Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Anxa8 |
T |
A |
14: 33,814,579 (GRCm39) |
|
probably null |
Het |
Ap4e1 |
A |
G |
2: 126,891,479 (GRCm39) |
I83M |
probably benign |
Het |
Arhgap44 |
G |
C |
11: 64,943,921 (GRCm39) |
P197A |
probably benign |
Het |
Asb1 |
T |
A |
1: 91,480,051 (GRCm39) |
V157E |
probably damaging |
Het |
B3gat1 |
T |
A |
9: 26,666,986 (GRCm39) |
Y73N |
probably benign |
Het |
Bmp8a |
G |
A |
4: 123,218,362 (GRCm39) |
T219I |
possibly damaging |
Het |
Cacna1c |
G |
A |
6: 118,728,502 (GRCm39) |
S285F |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,289,389 (GRCm39) |
D369G |
probably damaging |
Het |
Ckap2l |
C |
T |
2: 129,111,176 (GRCm39) |
G674R |
probably damaging |
Het |
Cog2 |
A |
G |
8: 125,262,190 (GRCm39) |
Y276C |
probably damaging |
Het |
Col16a1 |
A |
T |
4: 129,948,901 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
G |
A |
2: 27,901,353 (GRCm39) |
G1282R |
unknown |
Het |
Cyp2c29 |
A |
T |
19: 39,313,439 (GRCm39) |
M351L |
probably benign |
Het |
Cyp4f15 |
T |
A |
17: 32,911,554 (GRCm39) |
D145E |
probably benign |
Het |
Defb48 |
T |
C |
14: 63,221,906 (GRCm39) |
Y4C |
unknown |
Het |
Dnaaf3 |
T |
C |
7: 4,529,903 (GRCm39) |
Q292R |
probably benign |
Het |
Dnah11 |
T |
C |
12: 118,091,343 (GRCm39) |
M930V |
possibly damaging |
Het |
Dnaja2 |
A |
T |
8: 86,280,029 (GRCm39) |
I50K |
probably damaging |
Het |
Dnm2 |
A |
G |
9: 21,385,925 (GRCm39) |
N316S |
probably damaging |
Het |
Dusp12 |
A |
G |
1: 170,708,175 (GRCm39) |
Y181H |
possibly damaging |
Het |
Efemp1 |
T |
G |
11: 28,871,795 (GRCm39) |
F437V |
possibly damaging |
Het |
Eps8l3 |
T |
A |
3: 107,798,325 (GRCm39) |
V464D |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,175,886 (GRCm39) |
L1609Q |
probably benign |
Het |
Fbxw24 |
C |
T |
9: 109,453,910 (GRCm39) |
V79I |
probably benign |
Het |
Fgl2 |
A |
T |
5: 21,580,918 (GRCm39) |
Q420L |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,396 (GRCm39) |
K408E |
probably benign |
Het |
Fkbp9 |
A |
C |
6: 56,852,692 (GRCm39) |
I471L |
probably benign |
Het |
Fndc1 |
A |
T |
17: 7,972,538 (GRCm39) |
S1465T |
probably damaging |
Het |
Fry |
A |
T |
5: 150,322,998 (GRCm39) |
T1050S |
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,749,856 (GRCm39) |
V344I |
probably benign |
Het |
Gtf3c1 |
A |
G |
7: 125,262,712 (GRCm39) |
V1049A |
probably damaging |
Het |
Ireb2 |
A |
G |
9: 54,814,098 (GRCm39) |
E829G |
probably benign |
Het |
Itih5 |
G |
A |
2: 10,245,392 (GRCm39) |
V494I |
probably benign |
Het |
Krt75 |
A |
T |
15: 101,476,507 (GRCm39) |
D419E |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,116,266 (GRCm39) |
S2378P |
probably damaging |
Het |
Lcorl |
T |
A |
5: 45,904,623 (GRCm39) |
|
probably null |
Het |
Man2a1 |
A |
T |
17: 64,966,004 (GRCm39) |
H314L |
probably damaging |
Het |
Mthfd1l |
T |
A |
10: 3,957,840 (GRCm39) |
H292Q |
possibly damaging |
Het |
Ocm |
A |
T |
5: 143,960,686 (GRCm39) |
M87K |
possibly damaging |
Het |
Oplah |
A |
G |
15: 76,186,968 (GRCm39) |
Y616H |
probably damaging |
Het |
Or4s2b |
A |
T |
2: 88,508,366 (GRCm39) |
S56C |
probably benign |
Het |
Or52e4 |
A |
C |
7: 104,705,863 (GRCm39) |
I137L |
probably benign |
Het |
Or5b99 |
T |
C |
19: 12,976,533 (GRCm39) |
L61P |
probably damaging |
Het |
Or5p58 |
A |
C |
7: 107,694,666 (GRCm39) |
I37S |
probably damaging |
Het |
Or8c13 |
C |
A |
9: 38,091,546 (GRCm39) |
S191I |
probably damaging |
Het |
Or8g32 |
A |
G |
9: 39,305,932 (GRCm39) |
T282A |
probably benign |
Het |
Pde3a |
G |
A |
6: 141,404,812 (GRCm39) |
V346M |
probably damaging |
Het |
Pdlim1 |
T |
A |
19: 40,231,892 (GRCm39) |
E162V |
possibly damaging |
