Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,330,501 (GRCm39) |
T1385A |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,149,972 (GRCm39) |
D1646E |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,407,407 (GRCm39) |
R2098H |
probably benign |
Het |
Atl3 |
C |
A |
19: 7,509,592 (GRCm39) |
T435N |
possibly damaging |
Het |
Cdh22 |
G |
T |
2: 164,958,200 (GRCm39) |
T589K |
probably damaging |
Het |
Cnot3 |
T |
C |
7: 3,661,082 (GRCm39) |
L561S |
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,841,468 (GRCm39) |
D363G |
unknown |
Het |
Cyp24a1 |
T |
C |
2: 170,338,229 (GRCm39) |
D105G |
possibly damaging |
Het |
Dennd4a |
C |
A |
9: 64,758,491 (GRCm39) |
|
probably null |
Het |
Dnah8 |
A |
G |
17: 31,019,561 (GRCm39) |
K3878R |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,894,539 (GRCm39) |
S1900P |
probably benign |
Het |
Fancg |
A |
G |
4: 43,008,736 (GRCm39) |
L167P |
probably damaging |
Het |
Ighd2-8 |
A |
G |
12: 113,414,487 (GRCm39) |
S1P |
possibly damaging |
Het |
Kif28 |
A |
G |
1: 179,525,336 (GRCm39) |
|
probably null |
Het |
Mrpl55 |
T |
A |
11: 59,095,397 (GRCm39) |
C20* |
probably null |
Het |
Myo5a |
A |
G |
9: 75,079,001 (GRCm39) |
K920E |
possibly damaging |
Het |
Naa35 |
G |
A |
13: 59,770,680 (GRCm39) |
|
probably benign |
Het |
Olfm3 |
A |
G |
3: 114,890,573 (GRCm39) |
R76G |
probably damaging |
Het |
Or14a258 |
T |
C |
7: 86,035,521 (GRCm39) |
M116V |
probably damaging |
Het |
Or2ag1 |
T |
C |
7: 106,313,373 (GRCm39) |
R172G |
possibly damaging |
Het |
Pcdha12 |
A |
T |
18: 37,155,468 (GRCm39) |
D729V |
probably benign |
Het |
Phf11c |
T |
C |
14: 59,622,981 (GRCm39) |
|
probably null |
Het |
Phf20 |
T |
A |
2: 156,093,688 (GRCm39) |
|
probably null |
Het |
Plbd1 |
T |
A |
6: 136,593,987 (GRCm39) |
Y376F |
probably benign |
Het |
Poglut1 |
A |
G |
16: 38,352,173 (GRCm39) |
V257A |
probably damaging |
Het |
Reln |
A |
G |
5: 22,106,623 (GRCm39) |
I3249T |
probably benign |
Het |
Rgsl1 |
G |
A |
1: 153,701,639 (GRCm39) |
P272S |
possibly damaging |
Het |
Slc15a2 |
A |
T |
16: 36,592,472 (GRCm39) |
Y197* |
probably null |
Het |
Slc45a2 |
C |
T |
15: 11,012,693 (GRCm39) |
T232I |
probably benign |
Het |
Ssc5d |
T |
A |
7: 4,929,517 (GRCm39) |
|
probably null |
Het |
Them4 |
A |
T |
3: 94,238,851 (GRCm39) |
L219F |
possibly damaging |
Het |
Tmem30b |
G |
T |
12: 73,592,940 (GRCm39) |
N58K |
probably benign |
Het |
Trappc2b |
T |
C |
11: 51,576,799 (GRCm39) |
E33G |
probably benign |
Het |
Ttc29 |
G |
A |
8: 78,972,942 (GRCm39) |
E131K |
possibly damaging |
Het |
Vmn1r29 |
C |
G |
6: 58,284,676 (GRCm39) |
S132C |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,742 (GRCm39) |
A194V |
probably benign |
Het |
Wdr86 |
A |
T |
5: 24,923,085 (GRCm39) |
H202Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,347,239 (GRCm39) |
D3160G |
probably benign |
Het |
Xkr5 |
T |
C |
8: 18,983,982 (GRCm39) |
D520G |
probably benign |
Het |
Zfp607b |
T |
G |
7: 27,403,406 (GRCm39) |
C621G |
probably damaging |
Het |
|
Other mutations in Thbs2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Thbs2
|
APN |
17 |
14,889,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00764:Thbs2
|
APN |
17 |
14,910,514 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01370:Thbs2
|
APN |
17 |
14,910,327 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01604:Thbs2
|
APN |
17 |
