Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810030O07Rik |
A |
G |
X: 12,530,764 (GRCm39) |
V199A |
possibly damaging |
Het |
Aco1 |
T |
C |
4: 40,175,996 (GRCm39) |
M210T |
probably damaging |
Het |
Actr10 |
G |
A |
12: 70,990,289 (GRCm39) |
E114K |
probably benign |
Het |
Adam6b |
T |
C |
12: 113,454,764 (GRCm39) |
M527T |
probably benign |
Het |
Ahi1 |
C |
T |
10: 20,857,274 (GRCm39) |
T623M |
probably damaging |
Het |
Aldh8a1 |
T |
C |
10: 21,271,545 (GRCm39) |
W424R |
probably damaging |
Het |
Apeh |
A |
T |
9: 107,969,071 (GRCm39) |
S299T |
probably benign |
Het |
Bbs5 |
A |
C |
2: 69,485,895 (GRCm39) |
I147L |
probably benign |
Het |
Bmp2k |
T |
G |
5: 97,179,109 (GRCm39) |
|
probably benign |
Het |
C2cd6 |
A |
G |
1: 59,101,651 (GRCm39) |
F336S |
probably damaging |
Het |
Cd274 |
T |
A |
19: 29,359,938 (GRCm39) |
L248M |
probably damaging |
Het |
Chsy3 |
T |
A |
18: 59,542,383 (GRCm39) |
M507K |
possibly damaging |
Het |
Clip2 |
T |
C |
5: 134,531,984 (GRCm39) |
N572S |
probably damaging |
Het |
Commd9 |
A |
G |
2: 101,731,324 (GRCm39) |
T170A |
probably benign |
Het |
Cpt1c |
G |
A |
7: 44,609,580 (GRCm39) |
S674L |
probably damaging |
Het |
Dhx33 |
C |
A |
11: 70,878,030 (GRCm39) |
R671L |
probably damaging |
Het |
Dnah5 |
G |
A |
15: 28,299,386 (GRCm39) |
E1583K |
probably damaging |
Het |
Eed |
G |
T |
7: 89,621,493 (GRCm39) |
N51K |
probably damaging |
Het |
Efcab14 |
A |
G |
4: 115,617,261 (GRCm39) |
|
probably benign |
Het |
Ephb2 |
A |
C |
4: 136,384,762 (GRCm39) |
M884R |
probably damaging |
Het |
Foxn2 |
G |
T |
17: 88,770,479 (GRCm39) |
A109S |
probably benign |
Het |
Fut1 |
A |
T |
7: 45,268,871 (GRCm39) |
D220V |
probably damaging |
Het |
Gm6468 |
C |
T |
5: 95,429,066 (GRCm39) |
|
noncoding transcript |
Het |
Gm7964 |
A |
T |
7: 83,405,515 (GRCm39) |
|
noncoding transcript |
Het |
Gm9772 |
C |
T |
17: 22,226,031 (GRCm39) |
|
probably benign |
Het |
Golph3 |
G |
T |
15: 12,349,578 (GRCm39) |
M199I |
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,394,884 (GRCm39) |
N1666D |
probably damaging |
Het |
Itprid1 |
A |
G |
6: 55,944,922 (GRCm39) |
T548A |
unknown |
Het |
Kif12 |
C |
T |
4: 63,084,732 (GRCm39) |
E529K |
probably benign |
Het |
Lpp |
C |
T |
16: 24,580,895 (GRCm39) |
R204W |
probably damaging |
Het |
Lrrc52 |
T |
A |
1: 167,293,949 (GRCm39) |
N112I |
probably damaging |
Het |
Msi1 |
T |
A |
5: 115,579,506 (GRCm39) |
|
probably null |
Het |
Nasp |
T |
G |
4: 116,461,997 (GRCm39) |
E170A |
probably damaging |
Het |
Necab2 |
T |
A |
8: 120,189,391 (GRCm39) |
V187E |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,929,804 (GRCm39) |
E5790G |
probably damaging |
Het |
Or7e176 |
A |
T |
9: 20,171,511 (GRCm39) |
D125V |
probably damaging |
Het |
Or9a7 |
A |
G |
6: 40,520,980 (GRCm39) |
L311P |
probably damaging |
Het |
Pard3b |
C |
T |
1: 62,205,541 (GRCm39) |
T445I |
probably damaging |
Het |
Pcdh10 |
A |
G |
3: 45,335,377 (GRCm39) |
I564V |
probably benign |
Het |
Pcdhb22 |
T |
A |
18: 37,653,602 (GRCm39) |
L690Q |
probably damaging |
Het |
Pemt |
T |
A |
11: 59,867,680 (GRCm39) |
T115S |
probably damaging |
Het |
Plcl2 |
A |
G |
17: 50,913,669 (GRCm39) |
N226S |
possibly damaging |
Het |
Ppp6r1 |
A |
G |
7: 4,636,341 (GRCm39) |