Het |
Pdzd2 |
C |
G |
15: 12,374,681 (GRCm39) |
S1818T |
probably benign |
Het |
Phf24 |
G |
A |
4: 42,933,731 (GRCm39) |
G38S |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,907,186 (GRCm39) |
V701A |
probably benign |
Het |
Ppard |
C |
G |
17: 28,505,348 (GRCm39) |
R12G |
unknown |
Het |
Ptprz1 |
A |
G |
6: 23,001,545 (GRCm39) |
S1212G |
probably benign |
Het |
Rab3il1 |
C |
A |
19: 10,004,808 (GRCm39) |
Q110K |
possibly damaging |
Het |
Rin3 |
A |
T |
12: 102,327,642 (GRCm39) |
|
probably benign |
Het |
Rps6kb2 |
T |
A |
19: 4,208,677 (GRCm39) |
K280* |
probably null |
Het |
Slc27a6 |
G |
T |
18: 58,705,105 (GRCm39) |
L162F |
possibly damaging |
Het |
Slc6a19 |
T |
A |
13: 73,832,161 (GRCm39) |
I472F |
possibly damaging |
Het |
Spatc1l |
G |
A |
10: 76,405,206 (GRCm39) |
R196Q |
probably damaging |
Het |
Srp72 |
T |
C |
5: 77,132,231 (GRCm39) |
I273T |
probably damaging |
Het |
St8sia1 |
C |
A |
6: 142,813,649 (GRCm39) |
S171I |
probably benign |
Het |
Tas2r136 |
T |
C |
6: 132,754,455 (GRCm39) |
H224R |
probably damaging |
Het |
Tas2r140 |
A |
G |
6: 133,032,743 (GRCm39) |
V5A |
possibly damaging |
Het |
Tbce |
C |
T |
13: 14,194,446 (GRCm39) |
R71H |
probably damaging |
Het |
Tdrd9 |
A |
T |
12: 111,963,269 (GRCm39) |
K115* |
probably null |
Het |
Thada |
T |
A |
17: 84,580,245 (GRCm39) |
H1403L |
probably damaging |
Het |
Thap1 |
AGCAGCATCTGCTCG |
AG |
8: 26,650,882 (GRCm39) |
|
probably null |
Het |
Timm44 |
A |
G |
8: 4,317,932 (GRCm39) |
S159P |
probably damaging |
Het |
Tlk2 |
T |
A |
11: 105,171,926 (GRCm39) |
C699S |
probably damaging |
Het |
Tmem178b |
A |
G |
6: 39,981,160 (GRCm39) |
K65R |
probably damaging |
Het |
Ttc28 |
T |
C |
5: 111,425,329 (GRCm39) |
V1718A |
possibly damaging |
Het |
Ube2frt |
T |
A |
12: 36,140,729 (GRCm39) |
|
probably benign |
Het |
Unc13a |
C |
A |
8: 72,115,494 (GRCm39) |
|
probably null |
Het |
Vip |
A |
T |
10: 5,594,099 (GRCm39) |
I151F |
probably damaging |
Het |
Vps16 |
C |
T |
2: 130,280,030 (GRCm39) |
P85L |
probably benign |
Het |
Wdsub1 |
T |
C |
2: 59,700,743 (GRCm39) |
|
probably benign |
Het |
Zc3h12c |
T |
C |
9: 52,027,853 (GRCm39) |
D503G |
probably damaging |
Het |
|
Other mutations in Ttc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03278:Ttc6
|
APN |
12 |
57,668,812 (GRCm39) |
missense |
probably damaging |
0.99 |
polonius
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
tybalt
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02802:Ttc6
|
UTSW |
12 |
57,622,654 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4802001:Ttc6
|
UTSW |
12 |
57,772,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0698:Ttc6
|
UTSW |
12 |
57,720,002 (GRCm39) |
missense |
probably benign |
0.04 |
R0988:Ttc6
|
UTSW |
12 |
57,735,435 (GRCm39) |
splice site |
probably benign |
|
R1290:Ttc6
|
UTSW |
12 |
57,707,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1338:Ttc6
|
UTSW |
12 |
57,663,155 (GRCm39) |
missense |
probably benign |
0.10 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1481:Ttc6
|
UTSW |
12 |
57,783,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Ttc6
|
UTSW |
12 |
57,696,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1558:Ttc6
|
UTSW |
12 |
57,733,132 (GRCm39) |
missense |
probably benign |
0.14 |
R1570:Ttc6
|
UTSW |
12 |
57,721,549 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Ttc6
|
UTSW |
12 |
57,784,454 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1819:Ttc6
|
UTSW |
12 |
57,741,286 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Ttc6
|
UTSW |
12 |
57,707,033 (GRCm39) |
missense |
probably benign |
0.10 |
R1863:Ttc6
|
UTSW |
12 |
57,760,881 (GRCm39) |
