Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
C |
5: 114,383,153 (GRCm39) |
I2112T |
probably benign |
Het |
Agtpbp1 |
C |
A |
13: 59,598,132 (GRCm39) |
|
probably benign |
Het |
Ash1l |
T |
C |
3: 88,890,623 (GRCm39) |
M834T |
probably damaging |
Het |
Aspg |
A |
G |
12: 112,082,958 (GRCm39) |
T213A |
possibly damaging |
Het |
Chpf2 |
T |
C |
5: 24,794,646 (GRCm39) |
V272A |
possibly damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Ddah2 |
G |
T |
17: 35,280,503 (GRCm39) |
D215Y |
probably damaging |
Het |
Dna2 |
C |
T |
10: 62,784,966 (GRCm39) |
R28W |
probably benign |
Het |
Fbrsl1 |
T |
A |
5: 110,522,385 (GRCm39) |
M150L |
probably benign |
Het |
Hmces |
T |
A |
6: 87,913,164 (GRCm39) |
D306E |
probably benign |
Het |
Itga2 |
C |
T |
13: 115,002,691 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
T |
C |
10: 67,075,015 (GRCm39) |
|
probably benign |
Het |
Krr1 |
T |
A |
10: 111,811,562 (GRCm39) |
H85Q |
probably benign |
Het |
Krt87 |
C |
T |
15: 101,389,314 (GRCm39) |
R6Q |
probably benign |
Het |
Krtap24-1 |
T |
C |
16: 88,408,530 (GRCm39) |
M199V |
probably benign |
Het |
Krtap5-2 |
A |
T |
7: 141,728,620 (GRCm39) |
C353* |
probably null |
Het |
Myo7a |
T |
G |
7: 97,746,880 (GRCm39) |
I178L |
possibly damaging |
Het |
Myof |
G |
A |
19: 37,899,408 (GRCm39) |
T1043I |
probably damaging |
Het |
Noc4l |
C |
T |
5: 110,798,450 (GRCm39) |
E247K |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Or4p19 |
A |
T |
2: 88,242,890 (GRCm39) |
N37K |
probably damaging |
Het |
Or7e168 |
A |
G |
9: 19,719,928 (GRCm39) |
I105V |
probably benign |
Het |
Pank4 |
T |
C |
4: 155,062,630 (GRCm39) |
F584L |
probably damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,312,875 (GRCm39) |
F1198L |
probably damaging |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Tent5c |
T |
C |
3: 100,380,316 (GRCm39) |
T147A |
possibly damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Unc13a |
A |
G |
8: 72,107,630 (GRCm39) |
I554T |
probably damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,247,866 (GRCm39) |
D1023G |
probably damaging |
Het |
Zfp791 |
T |
A |
8: 85,837,583 (GRCm39) |
K94* |
probably null |
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 |
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 |
|