Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933406P04Rik |
G |
A |
10: 20,186,973 (GRCm39) |
|
probably benign |
Het |
Adam28 |
A |
T |
14: 68,844,049 (GRCm39) |
|
probably benign |
Het |
Adamts3 |
A |
G |
5: 90,009,334 (GRCm39) |
W110R |
possibly damaging |
Het |
Add1 |
T |
C |
5: 34,771,568 (GRCm39) |
V342A |
possibly damaging |
Het |
Aff3 |
A |
G |
1: 38,249,068 (GRCm39) |
S680P |
probably damaging |
Het |
Ak9 |
T |
C |
10: 41,221,135 (GRCm39) |
Y322H |
probably damaging |
Het |
Als2 |
A |
G |
1: 59,207,573 (GRCm39) |
L1528S |
probably benign |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Atp6v1a |
A |
C |
16: 43,931,859 (GRCm39) |
|
probably null |
Het |
Bpi |
T |
C |
2: 158,103,314 (GRCm39) |
L103P |
probably damaging |
Het |
Cd80 |
G |
A |
16: 38,303,056 (GRCm39) |
V168I |
probably benign |
Het |
Cfh |
T |
C |
1: 140,030,096 (GRCm39) |
S926G |
probably damaging |
Het |
Chrd |
A |
T |
16: 20,554,189 (GRCm39) |
T304S |
probably damaging |
Het |
Chsy3 |
A |
G |
18: 59,542,125 (GRCm39) |
Y421C |
probably damaging |
Het |
Cmbl |
T |
G |
15: 31,585,455 (GRCm39) |
V101G |
probably damaging |
Het |
Colgalt2 |
T |
A |
1: 152,371,543 (GRCm39) |
|
probably benign |
Het |
Coq4 |
C |
T |
2: 29,680,010 (GRCm39) |
Q101* |
probably null |
Het |
Cr2 |
T |
C |
1: 194,845,904 (GRCm39) |
|
probably benign |
Het |
Cry1 |
T |
C |
10: 85,020,223 (GRCm39) |
D38G |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,327,229 (GRCm39) |
D758G |
probably benign |
Het |
Epsti1 |
C |
T |
14: 78,164,677 (GRCm39) |
|
probably benign |
Het |
Fam24b |
T |
C |
7: 130,928,915 (GRCm39) |
|
probably benign |
Het |
Fem1c |
G |
A |
18: 46,638,227 (GRCm39) |
R592C |
probably benign |
Het |
Foxred1 |
T |
C |
9: 35,116,178 (GRCm39) |
Y490C |
possibly damaging |
Het |
Gm9875 |
A |
G |
2: 13,562,699 (GRCm39) |
K9R |
unknown |
Het |
Grid2ip |
T |
C |
5: 143,365,117 (GRCm39) |
S322P |
probably damaging |
Het |
Gucy1b2 |
A |
G |
14: 62,640,608 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,533,127 (GRCm39) |
|
probably null |
Het |
Hpdl |
C |
T |
4: 116,677,984 (GRCm39) |
S159N |
possibly damaging |
Het |
Hsd17b12 |
A |
T |
2: 93,863,987 (GRCm39) |
M285K |
probably benign |
Het |
Icam5 |
T |
C |
9: 20,943,493 (GRCm39) |
I23T |
probably benign |
Het |
Kat5 |
A |
G |
19: 5,658,364 (GRCm39) |
|
probably benign |
Het |
Lama3 |
A |
G |
18: 12,640,006 (GRCm39) |
N67S |
probably benign |
Het |
Lamb2 |
T |
C |
9: 108,363,304 (GRCm39) |
|
probably benign |
Het |
Lgals3bp |
A |
G |
11: 118,284,220 (GRCm39) |
F453S |
probably damaging |
Het |
Lypd4 |
A |
G |
7: 24,564,800 (GRCm39) |
Y113H |
probably damaging |
Het |
Mdm1 |
C |
T |
10: 117,982,506 (GRCm39) |
T47M |
probably damaging |
Het |
Mei1 |
C |
A |
15: 81,954,351 (GRCm39) |
T52K |
probably benign |
Het |
Meiob |
G |
A |
17: 25,037,236 (GRCm39) |
|
probably benign |
Het |
Ndufaf6 |
A |
G |
4: 11,051,224 (GRCm39) |
V292A |
probably damaging |
Het |
Neb |
T |
A |
2: 52,154,038 (GRCm39) |
M2358L |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,047,005 (GRCm39) |
S1119P |
possibly damaging |
Het |
Nsmaf |
A |
G |
4: 6,418,470 (GRCm39) |
|
probably null |
Het |
Ogfod1 |
T |
C |
8: 94,773,895 (GRCm39) |
|
probably benign |
Het |
Or5ae2 |
T |
C |
7: 84,506,345 (GRCm39) |
I256T |
probably damaging |
Het |
Or8h7 |
T |
C |
2: 86,720,763 (GRCm39) |
Y252C |
possibly damaging |
Het |
Or9s14 |
G |
T |
1: 92,535,618 (GRCm39) |
V20L |
probably benign |
Het |
Osbpl1a |
T |
A |
18: 13,015,336 (GRCm39) |
|
probably null |
Het |
Otud7b |
T |
A |
3: 96,052,270 (GRCm39) |
|
probably benign |
Het |
