93,117,888 (GRCm39) |
splice site |
probably null |
|
R8494:Crocc2
|
UTSW |
1 |
93,144,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R8856:Crocc2
|
UTSW |
1 |
93,120,847 (GRCm39) |
missense |
probably benign |
0.41 |
R8918:Crocc2
|
UTSW |
1 |
93,129,144 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8970:Crocc2
|
UTSW |
1 |
93,116,687 (GRCm39) |
missense |
probably benign |
0.02 |
R9458:Crocc2
|
UTSW |
1 |
93,145,516 (GRCm39) |
missense |
probably damaging |
0.97 |
R9482:Crocc2
|
UTSW |
1 |
93,143,106 (GRCm39) |
missense |
probably benign |
0.32 |
R9522:Crocc2
|
UTSW |
1 |
93,117,429 (GRCm39) |
missense |
probably benign |
0.02 |
R9597:Crocc2
|
UTSW |
1 |
93,118,217 (GRCm39) |
missense |
probably benign |
0.26 |
R9703:Crocc2
|
UTSW |
1 |
93,130,444 (GRCm39) |
missense |
probably benign |
|
Z1177:Crocc2
|
UTSW |
1 |
93,154,414 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Crocc2
|
UTSW |
1 |
93,141,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|