Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 8,957,267 (GRCm39) |
V132A |
possibly damaging |
Het |
Acp3 |
A |
T |
9: 104,184,174 (GRCm39) |
V292E |
probably damaging |
Het |
Adamts10 |
T |
C |
17: 33,747,870 (GRCm39) |
V102A |
possibly damaging |
Het |
Add2 |
A |
G |
6: 86,073,728 (GRCm39) |
T206A |
probably benign |
Het |
Alg12 |
A |
T |
15: 88,700,391 (GRCm39) |
L15Q |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,307,800 (GRCm39) |
D346E |
probably damaging |
Het |
Armc2 |
A |
T |
10: 41,799,790 (GRCm39) |
N689K |
probably damaging |
Het |
Best3 |
T |
A |
10: 116,860,460 (GRCm39) |
D573E |
probably benign |
Het |
Bltp1 |
T |
G |
3: 37,020,086 (GRCm39) |
N2108K |
probably damaging |
Het |
Ccdc80 |
A |
T |
16: 44,916,261 (GRCm39) |
Q339L |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,778,242 (GRCm39) |
V19A |
probably benign |
Het |
Cimap1a |
G |
A |
7: 140,428,398 (GRCm39) |
|
probably benign |
Het |
Cnksr1 |
A |
T |
4: 133,956,986 (GRCm39) |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,786,345 (GRCm39) |
V525E |
unknown |
Het |
Cplane1 |
T |
C |
15: 8,251,421 (GRCm39) |
S1898P |
probably benign |
Het |
Crebrf |
T |
C |
17: 26,961,394 (GRCm39) |
S172P |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 16,059,439 (GRCm39) |
I2099V |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,586,233 (GRCm39) |
M400K |
possibly damaging |
Het |
Dnah11 |
A |
T |
12: 117,958,935 (GRCm39) |
F2983I |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,735,733 (GRCm39) |
V1005A |
possibly damaging |
Het |
Dyrk2 |
C |
A |
10: 118,704,153 (GRCm39) |
G34C |
probably damaging |
Het |
Eif4a1 |
A |
T |
11: 69,559,423 (GRCm39) |
|
probably benign |
Het |
Eno4 |
G |
T |
19: 58,952,975 (GRCm39) |
D330Y |
probably damaging |
Het |
Faf1 |
G |
A |
4: 109,699,496 (GRCm39) |
C347Y |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,234,100 (GRCm39) |
Y124C |
probably damaging |
Het |
Fam227a |
G |
T |
15: 79,521,255 (GRCm39) |
F269L |
probably benign |
Het |
Fancm |
C |
A |
12: 65,122,605 (GRCm39) |
D42E |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,404,317 (GRCm39) |
I356N |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,509,869 (GRCm39) |
T1444S |
probably damaging |
Het |
Galr1 |
A |
G |
18: 82,412,065 (GRCm39) |
L267P |
probably damaging |
Het |
Gbx1 |
T |
C |
5: 24,709,837 (GRCm39) |
H336R |
probably damaging |
Het |
Gimap8 |
A |
T |
6: 48,636,281 (GRCm39) |
Q682L |
possibly damaging |
Het |
Gm2396 |
T |
G |
9: 88,813,281 (GRCm39) |
|
noncoding transcript |
Het |
Gm5798 |
T |
C |
14: 41,070,614 (GRCm39) |
L8S |
probably damaging |
Het |
Hmgcll1 |
C |
T |
9: 75,963,460 (GRCm39) |
S39F |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Il3ra |
A |
T |
14: 14,355,381 (GRCm38) |
E289D |
probably benign |
Het |
Isoc1 |
T |
A |
18: 58,806,350 (GRCm39) |
L220Q |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,990,302 (GRCm39) |
K918* |
probably null |
Het |
Kat6a |
C |
T |
8: 23,428,329 (GRCm39) |
T1228I |