14,899,031 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01936:Thbs2
|
APN |
17 |
14,908,076 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02061:Thbs2
|
APN |
17 |
14,900,176 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02255:Thbs2
|
APN |
17 |
14,910,047 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02342:Thbs2
|
APN |
17 |
14,896,578 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02402:Thbs2
|
APN |
17 |
14,891,716 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02499:Thbs2
|
APN |
17 |
14,904,328 (GRCm39) |
splice site |
probably benign |
|
IGL02572:Thbs2
|
APN |
17 |
14,897,275 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02701:Thbs2
|
APN |
17 |
14,903,623 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02871:Thbs2
|
APN |
17 |
14,906,048 (GRCm39) |
missense |
probably benign |
|
IGL03058:Thbs2
|
APN |
17 |
14,910,231 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03185:Thbs2
|
APN |
17 |
14,901,672 (GRCm39) |
nonsense |
probably null |
|
IGL03232:Thbs2
|
APN |
17 |
14,911,675 (GRCm39) |
start codon destroyed |
probably null |
|
IGL03289:Thbs2
|
APN |
17 |
14,910,384 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03407:Thbs2
|
APN |
17 |
14,893,535 (GRCm39) |
missense |
probably benign |
0.00 |
H8562:Thbs2
|
UTSW |
17 |
14,891,715 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02802:Thbs2
|
UTSW |
17 |
14,904,389 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4354001:Thbs2
|
UTSW |
17 |
14,910,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R0088:Thbs2
|
UTSW |
17 |
14,901,963 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0167:Thbs2
|
UTSW |
17 |
14,887,787 (GRCm39) |
splice site |
probably benign |
|
R0415:Thbs2
|
UTSW |
17 |
14,900,235 (GRCm39) |
missense |
probably benign |
|
R0658:Thbs2
|
UTSW |
17 |
14,900,587 (GRCm39) |
missense |
probably benign |
0.00 |
R0735:Thbs2
|
UTSW |
17 |
14,900,077 (GRCm39) |
missense |
probably benign |
0.00 |
R1582:Thbs2
|
UTSW |
17 |
14,891,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Thbs2
|
UTSW |
17 |
14,910,030 (GRCm39) |
missense |
probably benign |
0.00 |
R1608:Thbs2
|
UTSW |
17 |
14,906,043 (GRCm39) |
missense |
probably benign |
|
R1721:Thbs2
|
UTSW |
17 |
14,899,072 (GRCm39) |
missense |
probably benign |
0.00 |
R1724:Thbs2
|
UTSW |
17 |
14,906,162 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1791:Thbs2
|
UTSW |
17 |
14,906,075 (GRCm39) |
missense |
probably benign |
|
R1816:Thbs2
|
UTSW |
17 |
14,890,976 (GRCm39) |
missense |
probably benign |
0.00 |
R1816:Thbs2
|
UTSW |
17 |
14,890,975 (GRCm39) |
missense |
probably benign |
0.01 |
R1911:Thbs2
|
UTSW |
17 |
14,910,104 (GRCm39) |
missense |
probably benign |
0.38 |
R2137:Thbs2
|
UTSW |
17 |
14,893,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Thbs2
|
UTSW |
17 |
14,893,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2244:Thbs2
|
UTSW |
17 |
14,891,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2325:Thbs2
|
UTSW |
17 |
14,910,551 (GRCm39) |
splice site |
probably null |
|
R2509:Thbs2
|
UTSW |
17 |
14,906,105 (GRCm39) |
missense |
probably benign |
0.11 |
R3838:Thbs2
|
UTSW |
17 |
14,908,113 (GRCm39) |
missense |
probably benign |
|
R4173:Thbs2
|
UTSW |
17 |
14,901,893 (GRCm39) |
splice site |
probably null |
|
R4427:Thbs2
|
UTSW |
17 |
14,900,597 (GRCm39) |
missense |
probably benign |
|
R4495:Thbs2
|
UTSW |
17 |
