Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd46 |
A |
G |
15: 36,486,079 (GRCm39) |
V58A |
possibly damaging |
Het |
Dhx16 |
A |
G |
17: 36,194,949 (GRCm39) |
E492G |
probably damaging |
Het |
Dock1 |
T |
C |
7: 134,747,294 (GRCm39) |
M1535T |
probably damaging |
Het |
F2 |
A |
T |
2: 91,463,439 (GRCm39) |
H148Q |
probably benign |
Het |
Fam83e |
A |
T |
7: 45,373,345 (GRCm39) |
H237L |
probably benign |
Het |
Fscn3 |
A |
T |
6: 28,428,153 (GRCm39) |
|
probably null |
Het |
Gpr162 |
C |
A |
6: 124,838,123 (GRCm39) |
G176C |
probably damaging |
Het |
Icam5 |
A |
G |
9: 20,946,505 (GRCm39) |
D376G |
possibly damaging |
Het |
Ift172 |
T |
C |
5: 31,440,402 (GRCm39) |
K295R |
probably benign |
Het |
Irf3 |
A |
G |
7: 44,648,134 (GRCm39) |
|
probably benign |
Het |
Itga2 |
A |
T |
13: 115,001,845 (GRCm39) |
|
probably null |
Het |
Klhl11 |
A |
T |
11: 100,354,662 (GRCm39) |
D386E |
probably damaging |
Het |
Myh4 |
G |
T |
11: 67,136,373 (GRCm39) |
G417V |
probably damaging |
Het |
Nlrp3 |
A |
G |
11: 59,455,909 (GRCm39) |
T902A |
probably benign |
Het |
Or2y17 |
A |
G |
11: 49,232,018 (GRCm39) |
I220V |
probably benign |
Het |
Or4a72 |
A |
C |
2: 89,405,668 (GRCm39) |
M134R |
possibly damaging |
Het |
Or9g3 |
A |
T |
2: 85,590,503 (GRCm39) |
Y72* |
probably null |
Het |
Phf10 |
T |
C |
17: 15,174,361 (GRCm39) |
Y239C |
probably damaging |
Het |
Pla2g4e |
A |
G |
2: 120,017,717 (GRCm39) |
F203S |
probably benign |
Het |
Pramel1 |
T |
C |
4: 143,124,096 (GRCm39) |
F257S |
probably damaging |
Het |
Prodh2 |
A |
G |
7: 30,205,803 (GRCm39) |
H213R |
probably damaging |
Het |
Rgs7 |
C |
T |
1: 175,016,788 (GRCm39) |
D61N |
probably damaging |
Het |
Rhobtb1 |
T |
A |
10: 69,121,508 (GRCm39) |
|
probably benign |
Het |
Sct |
C |
A |
7: 140,858,530 (GRCm39) |
|
probably null |
Het |
Slc17a9 |
G |
A |
2: 180,382,536 (GRCm39) |
|
probably null |
Het |
Spire1 |
T |
C |
18: 67,639,725 (GRCm39) |
T263A |
probably benign |
Het |
Trpm1 |
A |
T |
7: 63,895,690 (GRCm39) |
|
probably null |
Het |
Trpm7 |
G |
T |
2: 126,649,282 (GRCm39) |
N1469K |
probably benign |
Het |
Zfp750 |
G |
T |
11: 121,402,837 (GRCm39) |
T637K |
probably benign |
Het |
Zswim5 |
T |
C |
4: 116,843,841 (GRCm39) |
C960R |
probably damaging |
Het |
Zwint |
T |
A |
10: 72,490,815 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Evpl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Evpl
|
APN |
11 |
116,125,331 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00896:Evpl
|
APN |
11 |
116,113,410 (GRCm39) |
nonsense |
probably null |
|
IGL00941:Evpl
|
APN |
11 |
116,118,727 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01443:Evpl
|
APN |
11 |
116,113,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Evpl
|
APN |
11 |
116,124,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01957:Evpl
|
APN |
11 |
116,114,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Evpl
|
APN |
11 |
116,117,841 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02457:Evpl
|
APN |
11 |
116,120,939 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02502:Evpl
|
APN |
11 |
116,113,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02536:Evpl
|
APN |
11 |
116,112,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Evpl
|
APN |
11 |
116,112,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Evpl
|
APN |
11 |
116,112,438 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03405:Evpl
|
APN |
11 |
116,118,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
A4554:Evpl
|
UTSW |
11 |
116,111,660 (GRCm39) |
missense |
probably damaging |
1.00 |
BB005:Evpl
|
UTSW |
11 |
116,113,359 (GRCm39) |
missense |
possibly damaging |
0.63 |
BB015:Evpl
|
UTSW |
11 |
116,113,359 (GRCm39) |
missense |
possibly damaging |
0.63 |
PIT4449001:Evpl
|
UTSW |
11 |
116,124,225 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0082:Evpl
|
UTSW |
11 |
116,125,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Evpl
|
UTSW |
11 |
116,111,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Evpl
|
UTSW |
11 |
116,114,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R0581:Evpl
|
UTSW |
11 |
116,120,316 (GRCm39) |
missense |
probably benign |
0.02 |
R0727:Evpl
|
UTSW |
11 |
116,123,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R0791:Evpl
|
UTSW |
11 |
116,118,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Evpl
|
UTSW |
11 |
116,118,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1079:Evpl
|
UTSW |
11 |
116,120,894 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1514:Evpl
