Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg5 |
C |
T |
8: 95,660,646 (GRCm39) |
T95I |
|
Het |
Arap2 |
C |
T |
5: 62,906,681 (GRCm39) |
V113I |
probably benign |
Het |
Atraid |
C |
T |
5: 31,209,590 (GRCm39) |
Q85* |
probably null |
Het |
Bcdin3d |
T |
C |
15: 99,368,344 (GRCm39) |
D285G |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,610 (GRCm39) |
I346K |
probably benign |
Het |
Carmil3 |
T |
C |
14: 55,736,069 (GRCm39) |
W604R |
probably damaging |
Het |
Ccl6 |
C |
T |
11: 83,480,582 (GRCm39) |
|
probably null |
Het |
Cct4 |
C |
T |
11: 22,940,616 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
C |
T |
17: 43,156,285 (GRCm39) |
R84Q |
possibly damaging |
Het |
Cdt1 |
T |
A |
8: 123,295,012 (GRCm39) |
|
probably null |
Het |
Cln3 |
C |
T |
7: 126,181,942 (GRCm39) |
G40D |
probably damaging |
Het |
Crlf3 |
T |
C |
11: 79,955,216 (GRCm39) |
S47G |
possibly damaging |
Het |
Csrp3 |
T |
C |
7: 48,480,385 (GRCm39) |
K193R |
probably benign |
Het |
Cxcl3 |
A |
C |
5: 90,934,219 (GRCm39) |
E33A |
probably damaging |
Het |
Cyp11b1 |
T |
C |
15: 74,708,708 (GRCm39) |
D362G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,321,935 (GRCm39) |
D3795G |
probably damaging |
Het |
Dnah3 |
G |
A |
7: 119,521,965 (GRCm39) |
A4076V |
probably damaging |
Het |
Dnaja3 |
T |
A |
16: 4,519,046 (GRCm39) |
I380N |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,546,246 (GRCm39) |
H785L |
probably benign |
Het |
Dop1b |
T |
G |
16: 93,607,023 (GRCm39) |
F2226V |
possibly damaging |
Het |
Dscaml1 |
A |
T |
9: 45,581,437 (GRCm39) |
I419F |
probably benign |
Het |
Dyrk4 |
T |
A |
6: 126,862,200 (GRCm39) |
I431F |
probably benign |
Het |
Endog |
C |
T |
2: 30,062,902 (GRCm39) |
R181C |
probably damaging |
Het |
Fam90a1a |
A |
T |
8: 22,453,641 (GRCm39) |
Y332F |
probably benign |
Het |
Fastkd3 |
T |
C |
13: 68,737,499 (GRCm39) |
I588T |
probably benign |
Het |
Galnt9 |
G |
A |
5: 110,737,694 (GRCm39) |
V217I |
probably benign |
Het |
Gm973 |
A |
T |
1: 59,601,888 (GRCm39) |
R501* |
probably null |
Het |
Gnptab |
C |
T |
10: 88,215,019 (GRCm39) |
|
probably benign |
Het |
Gpn1 |
T |
C |
5: 31,660,761 (GRCm39) |
F184S |
probably damaging |
Het |
Imp3 |
G |
T |
9: 56,845,007 (GRCm39) |
V73L |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,032,365 (GRCm39) |
D259G |
probably null |
Het |
Jag1 |
T |
C |
2: 136,948,802 (GRCm39) |
S142G |
probably benign |
Het |
Klhl5 |
A |
T |
5: 65,289,098 (GRCm39) |
E120V |
probably benign |
Het |
Lct |
C |
A |
1: 128,228,197 (GRCm39) |
V1099L |
probably benign |
Het |
Lrba |
G |
C |
3: 86,235,633 (GRCm39) |
W912C |
probably damaging |
Het |
Lss |
C |
T |
10: 76,383,305 (GRCm39) |
T535I |
probably damaging |
Het |
Mcts2 |
T |
C |
2: 152,529,297 (GRCm39) |
I36T |
probably benign |
Het |
Meikin |
T |
A |
11: 54,302,738 (GRCm39) |
N383K |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,461,055 (GRCm39) |
Y663C |
probably damaging |
Het |
Nadk2 |
T |
A |
15: 9,108,342 (GRCm39) |
M419K |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nfat5 |
T |
C |
8: 108,020,515 (GRCm39) |
S20P |
probably damaging |
Het |
Nlrp1a |
C |
T |
11: 71,014,119 (GRCm39) |
C377Y |
probably damaging |
Het |
Nlrp9a |
T |
C |
7: 26,250,463 (GRCm39) |
V76A |
probably damaging |
Het |
Nrap |
C |
A |
19: 56,366,567 (GRCm39) |
A341S |
probably benign |
Het |
Ntng2 |
T |
C |
2: 29,117,732 (GRCm39) |
S239G |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,197,566 (GRCm39) |
C207S |
possibly damaging |
Het |
Or10a4 |
T |
C |
7: 106,697,619 (GRCm39) |
*316R |
probably null |
Het |
Or10ak7 |
T |
A |
4: 118,791,146 (GRCm39) |
