Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr3 |
A |
T |
1: 125,322,874 (GRCm39) |
D364E |
probably benign |
Het |
Adra2c |
C |
T |
5: 35,437,423 (GRCm39) |
T65I |
probably damaging |
Het |
Agap2 |
T |
A |
10: 126,925,229 (GRCm39) |
|
probably null |
Het |
Ager |
T |
C |
17: 34,817,728 (GRCm39) |
V126A |
possibly damaging |
Het |
Arhgap39 |
T |
C |
15: 76,621,736 (GRCm39) |
I288M |
probably benign |
Het |
Arhgap45 |
A |
T |
10: 79,862,068 (GRCm39) |
S541C |
probably benign |
Het |
Asb4 |
A |
G |
6: 5,431,043 (GRCm39) |
Y426C |
probably damaging |
Het |
Azi2 |
C |
T |
9: 117,878,406 (GRCm39) |
T82I |
probably damaging |
Het |
Baz2b |
T |
A |
2: 59,778,567 (GRCm39) |
R764S |
probably damaging |
Het |
Ccdc146 |
A |
C |
5: 21,506,338 (GRCm39) |
I701S |
probably damaging |
Het |
Ccnq |
T |
C |
11: 78,642,056 (GRCm39) |
K145E |
probably damaging |
Het |
Cd55b |
T |
A |
1: 130,345,903 (GRCm39) |
I172F |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,718,647 (GRCm39) |
E199G |
probably benign |
Het |
Cntnap4 |
A |
T |
8: 113,478,921 (GRCm39) |
T216S |
possibly damaging |
Het |
D5Ertd579e |
A |
T |
5: 36,761,858 (GRCm39) |
N1336K |
possibly damaging |
Het |
Dlg5 |
T |
C |
14: 24,214,636 (GRCm39) |
N649S |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 49,979,653 (GRCm39) |
E96G |
probably benign |
Het |
Dscaml1 |
C |
T |
9: 45,579,458 (GRCm39) |
T335I |
possibly damaging |
Het |
Epb41l2 |
G |
T |
10: 25,378,022 (GRCm39) |
G695C |
probably damaging |
Het |
Erbb4 |
C |
T |
1: 68,599,735 (GRCm39) |
R114H |
probably damaging |
Het |
F2rl1 |
G |
T |
13: 95,650,446 (GRCm39) |
Y145* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,810,785 (GRCm39) |
Y2368F |
possibly damaging |
Het |
Galnt7 |
C |
T |
8: 57,989,612 (GRCm39) |
|
probably null |
Het |
Garre1 |
A |
T |
7: 33,941,802 (GRCm39) |
Y627* |
probably null |
Het |
Gm6811 |
T |
A |
17: 21,314,245 (GRCm39) |
|
noncoding transcript |
Het |
Gm6811 |
T |
G |
17: 21,314,952 (GRCm39) |
|
noncoding transcript |
Het |
H2-M1 |
G |
A |
17: 36,982,602 (GRCm39) |
T86M |
possibly damaging |
Het |
Hk2 |
T |
C |
6: 82,720,347 (GRCm39) |
D170G |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,614,432 (GRCm39) |
A1325T |
possibly damaging |
Het |
Insrr |
T |
A |
3: 87,707,826 (GRCm39) |
Y89* |
probably null |
Het |
Itga1 |
T |
C |
13: 115,117,388 (GRCm39) |
E871G |
probably benign |
Het |
Kat6a |
T |
C |
8: 23,429,421 (GRCm39) |
L1592P |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,500,979 (GRCm39) |
A756E |
probably benign |
Het |
Krt12 |
A |
T |
11: 99,312,728 (GRCm39) |
C105* |
probably null |
Het |
Lama1 |
G |
A |
17: 68,091,083 (GRCm39) |
|
probably null |
Het |
Lama3 |
A |
G |
18: 12,640,006 (GRCm39) |
N67S |
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,956,587 (GRCm39) |
|
probably null |
Het |
Lypd9 |
T |
A |
11: 58,337,192 (GRCm39) |
I94L |
possibly damaging |
Het |
Map2 |
T |
C |
1: 66,438,578 (GRCm39) |
V34A |
probably damaging |
Het |
Mroh6 |
A |
G |
15: 75,757,549 (GRCm39) |
L487P |
probably damaging |
Het |
Myo18b |
A |
T |
5: 112,959,508 (GRCm39) |
S1430T |
probably benign |
Het |
Or1e31 |
A |
T |
11: 73,690,229 (GRCm39) |
M118K |
probably damaging |
Het |
Palld |
C |
T |
8: 61,966,457 (GRCm39) |
A980T |
probably damaging |
Het |
Paxip1 |
A |
T |
5: 27,966,666 (GRCm39) |
I620N |
probably damaging |
Het |
Pcdha6 |
A |
G |
18: 37,102,820 (GRCm39) |
|
probably null |
Het |
Pcdhb11 |
G |
A |
18: 37,554,813 (GRCm39) |
V48M |
probably benign |
Het |
Pcdhga6 |
A |
G |
18: 37,840,697 (GRCm39) |
E139G |
probably benign |
Het |
Pck1 |
T |
C |
2: 172,999,112 (GRCm39) |
V426A |
probably damaging |
Het |
Pck2 |
T |
A |
14: 55,780,081 (GRCm39) |
I110N |
probably damaging |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Phactr3 |
G |
A |
