Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam28 |
T |
C |
14: 68,846,578 (GRCm39) |
E745G |
probably benign |
Het |
Adamts12 |
G |
T |
15: 11,286,877 (GRCm39) |
K827N |
probably benign |
Het |
Ang2 |
T |
C |
14: 51,433,164 (GRCm39) |
T73A |
probably benign |
Het |
Bbs10 |
T |
C |
10: 111,134,735 (GRCm39) |
L51P |
probably damaging |
Het |
Bean1 |
T |
C |
8: 104,943,856 (GRCm39) |
I137T |
probably benign |
Het |
Cimip1 |
A |
T |
2: 173,369,716 (GRCm39) |
S77C |
probably damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,434,629 (GRCm39) |
T410A |
probably benign |
Het |
Cyp4a10 |
A |
C |
4: 115,378,342 (GRCm39) |
I143L |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 92,087,231 (GRCm39) |
Q788L |
probably damaging |
Het |
Epha10 |
G |
A |
4: 124,775,707 (GRCm39) |
V14I |
probably benign |
Het |
Eprs1 |
G |
A |
1: 185,117,159 (GRCm39) |
D401N |
probably damaging |
Het |
Fam169a |
T |
C |
13: 97,234,070 (GRCm39) |
V114A |
probably damaging |
Het |
Fbn2 |
G |
A |
18: 58,333,682 (GRCm39) |
P178S |
possibly damaging |
Het |
Fcrl2 |
A |
C |
3: 87,169,484 (GRCm39) |
|
probably null |
Het |
Grm1 |
G |
T |
10: 10,565,142 (GRCm39) |
H1055Q |
probably benign |
Het |
Mcm6 |
T |
C |
1: 128,276,789 (GRCm39) |
N267S |
probably benign |
Het |
Or5an1c |
T |
C |
19: 12,218,866 (GRCm39) |
D53G |
probably damaging |
Het |
Phc3 |
T |
C |
3: 30,984,018 (GRCm39) |
I699V |
probably damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Pyroxd1 |
T |
C |
6: 142,304,874 (GRCm39) |
V367A |
probably benign |
Het |
R3hdm1 |
G |
A |
1: 128,159,142 (GRCm39) |
R939H |
probably benign |
Het |
Rhot1 |
T |
C |
11: 80,136,847 (GRCm39) |
C310R |
probably damaging |
Het |
Tnrc6a |
G |
A |
7: 122,783,474 (GRCm39) |
V1481M |
probably benign |
Het |
Vmn1r234 |
A |
T |
17: 21,449,172 (GRCm39) |
M29L |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,881,700 (GRCm39) |
I460T |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,660,465 (GRCm39) |
Y1240N |
probably damaging |
Het |
|
Other mutations in Rag1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00940:Rag1
|
APN |
2 |
101,472,733 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01125:Rag1
|
APN |
2 |
101,472,346 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01836:Rag1
|
APN |
2 |
101,472,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02216:Rag1
|
APN |
2 |
101,473,726 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02271:Rag1
|
APN |
2 |
101,473,733 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02293:Rag1
|
APN |
2 |
101,473,391 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02601:Rag1
|
APN |
2 |
101,473,018 (GRCm39) |
missense |
probably damaging |
1.00 |
Anne
|
UTSW |
2 |
101,473,861 (GRCm39) |
missense |
probably damaging |
0.99 |
busted
|
UTSW |
2 |
101,472,292 (GRCm39) |
missense |
probably damaging |
1.00 |
cloth
|
UTSW |
2 |
101,473,009 (GRCm39) |
missense |
probably damaging |
1.00 |
defective
|
UTSW |
2 |
101,473,055 (GRCm39) |
missense |
probably damaging |
1.00 |
doll
|
UTSW |
2 |
101,472,415 (GRCm39) |
missense |
probably damaging |
1.00 |
dysfunctional
|
UTSW |
2 |
101,474,629 (GRCm39) |
missense |
probably damaging |
1.00 |
furchte
|
UTSW |
2 |
101,474,852 (GRCm39) |
missense |
probably benign |
0.05 |
horrorshow
|
UTSW |
2 |
101,472,968 (GRCm39) |
missense |
probably damaging |
1.00 |
huckle
|
UTSW |
2 |
101,471,568 (GRCm39) |
intron |
probably benign |
|
maladaptive
|
UTSW |
2 |
101,645,647 (GRCm38) |
intron |
probably benign |
|
scarecrow
|
UTSW |
2 |
101,472,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Rag1
|
UTSW |
2 |
101,473,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1126:Rag1
|
UTSW |
2 |
101,473,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1177:Rag1
|
UTSW |
2 |
101,472,623 (GRCm39) |