I300F |
possibly damaging |
Het |
Or1j17 |
T |
C |
2: 36,578,107 (GRCm39) |
I31T |
probably benign |
Het |
Or2ag1 |
T |
C |
7: 106,473,474 (GRCm39) |
|
probably benign |
Het |
Or5b118 |
T |
A |
19: 13,448,337 (GRCm39) |
M1K |
probably null |
Het |
Or8c13 |
A |
C |
9: 38,091,318 (GRCm39) |
V267G |
probably damaging |
Het |
Or8k31-ps1 |
C |
T |
2: 86,356,150 (GRCm39) |
V124I |
probably damaging |
Het |
Pcdhgb2 |
C |
A |
18: 37,823,159 (GRCm39) |
A50E |
probably damaging |
Het |
Pgap1 |
A |
T |
1: 54,582,220 (GRCm39) |
M209K |
possibly damaging |
Het |
Plbd1 |
T |
A |
6: 136,589,829 (GRCm39) |
D463V |
probably damaging |
Het |
Plcg2 |
T |
A |
8: 118,310,288 (GRCm39) |
I380N |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,087,285 (GRCm39) |
W184R |
probably damaging |
Het |
Pptc7 |
G |
A |
5: 122,451,840 (GRCm39) |
V202I |
probably benign |
Het |
Prpf6 |
C |
T |
2: 181,282,389 (GRCm39) |
A510V |
probably damaging |
Het |
Prr5l |
T |
C |
2: 101,559,777 (GRCm39) |
Y235C |
probably benign |
Het |
Ptprk |
T |
C |
10: 28,450,905 (GRCm39) |
V1022A |
probably benign |
Het |
Rbl2 |
T |
C |
8: 91,810,057 (GRCm39) |
|
probably null |
Het |
Rmnd1 |
T |
C |
10: 4,360,753 (GRCm39) |
K348E |
probably benign |
Het |
Rsf1 |
CGGCGGC |
CGGCGGCGGGGGCGGC |
7: 97,229,136 (GRCm39) |
|
probably benign |
Het |
Sacs |
T |
A |
14: 61,429,241 (GRCm39) |
N433K |
probably benign |
Het |
Scyl1 |
T |
C |
19: 5,810,057 (GRCm39) |
T590A |
probably benign |
Het |
Sdhd |
A |
G |
9: 50,508,533 (GRCm39) |
V111A |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,827,509 (GRCm39) |
P330Q |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,848,128 (GRCm39) |
P31S |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,687,211 (GRCm39) |
R457W |
probably damaging |
Het |
Slc5a8 |
G |
A |
10: 88,755,364 (GRCm39) |
M490I |
probably benign |
Het |
Slx4 |
A |
G |
16: 3,806,844 (GRCm39) |
I533T |
probably benign |
Het |
Slx4ip |
T |
A |
2: 136,888,650 (GRCm39) |
F110L |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,652,359 (GRCm39) |
R2000G |
probably benign |
Het |
Snx8 |
T |
C |
5: 140,346,008 (GRCm39) |
E75G |
possibly damaging |
Het |
Stab2 |
C |
A |
10: 86,735,705 (GRCm39) |
C1292F |
probably damaging |
Het |
Swt1 |
A |
T |
1: 151,270,364 (GRCm39) |
M617K |
possibly damaging |
Het |
Tiam2 |
T |
A |
17: 3,568,687 (GRCm39) |
I1611N |
possibly damaging |
Het |
Tmem63b |
T |
G |
17: 45,972,748 (GRCm39) |
N682T |
probably benign |
Het |
Trio |
C |
T |
15: 27,871,273 (GRCm39) |
V674M |
probably damaging |
Het |
Trpc3 |
G |
A |
3: 36,704,286 (GRCm39) |
T557M |
possibly damaging |
Het |
Vac14 |
T |
G |
8: 111,397,674 (GRCm39) |
L463R |
probably damaging |
Het |
Vmn2r43 |
C |
T |
7: 8,256,379 (GRCm39) |
|
probably null |
Het |
Wdr49 |
A |
T |
3: 75,265,751 (GRCm39) |
Y232N |
possibly damaging |
Het |
Wdr90 |
T |
C |
17: 26,064,367 (GRCm39) |
M1835V |
probably benign |
Het |
Xpc |
T |
C |
6: 91,469,320 (GRCm39) |
E809G |
probably damaging |
Het |
Zfhx3 |
A |
T |
8: 109,675,493 (GRCm39) |
Q2181L |
probably damaging |
Het |
Zfp442 |
T |
C |
2: 150,251,201 (GRCm39) |
T234A |
probably benign |
Het |
Zfp764 |
A |
T |
7: 127,004,450 (GRCm39) |
M227K |
probably benign |
Het |
Zfp764l1 |
A |
G |
7: 126,990,695 (GRCm39) |
S431P |
probably benign |
Het |
Zfp957 |
A |
G |
14: 79,450,750 (GRCm39) |
S350P |
unknown |
Het |
Zscan29 |
T |
A |
2: 120,999,761 (GRCm39) |
K147* |
probably null |
Het |
|
Other mutations in Thoc2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01023:Thoc2l
|
APN |
5 |
104,668,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Thoc2l
|
APN |
5 |
