Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,772,383 (GRCm39) |
V524E |
probably damaging |
Het |
Acer2 |
T |
A |
4: 86,818,808 (GRCm39) |
M152K |
probably damaging |
Het |
Actn3 |
T |
C |
19: 4,921,876 (GRCm39) |
D130G |
probably damaging |
Het |
Ank1 |
T |
A |
8: 23,577,983 (GRCm39) |
F211Y |
probably damaging |
Het |
Ankfn1 |
C |
T |
11: 89,282,670 (GRCm39) |
A326T |
probably benign |
Het |
Ankrd11 |
G |
A |
8: 123,635,503 (GRCm39) |
R44C |
probably damaging |
Het |
Ankrd46 |
A |
G |
15: 36,484,217 (GRCm39) |
|
probably benign |
Het |
Aurkb |
G |
A |
11: 68,939,172 (GRCm39) |
E132K |
possibly damaging |
Het |
Bsdc1 |
C |
T |
4: 129,359,069 (GRCm39) |
T9I |
possibly damaging |
Het |
Card14 |
C |
T |
11: 119,230,428 (GRCm39) |
R767* |
probably null |
Het |
Ccdc82 |
T |
A |
9: 13,272,745 (GRCm39) |
F411L |
possibly damaging |
Het |
Col12a1 |
C |
T |
9: 79,552,973 (GRCm39) |
G2106D |
probably damaging |
Het |
Col27a1 |
T |
A |
4: 63,237,701 (GRCm39) |
|
probably benign |
Het |
Cox10 |
A |
G |
11: 63,855,198 (GRCm39) |
L361P |
probably damaging |
Het |
Cox18 |
A |
G |
5: 90,371,548 (GRCm39) |
I84T |
probably benign |
Het |
Dhrs3 |
T |
C |
4: 144,646,522 (GRCm39) |
S125P |
probably damaging |
Het |
Fbxl15 |
A |
G |
19: 46,317,765 (GRCm39) |
H149R |
probably benign |
Het |
Flg2 |
T |
A |
3: 93,127,789 (GRCm39) |
S2234T |
unknown |
Het |
Gtf2e1 |
A |
C |
16: 37,356,698 (GRCm39) |
|
probably null |
Het |
H2-Q7 |
A |
T |
17: 35,658,655 (GRCm39) |
S98C |
probably damaging |
Het |
Hcn2 |
G |
T |
10: 79,569,607 (GRCm39) |
E536* |
probably null |
Het |
Kat6b |
A |
T |
14: 21,720,748 (GRCm39) |
H1700L |
probably damaging |
Het |
Klhl3 |
C |
T |
13: 58,248,192 (GRCm39) |
V35I |
probably benign |
Het |
Krt34 |
A |
T |
11: 99,930,916 (GRCm39) |
L162Q |
probably damaging |
Het |
Ly9 |
A |
G |
1: 171,416,663 (GRCm39) |
S644P |
probably damaging |
Het |
Magi1 |
A |
T |
6: 93,676,620 (GRCm39) |
V685E |
probably damaging |
Het |
Malrd1 |
A |
G |
2: 15,531,408 (GRCm39) |
|
probably benign |
Het |
Malrd1 |
A |
T |
2: 15,672,740 (GRCm39) |
H599L |
probably benign |
Het |
Matn2 |
T |
A |
15: 34,426,380 (GRCm39) |
C631S |
probably damaging |
Het |
Megf8 |
A |
T |
7: 25,049,120 (GRCm39) |
D1739V |
probably damaging |
Het |
Mlf1 |
G |
A |
3: 67,300,277 (GRCm39) |
R98Q |
probably benign |
Het |
Mprip |
T |
A |
11: 59,649,815 (GRCm39) |
I1173K |
possibly damaging |
Het |
Mrc1 |
A |
G |
2: 14,275,016 (GRCm39) |
D439G |
probably damaging |
Het |
Mroh5 |
A |
T |
15: 73,662,691 (GRCm39) |
W208R |
probably damaging |
Het |
Ms4a5 |
T |
G |
19: 11,256,646 (GRCm39) |
I84L |
probably benign |
Het |
Myt1 |
G |
A |
2: 181,405,218 (GRCm39) |
|
probably null |
Het |
Nbea |
T |
A |
3: 55,907,990 (GRCm39) |
H1374L |
probably damaging |
Het |
Nbeal1 |
T |
A |
1: 60,292,633 (GRCm39) |
I1095K |
probably benign |
Het |
Nolc1 |
A |
G |
19: 46,071,509 (GRCm39) |
|
probably benign |
Het |
Nr5a2 |
A |
G |
1: 136,887,976 (GRCm39) |
L18P |
probably benign |
Het |
Nup188 |
G |
T |
2: 30,212,199 (GRCm39) |
C562F |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,971,597 (GRCm39) |
V2415A |
probably damaging |
Het |
Pacsin2 |
A |
T |
15: 83,263,879 (GRCm39) |
|
probably null |
Het |
Pias3 |
A |
G |
3: 96,606,839 (GRCm39) |
H34R |
possibly damaging |
Het |
Ppfia2 |
T |
C |
10: 106,729,361 (GRCm39) |
V903A |
probably damaging |
Het |
Pramel1 |
T |
A |
4: 143,123,275 (GRCm39) |
L84Q |
probably damaging |
Het |
Pramel6 |
G |
A |
2: 87,339,782 (GRCm39) |
C182Y |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,743,896 (GRCm39) |
Y120H |
probably damaging |
Het |
Prss28 |
A |
G |
17: 25,530,331 (GRCm39) |
M212V |
probably benign |
Het |
Rbp3 |
G |
T |
14: 33,677,224 (GRCm39) |
G391* |
probably null |
Het |
Rc3h2 |
C |
T |
2: 37,301,151 (GRCm39) |
|
probably null |
Het |
Ret |
A |
G |
6: 118,150,582 (GRCm39) |
F645L |
probably benign |
Het |
Saxo5 |
T |
C |
8: 3,529,268 (GRCm39) |
L251P |
