Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl11 |
T |
C |
9: 107,808,434 (GRCm39) |
V919A |
probably damaging |
Het |
Adam28 |
G |
A |
14: 68,845,387 (GRCm39) |
P761L |
possibly damaging |
Het |
Aoc1l3 |
T |
A |
6: 48,965,566 (GRCm39) |
C525S |
possibly damaging |
Het |
Aplf |
G |
A |
6: 87,623,065 (GRCm39) |
P338L |
probably benign |
Het |
Arl5b |
T |
A |
2: 15,077,942 (GRCm39) |
I89N |
probably damaging |
Het |
Asap2 |
T |
C |
12: 21,297,320 (GRCm39) |
V596A |
probably damaging |
Het |
Baz1b |
T |
G |
5: 135,273,076 (GRCm39) |
F1400C |
probably damaging |
Het |
Ccdc149 |
A |
T |
5: 52,542,497 (GRCm39) |
L365Q |
probably damaging |
Het |
Ccdc60 |
A |
G |
5: 116,318,870 (GRCm39) |
S149P |
probably damaging |
Het |
Ces1b |
A |
G |
8: 93,794,775 (GRCm39) |
C275R |
probably damaging |
Het |
Creb3 |
T |
C |
4: 43,563,509 (GRCm39) |
L163P |
probably damaging |
Het |
Dhx37 |
T |
G |
5: 125,500,496 (GRCm39) |
N570T |
probably benign |
Het |
Epc1 |
T |
C |
18: 6,453,657 (GRCm39) |
N223D |
probably damaging |
Het |
Gbp5 |
C |
T |
3: 142,208,885 (GRCm39) |
H143Y |
possibly damaging |
Het |
Gfod1 |
A |
T |
13: 43,456,905 (GRCm39) |
D23E |
probably benign |
Het |
Gm7361 |
A |
T |
5: 26,467,051 (GRCm39) |
E223D |
possibly damaging |
Het |
Izumo1 |
A |
G |
7: 45,274,415 (GRCm39) |
K161E |
probably damaging |
Het |
Kcnh2 |
C |
T |
5: 24,527,670 (GRCm39) |
R894H |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,158,366 (GRCm39) |
N1617S |
possibly damaging |
Het |
Med13l |
A |
T |
5: 118,892,350 (GRCm39) |
E1924D |
possibly damaging |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Mtg2 |
T |
G |
2: 179,725,221 (GRCm39) |
S145A |
probably benign |
Het |
Mug2 |
G |
A |
6: 122,062,454 (GRCm39) |
S1442N |
probably benign |
Het |
Myo1b |
A |
T |
1: 51,836,246 (GRCm39) |
I315N |
probably damaging |
Het |
Naip2 |
G |
A |
13: 100,291,386 (GRCm39) |
T1184M |
probably benign |
Het |
Naip2 |
T |
A |
13: 100,291,419 (GRCm39) |
H1173L |
probably benign |
Het |
Nsrp1 |
G |
A |
11: 76,937,285 (GRCm39) |
R304* |
probably null |
Het |
Or2a56 |
G |
T |
6: 42,932,686 (GRCm39) |
V85L |
probably benign |
Het |
Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
Parp4 |
T |
C |
14: 56,885,576 (GRCm39) |
F1552L |
unknown |
Het |
Pigw |
G |
A |
11: 84,769,033 (GRCm39) |
H99Y |
probably benign |
Het |
Ppp6r2 |
G |
A |
15: 89,158,379 (GRCm39) |
M444I |
possibly damaging |
Het |
Rchy1 |
A |
G |
5: 92,105,476 (GRCm39) |
F82L |
probably damaging |
Het |
Reln |
A |
C |
5: 22,432,626 (GRCm39) |
F125V |
probably damaging |
Het |
Riok1 |
G |
A |
13: 38,241,149 (GRCm39) |
E435K |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,343,407 (GRCm39) |
R3590G |
probably damaging |
Het |
Scart2 |
A |
G |
7: 139,874,704 (GRCm39) |
E394G |
probably damaging |
Het |
Scrib |
G |
C |
15: 75,923,310 (GRCm39) |
P1249A |
probably benign |
Het |
Shc4 |
C |
T |
2: 125,520,607 (GRCm39) |
|
probably null |
Het |
Slc12a2 |
T |
A |
18: 58,037,450 (GRCm39) |
I520N |
probably damaging |
Het |
Slc26a5 |
A |
G |
5: 22,021,959 (GRCm39) |