S750P |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,758,771 (GRCm39) |
V375A |
probably damaging |
Het |
Psd3 |
A |
C |
8: 68,356,797 (GRCm39) |
M673R |
probably damaging |
Het |
Ptprt |
T |
C |
2: 161,372,437 (GRCm39) |
I1392V |
probably damaging |
Het |
Rlf |
G |
A |
4: 121,039,811 (GRCm39) |
T200I |
probably benign |
Het |
Robo1 |
G |
A |
16: 72,768,872 (GRCm39) |
G479D |
possibly damaging |
Het |
Rpe65 |
A |
G |
3: 159,309,988 (GRCm39) |
D87G |
possibly damaging |
Het |
Sema3g |
T |
C |
14: 30,943,181 (GRCm39) |
V148A |
probably damaging |
Het |
Sgms2 |
G |
A |
3: 131,116,833 (GRCm39) |
P341S |
probably benign |
Het |
Skint7 |
A |
T |
4: 111,839,225 (GRCm39) |
Q173L |
possibly damaging |
Het |
Slc2a9 |
G |
A |
5: 38,594,013 (GRCm39) |
A150V |
probably benign |
Het |
Slc35c2 |
A |
G |
2: 165,124,801 (GRCm39) |
L58P |
probably damaging |
Het |
Slc7a6 |
G |
A |
8: 106,923,206 (GRCm39) |
C495Y |
possibly damaging |
Het |
Smurf1 |
G |
A |
5: 144,823,248 (GRCm39) |
P458L |
probably damaging |
Het |
Spag1 |
C |
T |
15: 36,221,710 (GRCm39) |
T601I |
probably benign |
Het |
Spink8 |
A |
T |
9: 109,649,665 (GRCm39) |
Q49L |
possibly damaging |
Het |
Spout1 |
A |
T |
2: 30,065,266 (GRCm39) |
Y284N |
probably damaging |
Het |
Srrm1 |
A |
T |
4: 135,080,427 (GRCm39) |
M1K |
probably null |
Het |
Stxbp5l |
A |
G |
16: 37,150,257 (GRCm39) |
L116P |
probably damaging |
Het |
Tmem41b |
A |
G |
7: 109,577,960 (GRCm39) |
V108A |
probably damaging |
Het |
Tra2b |
A |
G |
16: 22,067,790 (GRCm39) |
|
probably benign |
Het |
Trio |
G |
T |
15: 27,902,647 (GRCm39) |
H271Q |
probably benign |
Het |
Ttn |
A |
G |
2: 76,723,263 (GRCm39) |
|
probably benign |
Het |
Usp51 |
A |
T |
X: 151,791,669 (GRCm39) |
H421L |
probably damaging |
Het |
Vmn2r29 |
A |
T |
7: 7,244,810 (GRCm39) |
W355R |
probably damaging |
Het |
Vpreb1a |
T |
C |
16: 16,686,603 (GRCm39) |
N96D |
possibly damaging |
Het |
Zfp318 |
C |
T |
17: 46,707,736 (GRCm39) |
R265* |
probably null |
Het |
Zp3r |
C |
A |
1: 130,524,404 (GRCm39) |
C213F |
probably damaging |
Het |
|
Other mutations in Tlr9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00864:Tlr9
|
APN |
9 |
106,102,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01764:Tlr9
|
APN |
9 |
106,103,004 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:Tlr9
|
APN |
9 |
106,102,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02851:Tlr9
|
APN |
9 |
106,101,929 (GRCm39) |
nonsense |
probably null |
|
Asura
|
UTSW |
9 |
106,101,846 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg1
|
UTSW |
9 |
106,102,206 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg11
|
UTSW |
9 |
106,101,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg2
|
UTSW |
9 |
106,103,664 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg3
|
UTSW |
9 |
106,101,351 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg5
|
UTSW |
9 |
106,101,888 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg6
|
UTSW |
9 |
106,103,792 (GRCm39) |
missense |
probably damaging |
1.00 |
cpg7
|
UTSW |
9 |
106,102,548 (GRCm39) |
missense |
probably benign |
0.00 |
Meager
|
UTSW |
9 |
106,101,338 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Tlr9
|
UTSW |
9 |
106,100,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Tlr9
|
UTSW |
9 |