104,669,612 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01133:Thoc2l
|
APN |
5 |
104,665,528 (GRCm39) |
missense |
probably benign |
|
IGL01564:Thoc2l
|
APN |
5 |
104,668,529 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01727:Thoc2l
|
APN |
5 |
104,667,379 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02086:Thoc2l
|
APN |
5 |
104,666,867 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02153:Thoc2l
|
APN |
5 |
104,668,949 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02256:Thoc2l
|
APN |
5 |
104,668,149 (GRCm39) |
nonsense |
probably null |
|
IGL02436:Thoc2l
|
APN |
5 |
104,669,021 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02969:Thoc2l
|
APN |
5 |
104,667,209 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03275:Thoc2l
|
APN |
5 |
104,666,143 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03357:Thoc2l
|
APN |
5 |
104,668,334 (GRCm39) |
missense |
probably damaging |
1.00 |
Magnetar
|
UTSW |
5 |
104,668,145 (GRCm39) |
missense |
probably damaging |
0.99 |
F2404:Thoc2l
|
UTSW |
5 |
104,668,096 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0318:Thoc2l
|
UTSW |
5 |
104,665,619 (GRCm39) |
missense |
probably benign |
0.00 |
R0349:Thoc2l
|
UTSW |
5 |
104,667,842 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0454:Thoc2l
|
UTSW |
5 |
104,666,077 (GRCm39) |
missense |
probably benign |
0.45 |
R0742:Thoc2l
|
UTSW |
5 |
104,670,020 (GRCm39) |
missense |
probably benign |
0.00 |
R0842:Thoc2l
|
UTSW |
5 |
104,667,066 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0882:Thoc2l
|
UTSW |
5 |
104,666,875 (GRCm39) |
missense |
probably benign |
0.05 |
R1123:Thoc2l
|
UTSW |
5 |
104,666,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Thoc2l
|
UTSW |
5 |
104,668,769 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1205:Thoc2l
|
UTSW |
5 |
104,668,079 (GRCm39) |
missense |
probably benign |
0.28 |
R1261:Thoc2l
|
UTSW |
5 |
104,668,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R1432:Thoc2l
|
UTSW |
5 |
104,665,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1447:Thoc2l
|
UTSW |
5 |
104,670,070 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1466:Thoc2l
|
UTSW |
5 |
104,666,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Thoc2l
|
UTSW |
5 |
104,666,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R1584:Thoc2l
|
UTSW |
5 |
104,666,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R1636:Thoc2l
|
UTSW |
5 |
104,668,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R1686:Thoc2l
|
UTSW |
5 |
104,667,789 (GRCm39) |
nonsense |
probably null |
|
R1698:Thoc2l
|
UTSW |
5 |
104,668,376 (GRCm39) |
missense |
probably benign |
0.09 |
R1816:Thoc2l
|
UTSW |
5 |
104,665,700 (GRCm39) |
missense |
probably benign |
0.16 |
R1903:Thoc2l
|
UTSW |
5 |
104,666,196 (GRCm39) |
missense |
probably benign |
0.00 |
R2096:Thoc2l
|
UTSW |
5 |
104,667,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2146:Thoc2l
|
UTSW |
5 |
104,666,857 (GRCm39) |
missense |
probably benign |
|
R2226:Thoc2l
|
UTSW |
5 |
104,667,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Thoc2l
|
UTSW |
5 |
104,667,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R2383:Thoc2l
|
UTSW |
5 |
104,666,854 (GRCm39) |
missense |
probably benign |
0.23 |
R2656:Thoc2l
|
UTSW |
5 |
104,667,181 (GRCm39) |
missense |
probably benign |
0.05 |
R3982:Thoc2l
|
UTSW |
5 |
104,668,889 (GRCm39) |
missense |
probably benign |
0.29 |
R3983:Thoc2l
|
UTSW |
5 |
104,668,889 (GRCm39) |
missense |
probably benign |
0.29 |
R4115:Thoc2l
|
UTSW |
5 |
104,667,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4345:Thoc2l
