Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap2a2 |
T |
A |
7: 141,209,186 (GRCm39) |
S793T |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,727,153 (GRCm39) |
D459G |
probably damaging |
Het |
Cacna1g |
C |
A |
11: 94,347,977 (GRCm39) |
D704Y |
probably damaging |
Het |
Cby2 |
A |
G |
14: 75,820,829 (GRCm39) |
S299P |
probably benign |
Het |
Cry2 |
A |
G |
2: 92,244,060 (GRCm39) |
I371T |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,882,632 (GRCm39) |
F384I |
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,187,301 (GRCm39) |
|
probably null |
Het |
Hecw1 |
G |
T |
13: 14,552,382 (GRCm39) |
D72E |
probably damaging |
Het |
Htt |
T |
A |
5: 35,064,924 (GRCm39) |
W3046R |
probably damaging |
Het |
Hydin |
A |
T |
8: 110,993,995 (GRCm39) |
N10Y |
unknown |
Het |
Ighv8-8 |
T |
A |
12: 115,257,760 (GRCm39) |
T94S |
probably benign |
Het |
Igkv4-58 |
A |
G |
6: 69,477,538 (GRCm39) |
S20P |
probably damaging |
Het |
Il4i1 |
T |
C |
7: 44,486,919 (GRCm39) |
|
probably benign |
Het |
Kif13a |
A |
T |
13: 46,918,099 (GRCm39) |
S403T |
probably benign |
Het |
Klhl40 |
T |
C |
9: 121,612,446 (GRCm39) |
L616P |
probably damaging |
Het |
Krt7 |
T |
C |
15: 101,325,491 (GRCm39) |
L440P |
possibly damaging |
Het |
Lpin1 |
A |
G |
12: 16,594,678 (GRCm39) |
L755P |
probably damaging |
Het |
Magee2 |
C |
A |
X: 103,899,134 (GRCm39) |
E506* |
probably null |
Het |
Mast3 |
G |
A |
8: 71,234,207 (GRCm39) |
R143* |
probably null |
Het |
Med12 |
T |
A |
X: 100,321,695 (GRCm39) |
H459Q |
probably benign |
Het |
Mmp3 |
T |
C |
9: 7,450,149 (GRCm39) |
S294P |
probably benign |
Het |
Muc6 |
T |
C |
7: 141,234,349 (GRCm39) |
Y714C |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,074,349 (GRCm39) |
L662S |
probably damaging |
Het |
Nprl3 |
A |
G |
11: 32,200,256 (GRCm39) |
I20T |
probably damaging |
Het |
Or10ag2 |
A |
T |
2: 87,248,587 (GRCm39) |
D65V |
possibly damaging |
Het |
Pcdhb19 |
A |
G |
18: 37,631,665 (GRCm39) |
T487A |
possibly damaging |
Het |
Phlpp2 |
A |
G |
8: 110,667,467 (GRCm39) |
E1332G |
probably benign |
Het |
Pick1 |
T |
C |
15: 79,125,481 (GRCm39) |
S113P |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,507,178 (GRCm39) |
E1023G |
probably damaging |
Het |
Rspry1 |
A |
C |
8: 95,376,962 (GRCm39) |
I382L |
probably benign |
Het |
Sf3b3 |
A |
C |
8: 111,566,586 (GRCm39) |
V248G |
probably damaging |
Het |
Smg5 |
T |
A |
3: 88,253,759 (GRCm39) |
Y126* |
probably null |
Het |
Spin1 |
T |
C |
13: 51,281,973 (GRCm39) |
V22A |
probably benign |
Het |
Stab1 |
C |
T |
14: 30,872,220 (GRCm39) |
R1189Q |
possibly damaging |
Het |
Sytl5 |
A |
G |
X: 9,829,939 (GRCm39) |
D538G |
probably damaging |
Het |
Taar7e |
T |
A |
10: 23,913,813 (GRCm39) |
M101K |
probably damaging |
Het |
Taf4 |
A |
G |
2: 179,576,847 (GRCm39) |
V578A |
probably damaging |
Het |
Tmem266 |
G |
T |
9: 55,344,517 (GRCm39) |
C383F |
probably benign |
Het |
Trim34a |
T |
C |
7: 103,910,140 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
T |
C |
17: 20,249,866 (GRCm39) |
T802A |
probably damaging |
Het |
Vmn2r32 |
A |
C |
7: 7,467,029 (GRCm39) |
I833S |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,262,328 (GRCm39) |
D137G |
probably benign |
Het |
Vps13c |
C |
T |
9: 67,853,308 (GRCm39) |
S2467L |
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 |
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 |
R8776-TAIL: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 |
|