I484T |
probably benign |
Het |
Slc39a11 |
G |
T |
11: 113,354,899 (GRCm39) |
T110K |
probably benign |
Het |
Snd1 |
T |
A |
6: 28,884,970 (GRCm39) |
S774T |
probably benign |
Het |
Spata31d1c |
C |
T |
13: 65,184,129 (GRCm39) |
P557L |
probably damaging |
Het |
Tada1 |
A |
G |
1: 166,216,198 (GRCm39) |
D133G |
probably benign |
Het |
Tg |
A |
T |
15: 66,579,859 (GRCm39) |
T1555S |
probably damaging |
Het |
Thra |
A |
G |
11: 98,644,455 (GRCm39) |
E15G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,625,440 (GRCm39) |
I15128F |
probably damaging |
Het |
Ube2r2 |
A |
G |
4: 41,174,066 (GRCm39) |
Y68C |
probably damaging |
Het |
Uncx |
A |
T |
5: 139,532,442 (GRCm39) |
N169I |
probably damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,743,786 (GRCm39) |
Y483C |
possibly damaging |
Het |
Xkr4 |
T |
C |
1: 3,286,897 (GRCm39) |
D431G |
probably damaging |
Het |
Xylb |
C |
A |
9: 119,209,091 (GRCm39) |
A311E |
possibly damaging |
Het |
Zbtb39 |
C |
G |
10: 127,578,175 (GRCm39) |
Q250E |
probably benign |
Het |
Zbtb39 |
C |
A |
10: 127,578,931 (GRCm39) |
H502N |
probably damaging |
Het |
Zfp82 |
A |
G |
7: 29,755,876 (GRCm39) |
L402P |
probably damaging |
Het |
Zpbp2 |
G |
A |
11: 98,448,451 (GRCm39) |
R256Q |
probably benign |
Het |
|
Other mutations in Timd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
BB009:Timd5
|
UTSW |
11 |
46,426,366 (GRCm39) |
missense |
probably benign |
0.13 |
BB019:Timd5
|
UTSW |
11 |
46,426,366 (GRCm39) |
missense |
probably benign |
0.13 |
R0314:Timd5
|
UTSW |
11 |
46,419,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R1602:Timd5
|
UTSW |
11 |
46,426,415 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Timd5
|
UTSW |
11 |
46,417,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Timd5
|
UTSW |
11 |
46,419,358 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1918:Timd5
|
UTSW |
11 |
46,419,358 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1919:Timd5
|
UTSW |
11 |
46,419,358 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2202:Timd5
|
UTSW |
11 |
46,419,394 (GRCm39) |
missense |
probably benign |
0.06 |
R2205:Timd5
|
UTSW |
11 |
46,419,394 (GRCm39) |
missense |
probably benign |
0.06 |
R3964:Timd5
|
UTSW |
11 |
46,426,340 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3965:Timd5
|
UTSW |
11 |
46,426,340 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3966:Timd5
|
UTSW |
11 |
46,426,340 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5022:Timd5
|
UTSW |
11 |
46,419,359 (GRCm39) |
missense |
probably damaging |
0.97 |
R5023:Timd5
|
UTSW |
11 |
46,419,359 (GRCm39) |
missense |
probably damaging |
0.97 |
R7294:Timd5
|
UTSW |
11 |
46,426,439 (GRCm39) |
missense |
probably benign |
0.41 |
R7441:Timd5
|
UTSW |
11 |
46,419,382 (GRCm39) |
nonsense |
probably null |
|
R7932:Timd5
|
UTSW |
11 |
46,426,366 (GRCm39) |
missense |
probably benign |
0.13 |
R8027:Timd5
|
UTSW |
11 |
46,428,744 (GRCm39) |
missense |
probably benign |
|
R9306:Timd5
|
UTSW |
11 |
46,419,519 (GRCm39) |
missense |
probably benign |
0.03 |
|