Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,051,359 (GRCm39) |
K112N |
probably benign |
Het |
Brwd1 |
A |
G |
16: 95,866,087 (GRCm39) |
S232P |
probably damaging |
Het |
Calm5 |
A |
T |
13: 3,904,629 (GRCm39) |
M108L |
possibly damaging |
Het |
Ces1g |
A |
T |
8: 94,055,094 (GRCm39) |
V201D |
probably damaging |
Het |
Cltc |
C |
A |
11: 86,598,312 (GRCm39) |
V1017L |
probably benign |
Het |
Cpt1c |
C |
T |
7: 44,616,516 (GRCm39) |
R245Q |
probably damaging |
Het |
Csrnp1 |
C |
A |
9: 119,806,158 (GRCm39) |
A39S |
probably benign |
Het |
Elf1 |
A |
G |
14: 79,808,322 (GRCm39) |
D258G |
possibly damaging |
Het |
Entrep1 |
A |
C |
19: 23,972,168 (GRCm39) |
S179A |
possibly damaging |
Het |
Glipr1l1 |
A |
T |
10: 111,896,300 (GRCm39) |
D29V |
probably benign |
Het |
Gm4340 |
T |
C |
10: 104,031,820 (GRCm39) |
V188A |
probably benign |
Het |
Gsdma2 |
T |
C |
11: 98,540,375 (GRCm39) |
M98T |
probably benign |
Het |
Hars1 |
A |
T |
18: 36,903,476 (GRCm39) |
D315E |
probably benign |
Het |
Hsph1 |
A |
C |
5: 149,555,540 (GRCm39) |
Y89D |
probably damaging |
Het |
Ighv11-2 |
T |
A |
12: 114,012,008 (GRCm39) |
D69V |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,995,528 (GRCm39) |
G438D |
possibly damaging |
Het |
Krt6a |
G |
T |
15: 101,600,187 (GRCm39) |
T355K |
possibly damaging |
Het |
Lce1m |
T |
C |
3: 92,925,177 (GRCm39) |
|
probably null |
Het |
Lmbrd1 |
A |
T |
1: 24,767,625 (GRCm39) |
|
probably null |
Het |
Lmtk3 |
A |
G |
7: 45,442,841 (GRCm39) |
E508G |
probably damaging |
Het |
Lrrc2 |
G |
A |
9: 110,809,899 (GRCm39) |
V312I |
probably benign |
Het |
Lyn |
A |
T |
4: 3,789,834 (GRCm39) |
K477* |
probably null |
Het |
Nfe2l2 |
T |
C |
2: 75,509,757 (GRCm39) |
D21G |
probably damaging |
Het |
Or14c45 |
G |
A |
7: 86,176,280 (GRCm39) |
C105Y |
probably benign |
Het |
Or4f14d |
T |
C |
2: 111,960,926 (GRCm39) |
T77A |
probably benign |
Het |
Or55b3 |
G |
A |
7: 102,126,472 (GRCm39) |
R202C |
possibly damaging |
Het |
Or8c15 |
T |
C |
9: 38,120,447 (GRCm39) |
F31L |
probably benign |
Het |
Pgap6 |
C |
A |
17: 26,336,865 (GRCm39) |
P261Q |
probably benign |
Het |
Pkm |
T |
A |
9: 59,585,441 (GRCm39) |
C474* |
probably null |
Het |
Prr36 |
T |
A |
8: 4,263,150 (GRCm39) |
I839F |
unknown |
Het |
Qtrt2 |
A |
G |
16: 43,689,303 (GRCm39) |
|
probably null |
Het |
Ripk4 |
A |
T |
16: 97,547,125 (GRCm39) |
V379E |
probably damaging |
Het |
Rreb1 |
C |
A |
13: 38,133,042 (GRCm39) |
P304Q |
|
Het |
Saxo2 |
A |
T |
7: 82,297,625 (GRCm39) |
C5S |
possibly damaging |
Het |
Scart2 |
G |
A |
7: 139,876,742 (GRCm39) |
G711D |
probably damaging |
Het |
Sema5a |
C |
A |
15: 32,609,378 (GRCm39) |
T428N |
possibly damaging |
Het |
Setd5 |
C |
A |
6: 113,121,010 (GRCm39) |
P1073Q |
possibly damaging |
Het |
Sh2d5 |
T |
G |
4: 137,984,150 (GRCm39) |
C173G |
probably benign |
Het |
Slc4a10 |
T |
G |
2: 62,080,823 (GRCm39) |
V350G |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,106,743 (GRCm39) |
C15R |
probably damaging |
Het |
Smg7 |
A |
T |
1: 152,717,295 (GRCm39) |
F940Y |
possibly damaging |
Het |
Spata17 |
T |
A |
1: 186,854,833 (GRCm39) |
|
probably null |
Het |
Specc1 |
A |
G |
11: 62,019,210 (GRCm39) |
N603S |
possibly damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,421,673 (GRCm39) |
D355G |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,754,934 (GRCm39) |
T174A |
probably benign |
Het |
Vmn2r52 |
A |
G |
7: 9,907,274 (GRCm39) |
Y151H |
probably benign |
Het |
Wdr12 |
G |
A |
1: 60,136,748 (GRCm39) |
|
probably benign |
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 |
R5649:Thbs2
|
UTSW |
17 |
14,910,215 (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 |
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 |
|