missense |
probably benign |
0.04 |
R1872:Ttc6
|
UTSW |
12 |
57,751,338 (GRCm39) |
critical splice donor site |
probably null |
|
R1887:Ttc6
|
UTSW |
12 |
57,720,044 (GRCm39) |
missense |
probably benign |
0.04 |
R1937:Ttc6
|
UTSW |
12 |
57,663,109 (GRCm39) |
missense |
probably benign |
0.02 |
R2014:Ttc6
|
UTSW |
12 |
57,623,003 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2056:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2058:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2059:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2152:Ttc6
|
UTSW |
12 |
57,752,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R2179:Ttc6
|
UTSW |
12 |
57,719,904 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2275:Ttc6
|
UTSW |
12 |
57,749,084 (GRCm39) |
missense |
probably benign |
0.01 |
R2432:Ttc6
|
UTSW |
12 |
57,668,821 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2474:Ttc6
|
UTSW |
12 |
57,622,713 (GRCm39) |
missense |
probably benign |
0.37 |
R2853:Ttc6
|
UTSW |
12 |
57,622,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R3848:Ttc6
|
UTSW |
12 |
57,723,932 (GRCm39) |
missense |
probably damaging |
0.97 |
R3853:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3950:Ttc6
|
UTSW |
12 |
57,696,292 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3955:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3957:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R4135:Ttc6
|
UTSW |
12 |
57,679,581 (GRCm39) |
intron |
probably benign |
|
R4387:Ttc6
|
UTSW |
12 |
57,689,836 (GRCm39) |
missense |
probably benign |
0.00 |
R4577:Ttc6
|
UTSW |
12 |
57,623,441 (GRCm39) |
missense |
probably benign |
0.22 |
R4747:Ttc6
|
UTSW |
12 |
57,721,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4779:Ttc6
|
UTSW |
12 |
57,776,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Ttc6
|
UTSW |
12 |
57,749,142 (GRCm39) |
missense |
probably damaging |
0.96 |
R4898:Ttc6
|
UTSW |
12 |
57,707,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4930:Ttc6
|
UTSW |
12 |
57,720,609 (GRCm39) |
critical splice donor site |
probably null |
|
R4946:Ttc6
|
UTSW |
12 |
57,689,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5257:Ttc6
|
UTSW |
12 |
57,749,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5303:Ttc6
|
UTSW |
12 |
57,622,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Ttc6
|
UTSW |
12 |
57,689,821 (GRCm39) |
splice site |
probably null |
|
R5402:Ttc6
|
UTSW |
12 |
57,783,817 (GRCm39) |
nonsense |
probably null |
|
R5428:Ttc6
|
UTSW |
12 |
57,736,620 (GRCm39) |
missense |
probably null |
0.98 |
R5436:Ttc6
|
UTSW |
12 |
57,721,380 (GRCm39) |
splice site |
probably null |
|
R5646:Ttc6
|
UTSW |
12 |
57,622,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Ttc6
|
UTSW |
12 |
57,724,000 (GRCm39) |
missense |
probably benign |
0.22 |
R5792:Ttc6
|
UTSW |
12 |
57,719,990 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5808:Ttc6
|
UTSW |
12 |
57,664,397 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5842:Ttc6
|
UTSW |
12 |
57,783,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Ttc6
|
UTSW |
12 |
57,720,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R6144:Ttc6
|
UTSW |
12 |
57,719,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6155:Ttc6
|
UTSW |
12 |
57,784,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6283:Ttc6
|
UTSW |
12 |
57,749,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6371:Ttc6
|
UTSW |
12 |
57,775,249 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Ttc6
|
UTSW |
12 |
57,721,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ttc6
|
UTSW |
12 |