106,102,164 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0058:Tlr9
|
UTSW |
9 |
106,102,164 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0071:Tlr9
|
UTSW |
9 |
106,100,777 (GRCm39) |
missense |
probably benign |
|
R0071:Tlr9
|
UTSW |
9 |
106,100,777 (GRCm39) |
missense |
probably benign |
|
R0126:Tlr9
|
UTSW |
9 |
106,102,881 (GRCm39) |
missense |
probably benign |
0.01 |
R0165:Tlr9
|
UTSW |
9 |
106,103,286 (GRCm39) |
missense |
probably benign |
0.10 |
R0534:Tlr9
|
UTSW |
9 |
106,102,086 (GRCm39) |
missense |
probably benign |
0.01 |
R0585:Tlr9
|
UTSW |
9 |
106,102,275 (GRCm39) |
missense |
probably benign |
0.01 |
R1527:Tlr9
|
UTSW |
9 |
106,100,949 (GRCm39) |
missense |
probably benign |
0.09 |
R1712:Tlr9
|
UTSW |
9 |
106,101,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1817:Tlr9
|
UTSW |
9 |
106,102,142 (GRCm39) |
missense |
probably benign |
|
R1940:Tlr9
|
UTSW |
9 |
106,101,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Tlr9
|
UTSW |
9 |
106,102,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Tlr9
|
UTSW |
9 |
106,101,140 (GRCm39) |
missense |
probably benign |
0.05 |
R3700:Tlr9
|
UTSW |
9 |
106,101,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Tlr9
|
UTSW |
9 |
106,101,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R4608:Tlr9
|
UTSW |
9 |
106,102,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R4612:Tlr9
|
UTSW |
9 |
106,101,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Tlr9
|
UTSW |
9 |
106,101,876 (GRCm39) |
missense |
probably benign |
|
R5173:Tlr9
|
UTSW |
9 |
106,103,151 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5472:Tlr9
|
UTSW |
9 |
106,101,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5572:Tlr9
|
UTSW |
9 |
106,102,836 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5618:Tlr9
|
UTSW |
9 |
106,101,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5820:Tlr9
|
UTSW |
9 |
106,099,906 (GRCm39) |
critical splice donor site |
probably null |
|
R6393:Tlr9
|
UTSW |
9 |
106,102,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Tlr9
|
UTSW |
9 |
106,102,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Tlr9
|
UTSW |
9 |
106,101,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7385:Tlr9
|
UTSW |
9 |
106,102,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Tlr9
|
UTSW |
9 |
106,101,729 (GRCm39) |
missense |
probably benign |
0.00 |
R7561:Tlr9
|
UTSW |
9 |
106,103,148 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Tlr9
|
UTSW |
9 |
106,099,834 (GRCm39) |
start gained |
probably benign |
|
R8892:Tlr9
|
UTSW |
9 |
106,099,834 (GRCm39) |
start gained |
probably benign |
|
R8926:Tlr9
|
UTSW |
9 |
106,103,213 (GRCm39) |
missense |
probably benign |
|
R9221:Tlr9
|
UTSW |
9 |
106,101,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Tlr9
|
UTSW |
9 |
106,102,752 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9581:Tlr9
|
UTSW |
9 |
106,101,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Tlr9
|
UTSW |
9 |
106,100,721 (GRCm39) |
missense |
probably benign |
0.00 |
R9697:Tlr9
|
UTSW |
9 |
106,100,723 (GRCm39) |
nonsense |
probably null |
|
R9788:Tlr9
|
UTSW |
9 |
106,101,006 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tlr9
|
UTSW |
9 |
106,100,862 (GRCm39) |
missense |
probably benign |
0.03 |
|