14,891,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Thbs2
|
UTSW |
17 |
14,891,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Thbs2
|
UTSW |
17 |
14,899,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R5058:Thbs2
|
UTSW |
17 |
14,896,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Thbs2
|
UTSW |
17 |
14,890,852 (GRCm39) |
splice site |
probably null |
|
R5619:Thbs2
|
UTSW |
17 |
14,901,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5664:Thbs2
|
UTSW |
17 |
14,910,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Thbs2
|
UTSW |
17 |
14,908,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R5816:Thbs2
|
UTSW |
17 |
14,904,333 (GRCm39) |
critical splice donor site |
probably null |
|
R5840:Thbs2
|
UTSW |
17 |
14,901,692 (GRCm39) |
splice site |
probably null |
|
R6149:Thbs2
|
UTSW |
17 |
14,899,942 (GRCm39) |
critical splice donor site |
probably null |
|
R6166:Thbs2
|
UTSW |
17 |
14,900,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R6412:Thbs2
|
UTSW |
17 |
14,897,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6473:Thbs2
|
UTSW |
17 |
14,906,058 (GRCm39) |
missense |
probably benign |
0.23 |
R6640:Thbs2
|
UTSW |
17 |
14,893,630 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6695:Thbs2
|
UTSW |
17 |
14,894,426 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6711:Thbs2
|
UTSW |
17 |
14,910,527 (GRCm39) |
missense |
probably benign |
0.00 |
R6947:Thbs2
|
UTSW |
17 |
14,910,029 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6962:Thbs2
|
UTSW |
17 |
14,902,082 (GRCm39) |
missense |
probably benign |
0.00 |
R7183:Thbs2
|
UTSW |
17 |
14,910,378 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7203:Thbs2
|
UTSW |
17 |
14,891,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R7386:Thbs2
|
UTSW |
17 |
14,893,412 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7621:Thbs2
|
UTSW |
17 |
14,894,426 (GRCm39) |
missense |
probably benign |
|
R7747:Thbs2
|
UTSW |
17 |
14,890,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7759:Thbs2
|
UTSW |
17 |
14,897,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Thbs2
|
UTSW |
17 |
14,896,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R7895:Thbs2
|
UTSW |
17 |
14,896,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Thbs2
|
UTSW |
17 |
14,900,584 (GRCm39) |
missense |
probably benign |
0.00 |
R8332:Thbs2
|
UTSW |
17 |
14,900,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Thbs2
|
UTSW |
17 |
14,900,666 (GRCm39) |
missense |
probably benign |
0.00 |
R8695:Thbs2
|
UTSW |
17 |
14,899,963 (GRCm39) |
missense |
probably benign |
|
R8707:Thbs2
|
UTSW |
17 |
14,911,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Thbs2
|
UTSW |
17 |
14,889,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Thbs2
|
UTSW |
17 |
14,900,587 (GRCm39) |
missense |
probably benign |
0.00 |
R9183:Thbs2
|
UTSW |
17 |
14,896,526 (GRCm39) |
missense |
probably benign |
0.03 |
R9461:Thbs2
|
UTSW |
17 |
14,910,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Thbs2
|
UTSW |
17 |
14,890,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Thbs2
|
UTSW |
17 |
14,910,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Thbs2
|
UTSW |
17 |
14,899,083 (GRCm39) |
missense |
probably damaging |
1.00 |
S24628:Thbs2
|
UTSW |
17 |
14,900,235 (GRCm39) |
missense |
probably benign |
|
X0025:Thbs2
|
UTSW |
17 |
14,902,062 (GRCm39) |
missense |
probably damaging |
0.97 |
|