missense |
probably benign |
0.10 |
R1513:Rag1
|
UTSW |
2 |
101,473,336 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1859:Rag1
|
UTSW |
2 |
101,474,407 (GRCm39) |
missense |
probably benign |
0.03 |
R2218:Rag1
|
UTSW |
2 |
101,474,491 (GRCm39) |
missense |
probably benign |
|
R3932:Rag1
|
UTSW |
2 |
101,473,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4127:Rag1
|
UTSW |
2 |
101,472,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R4365:Rag1
|
UTSW |
2 |
101,473,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4620:Rag1
|
UTSW |
2 |
101,474,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Rag1
|
UTSW |
2 |
101,473,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Rag1
|
UTSW |
2 |
101,472,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Rag1
|
UTSW |
2 |
101,474,560 (GRCm39) |
missense |
probably benign |
0.01 |
R5239:Rag1
|
UTSW |
2 |
101,473,300 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5390:Rag1
|
UTSW |
2 |
101,473,079 (GRCm39) |
missense |
probably benign |
|
R5607:Rag1
|
UTSW |
2 |
101,474,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Rag1
|
UTSW |
2 |
101,474,797 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6412:Rag1
|
UTSW |
2 |
101,472,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R6633:Rag1
|
UTSW |
2 |
101,473,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R6679:Rag1
|
UTSW |
2 |
101,474,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R6723:Rag1
|
UTSW |
2 |
101,473,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R6853:Rag1
|
UTSW |
2 |
101,472,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R6867:Rag1
|
UTSW |
2 |
101,472,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6974:Rag1
|
UTSW |
2 |
101,472,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R7071:Rag1
|
UTSW |
2 |
101,473,807 (GRCm39) |
missense |
probably damaging |
0.99 |
R7124:Rag1
|
UTSW |
2 |
101,474,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R7248:Rag1
|
UTSW |
2 |
101,472,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R7256:Rag1
|
UTSW |
2 |
101,472,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R7567:Rag1
|
UTSW |
2 |
101,474,006 (GRCm39) |
missense |
probably damaging |
0.98 |
R7581:Rag1
|
UTSW |
2 |
101,473,649 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7830:Rag1
|
UTSW |
2 |
101,472,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Rag1
|
UTSW |
2 |
101,472,691 (GRCm39) |
missense |
probably benign |
0.24 |
R8024:Rag1
|
UTSW |
2 |
101,472,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R8434:Rag1
|
UTSW |
2 |
101,473,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Rag1
|
UTSW |
2 |
101,472,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R8918:Rag1
|
UTSW |
2 |
101,472,098 (GRCm39) |
missense |
probably benign |
|
R9116:Rag1
|
UTSW |
2 |
101,475,137 (GRCm39) |
missense |
probably benign |
0.38 |
R9116:Rag1
|
UTSW |
2 |
101,472,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Rag1
|
UTSW |
2 |
101,474,852 (GRCm39) |
missense |
probably benign |
0.05 |
R9409:Rag1
|
UTSW |
2 |
101,473,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Rag1
|
UTSW |
2 |
101,473,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Rag1
|
UTSW |
2 |
101,473,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R9594:Rag1
|
UTSW |
2 |
101,474,701 (GRCm39) |
missense |
probably benign |
|
R9658:Rag1
|
UTSW |
2 |
101,473,229 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9779:Rag1
|
UTSW |
2 |
101,474,153 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Rag1
|
UTSW |
2 |
101,474,892 (GRCm39) |
missense |
probably damaging |
0.99 |
X0018:Rag1
|
UTSW |
2 |
101,473,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rag1
|
UTSW |
2 |
101,473,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|