probably benign |
Het |
Klhl30 |
T |
A |
1: 91,287,046 (GRCm39) |
|
probably null |
Het |
Krtap6-2 |
A |
T |
16: 89,216,806 (GRCm39) |
C54S |
unknown |
Het |
Lmf2 |
G |
A |
15: 89,236,003 (GRCm39) |
P634S |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,490,906 (GRCm39) |
V175A |
possibly damaging |
Het |
Mcm3 |
A |
C |
1: 20,890,480 (GRCm39) |
|
probably benign |
Het |
Mon1b |
T |
C |
8: 114,365,859 (GRCm39) |
S396P |
probably damaging |
Het |
Mroh2a |
T |
C |
1: 88,184,476 (GRCm39) |
V1453A |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,126,404 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
T |
G |
8: 95,247,844 (GRCm39) |
|
probably benign |
Het |
Nlrp14 |
GT |
GTT |
7: 106,796,386 (GRCm39) |
|
probably null |
Het |
Nwd2 |
T |
G |
5: 63,962,151 (GRCm39) |
S578R |
probably damaging |
Het |
Or12k7 |
A |
G |
2: 36,958,422 (GRCm39) |
Y35C |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,005 (GRCm39) |
V105I |
possibly damaging |
Het |
Otoa |
C |
A |
7: 120,701,902 (GRCm39) |
P194T |
probably damaging |
Het |
Pde1b |
A |
C |
15: 103,429,801 (GRCm39) |
D98A |
probably damaging |
Het |
Pi4ka |
A |
T |
16: 17,195,033 (GRCm39) |
C122S |
probably damaging |
Het |
Pole2 |
C |
T |
12: 69,269,924 (GRCm39) |
V67M |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,393,736 (GRCm39) |
D312E |
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,436,745 (GRCm39) |
D453G |
probably damaging |
Het |
Prrc1 |
T |
A |
18: 57,507,626 (GRCm39) |
V260E |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,444,793 (GRCm39) |
Y62N |
probably benign |
Het |
Reln |
C |
T |
5: 22,160,236 (GRCm39) |
G2111E |
probably damaging |
Het |
Rsph6a |
A |
T |
7: 18,791,665 (GRCm39) |
E278V |
possibly damaging |
Het |
Scpep1 |
T |
A |
11: 88,832,122 (GRCm39) |
I203F |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,148,596 (GRCm39) |
C747R |
probably damaging |
Het |
Sec31a |
A |
T |
5: 100,516,192 (GRCm39) |
N967K |
probably damaging |
Het |
Sell |
T |
C |
1: 163,890,631 (GRCm39) |
W5R |
probably benign |
Het |
Siglec1 |
C |
T |
2: 130,911,789 (GRCm39) |
V1697M |
probably benign |
Het |
Sinhcaf |
A |
G |
6: 148,834,498 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
T |
A |
19: 7,768,419 (GRCm39) |
I213L |
probably benign |
Het |
Slc2a13 |
G |
A |
15: 91,296,415 (GRCm39) |
P300S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,231 (GRCm39) |
Y461H |
possibly damaging |
Het |
Slco3a1 |
G |
C |
7: 73,970,304 (GRCm39) |
C434W |
probably null |
Het |
Sp3 |
A |
T |
2: 72,768,633 (GRCm39) |
V666D |
probably benign |
Het |
Spidr |
A |
T |
16: 15,936,806 (GRCm39) |
W100R |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,926,802 (GRCm39) |
M286L |
probably damaging |
Het |
Sult1c2 |
T |
A |
17: 54,139,163 (GRCm39) |
I183F |
probably benign |
Het |
Svep1 |
G |
T |
4: 58,087,751 (GRCm39) |
T1776K |
probably benign |
Het |
Tesk2 |
A |
G |
4: 116,660,190 (GRCm39) |
H436R |
probably benign |
Het |
Timm10 |
T |
C |
2: 84,660,192 (GRCm39) |
S44P |