2: 177,920,812 (GRCm39) |
E222K |
probably damaging |
Het |
Ppip5k1 |
A |
T |
2: 121,153,684 (GRCm39) |
|
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,206,076 (GRCm39) |
H278R |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,349,886 (GRCm39) |
H91Q |
probably damaging |
Het |
Slc13a2 |
CGTTATCTGT |
CGT |
11: 78,294,306 (GRCm39) |
|
probably benign |
Het |
Smn1 |
A |
G |
13: 100,264,503 (GRCm39) |
N78S |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,046,078 (GRCm39) |
I1614N |
probably damaging |
Het |
Syt17 |
T |
C |
7: 118,033,513 (GRCm39) |
D165G |
probably damaging |
Het |
Tbck |
A |
G |
3: 132,448,766 (GRCm39) |
Y593C |
probably damaging |
Het |
Tcaf2 |
G |
C |
6: 42,606,687 (GRCm39) |
F422L |
probably benign |
Het |
Tex15 |
T |
A |
8: 34,067,217 (GRCm39) |
F2216I |
possibly damaging |
Het |
Trpc4 |
A |
G |
3: 54,225,441 (GRCm39) |
E846G |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,580,313 (GRCm39) |
I753T |
probably benign |
Het |
Vdac1 |
C |
T |
11: 52,267,309 (GRCm39) |
T70M |
possibly damaging |
Het |
Vmn1r124 |
A |
C |
7: 20,994,104 (GRCm39) |
F147V |
probably benign |
Het |
Vmn1r220 |
T |
C |
13: 23,368,465 (GRCm39) |
D77G |
probably damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,493,730 (GRCm39) |
H72R |
probably benign |
Het |
Vmn2r78 |
A |
T |
7: 86,570,318 (GRCm39) |
I279L |
probably benign |
Het |
Vmn2r95 |
G |
T |
17: 18,671,732 (GRCm39) |
A490S |
possibly damaging |
Het |
Wdfy4 |
C |
T |
14: 32,831,482 (GRCm39) |
A915T |
possibly damaging |
Het |
Zmiz2 |
G |
T |
11: 6,345,604 (GRCm39) |
|
probably null |
Het |
Zscan2 |
A |
G |
7: 80,525,557 (GRCm39) |
N426S |
probably benign |
Het |
|
Other mutations in Notch3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Notch3
|
APN |
17 |
32,377,088 (GRCm39) |
nonsense |
probably null |
|
IGL01065:Notch3
|
APN |
17 |
32,365,390 (GRCm39) |
nonsense |
probably null |
|
IGL01296:Notch3
|
APN |
17 |
32,385,731 (GRCm39) |
missense |
unknown |
|
IGL01322:Notch3
|
APN |
17 |
32,363,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Notch3
|
APN |
17 |
32,362,410 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01358:Notch3
|
APN |
17 |
32,363,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01600:Notch3
|
APN |
17 |
32,363,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Notch3
|
APN |
17 |
32,377,844 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01623:Notch3
|
APN |
17 |
32,377,844 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01971:Notch3
|
APN |
17 |
32,343,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Notch3
|
APN |
17 |
32,341,716 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02072:Notch3
|
APN |
17 |
32,366,048 (GRCm39) |
nonsense |
probably null |
|
IGL02145:Notch3
|
APN |
17 |
32,373,715 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02256:Notch3
|
APN |
17 |
32,351,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Notch3
|
APN |
17 |
32,363,179 (GRCm39) |
missense |
probably benign |
|
IGL02476:Notch3
|
APN |
17 |
32,377,612 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02502:Notch3
|
APN |
17 |
32,377,252 (GRCm39) |
nonsense |
probably null |
|
IGL02551:Notch3
|
APN |
17 |
32,373,705 (GRCm39) |
splice site |
probably benign |
|
divide
|
UTSW |
17 |
32,356,787 (GRCm39) |
splice site |
probably null |
|
impressed
|
UTSW |
17 |
32,385,652 (GRCm39) |
missense |
probably benign |
|
indented
|
UTSW |
17 |
32,366,937 (GRCm39) |
missense |
probably benign |
0.00 |
Lopressor
|
UTSW |
17 |
32,372,858 (GRCm39) |
missense |
probably damaging |
1.00 |
marginal
|
UTSW |
17 |
32,383,198 (GRCm39) |
missense |
probably benign |
|
PIT4486001:Notch3
|
UTSW |
17 |
32,373,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Notch3
|
UTSW |
17 |
32,352,436 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0201:Notch3
