Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
A |
G |
2: 35,245,002 (GRCm39) |
Y117H |
probably benign |
Het |
a |
A |
G |
2: 154,892,612 (GRCm39) |
D97G |
probably damaging |
Het |
Cdca7l |
T |
C |
12: 117,836,098 (GRCm39) |
S190P |
probably damaging |
Het |
Chst9 |
T |
A |
18: 15,586,086 (GRCm39) |
Y159F |
possibly damaging |
Het |
Col26a1 |
G |
A |
5: 136,911,708 (GRCm39) |
R52C |
probably damaging |
Het |
Dchs2 |
A |
T |
3: 83,263,701 (GRCm39) |
D3323V |
possibly damaging |
Het |
Dqx1 |
T |
A |
6: 83,035,619 (GRCm39) |
I44N |
probably damaging |
Het |
Edc4 |
A |
G |
8: 106,613,992 (GRCm39) |
D415G |
probably damaging |
Het |
Enpp3 |
T |
A |
10: 24,650,733 (GRCm39) |
D801V |
probably damaging |
Het |
Fam13b |
G |
A |
18: 34,584,446 (GRCm39) |
R573C |
probably damaging |
Het |
Fgfr2 |
A |
T |
7: 129,798,002 (GRCm39) |
I415N |
possibly damaging |
Het |
Gm32742 |
T |
A |
9: 51,067,230 (GRCm39) |
M366L |
probably benign |
Het |
Gm49336 |
A |
T |
14: 60,457,515 (GRCm39) |
S563T |
possibly damaging |
Het |
Gm5475 |
T |
C |
15: 100,324,892 (GRCm39) |
F107L |
unknown |
Het |
Lamp3 |
T |
C |
16: 19,474,252 (GRCm39) |
D374G |
probably damaging |
Het |
Lin9 |
T |
C |
1: 180,496,450 (GRCm39) |
|
probably null |
Het |
Mef2d |
T |
C |
3: 88,074,956 (GRCm39) |
S381P |
probably benign |
Het |
Mfsd9 |
A |
G |
1: 40,812,915 (GRCm39) |
*467Q |
probably null |
Het |
Mpo |
A |
G |
11: 87,693,538 (GRCm39) |
I639V |
possibly damaging |
Het |
Mrgprh |
T |
C |
17: 13,096,375 (GRCm39) |
I205T |
probably benign |
Het |
Ncapd2 |
T |
C |
6: 125,154,476 (GRCm39) |
D580G |
probably benign |
Het |
Nkain4 |
T |
A |
2: 180,585,920 (GRCm39) |
I48F |
probably damaging |
Het |
Nr6a1 |
A |
G |
2: 38,650,244 (GRCm39) |
Y129H |
probably damaging |
Het |
Or7g19 |
T |
A |
9: 18,856,286 (GRCm39) |
I114N |
possibly damaging |
Het |
Robo1 |
G |
T |
16: 72,821,141 (GRCm39) |
E1294* |
probably null |
Het |
Septin8 |
A |
G |
11: 53,428,343 (GRCm39) |
K331R |
probably benign |
Het |
Shmt2 |
A |
G |
10: 127,356,785 (GRCm39) |
|
probably null |
Het |
Skint6 |
A |
C |
4: 112,661,885 (GRCm39) |
L1233R |
possibly damaging |
Het |
Slc41a3 |
A |
T |
6: 90,621,165 (GRCm39) |
T402S |
probably benign |
Het |
Slc9a2 |
A |
G |
1: 40,781,889 (GRCm39) |
T373A |
probably damaging |
Het |
Spata31d1b |
T |
C |
13: 59,863,283 (GRCm39) |
C144R |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,181,783 (GRCm39) |
V4184A |
possibly damaging |
Het |
Tenm4 |
G |
A |
7: 96,544,239 (GRCm39) |
R2122H |
probably damaging |
Het |
Tlnrd1 |
A |
T |
7: 83,532,316 (GRCm39) |
D38E |
probably benign |
Het |
Tnnc2 |
C |
T |
2: 164,620,135 (GRCm39) |
A6T |
probably benign |
Het |
Usp9y |
A |
G |
Y: 1,356,320 (GRCm39) |
V1127A |
probably benign |
Het |
Ylpm1 |
T |
C |
12: 85,077,195 (GRCm39) |
Y1307H |
probably damaging |
Het |
Zfp266 |
T |
C |
9: 20,411,509 (GRCm39) |
S223G |
probably benign |
Het |
|
Other mutations in Notch4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00904:Notch4
|
APN |
17 |
34,794,535 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01022:Notch4
|
APN |
17 |
34,784,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01356:Notch4
|
APN |
17 |
34,800,000 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01634:Notch4
|
APN |
17 |
34,791,562 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Notch4
|
APN |
17 |
34,803,587 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02248:Notch4
|
APN |
17 |
34,806,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Notch4
|
APN |
17 |