possibly damaging |
Het |
Tmed11 |
C |
A |
5: 108,943,048 (GRCm39) |
|
probably null |
Het |
Trim12c |
G |
A |
7: 103,990,155 (GRCm39) |
R441C |
probably damaging |
Het |
Trmt2a |
A |
G |
16: 18,070,793 (GRCm39) |
K509E |
probably damaging |
Het |
Upk3a |
A |
G |
15: 84,903,624 (GRCm39) |
T108A |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,965,158 (GRCm39) |
M334V |
probably benign |
Het |
Vash1 |
A |
G |
12: 86,726,916 (GRCm39) |
D52G |
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,368,246 (GRCm39) |
T249P |
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,247,848 (GRCm39) |
F772I |
probably damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,820,787 (GRCm39) |
S49Y |
probably benign |
Het |
Xdh |
T |
C |
17: 74,217,238 (GRCm39) |
T677A |
probably damaging |
Het |
Zan |
A |
G |
5: 137,384,718 (GRCm39) |
L5102P |
unknown |
Het |
Zfp160 |
T |
A |
17: 21,240,343 (GRCm39) |
S9T |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,673 (GRCm39) |
H267L |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,365,038 (GRCm39) |
I179K |
probably benign |
Het |
Zfp975 |
T |
C |
7: 42,311,716 (GRCm39) |
Y299C |
probably damaging |
Het |
|
Other mutations in Tex2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Tex2
|
APN |
11 |
106,459,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01380:Tex2
|
APN |
11 |
106,435,141 (GRCm39) |
nonsense |
probably null |
|
IGL02607:Tex2
|
APN |
11 |
106,437,573 (GRCm39) |
missense |
unknown |
|
IGL02680:Tex2
|
APN |
11 |
106,459,058 (GRCm39) |
unclassified |
probably benign |
|
IGL02699:Tex2
|
APN |
11 |
106,459,259 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03187:Tex2
|
APN |
11 |
106,458,903 (GRCm39) |
unclassified |
probably benign |
|
IGL03398:Tex2
|
APN |
11 |
106,459,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Tex2
|
UTSW |
11 |
106,410,781 (GRCm39) |
nonsense |
probably null |
|
R0242:Tex2
|
UTSW |
11 |
106,410,781 (GRCm39) |
nonsense |
probably null |
|
R1085:Tex2
|
UTSW |
11 |
106,459,313 (GRCm39) |
missense |
probably damaging |
0.98 |
R1491:Tex2
|
UTSW |
11 |
106,394,466 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1664:Tex2
|
UTSW |
11 |
106,458,608 (GRCm39) |
unclassified |
probably benign |
|
R1794:Tex2
|
UTSW |
11 |
106,458,728 (GRCm39) |
unclassified |
probably benign |
|
R1855:Tex2
|
UTSW |
11 |
106,437,702 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2077:Tex2
|
UTSW |
11 |
106,397,690 (GRCm39) |
splice site |
probably null |
|
R2151:Tex2
|
UTSW |
11 |
106,458,161 (GRCm39) |
unclassified |
probably benign |
|
R2175:Tex2
|
UTSW |
11 |
106,394,513 (GRCm39) |
missense |
unknown |
|
R2984:Tex2
|
UTSW |
11 |
106,437,489 (GRCm39) |
critical splice donor site |
probably null |
|
R3156:Tex2
|
UTSW |
11 |
106,424,695 (GRCm39) |
critical splice donor site |
probably null |
|
R3722:Tex2
|
UTSW |
11 |
106,437,566 (GRCm39) |
nonsense |
probably null |
|
R3724:Tex2
|
UTSW |
11 |
106,420,156 (GRCm39) |
missense |
unknown |
|
R3770:Tex2
|
UTSW |
11 |
