Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
C2cd6 |
T |
C |
1: 59,133,997 (GRCm39) |
N8S |
probably benign |
Het |
Cdh8 |
G |
A |
8: 99,757,387 (GRCm39) |
T737M |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,711,920 (GRCm39) |
|
probably benign |
Het |
Cenph |
T |
A |
13: 100,909,269 (GRCm39) |
Q46L |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,200,277 (GRCm39) |
C1395R |
probably damaging |
Het |
Dnah8 |
C |
T |
17: 31,037,025 (GRCm39) |
|
probably benign |
Het |
Dolk |
T |
C |
2: 30,175,740 (GRCm39) |
N102D |
probably benign |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Farp2 |
G |
A |
1: 93,505,372 (GRCm39) |
R368Q |
probably damaging |
Het |
Fermt3 |
A |
T |
19: 6,996,183 (GRCm39) |
M4K |
probably benign |
Het |
Fndc8 |
A |
C |
11: 82,789,429 (GRCm39) |
T196P |
probably damaging |
Het |
Galc |
G |
A |
12: 98,173,672 (GRCm39) |
T630I |
probably damaging |
Het |
Gm21970 |
T |
G |
16: 91,211,545 (GRCm39) |
S128A |
possibly damaging |
Het |
Gpr146 |
T |
C |
5: 139,378,533 (GRCm39) |
S112P |
probably damaging |
Het |
Grip2 |
A |
G |
6: 91,764,276 (GRCm39) |
S51P |
probably damaging |
Het |
Htra2 |
G |
T |
6: 83,031,280 (GRCm39) |
T43N |
possibly damaging |
Het |
Lnpep |
T |
C |
17: 17,799,445 (GRCm39) |
Y70C |
possibly damaging |
Het |
Med17 |
G |
A |
9: 15,188,963 (GRCm39) |
R101* |
probably null |
Het |
Mtdh |
A |
T |
15: 34,099,723 (GRCm39) |
N158Y |
probably damaging |
Het |
Neo1 |
A |
T |
9: 58,833,094 (GRCm39) |
H550Q |
possibly damaging |
Het |
Or2h1b |
C |
T |
17: 37,461,979 (GRCm39) |
V295I |
probably benign |
Het |
Or5p57 |
A |
C |
7: 107,665,710 (GRCm39) |
F68L |
probably benign |
Het |
Pex1 |
C |
T |
5: 3,655,952 (GRCm39) |
Q260* |
probably null |
Het |
Pex6 |
T |
C |
17: 47,034,425 (GRCm39) |
V758A |
probably damaging |
Het |
Qsox1 |
T |
C |
1: 155,688,346 (GRCm39) |
E67G |
probably damaging |
Het |
Rimbp2 |
C |
T |
5: 128,848,861 (GRCm39) |
S895N |
probably benign |
Het |
Rnls |
A |
G |
19: 33,180,012 (GRCm39) |
V28A |
possibly damaging |
Het |
Spidr |
T |
C |
16: 15,707,494 (GRCm39) |
*934W |
probably null |
Het |
Spta1 |
A |
T |
1: 174,046,380 (GRCm39) |
M1654L |
probably damaging |
Het |
Srbd1 |
C |
A |
17: 86,295,801 (GRCm39) |
V870F |
probably benign |
Het |
Suco |
A |
T |
1: 161,662,136 (GRCm39) |
M765K |
probably benign |
Het |
Taok1 |
A |
G |
11: 77,440,178 (GRCm39) |
Y610H |
probably benign |
Het |
Them7 |
T |
A |
2: 105,209,220 (GRCm39) |
L180* |
probably null |
Het |
Trim45 |
A |
G |
3: 100,832,621 (GRCm39) |
I285V |
probably benign |
Het |
Trim66 |
T |
C |
7: 109,059,481 (GRCm39) |
K921R |
probably benign |
Het |
Ttn |
A |
G |
2: 76,601,887 (GRCm39) |
S10265P |
probably damaging |
Het |
Vgll3 |
A |
T |
16: 65,612,556 (GRCm39) |
Y13F |
probably damaging |
Het |
Ylpm1 |
T |
A |
12: 85,061,731 (GRCm39) |
M544K |
unknown |
Het |
Ypel1 |
T |
C |
16: 16,906,702 (GRCm39) |
T500A |
probably benign |
Het |
Zmym1 |
T |
A |
4: 126,942,256 (GRCm39) |
S711C |
probably damaging |
Het |
|
Other mutations in Thbs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00801:Thbs1
|
APN |
2 |
117,953,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00920:Thbs1
|
APN |
2 |
117,943,682 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01295:Thbs1
|
APN |
2 |
117,948,808 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01649:Thbs1
|
APN |
2 |
117,945,463 (GRCm39) |
missense |
probably benign |
|
IGL02077:Thbs1
|
APN |
2 |
117,943,591 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02251:Thbs1
|
APN |
2 |
117,943,999 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02263:Thbs1
|
APN |
2 |
117,950,361 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02393:Thbs1
|
APN |
2 |
117,953,580 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02411:Thbs1
|
APN |
2 |
117,945,451 (GRCm39) |
missense |
probably benign |
|
IGL02659:Thbs1
|
APN |
2 |
117,945,273 (GRCm39) |
missense |
probably benign |
0.29 |
Stark
|
UTSW |
2 |
117,951,718 (GRCm39) |
critical splice donor site |
probably null |
|
R0014:Thbs1
|
UTSW |
2 |
117,943,831 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0042:Thbs1
|
UTSW |
2 |
117,953,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Thbs1
|
UTSW |
2 |
117,954,395 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0240:Thbs1
|
UTSW |
2 |
117,944,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Thbs1
|
UTSW |
2 |
117,944,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Thbs1
|
UTSW |
2 |
117,948,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Thbs1
|
UTSW |
2 |
117,943,472 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0678:Thbs1
|
UTSW |
2 |
117,953,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1037:Thbs1
|
UTSW |
2 |
117,953,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Thbs1
|
UTSW |
2 |
117,944,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Thbs1
|
UTSW |
2 |
117,953,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1571:Thbs1
|
UTSW |
2 |