P3h3 |
T |
A |
6: 124,832,998 (GRCm39) |
H185L |
probably damaging |
Het |
P4htm |
G |
A |
9: 108,460,923 (GRCm39) |
A183V |
probably null |
Het |
Peak1 |
C |
T |
9: 56,134,382 (GRCm39) |
|
probably benign |
Het |
Phf20l1 |
A |
G |
15: 66,466,971 (GRCm39) |
K88R |
probably damaging |
Het |
Phlpp2 |
A |
G |
8: 110,659,843 (GRCm39) |
N721S |
probably benign |
Het |
Plagl2 |
T |
C |
2: 153,077,864 (GRCm39) |
K39R |
probably benign |
Het |
Plppr1 |
A |
T |
4: 49,323,466 (GRCm39) |
N252I |
probably damaging |
Het |
Pom121l2 |
C |
T |
13: 22,166,206 (GRCm39) |
A159V |
probably damaging |
Het |
Prom2 |
C |
A |
2: 127,381,915 (GRCm39) |
|
probably null |
Het |
Prrc2c |
T |
C |
1: 162,509,995 (GRCm39) |
T1017A |
probably damaging |
Het |
Rimbp3 |
G |
T |
16: 17,029,563 (GRCm39) |
A996S |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,322,543 (GRCm39) |
T1387A |
probably benign |
Het |
Scaper |
A |
T |
9: 55,722,802 (GRCm39) |
|
probably benign |
Het |
Scara5 |
A |
G |
14: 65,997,097 (GRCm39) |
E403G |
possibly damaging |
Het |
Scrib |
T |
C |
15: 75,939,402 (GRCm39) |
I94V |
possibly damaging |
Het |
Shank3 |
T |
C |
15: 89,408,350 (GRCm39) |
F67L |
possibly damaging |
Het |
Shprh |
T |
C |
10: 11,082,856 (GRCm39) |
F1562L |
probably damaging |
Het |
Src |
C |
T |
2: 157,311,841 (GRCm39) |
T529M |
probably damaging |
Het |
Sycp2l |
T |
A |
13: 41,296,942 (GRCm39) |
M341K |
probably benign |
Het |
Syde1 |
T |
C |
10: 78,424,929 (GRCm39) |
|
probably benign |
Het |
Tle6 |
T |
A |
10: 81,430,180 (GRCm39) |
H324L |
probably damaging |
Het |
Tnfaip8 |
ACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
ACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
18: 50,179,912 (GRCm39) |
|
probably benign |
Het |
Tnfrsf14 |
T |
A |
4: 155,009,837 (GRCm39) |
K115* |
probably null |
Het |
Trappc10 |
T |
C |
10: 78,037,331 (GRCm39) |
N824S |
possibly damaging |
Het |
Tsc1 |
C |
T |
2: 28,561,790 (GRCm39) |
S309F |
probably damaging |
Het |
Ttc21a |
A |
G |
9: 119,790,908 (GRCm39) |
I885V |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,570,797 (GRCm39) |
A26699T |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,778,715 (GRCm39) |
Y1262C |
unknown |
Het |
Usp49 |
T |
C |
17: 47,985,851 (GRCm39) |
|
probably null |
Het |
Vmn1r226 |
A |
T |
17: 20,908,133 (GRCm39) |
T122S |
probably benign |
Het |
Vps8 |
A |
T |
16: 21,378,087 (GRCm39) |
T1033S |
probably benign |
Het |
Vwf |
C |
A |
6: 125,662,800 (GRCm39) |
T2728K |
probably benign |
Het |
Wdr5b |
T |
C |
16: 35,862,366 (GRCm39) |
S162P |
probably benign |
Het |
Xrn1 |
C |
T |
9: 95,908,930 (GRCm39) |
Q1235* |
probably null |
Het |
Zfp1005 |
A |
G |
2: 150,110,523 (GRCm39) |
I404M |
unknown |
Het |
|
Other mutations in Tars3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Tars3
|
APN |
7 |
65,302,007 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00470:Tars3
|
APN |
7 |
65,338,656 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00594:Tars3
|
APN |
7 |
65,325,880 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01352:Tars3
|
APN |
7 |
65,308,658 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01519:Tars3
|
APN |
7 |
65,313,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Tars3
|
APN |
7 |
65,332,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02370:Tars3
|
APN |
7 |
65,310,913 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02729:Tars3
|
APN |
7 |
65,332,567 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03234:Tars3
|
APN |
7 |
65,302,026 (GRCm39) |
missense |
probably benign |
0.06 |
gary