|
UTSW |
17 |
32,375,122 (GRCm39) |
splice site |
probably benign |
|
R0630:Notch3
|
UTSW |
17 |
32,366,446 (GRCm39) |
splice site |
probably benign |
|
R1167:Notch3
|
UTSW |
17 |
32,341,719 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1432:Notch3
|
UTSW |
17 |
32,383,198 (GRCm39) |
missense |
probably benign |
|
R1567:Notch3
|
UTSW |
17 |
32,377,554 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1623:Notch3
|
UTSW |
17 |
32,358,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Notch3
|
UTSW |
17 |
32,375,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Notch3
|
UTSW |
17 |
32,377,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1789:Notch3
|
UTSW |
17 |
32,377,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Notch3
|
UTSW |
17 |
32,362,402 (GRCm39) |
missense |
probably benign |
0.08 |
R1837:Notch3
|
UTSW |
17 |
32,343,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Notch3
|
UTSW |
17 |
32,362,402 (GRCm39) |
missense |
probably benign |
0.08 |
R1937:Notch3
|
UTSW |
17 |
32,372,826 (GRCm39) |
missense |
probably benign |
0.03 |
R1954:Notch3
|
UTSW |
17 |
32,385,652 (GRCm39) |
missense |
probably benign |
|
R2014:Notch3
|
UTSW |
17 |
32,376,974 (GRCm39) |
missense |
probably benign |
0.00 |
R2058:Notch3
|
UTSW |
17 |
32,362,618 (GRCm39) |
missense |
probably benign |
|
R2068:Notch3
|
UTSW |
17 |
32,354,482 (GRCm39) |
missense |
probably benign |
0.00 |
R2097:Notch3
|
UTSW |
17 |
32,341,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Notch3
|
UTSW |
17 |
32,363,584 (GRCm39) |
missense |
probably benign |
0.19 |
R2156:Notch3
|
UTSW |
17 |
32,366,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Notch3
|
UTSW |
17 |
32,366,952 (GRCm39) |
missense |
probably benign |
0.00 |
R2324:Notch3
|
UTSW |
17 |
32,369,108 (GRCm39) |
splice site |
probably benign |
|
R2432:Notch3
|
UTSW |
17 |
32,372,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R3117:Notch3
|
UTSW |
17 |
32,377,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Notch3
|
UTSW |
17 |
32,377,435 (GRCm39) |
missense |
probably damaging |
0.96 |
R3409:Notch3
|
UTSW |
17 |
32,369,676 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3434:Notch3
|
UTSW |
17 |
32,377,592 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3435:Notch3
|
UTSW |
17 |
32,377,592 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3438:Notch3
|
UTSW |
17 |
32,372,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Notch3
|
UTSW |
17 |
32,372,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4087:Notch3
|
UTSW |
17 |
32,377,087 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4115:Notch3
|
UTSW |
17 |
32,377,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Notch3
|
UTSW |
17 |
32,351,181 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4234:Notch3
|
UTSW |
17 |
32,360,315 (GRCm39) |
missense |
probably damaging |
0.97 |
R4242:Notch3
|
UTSW |
17 |
32,362,719 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4658:Notch3
|
UTSW |
17 |
32,373,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Notch3
|
UTSW |
17 |
32,366,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Notch3
|
UTSW |
17 |
32,366,937 (GRCm39) |
missense |
probably benign |
0.00 |
R4885:Notch3
|
UTSW |
17 |
32,360,351 (GRCm39) |
missense |
probably damaging |
0.98 |
R4924:Notch3
|
UTSW |
17 |
32,363,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Notch3
|
UTSW |
17 |
32,376,864 (GRCm39) |
critical splice donor site |
probably null |
|
R5086:Notch3
|
UTSW |
17 |
32,362,308 (GRCm39) |
missense |
probably benign |
0.13 |
R5343:Notch3
|
UTSW |
17 |
32,362,257 (GRCm39) |
missense |
probably benign |
0.03 |
R5389:Notch3
|
UTSW |
17 |
32,358,163 (GRCm39) |
missense |
probably benign |
|
R5503:Notch3
|
UTSW |
17 |
