Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi1 |
T |
C |
2: 22,843,555 (GRCm39) |
T297A |
probably benign |
Het |
Acadl |
G |
T |
1: 66,892,337 (GRCm39) |
T162K |
probably benign |
Het |
Aldoart2 |
A |
T |
12: 55,612,536 (GRCm39) |
I154F |
probably damaging |
Het |
Alkbh8 |
G |
A |
9: 3,385,478 (GRCm39) |
R625H |
probably damaging |
Het |
Ankrd31 |
T |
A |
13: 96,969,036 (GRCm39) |
V891E |
probably benign |
Het |
Aopep |
G |
A |
13: 63,216,065 (GRCm39) |
V446I |
probably damaging |
Het |
Atp8b5 |
C |
T |
4: 43,356,982 (GRCm39) |
R577* |
probably null |
Het |
Capn3 |
G |
T |
2: 120,316,867 (GRCm39) |
E285D |
probably benign |
Het |
Cd79b |
G |
T |
11: 106,204,526 (GRCm39) |
P87T |
probably damaging |
Het |
Celsr2 |
T |
G |
3: 108,319,971 (GRCm39) |
D947A |
probably damaging |
Het |
Csmd3 |
A |
C |
15: 47,569,783 (GRCm39) |
S1213R |
|
Het |
Cyp2j5 |
T |
C |
4: 96,552,241 (GRCm39) |
M3V |
probably benign |
Het |
Ddi1 |
C |
T |
9: 6,265,787 (GRCm39) |
R194K |
probably benign |
Het |
Decr1 |
T |
C |
4: 15,933,019 (GRCm39) |
K49R |
probably benign |
Het |
Dnah10 |
A |
C |
5: 124,905,575 (GRCm39) |
E4130A |
probably benign |
Het |
Dst |
A |
G |
1: 34,323,444 (GRCm39) |
D4648G |
probably damaging |
Het |
Ecd |
A |
G |
14: 20,380,020 (GRCm39) |
|
probably null |
Het |
Erbin |
A |
T |
13: 103,970,864 (GRCm39) |
Y917* |
probably null |
Het |
Evpl |
T |
C |
11: 116,113,989 (GRCm39) |
K1234E |
probably benign |
Het |
F11r |
T |
A |
1: 171,289,191 (GRCm39) |
Y218N |
possibly damaging |
Het |
Fam43a |
C |
G |
16: 30,420,622 (GRCm39) |
T402S |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,457,064 (GRCm39) |
N2096S |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,196,962 (GRCm39) |
Y172* |
probably null |
Het |
Hscb |
A |
G |
5: 110,983,844 (GRCm39) |
V90A |
probably benign |
Het |
Iqgap2 |
T |
C |
13: 95,794,387 (GRCm39) |
D1195G |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,950,900 (GRCm39) |
I115T |
probably damaging |
Het |
Mast2 |
C |
T |
4: 116,170,172 (GRCm39) |
R707H |
probably damaging |
Het |
Mindy4 |
A |
G |
6: 55,277,977 (GRCm39) |
N607S |
probably damaging |
Het |
Mrpl9 |
T |
A |
3: 94,351,050 (GRCm39) |
Y77N |
probably damaging |
Het |
Muc16 |
G |
A |
9: 18,570,347 (GRCm39) |
T724I |
unknown |
Het |
Nat3 |
A |
T |
8: 68,000,478 (GRCm39) |
Y119F |
possibly damaging |
Het |
Nol7 |
T |
C |
13: 43,554,990 (GRCm39) |
S208P |
probably damaging |
Het |
Nup50l |
TCC |
TCCGCC |
6: 96,142,078 (GRCm39) |
|
probably benign |
Het |
Nup50l |
TCC |
TCCCCC |
6: 96,142,084 (GRCm39) |
|
probably benign |
Het |
Or13j1 |
A |
T |
4: 43,705,884 (GRCm39) |
V228E |
probably damaging |
Het |
Or3a4 |
T |
A |
11: 73,945,301 (GRCm39) |
I95F |
probably benign |
Het |
Or5al5 |
A |
T |
2: 85,961,721 (GRCm39) |
Y95* |
probably null |
Het |
Or8g17 |
G |
T |
9: 38,930,783 (GRCm39) |
