Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adh6a |
A |
G |
3: 138,019,097 (GRCm39) |
|
probably benign |
Het |
Atp1a1 |
C |
T |
3: 101,498,730 (GRCm39) |
G188R |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,522,311 (GRCm38) |
Y618H |
probably damaging |
Het |
Dot1l |
T |
C |
10: 80,621,700 (GRCm39) |
S451P |
probably benign |
Het |
Dpysl4 |
G |
A |
7: 138,676,089 (GRCm39) |
V294I |
possibly damaging |
Het |
Ehmt1 |
T |
A |
2: 24,753,232 (GRCm39) |
|
probably null |
Het |
Eps8 |
C |
T |
6: 137,460,539 (GRCm39) |
|
probably null |
Het |
Gm7247 |
T |
A |
14: 51,602,853 (GRCm39) |
I63K |
probably damaging |
Het |
Gsdme |
T |
A |
6: 50,199,769 (GRCm39) |
D270V |
probably damaging |
Het |
Kel |
T |
A |
6: 41,674,372 (GRCm39) |
T353S |
possibly damaging |
Het |
Krt73 |
T |
C |
15: 101,704,331 (GRCm39) |
H403R |
probably benign |
Het |
Mrnip |
A |
G |
11: 50,090,675 (GRCm39) |
T280A |
probably benign |
Het |
Or1j14 |
C |
T |
2: 36,417,837 (GRCm39) |
Q138* |
probably null |
Het |
Pkdrej |
A |
G |
15: 85,705,159 (GRCm39) |
L259P |
probably damaging |
Het |
Plod2 |
T |
C |
9: 92,488,551 (GRCm39) |
|
probably benign |
Het |
Rad54l2 |
A |
G |
9: 106,593,356 (GRCm39) |
S415P |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,115,433 (GRCm39) |
S931P |
probably damaging |
Het |
Sec23a |
T |
C |
12: 59,018,073 (GRCm39) |
I618V |
probably damaging |
Het |
Smtnl1 |
A |
T |
2: 84,645,714 (GRCm39) |
F386I |
probably damaging |
Het |
Sppl2b |
C |
T |
10: 80,697,220 (GRCm39) |
T30I |
probably benign |
Het |
Srf |
T |
C |
17: 46,860,108 (GRCm39) |
|
probably benign |
Het |
Tbc1d22b |
A |
G |
17: 29,818,932 (GRCm39) |
T429A |
probably damaging |
Het |
Tcf20 |
A |
T |
15: 82,739,356 (GRCm39) |
D698E |
probably damaging |
Het |
Tmem106c |
C |
A |
15: 97,867,567 (GRCm39) |
S250R |
probably benign |
Het |
Tmprss3 |
A |
G |
17: 31,410,018 (GRCm39) |
S199P |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,492,060 (GRCm39) |
|
probably benign |
Het |
Zfp595 |
A |
G |
13: 67,480,525 (GRCm39) |
|
probably benign |
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 |
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 |
R1319:Rag1
|
UTSW |
2 |
101,473,537 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|