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 |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly 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 |
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 Egf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Egf
|
APN |
3 |
129,505,098 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00579:Egf
|
APN |
3 |
129,491,447 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01307:Egf
|
APN |
3 |
129,533,642 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01314:Egf
|
APN |
3 |
129,479,909 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01360:Egf
|
APN |
3 |
129,533,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Egf
|
APN |
3 |
129,496,104 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01610:Egf
|
APN |
3 |
129,499,909 (GRCm39) |
splice site |
probably benign |
|
IGL01721:Egf
|
APN |
3 |
129,491,371 (GRCm39) |
nonsense |
probably null |
|
IGL01803:Egf
|
APN |
3 |
129,530,415 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01866:Egf
|
APN |
3 |
129,529,529 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02001:Egf
|
APN |
3 |
129,510,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Egf
|
APN |
3 |
129,533,631 (GRCm39) |
nonsense |
probably null |
|
IGL02209:Egf
|
APN |
3 |
129,500,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02347:Egf
|
APN |
3 |
129,472,026 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02821:Egf
|
APN |
3 |
129,496,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Egf
|
APN |
3 |
129,474,796 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03114:Egf
|
APN |
3 |
129,530,529 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4151001:Egf
|
UTSW |
3 |
129,496,198 (GRCm39) |
missense |
probably benign |
0.00 |
R0200:Egf
|
UTSW |
3 |
129,531,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Egf
|
UTSW |
3 |
129,499,882 (GRCm39) |
missense |
probably benign |
0.00 |
R0463:Egf
|
UTSW |
3 |
129,531,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Egf
|
UTSW |
3 |
129,499,882 (GRCm39) |
missense |
probably benign |
0.00 |
R0507:Egf
|
UTSW |
3 |
129,474,828 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0801:Egf
|
UTSW |
3 |
129,496,234 (GRCm39) |
splice site |
probably benign |
|
R1495:Egf
|
UTSW |
3 |
129,506,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Egf
|
UTSW |
3 |
129,484,427 (GRCm39) |
missense |
probably benign |
0.00 |
R1626:Egf
|
UTSW |
3 |
129,479,864 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1702:Egf
|
UTSW |
3 |
129,484,460 (GRCm39) |
missense |
probably benign |
0.17 |
R1906:Egf
|
UTSW |
3 |
129,518,873 (GRCm39) |
missense |
probably benign |
0.01 |
R2184:Egf
|
UTSW |
3 |
129,517,007 (GRCm39) |
nonsense |
probably null |
|
R3842:Egf
|
UTSW |
3 |
129,491,442 (GRCm39) |
nonsense |
probably null |
|
R3918:Egf
|
UTSW |
3 |
129,490,509 (GRCm39) |
missense |
probably null |
0.22 |
R4073:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4074:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4075:Egf
|
UTSW |
3 |
129,529,618 (GRCm39) |
missense |
probably benign |
0.01 |
R4307:Egf
|
UTSW |
3 |
129,512,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R4321:Egf
|
UTSW |
3 |
129,499,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R4617:Egf
|
UTSW |
3 |
129,484,442 (GRCm39) |
missense |
probably benign |
0.02 |
R4674:Egf
|
UTSW |
3 |
129,511,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Egf
|
UTSW |
3 |
129,510,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Egf
|
UTSW |
3 |
129,505,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Egf
|
UTSW |
3 |
129,505,179 (GRCm39) |
splice site |
probably null |
|
R5166:Egf
|
UTSW |
3 |
129,529,489 (GRCm39) |
missense |
probably benign |
|
R5179:Egf
|
UTSW |
3 |
129,479,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R5230:Egf
|
UTSW |
3 |
129,511,673 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6043:Egf
|
UTSW |
3 |
129,530,434 (GRCm39) |
missense |
probably benign |
0.09 |
R6119:Egf
|
UTSW |
3 |
129,530,421 (GRCm39) |
missense |
probably benign |
0.00 |
R6493:Egf
|
UTSW |
3 |
129,512,737 (GRCm39) |
start gained |
probably benign |
|
R6639:Egf
|
UTSW |
3 |
129,530,481 (GRCm39) |
missense |
probably benign |
0.22 |
R6936:Egf
|
UTSW |
3 |
129,474,853 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7019:Egf
|
UTSW |
3 |
129,511,713 (GRCm39) |
splice site |
probably null |
|
R7046:Egf
|
UTSW |
3 |
129,548,607 (GRCm39) |
missense |
unknown |
|
R7463:Egf
|
UTSW |
3 |
129,533,664 (GRCm39) |
missense |
probably benign |
0.39 |
R7472:Egf
|
UTSW |
3 |
129,479,912 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7723:Egf
|
UTSW |
3 |
129,499,786 (GRCm39) |
missense |
probably benign |
0.00 |
R7920:Egf
|
UTSW |
3 |
129,529,489 (GRCm39) |
missense |
probably benign |
|
R7952:Egf
|
UTSW |
3 |
129,533,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Egf
|
UTSW |
3 |
129,484,486 (GRCm39) |
missense |
probably benign |
0.09 |
R8344:Egf
|
UTSW |
3 |
129,548,592 (GRCm39) |
missense |
unknown |
|
R8557:Egf
|
UTSW |
3 |
129,548,600 (GRCm39) |
missense |
unknown |
|
R8912:Egf
|
UTSW |
3 |
129,531,164 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9091:Egf
|
UTSW |
3 |
129,529,449 (GRCm39) |
critical splice donor site |
probably null |
|
R9159:Egf
|
UTSW |
3 |
129,472,026 (GRCm39) |
missense |
probably benign |
0.17 |
R9270:Egf
|
UTSW |
3 |
129,529,449 (GRCm39) |
critical splice donor site |
probably null |
|
R9526:Egf
|
UTSW |
3 |
129,491,421 (GRCm39) |
missense |
probably benign |
|
R9544:Egf
|
UTSW |
3 |
129,511,617 (GRCm39) |
missense |
probably benign |
0.16 |
R9588:Egf
|
UTSW |
3 |
129,511,617 (GRCm39) |
missense |
probably benign |
0.16 |
R9630:Egf
|
UTSW |
3 |
129,518,844 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9639:Egf
|
UTSW |
3 |
129,513,949 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9751:Egf
|
UTSW |
3 |
129,548,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R9772:Egf
|
UTSW |
3 |
129,499,756 (GRCm39) |
missense |
probably benign |
0.01 |
R9776:Egf
|
UTSW |
3 |
129,530,514 (GRCm39) |
missense |
probably damaging |
0.99 |
X0011:Egf
|
UTSW |
3 |
129,504,947 (GRCm39) |
missense |
probably benign |
0.19 |
Z1176:Egf
|
UTSW |
3 |
129,491,366 (GRCm39) |
critical splice donor site |
probably null |
|
|