|
UTSW |
11 |
116,114,661 (GRCm39) |
missense |
probably benign |
|
R1699:Evpl
|
UTSW |
11 |
116,118,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Evpl
|
UTSW |
11 |
116,116,318 (GRCm39) |
missense |
probably benign |
0.06 |
R1775:Evpl
|
UTSW |
11 |
116,114,486 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1886:Evpl
|
UTSW |
11 |
116,118,402 (GRCm39) |
missense |
probably damaging |
0.97 |
R1903:Evpl
|
UTSW |
11 |
116,117,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R2081:Evpl
|
UTSW |
11 |
116,125,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Evpl
|
UTSW |
11 |
116,112,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R2571:Evpl
|
UTSW |
11 |
116,128,795 (GRCm39) |
missense |
unknown |
|
R3081:Evpl
|
UTSW |
11 |
116,111,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4097:Evpl
|
UTSW |
11 |
116,114,003 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4541:Evpl
|
UTSW |
11 |
116,123,470 (GRCm39) |
missense |
probably benign |
0.01 |
R4562:Evpl
|
UTSW |
11 |
116,124,225 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4703:Evpl
|
UTSW |
11 |
116,113,331 (GRCm39) |
missense |
probably damaging |
0.98 |
R4947:Evpl
|
UTSW |
11 |
116,114,201 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5243:Evpl
|
UTSW |
11 |
116,113,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5325:Evpl
|
UTSW |
11 |
116,112,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R5416:Evpl
|
UTSW |
11 |
116,125,085 (GRCm39) |
missense |
probably benign |
0.13 |
R5580:Evpl
|
UTSW |
11 |
116,125,058 (GRCm39) |
missense |
probably benign |
0.14 |
R5873:Evpl
|
UTSW |
11 |
116,125,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Evpl
|
UTSW |
11 |
116,121,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6438:Evpl
|
UTSW |
11 |
116,120,927 (GRCm39) |
missense |
probably benign |
0.00 |
R6742:Evpl
|
UTSW |
11 |
116,113,640 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6753:Evpl
|
UTSW |
11 |
116,128,732 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6764:Evpl
|
UTSW |
11 |
116,113,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R6846:Evpl
|
UTSW |
11 |
116,114,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Evpl
|
UTSW |
11 |
116,113,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7288:Evpl
|
UTSW |
11 |
116,114,775 (GRCm39) |
missense |
probably benign |
|
R7395:Evpl
|
UTSW |
11 |
116,117,905 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7441:Evpl
|
UTSW |
11 |
116,113,782 (GRCm39) |
nonsense |
probably null |
|
R7505:Evpl
|
UTSW |
11 |
116,117,813 (GRCm39) |
critical splice donor site |
probably null |
|
R7674:Evpl
|
UTSW |
11 |
116,113,394 (GRCm39) |
missense |
probably benign |
0.40 |
R7772:Evpl
|
UTSW |
11 |
116,112,261 (GRCm39) |
missense |
probably benign |
0.00 |
R7780:Evpl
|
UTSW |
11 |
116,125,000 (GRCm39) |
missense |
not run |
|
R7861:Evpl
|
UTSW |
11 |
116,118,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7928:Evpl
|
UTSW |
11 |
116,113,359 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8008:Evpl
|
UTSW |
11 |
116,121,298 (GRCm39) |
missense |
probably null |
0.21 |
R8040:Evpl
|
UTSW |
11 |
116,113,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R8052:Evpl
|
UTSW |
11 |
116,113,989 (GRCm39) |
missense |
probably benign |
0.00 |
R8402:Evpl
|
UTSW |
11 |
116,116,197 (GRCm39) |
missense |
probably benign |
0.03 |
R8513:Evpl
|
UTSW |
11 |
116,120,570 (GRCm39) |
critical splice donor site |
probably null |
|
R8695:Evpl
|
UTSW |
11 |
116,114,489 (GRCm39) |
missense |
probably benign |
0.02 |
R8725:Evpl
|
UTSW |
11 |
116,113,019 (GRCm39) |
missense |
probably benign |
0.25 |
R8749:Evpl
|
UTSW |
11 |
116,120,232 (GRCm39) |
missense |
probably benign |
0.01 |
R8807:Evpl
|
UTSW |
11 |
116,111,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Evpl
|
UTSW |
11 |
116,121,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R8947:Evpl
|
UTSW |
11 |
116,112,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R9123:Evpl
|
UTSW |
11 |
116,115,008 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9314:Evpl
|
UTSW |
11 |
116,118,503 (GRCm39) |
missense |
probably benign |
0.13 |
R9581:Evpl
|
UTSW |
11 |
116,120,660 (GRCm39) |
missense |
probably benign |
0.30 |
R9665:Evpl
|
UTSW |
11 |
116,123,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Evpl
|
UTSW |
11 |
116,124,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Evpl
|
UTSW |
11 |
116,112,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|