probably damaging |
Het |
Sgsm2 |
A |
G |
11: 74,755,995 (GRCm39) |
S402P |
possibly damaging |
Het |
Shc3 |
T |
A |
13: 51,636,915 (GRCm39) |
|
probably null |
Het |
Slc25a16 |
A |
G |
10: 62,776,938 (GRCm39) |
N246S |
probably benign |
Het |
Snrpd1 |
T |
A |
18: 10,623,694 (GRCm39) |
H26Q |
probably benign |
Het |
Thsd1 |
A |
G |
8: 22,733,363 (GRCm39) |
T137A |
probably damaging |
Het |
Tnik |
A |
T |
3: 28,593,597 (GRCm39) |
H151L |
probably damaging |
Het |
Tns1 |
T |
A |
1: 73,957,209 (GRCm39) |
K1725N |
probably damaging |
Het |
Tomm40l |
T |
A |
1: 171,048,161 (GRCm39) |
T147S |
probably damaging |
Het |
Tomm6 |
G |
T |
17: 47,998,932 (GRCm39) |
|
probably benign |
Het |
Trp53 |
G |
A |
11: 69,480,440 (GRCm39) |
C272Y |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,649,214 (GRCm39) |
V1492E |
probably benign |
Het |
Uvrag |
A |
G |
7: 98,555,726 (GRCm39) |
F456S |
probably damaging |
Het |
Vmn1r86 |
A |
T |
7: 12,836,279 (GRCm39) |
M199K |
possibly damaging |
Het |
Vmn2r4 |
C |
T |
3: 64,317,378 (GRCm39) |
C120Y |
probably damaging |
Het |
|
Other mutations in Tsen2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01319:Tsen2
|
APN |
6 |
115,553,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01409:Tsen2
|
APN |
6 |
115,536,555 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02002:Tsen2
|
APN |
6 |
115,536,568 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03301:Tsen2
|
APN |
6 |
115,545,732 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Tsen2
|
UTSW |
6 |
115,537,030 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Tsen2
|
UTSW |
6 |
115,537,030 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Tsen2
|
UTSW |
6 |
115,537,027 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Tsen2
|
UTSW |
6 |
115,537,033 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Tsen2
|
UTSW |
6 |
115,537,029 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Tsen2
|
UTSW |
6 |
115,537,038 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Tsen2
|
UTSW |
6 |
115,537,027 (GRCm39) |
small insertion |
probably benign |
|
R0141:Tsen2
|
UTSW |
6 |
115,545,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R1165:Tsen2
|
UTSW |
6 |
115,538,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R1528:Tsen2
|
UTSW |
6 |
115,536,989 (GRCm39) |
missense |
probably benign |
0.01 |
R2152:Tsen2
|
UTSW |
6 |
115,524,936 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4022:Tsen2
|
UTSW |
6 |
115,524,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4246:Tsen2
|
UTSW |
6 |
115,524,785 (GRCm39) |
splice site |
probably benign |
|
R4247:Tsen2
|
UTSW |
6 |
115,524,785 (GRCm39) |
splice site |
probably benign |
|
R4249:Tsen2
|
UTSW |
6 |
115,524,785 (GRCm39) |
splice site |
probably benign |
|
R4774:Tsen2
|
UTSW |
6 |
115,552,894 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5511:Tsen2
|
UTSW |
6 |
115,538,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Tsen2
|
UTSW |
6 |
115,554,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Tsen2
|
UTSW |
6 |
115,536,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Tsen2
|
UTSW |
6 |
115,537,036 (GRCm39) |
missense |
probably benign |
0.35 |
R6750:Tsen2
|
UTSW |
6 |
115,526,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Tsen2
|
UTSW |
6 |
115,524,933 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7438:Tsen2
|
UTSW |
6 |
115,536,943 (GRCm39) |
nonsense |
probably null |
|
R9254:Tsen2
|
UTSW |
6 |
115,553,864 (GRCm39) |
missense |
probably damaging |
0.97 |
RF030:Tsen2
|
UTSW |
6 |
115,537,028 (GRCm39) |
small insertion |
probably benign |
|
RF035:Tsen2
|
UTSW |
6 |
115,537,028 (GRCm39) |
small insertion |
probably benign |
|
RF042:Tsen2
|
UTSW |
6 |
115,537,028 (GRCm39) |
small insertion |
probably benign |
|
RF056:Tsen2
|
UTSW |
6 |
115,537,025 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Tsen2
|
UTSW |
6 |
115,536,877 (GRCm39) |
frame shift |
probably null |
|
|