106,435,078 (GRCm39) |
missense |
unknown |
|
R3771:Tex2
|
UTSW |
11 |
106,437,720 (GRCm39) |
missense |
unknown |
|
R3813:Tex2
|
UTSW |
11 |
106,402,770 (GRCm39) |
missense |
unknown |
|
R3947:Tex2
|
UTSW |
11 |
106,410,829 (GRCm39) |
missense |
unknown |
|
R4206:Tex2
|
UTSW |
11 |
106,458,398 (GRCm39) |
unclassified |
probably benign |
|
R4342:Tex2
|
UTSW |
11 |
106,457,832 (GRCm39) |
unclassified |
probably benign |
|
R4554:Tex2
|
UTSW |
11 |
106,435,212 (GRCm39) |
missense |
unknown |
|
R5207:Tex2
|
UTSW |
11 |
106,437,666 (GRCm39) |
missense |
unknown |
|
R5249:Tex2
|
UTSW |
11 |
106,437,615 (GRCm39) |
missense |
unknown |
|
R5257:Tex2
|
UTSW |
11 |
106,458,585 (GRCm39) |
unclassified |
probably benign |
|
R5258:Tex2
|
UTSW |
11 |
106,458,585 (GRCm39) |
unclassified |
probably benign |
|
R5278:Tex2
|
UTSW |
11 |
106,458,639 (GRCm39) |
missense |
probably benign |
0.34 |
R5702:Tex2
|
UTSW |
11 |
106,435,221 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5835:Tex2
|
UTSW |
11 |
106,410,739 (GRCm39) |
missense |
unknown |
|
R6150:Tex2
|
UTSW |
11 |
106,457,906 (GRCm39) |
missense |
probably benign |
0.34 |
R6785:Tex2
|
UTSW |
11 |
106,424,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6879:Tex2
|
UTSW |
11 |
106,424,836 (GRCm39) |
missense |
unknown |
|
R7038:Tex2
|
UTSW |
11 |
106,402,726 (GRCm39) |
critical splice donor site |
probably null |
|
R7117:Tex2
|
UTSW |
11 |
106,435,071 (GRCm39) |
missense |
unknown |
|
R7336:Tex2
|
UTSW |
11 |
106,439,685 (GRCm39) |
missense |
unknown |
|
R7568:Tex2
|
UTSW |
11 |
106,439,562 (GRCm39) |
missense |
unknown |
|
R7622:Tex2
|
UTSW |
11 |
106,437,721 (GRCm39) |
missense |
unknown |
|
R8228:Tex2
|
UTSW |
11 |
106,457,997 (GRCm39) |
missense |
probably benign |
0.34 |
R8407:Tex2
|
UTSW |
11 |
106,459,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8807:Tex2
|
UTSW |
11 |
106,458,414 (GRCm39) |
missense |
unknown |
|
R8807:Tex2
|
UTSW |
11 |
106,435,194 (GRCm39) |
missense |
unknown |
|
R8882:Tex2
|
UTSW |
11 |
106,435,062 (GRCm39) |
missense |
unknown |
|
R8926:Tex2
|
UTSW |
11 |
106,459,230 (GRCm39) |
missense |
|
|
R8936:Tex2
|
UTSW |
11 |
106,458,144 (GRCm39) |
nonsense |
probably null |
|
R8988:Tex2
|
UTSW |
11 |
106,402,731 (GRCm39) |
missense |
unknown |
|
R9165:Tex2
|
UTSW |
11 |
106,458,095 (GRCm39) |
missense |
unknown |
|
R9294:Tex2
|
UTSW |
11 |
106,459,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Tex2
|
UTSW |
11 |
106,435,075 (GRCm39) |
missense |
unknown |
|
R9405:Tex2
|
UTSW |
11 |
106,435,214 (GRCm39) |
missense |
unknown |
|
R9419:Tex2
|
UTSW |
11 |
106,457,835 (GRCm39) |
nonsense |
probably null |
|
R9477:Tex2
|
UTSW |
11 |
106,410,706 (GRCm39) |
critical splice donor site |
probably null |
|
R9626:Tex2
|
UTSW |
11 |
106,437,579 (GRCm39) |
missense |
unknown |
|
R9634:Tex2
|
UTSW |
11 |
106,458,978 (GRCm39) |
missense |
unknown |
|
T0970:Tex2
|
UTSW |
11 |
106,437,772 (GRCm39) |
missense |
unknown |
|
Z1177:Tex2
|
UTSW |
11 |
106,424,834 (GRCm39) |
missense |
unknown |
|
|