T18K |
probably damaging |
Het |
Osbpl3 |
A |
C |
6: 50,322,995 (GRCm39) |
L288R |
probably damaging |
Het |
Oscp1 |
A |
C |
4: 125,982,116 (GRCm39) |
D352A |
possibly damaging |
Het |
Pcdh9 |
G |
A |
14: 94,123,222 (GRCm39) |
R983C |
probably benign |
Het |
Pcdhgb8 |
T |
C |
18: 37,896,555 (GRCm39) |
S542P |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,174,030 (GRCm39) |
T490A |
|
Het |
Pkd1l1 |
A |
T |
11: 8,897,315 (GRCm39) |
D531E |
|
Het |
Potefam3d |
A |
T |
8: 69,975,404 (GRCm39) |
Y21N |
possibly damaging |
Het |
Prr3 |
G |
T |
17: 36,290,053 (GRCm39) |
D26E |
possibly damaging |
Het |
Psmd8 |
T |
C |
7: 28,880,001 (GRCm39) |
K24E |
probably benign |
Het |
Rasgrp4 |
G |
A |
7: 28,849,362 (GRCm39) |
C583Y |
probably damaging |
Het |
Rest |
A |
G |
5: 77,416,171 (GRCm39) |
I128M |
probably benign |
Het |
Rftn1 |
A |
T |
17: 50,393,607 (GRCm39) |
F144I |
probably damaging |
Het |
Rusc2 |
T |
C |
4: 43,421,851 (GRCm39) |
F757S |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,782,810 (GRCm39) |
S1942P |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,745,177 (GRCm39) |
R706Q |
probably damaging |
Het |
Sergef |
G |
T |
7: 46,264,062 (GRCm39) |
T275K |
probably damaging |
Het |
Serpina10 |
T |
C |
12: 103,594,569 (GRCm39) |
T217A |
probably damaging |
Het |
Shd |
G |
C |
17: 56,283,235 (GRCm39) |
S288T |
probably damaging |
Het |
Siglec15 |
C |
A |
18: 78,091,803 (GRCm39) |
A133S |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,118,932 (GRCm39) |
P325L |
probably damaging |
Het |
Syt8 |
G |
A |
7: 141,993,881 (GRCm39) |
G344D |
probably damaging |
Het |
Tes |
A |
G |
6: 17,097,291 (GRCm39) |
E133G |
probably benign |
Het |
Tmprss2 |
T |
C |
16: 97,369,616 (GRCm39) |
Y386C |
probably damaging |
Het |
Tnfrsf11b |
A |
T |
15: 54,115,502 (GRCm39) |
L365Q |
probably damaging |
Het |
Tns1 |
T |
A |
1: 73,992,596 (GRCm39) |
D67V |
probably damaging |
Het |
Tns2 |
T |
C |
15: 102,021,280 (GRCm39) |
S982P |
probably damaging |
Het |
Tpcn2 |
A |
T |
7: 144,814,683 (GRCm39) |
F473I |
probably benign |
Het |
Tsg101 |
A |
T |
7: 46,542,257 (GRCm39) |
I232N |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,268,848 (GRCm39) |
S1977P |
probably benign |
Het |
Ttll11 |
T |
A |
2: 35,869,527 (GRCm39) |
E37V |
unknown |
Het |
Ttn |
A |
T |
2: 76,649,160 (GRCm39) |
V12716E |
possibly damaging |
Het |
Vmn2r70 |
A |
C |
7: 85,212,923 (GRCm39) |
S495A |
probably benign |
Het |
Zfp974 |
A |
G |
7: 27,610,697 (GRCm39) |
C343R |
probably damaging |
Het |
Zfy1 |
A |
T |
Y: 726,004 (GRCm39) |
I587N |
possibly damaging |
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 |
|
R6276:Notch3
|
UTSW |
17 |
32,373,723 (GRCm39) |
missense |
probably benign |
0.10 |
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 |
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 |
|
|