57,735,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6795:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6959:Ttc6
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
R7053:Ttc6
|
UTSW |
12 |
57,707,318 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Ttc6
|
UTSW |
12 |
57,623,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7259:Ttc6
|
UTSW |
12 |
57,622,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Ttc6
|
UTSW |
12 |
57,622,837 (GRCm39) |
missense |
probably damaging |
0.96 |
R7369:Ttc6
|
UTSW |
12 |
57,719,717 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Ttc6
|
UTSW |
12 |
57,743,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R7429:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7430:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Ttc6
|
UTSW |
12 |
57,719,922 (GRCm39) |
missense |
probably benign |
0.02 |
R7535:Ttc6
|
UTSW |
12 |
57,623,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7866:Ttc6
|
UTSW |
12 |
57,721,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R7901:Ttc6
|
UTSW |
12 |
57,735,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7945:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7965:Ttc6
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8062:Ttc6
|
UTSW |
12 |
57,783,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8119:Ttc6
|
UTSW |
12 |
57,752,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8142:Ttc6
|
UTSW |
12 |
57,744,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8154:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ttc6
|
UTSW |
12 |
57,720,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ttc6
|
UTSW |
12 |
57,707,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Ttc6
|
UTSW |
12 |
57,707,282 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8696:Ttc6
|
UTSW |
12 |
57,784,492 (GRCm39) |
missense |
probably benign |
0.20 |
R8875:Ttc6
|
UTSW |
12 |
57,776,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8875:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R8876:Ttc6
|
UTSW |
12 |
57,784,489 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8924:Ttc6
|
UTSW |
12 |
57,697,790 (GRCm39) |
nonsense |
probably null |
|
R8944:Ttc6
|
UTSW |
12 |
57,689,826 (GRCm39) |
missense |
|
|
R8956:Ttc6
|
UTSW |
12 |
57,775,196 (GRCm39) |
nonsense |
probably null |
|
R9009:Ttc6
|
UTSW |
12 |
57,744,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Ttc6
|
UTSW |
12 |
57,752,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ttc6
|
UTSW |
12 |
57,783,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Ttc6
|
UTSW |
12 |
57,622,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Ttc6
|
UTSW |
12 |
57,776,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Ttc6
|
UTSW |
12 |
57,753,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9331:Ttc6
|
UTSW |
12 |
57,720,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Ttc6
|
UTSW |
12 |
57,784,404 (GRCm39) |
nonsense |
probably null |
|
R9430:Ttc6
|
UTSW |
12 |
57,733,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Ttc6
|
UTSW |
12 |
57,664,299 (GRCm39) |
missense |
probably benign |
|
R9688:Ttc6
|
UTSW |
12 |
57,720,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9732:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
probably benign |
0.36 |
R9740:Ttc6
|
UTSW |
12 |
57,736,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Ttc6
|
UTSW |
12 |
57,701,559 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ttc6
|
UTSW |
12 |
57,622,904 (GRCm39) |
missense |
probably damaging |
0.96 |
X0058:Ttc6
|
UTSW |
12 |
57,753,637 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ttc6
|
UTSW |
12 |
57,744,161 (GRCm39) |
missense |
probably benign |
0.08 |
|