34,787,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Notch4
|
APN |
17 |
34,796,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02561:Notch4
|
APN |
17 |
34,787,134 (GRCm39) |
splice site |
probably benign |
|
IGL02604:Notch4
|
APN |
17 |
34,784,362 (GRCm39) |
splice site |
probably null |
|
IGL03323:Notch4
|
APN |
17 |
34,801,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03366:Notch4
|
APN |
17 |
34,791,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03408:Notch4
|
APN |
17 |
34,784,542 (GRCm39) |
missense |
probably benign |
0.03 |
K3955:Notch4
|
UTSW |
17 |
34,787,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Notch4
|
UTSW |
17 |
34,784,337 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0366:Notch4
|
UTSW |
17 |
34,800,473 (GRCm39) |
splice site |
probably benign |
|
R0446:Notch4
|
UTSW |
17 |
34,784,337 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0490:Notch4
|
UTSW |
17 |
34,801,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Notch4
|
UTSW |
17 |
34,794,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Notch4
|
UTSW |
17 |
34,802,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R0702:Notch4
|
UTSW |
17 |
34,794,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Notch4
|
UTSW |
17 |
34,784,306 (GRCm39) |
nonsense |
probably null |
|
R0854:Notch4
|
UTSW |
17 |
34,787,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Notch4
|
UTSW |
17 |
34,806,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R1196:Notch4
|
UTSW |
17 |
34,787,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R1316:Notch4
|
UTSW |
17 |
34,786,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Notch4
|
UTSW |
17 |
34,786,656 (GRCm39) |
nonsense |
probably null |
|
R1527:Notch4
|
UTSW |
17 |
34,784,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Notch4
|
UTSW |
17 |
34,787,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R1718:Notch4
|
UTSW |
17 |
34,795,737 (GRCm39) |
splice site |
probably benign |
|
R1855:Notch4
|
UTSW |
17 |
34,799,936 (GRCm39) |
missense |
probably benign |
0.05 |
R1988:Notch4
|
UTSW |
17 |
34,806,562 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2022:Notch4
|
UTSW |
17 |
34,806,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Notch4
|
UTSW |
17 |
34,806,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R2078:Notch4
|
UTSW |
17 |
34,787,689 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2369:Notch4
|
UTSW |
17 |
34,804,924 (GRCm39) |
missense |
probably benign |
0.15 |
R3846:Notch4
|
UTSW |
17 |
34,797,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Notch4
|
UTSW |
17 |
34,797,043 (GRCm39) |
nonsense |
probably null |
|
R4087:Notch4
|
UTSW |
17 |
34,803,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4456:Notch4
|
UTSW |
17 |
34,802,807 (GRCm39) |
missense |
probably damaging |
0.99 |
R4628:Notch4
|
UTSW |
17 |
34,789,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Notch4
|
UTSW |
17 |
34,789,179 (GRCm39) |
missense |
probably benign |
0.00 |
R4778:Notch4
|
UTSW |
17 |
34,801,485 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4818:Notch4
|
UTSW |
17 |
34,797,690 (GRCm39) |
splice site |
probably benign |
|
R4828:Notch4
|
UTSW |
17 |
34,789,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R4830:Notch4
|
UTSW |
17 |
34,789,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R4859:Notch4
|
UTSW |
17 |
34,806,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Notch4
|
UTSW |
17 |
34,796,536 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5090:Notch4
|
