Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,381,750 (GRCm39) |
D1405V |
probably damaging |
Het |
Acsl6 |
A |
G |
11: 54,236,034 (GRCm39) |
I514V |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,593,462 (GRCm39) |
R4175H |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,987,026 (GRCm39) |
V2770A |
possibly damaging |
Het |
B4galt1 |
A |
G |
4: 40,812,787 (GRCm39) |
V246A |
probably damaging |
Het |
Cdr2l |
T |
C |
11: 115,284,939 (GRCm39) |
V425A |
probably benign |
Het |
Celsr1 |
T |
A |
15: 85,816,501 (GRCm39) |
D1814V |
probably damaging |
Het |
Exoc2 |
A |
G |
13: 31,061,556 (GRCm39) |
V495A |
probably benign |
Het |
Ifi47 |
A |
G |
11: 48,986,637 (GRCm39) |
T135A |
possibly damaging |
Het |
Klhl23 |
T |
C |
2: 69,654,496 (GRCm39) |
V122A |
probably damaging |
Het |
Klri2 |
T |
A |
6: 129,710,694 (GRCm39) |
N142Y |
probably damaging |
Het |
Kmt2c |
A |
T |
5: 25,509,692 (GRCm39) |
F3161L |
probably null |
Het |
Mgl2 |
A |
G |
11: 70,026,785 (GRCm39) |
T144A |
probably benign |
Het |
Mpp3 |
T |
C |
11: 101,899,453 (GRCm39) |
E356G |
probably benign |
Het |
Neb |
T |
G |
2: 52,117,420 (GRCm39) |
T872P |
|
Het |
Nek9 |
A |
G |
12: 85,376,727 (GRCm39) |
M218T |
probably damaging |
Het |
Or10a49 |
A |
T |
7: 108,468,046 (GRCm39) |
L105H |
probably damaging |
Het |
Or4f14 |
A |
G |
2: 111,742,724 (GRCm39) |
F184L |
probably benign |
Het |
Or51k2 |
T |
G |
7: 103,596,610 (GRCm39) |
I279S |
possibly damaging |
Het |
Pabpc1l |
G |
A |
2: 163,869,568 (GRCm39) |
G123R |
probably damaging |
Het |
Parp3 |
T |
C |
9: 106,352,069 (GRCm39) |
|
probably null |
Het |
Pcdhga1 |
A |
T |
18: 37,796,376 (GRCm39) |
Y460F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,725,311 (GRCm39) |
T1390A |
unknown |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pex6 |
T |
C |
17: 47,023,060 (GRCm39) |
L212P |
possibly damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
Ppib |
T |
C |
9: 65,968,755 (GRCm39) |
F48L |
probably damaging |
Het |
Psme4 |
A |
G |
11: 30,793,583 (GRCm39) |
E1228G |
probably benign |
Het |
Ptpdc1 |
G |
T |
13: 48,751,390 (GRCm39) |
H37N |
probably benign |
Het |
Rab31 |
A |
T |
17: 66,003,269 (GRCm39) |
I126N |
possibly damaging |
Het |
Rsad2 |
A |
T |
12: 26,506,405 (GRCm39) |
V5E |
probably benign |
Het |
Sbsn |
T |
A |
7: 30,451,366 (GRCm39) |
I127N |
possibly damaging |
Het |
Scart2 |
C |
T |
7: 139,876,231 (GRCm39) |
Q568* |
probably null |
Het |
Selenoh |
G |
T |
2: 84,500,691 (GRCm39) |
Q50K |
probably damaging |
Het |
Simc1 |
GCAGTCACTAAGAAGTGTAATGCAGTCATCAGGAGGTGTGACACAGTCACTAAGAAGTGTGATGCAGTCACCAGGAGGTGTGA |
GCAGTCACTAAGAAGTGTGATGCAGTCACCAGGAGGTGTGA |
13: 54,673,177 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
A |
T |
2: 26,841,515 (GRCm39) |
I487L |
probably benign |
Het |
Tep1 |
T |
A |
14: 51,085,162 (GRCm39) |
I874F |
possibly damaging |
Het |
Tmem43 |
T |
C |
6: 91,455,746 (GRCm39) |
V119A |
possibly damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,007,550 (GRCm39) |
W509R |
probably damaging |
Het |
Xpr1 |
A |
C |
1: 155,189,001 (GRCm39) |
Y290* |
probably null |
Het |
Zfp160 |
T |
C |
17: 21,246,313 (GRCm39) |
C288R |
probably damaging |
Het |
Zfp955a |
C |
T |
17: 33,463,087 (GRCm39) |
V15M |
probably damaging |
Het |
|
Other mutations in S1pr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01759:S1pr3
|
APN |
13 |
51,573,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01997:S1pr3
|
APN |
13 |
51,573,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02270:S1pr3
|
APN |
13 |
51,573,092 (GRCm39) |
missense |
probably benign |
0.03 |
R0242:S1pr3
|
UTSW |
13 |
51,572,938 (GRCm39) |
missense |
probably benign |
0.00 |
R0242:S1pr3
|
UTSW |
13 |
51,572,938 (GRCm39) |
missense |
probably benign |
0.00 |
R0584:S1pr3
|
UTSW |
13 |
51,573,697 (GRCm39) |
missense |
probably benign |
0.00 |
R1869:S1pr3
|
UTSW |
13 |
51,573,952 (GRCm39) |
missense |
probably benign |
0.01 |
R1870:S1pr3
|
UTSW |
13 |
51,573,952 (GRCm39) |
missense |
probably benign |
0.01 |
R2338:S1pr3
|
UTSW |
13 |
51,573,614 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5472:S1pr3
|
UTSW |
13 |
51,573,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6006:S1pr3
|
UTSW |
13 |
51,573,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:S1pr3
|
UTSW |
13 |
51,573,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:S1pr3
|
UTSW |
13 |
51,573,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:S1pr3
|
UTSW |
13 |
51,573,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:S1pr3
|
UTSW |
13 |
51,573,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8066:S1pr3
|
UTSW |
13 |
51,573,955 (GRCm39) |
makesense |
probably null |
|
R8964:S1pr3
|
UTSW |
13 |
51,573,248 (GRCm39) |
missense |
probably damaging |
0.96 |
R9341:S1pr3
|
UTSW |
13 |
51,573,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R9343:S1pr3
|
UTSW |
13 |
51,573,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|