117,949,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R1702:Thbs1
|
UTSW |
2 |
117,943,923 (GRCm39) |
missense |
probably benign |
|
R2035:Thbs1
|
UTSW |
2 |
117,948,821 (GRCm39) |
critical splice donor site |
probably null |
|
R2068:Thbs1
|
UTSW |
2 |
117,954,018 (GRCm39) |
nonsense |
probably null |
|
R2171:Thbs1
|
UTSW |
2 |
117,953,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R2844:Thbs1
|
UTSW |
2 |
117,948,109 (GRCm39) |
missense |
probably benign |
0.00 |
R2870:Thbs1
|
UTSW |
2 |
117,949,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Thbs1
|
UTSW |
2 |
117,949,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Thbs1
|
UTSW |
2 |
117,951,640 (GRCm39) |
missense |
probably benign |
0.05 |
R3621:Thbs1
|
UTSW |
2 |
117,951,640 (GRCm39) |
missense |
probably benign |
0.05 |
R3726:Thbs1
|
UTSW |
2 |
117,945,191 (GRCm39) |
missense |
probably benign |
0.02 |
R4499:Thbs1
|
UTSW |
2 |
117,950,431 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4524:Thbs1
|
UTSW |
2 |
117,953,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Thbs1
|
UTSW |
2 |
117,949,897 (GRCm39) |
missense |
probably damaging |
0.97 |
R4596:Thbs1
|
UTSW |
2 |
117,945,236 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4646:Thbs1
|
UTSW |
2 |
117,948,810 (GRCm39) |
missense |
probably benign |
0.15 |
R4783:Thbs1
|
UTSW |
2 |
117,945,273 (GRCm39) |
missense |
probably benign |
0.04 |
R4836:Thbs1
|
UTSW |
2 |
117,945,499 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4943:Thbs1
|
UTSW |
2 |
117,943,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Thbs1
|
UTSW |
2 |
117,945,259 (GRCm39) |
missense |
probably benign |
|
R5014:Thbs1
|
UTSW |
2 |
117,950,518 (GRCm39) |
critical splice donor site |
probably null |
|
R5062:Thbs1
|
UTSW |
2 |
117,951,718 (GRCm39) |
critical splice donor site |
probably null |
|
R5363:Thbs1
|
UTSW |
2 |
117,953,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Thbs1
|
UTSW |
2 |
117,943,636 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5432:Thbs1
|
UTSW |
2 |
117,945,164 (GRCm39) |
missense |
probably benign |
0.25 |
R5788:Thbs1
|
UTSW |
2 |
117,952,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Thbs1
|
UTSW |
2 |
117,950,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:Thbs1
|
UTSW |
2 |
117,943,137 (GRCm39) |
missense |
unknown |
|
R6466:Thbs1
|
UTSW |
2 |
117,950,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Thbs1
|
UTSW |
2 |
117,949,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R6794:Thbs1
|
UTSW |
2 |
117,950,519 (GRCm39) |
splice site |
probably null |
|
R6983:Thbs1
|
UTSW |
2 |
117,950,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7284:Thbs1
|
UTSW |
2 |
117,949,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Thbs1
|
UTSW |
2 |
117,945,438 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7467:Thbs1
|
UTSW |
2 |
117,948,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Thbs1
|
UTSW |
2 |
117,951,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7552:Thbs1
|
UTSW |
2 |
117,943,843 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7575:Thbs1
|
UTSW |
2 |
117,953,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7870:Thbs1
|
UTSW |
2 |
117,945,508 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7943:Thbs1
|
UTSW |
2 |
117,950,098 (GRCm39) |
splice site |
probably null |
|
R8267:Thbs1
|
UTSW |
2 |
117,952,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R8402:Thbs1
|
UTSW |
2 |
117,946,359 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8672:Thbs1
|
UTSW |
2 |
117,943,719 (GRCm39) |
missense |
probably benign |
|
R8726:Thbs1
|
UTSW |
2 |
117,949,957 (GRCm39) |
critical splice donor site |
probably null |
|
R8784:Thbs1
|
UTSW |
2 |
117,943,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R9010:Thbs1
|
UTSW |
2 |
117,953,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9353:Thbs1
|
UTSW |
2 |
117,953,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Thbs1
|
UTSW |
2 |
117,947,983 (GRCm39) |
missense |
probably benign |
0.11 |
R9474:Thbs1
|
UTSW |
2 |
117,950,518 (GRCm39) |
critical splice donor site |
probably null |
|
R9544:Thbs1
|
UTSW |
2 |
117,953,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Thbs1
|
UTSW |
2 |
117,949,897 (GRCm39) |
missense |
probably damaging |
0.97 |
R9701:Thbs1
|
UTSW |
2 |
117,950,716 (GRCm39) |
missense |
probably benign |
0.05 |
RF039:Thbs1
|
UTSW |
2 |
117,953,346 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF054:Thbs1
|
UTSW |
2 |
117,953,346 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0019:Thbs1
|
UTSW |
2 |
117,943,463 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Thbs1
|
UTSW |
2 |
117,953,403 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Thbs1
|
UTSW |
2 |
117,951,458 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Thbs1
|
UTSW |
2 |
117,943,960 (GRCm39) |
missense |
probably benign |
0.34 |
Z1177:Thbs1
|
UTSW |
2 |
117,948,139 (GRCm39) |
critical splice donor site |
probably null |
|
|