UTSW |
17 |
34,799,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R5290:Notch4
|
UTSW |
17 |
34,784,263 (GRCm39) |
missense |
probably benign |
0.01 |
R5363:Notch4
|
UTSW |
17 |
34,806,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Notch4
|
UTSW |
17 |
34,801,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Notch4
|
UTSW |
17 |
34,786,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Notch4
|
UTSW |
17 |
34,792,788 (GRCm39) |
missense |
probably null |
0.16 |
R6422:Notch4
|
UTSW |
17 |
34,803,533 (GRCm39) |
missense |
probably benign |
|
R6645:Notch4
|
UTSW |
17 |
34,806,790 (GRCm39) |
missense |
probably benign |
0.00 |
R6836:Notch4
|
UTSW |
17 |
34,805,074 (GRCm39) |
missense |
probably damaging |
0.96 |
R6943:Notch4
|
UTSW |
17 |
34,802,577 (GRCm39) |
missense |
probably benign |
|
R6991:Notch4
|
UTSW |
17 |
34,803,774 (GRCm39) |
nonsense |
probably null |
|
R7078:Notch4
|
UTSW |
17 |
34,801,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7168:Notch4
|
UTSW |
17 |
34,791,667 (GRCm39) |
missense |
probably benign |
0.05 |
R7182:Notch4
|
UTSW |
17 |
34,802,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Notch4
|
UTSW |
17 |
34,795,445 (GRCm39) |
missense |
probably benign |
0.00 |
R7247:Notch4
|
UTSW |
17 |
34,791,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7556:Notch4
|
UTSW |
17 |
34,794,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Notch4
|
UTSW |
17 |
34,802,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R7697:Notch4
|
UTSW |
17 |
34,789,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Notch4
|
UTSW |
17 |
34,801,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7994:Notch4
|
UTSW |
17 |
34,797,064 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8139:Notch4
|
UTSW |
17 |
34,803,774 (GRCm39) |
nonsense |
probably null |
|
R8171:Notch4
|
UTSW |
17 |
34,801,483 (GRCm39) |
nonsense |
probably null |
|
R8375:Notch4
|
UTSW |
17 |
34,787,228 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8448:Notch4
|
UTSW |
17 |
34,805,763 (GRCm39) |
splice site |
probably null |
|
R8543:Notch4
|
UTSW |
17 |
34,787,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8776:Notch4
|
UTSW |
17 |
34,806,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R8847:Notch4
|
UTSW |
17 |
34,803,962 (GRCm39) |
splice site |
probably benign |
|
R8885:Notch4
|
UTSW |
17 |
34,803,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9126:Notch4
|
UTSW |
17 |
34,800,080 (GRCm39) |
missense |
probably benign |
0.00 |
R9184:Notch4
|
UTSW |
17 |
34,806,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R9425:Notch4
|
UTSW |
17 |
34,795,801 (GRCm39) |
missense |
probably benign |
0.42 |
R9434:Notch4
|
UTSW |
17 |
34,801,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Notch4
|
UTSW |
17 |
34,806,667 (GRCm39) |
missense |
probably benign |
0.00 |
R9664:Notch4
|
UTSW |
17 |
34,784,601 (GRCm39) |
missense |
probably benign |
0.07 |
R9772:Notch4
|
UTSW |
17 |
34,792,883 (GRCm39) |
critical splice donor site |
probably null |
|
X0054:Notch4
|
UTSW |
17 |
34,803,469 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Notch4
|
UTSW |
17 |
34,805,058 (GRCm39) |
nonsense |
probably null |
|
Z1088:Notch4
|
UTSW |
17 |
34,806,889 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Notch4
|
UTSW |
17 |
34,806,883 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Notch4
|
UTSW |
17 |
34,806,882 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Notch4
|
UTSW |
17 |
34,794,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|