|
UTSW |
5 |
104,669,315 (GRCm39) |
missense |
probably benign |
0.21 |
R4697:Thoc2l
|
UTSW |
5 |
104,670,106 (GRCm39) |
missense |
probably benign |
0.00 |
R4711:Thoc2l
|
UTSW |
5 |
104,667,527 (GRCm39) |
missense |
probably damaging |
0.98 |
R4742:Thoc2l
|
UTSW |
5 |
104,666,723 (GRCm39) |
missense |
probably benign |
0.17 |
R4758:Thoc2l
|
UTSW |
5 |
104,668,265 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4863:Thoc2l
|
UTSW |
5 |
104,665,616 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4867:Thoc2l
|
UTSW |
5 |
104,668,868 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5024:Thoc2l
|
UTSW |
5 |
104,670,124 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5114:Thoc2l
|
UTSW |
5 |
104,667,742 (GRCm39) |
missense |
probably damaging |
0.99 |
R5117:Thoc2l
|
UTSW |
5 |
104,668,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Thoc2l
|
UTSW |
5 |
104,667,523 (GRCm39) |
missense |
probably benign |
0.03 |
R5341:Thoc2l
|
UTSW |
5 |
104,665,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Thoc2l
|
UTSW |
5 |
104,666,225 (GRCm39) |
missense |
probably damaging |
0.99 |
R5421:Thoc2l
|
UTSW |
5 |
104,666,261 (GRCm39) |
missense |
probably benign |
0.01 |
R5422:Thoc2l
|
UTSW |
5 |
104,667,512 (GRCm39) |
missense |
probably damaging |
0.98 |
R5606:Thoc2l
|
UTSW |
5 |
104,669,744 (GRCm39) |
missense |
probably benign |
0.00 |
R5939:Thoc2l
|
UTSW |
5 |
104,667,073 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6104:Thoc2l
|
UTSW |
5 |
104,666,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Thoc2l
|
UTSW |
5 |
104,666,262 (GRCm39) |
missense |
probably benign |
0.00 |
R6316:Thoc2l
|
UTSW |
5 |
104,667,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Thoc2l
|
UTSW |
5 |
104,668,064 (GRCm39) |
missense |
probably benign |
0.11 |
R6408:Thoc2l
|
UTSW |
5 |
104,666,643 (GRCm39) |
missense |
probably benign |
0.19 |
R6458:Thoc2l
|
UTSW |
5 |
104,670,169 (GRCm39) |
missense |
probably benign |
0.02 |
R6722:Thoc2l
|
UTSW |
5 |
104,668,145 (GRCm39) |
missense |
probably damaging |
0.99 |
R6789:Thoc2l
|
UTSW |
5 |
104,665,555 (GRCm39) |
missense |
probably benign |
0.00 |
R7494:Thoc2l
|
UTSW |
5 |
104,666,284 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7733:Thoc2l
|
UTSW |
5 |
104,667,826 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7884:Thoc2l
|
UTSW |
5 |
104,669,212 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7945:Thoc2l
|
UTSW |
5 |
104,666,413 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8112:Thoc2l
|
UTSW |
5 |
104,669,501 (GRCm39) |
missense |
probably benign |
|
R8131:Thoc2l
|
UTSW |
5 |
104,669,027 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8418:Thoc2l
|
UTSW |
5 |
104,667,724 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8963:Thoc2l
|
UTSW |
5 |
104,665,652 (GRCm39) |
missense |
probably benign |
0.00 |
R9051:Thoc2l
|
UTSW |
5 |
104,666,818 (GRCm39) |
missense |
probably benign |
0.07 |
R9169:Thoc2l
|
UTSW |
5 |
104,666,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Thoc2l
|
UTSW |
5 |
104,667,320 (GRCm39) |
missense |
probably benign |
0.00 |
R9358:Thoc2l
|
UTSW |
5 |
104,667,826 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9451:Thoc2l
|
UTSW |
5 |
104,668,644 (GRCm39) |
missense |
probably benign |
0.07 |
R9452:Thoc2l
|
UTSW |
5 |
104,669,610 (GRCm39) |
missense |
probably benign |
0.00 |
R9567:Thoc2l
|
UTSW |
5 |
104,669,644 (GRCm39) |
missense |
probably benign |
0.00 |
R9760:Thoc2l
|
UTSW |
5 |
104,667,101 (GRCm39) |
missense |
probably benign |
|
Z1176:Thoc2l
|
UTSW |
5 |
104,668,058 (GRCm39) |
missense |
possibly damaging |
0.69 |
|