32,366,029 (GRCm39) |
missense |
probably benign |
0.00 |
R5698:Notch3
|
UTSW |
17 |
32,376,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5824:Notch3
|
UTSW |
17 |
32,372,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5969:Notch3
|
UTSW |
17 |
32,372,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Notch3
|
UTSW |
17 |
32,362,501 (GRCm39) |
missense |
probably benign |
|
R6274:Notch3
|
UTSW |
17 |
32,366,264 (GRCm39) |
missense |
probably benign |
|
R6313:Notch3
|
UTSW |
17 |
32,370,128 (GRCm39) |
splice site |
probably null |
|
R6316:Notch3
|
UTSW |
17 |
32,356,787 (GRCm39) |
splice site |
probably null |
|
R6380:Notch3
|
UTSW |
17 |
32,363,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6401:Notch3
|
UTSW |
17 |
32,377,597 (GRCm39) |
missense |
probably benign |
0.01 |
R6502:Notch3
|
UTSW |
17 |
32,377,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Notch3
|
UTSW |
17 |
32,362,458 (GRCm39) |
missense |
probably benign |
0.16 |
R7131:Notch3
|
UTSW |
17 |
32,363,191 (GRCm39) |
missense |
probably benign |
|
R7140:Notch3
|
UTSW |
17 |
32,375,351 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7162:Notch3
|
UTSW |
17 |
32,365,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R7171:Notch3
|
UTSW |
17 |
32,377,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Notch3
|
UTSW |
17 |
32,376,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Notch3
|
UTSW |
17 |
32,360,365 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7554:Notch3
|
UTSW |
17 |
32,341,345 (GRCm39) |
missense |
probably benign |
0.03 |
R7575:Notch3
|
UTSW |
17 |
32,373,793 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7632:Notch3
|
UTSW |
17 |
32,377,480 (GRCm39) |
missense |
probably benign |
|
R7633:Notch3
|
UTSW |
17 |
32,377,596 (GRCm39) |
missense |
probably benign |
0.17 |
R7860:Notch3
|
UTSW |
17 |
32,341,747 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8052:Notch3
|
UTSW |
17 |
32,365,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R8250:Notch3
|
UTSW |
17 |
32,351,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Notch3
|
UTSW |
17 |
32,341,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R8306:Notch3
|
UTSW |
17 |
32,377,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R8458:Notch3
|
UTSW |
17 |
32,375,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8539:Notch3
|
UTSW |
17 |
32,375,329 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8865:Notch3
|
UTSW |
17 |
32,341,090 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Notch3
|
UTSW |
17 |
32,372,792 (GRCm39) |
missense |
probably benign |
0.14 |
R8927:Notch3
|
UTSW |
17 |
32,372,792 (GRCm39) |
missense |
probably benign |
0.14 |
R9062:Notch3
|
UTSW |
17 |
32,341,692 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9079:Notch3
|
UTSW |
17 |
32,383,033 (GRCm39) |
intron |
probably benign |
|
R9089:Notch3
|
UTSW |
17 |
32,370,521 (GRCm39) |
missense |
probably benign |
0.00 |
R9260:Notch3
|
UTSW |
17 |
32,362,216 (GRCm39) |
critical splice donor site |
probably null |
|
R9289:Notch3
|
UTSW |
17 |
32,377,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R9294:Notch3
|
UTSW |
17 |
32,362,665 (GRCm39) |
missense |
probably benign |
0.03 |
R9661:Notch3
|
UTSW |
17 |
32,373,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9779:Notch3
|
UTSW |
17 |
32,372,757 (GRCm39) |
missense |
probably damaging |
1.00 |
T0975:Notch3
|
UTSW |
17 |
32,365,391 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Notch3
|
UTSW |
17 |
32,377,626 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Notch3
|
UTSW |
17 |
32,370,344 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Notch3
|
UTSW |
17 |
32,360,490 (GRCm39) |
missense |
probably benign |
0.12 |
Z1177:Notch3
|
UTSW |
17 |
32,385,668 (GRCm39) |
missense |
probably benign |
|
|