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R8254_tarsl2_650
|
UTSW |
7 |
65,325,809 (GRCm39) |
missense |
probably benign |
|
smart_money
|
UTSW |
7 |
65,327,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Tars3
|
UTSW |
7 |
65,314,717 (GRCm39) |
missense |
probably benign |
0.19 |
R0153:Tars3
|
UTSW |
7 |
65,333,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Tars3
|
UTSW |
7 |
65,297,244 (GRCm39) |
missense |
probably benign |
0.01 |
R1467:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Tars3
|
UTSW |
7 |
65,308,645 (GRCm39) |
missense |
probably benign |
|
R2143:Tars3
|
UTSW |
7 |
65,305,539 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2144:Tars3
|
UTSW |
7 |
65,305,539 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2145:Tars3
|
UTSW |
7 |
65,305,539 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2208:Tars3
|
UTSW |
7 |
65,332,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Tars3
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R3715:Tars3
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R3914:Tars3
|
UTSW |
7 |
65,333,556 (GRCm39) |
missense |
probably benign |
0.05 |
R3929:Tars3
|
UTSW |
7 |
65,333,791 (GRCm39) |
splice site |
probably null |
|
R4008:Tars3
|
UTSW |
7 |
65,327,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Tars3
|
UTSW |
7 |
65,302,018 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4367:Tars3
|
UTSW |
7 |
65,332,567 (GRCm39) |
missense |
probably damaging |
0.97 |
R4652:Tars3
|
UTSW |
7 |
65,339,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Tars3
|
UTSW |
7 |
65,297,302 (GRCm39) |
missense |
probably benign |
0.38 |
R4901:Tars3
|
UTSW |
7 |
65,341,042 (GRCm39) |
missense |
probably benign |
0.05 |
R4999:Tars3
|
UTSW |
7 |
65,308,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R5423:Tars3
|
UTSW |
7 |
65,333,567 (GRCm39) |
missense |
probably benign |
0.00 |
R5756:Tars3
|
UTSW |
7 |
65,325,724 (GRCm39) |
missense |
probably benign |
0.22 |
R5772:Tars3
|
UTSW |
7 |
65,333,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Tars3
|
UTSW |
7 |
65,332,527 (GRCm39) |
missense |
probably benign |
0.32 |
R6230:Tars3
|
UTSW |
7 |
65,336,184 (GRCm39) |
splice site |
probably null |
|
R6424:Tars3
|
UTSW |
7 |
65,305,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6615:Tars3
|
UTSW |
7 |
65,327,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Tars3
|
UTSW |
7 |
65,312,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7350:Tars3
|
UTSW |
7 |
65,308,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Tars3
|
UTSW |
7 |
65,297,341 (GRCm39) |
missense |
probably damaging |
0.96 |
R7592:Tars3
|
UTSW |
7 |
65,308,619 (GRCm39) |
missense |
probably benign |
0.01 |
R7634:Tars3
|
UTSW |
7 |
65,325,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R7710:Tars3
|
UTSW |
7 |
65,314,717 (GRCm39) |
missense |
probably benign |
0.19 |
R7808:Tars3
|
UTSW |
7 |
65,302,009 (GRCm39) |
missense |
probably benign |
0.01 |
R7875:Tars3
|
UTSW |
7 |
65,327,899 (GRCm39) |
missense |
probably benign |
0.05 |
R8254:Tars3
|
UTSW |
7 |
65,325,809 (GRCm39) |
missense |
probably benign |
|
R8793:Tars3
|
UTSW |
7 |
65,294,673 (GRCm39) |
start gained |
probably benign |
|
R9162:Tars3
|
UTSW |
7 |
65,332,518 (GRCm39) |
missense |
probably benign |
0.01 |
R9200:Tars3
|
UTSW |
7 |
65,302,013 (GRCm39) |
missense |
probably benign |
|
R9461:Tars3
|
UTSW |
7 |
65,339,719 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9533:Tars3
|
UTSW |
7 |
65,333,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Tars3
|
UTSW |
7 |
65,302,012 (GRCm39) |
nonsense |
probably null |
|
|