Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
A |
G |
1: 179,580,887 (GRCm39) |
S1772P |
probably benign |
Het |
Cstdc3 |
T |
A |
16: 36,131,591 (GRCm39) |
Y34N |
probably damaging |
Het |
Epsti1 |
T |
C |
14: 78,210,052 (GRCm39) |
|
probably null |
Het |
Mtrr |
A |
T |
13: 68,719,266 (GRCm39) |
L325Q |
probably damaging |
Het |
Neb |
T |
C |
2: 52,186,367 (GRCm39) |
K902E |
possibly damaging |
Het |
Nfkbie |
T |
C |
17: 45,867,189 (GRCm39) |
L108P |
probably damaging |
Het |
Or2n1d |
T |
A |
17: 38,646,470 (GRCm39) |
C141S |
probably damaging |
Het |
Or4c52 |
A |
T |
2: 89,845,655 (GRCm39) |
Y127F |
probably damaging |
Het |
Pcdh15 |
A |
G |
10: 74,286,115 (GRCm39) |
D712G |
probably benign |
Het |
Polr3k |
T |
C |
2: 181,506,251 (GRCm39) |
|
probably benign |
Het |
Shkbp1 |
A |
C |
7: 27,041,875 (GRCm39) |
F660V |
possibly damaging |
Het |
Smchd1 |
T |
C |
17: 71,698,413 (GRCm39) |
D1121G |
probably damaging |
Het |
Srgap3 |
A |
T |
6: 112,699,983 (GRCm39) |
D998E |
probably benign |
Het |
Stab1 |
T |
C |
14: 30,861,765 (GRCm39) |
D14G |
probably damaging |
Het |
Tap1 |
T |
C |
17: 34,415,578 (GRCm39) |
S641P |
probably benign |
Het |
Tgm6 |
T |
C |
2: 129,993,354 (GRCm39) |
|
probably benign |
Het |
Tmco5 |
A |
T |
2: 116,717,781 (GRCm39) |
E194D |
probably damaging |
Het |
Treml4 |
T |
A |
17: 48,571,732 (GRCm39) |
V45E |
probably damaging |
Het |
Uggt2 |
A |
T |
14: 119,319,146 (GRCm39) |
M292K |
probably damaging |
Het |
Usp5 |
A |
T |
6: 124,801,189 (GRCm39) |
D179E |
possibly damaging |
Het |
Ythdf1 |
A |
G |
2: 180,553,486 (GRCm39) |
L216P |
probably damaging |
Het |
Zfp948 |
C |
T |
17: 21,807,333 (GRCm39) |
A175V |
probably benign |
Het |
|
Other mutations in Tgm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Tgm3
|
APN |
2 |
129,880,333 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00924:Tgm3
|
APN |
2 |
129,880,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01469:Tgm3
|
APN |
2 |
129,866,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01722:Tgm3
|
APN |
2 |
129,886,488 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02269:Tgm3
|
APN |
2 |
129,866,438 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02437:Tgm3
|
APN |
2 |
129,871,961 (GRCm39) |
splice site |
probably null |
|
IGL02449:Tgm3
|
APN |
2 |
129,880,529 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02992:Tgm3
|
APN |
2 |
129,883,899 (GRCm39) |
missense |
probably damaging |
1.00 |
tortellini
|
UTSW |
2 |
129,866,505 (GRCm39) |
critical splice donor site |
probably benign |
|
ANU74:Tgm3
|
UTSW |
2 |
129,890,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R0523:Tgm3
|
UTSW |
2 |
129,886,582 (GRCm39) |
critical splice donor site |
probably null |
|
R0833:Tgm3
|
UTSW |
2 |
129,868,602 (GRCm39) |
splice site |
probably benign |
|
R0834:Tgm3
|
UTSW |
2 |
129,868,677 (GRCm39) |
missense |
probably benign |
0.00 |
R0836:Tgm3
|
UTSW |
2 |
129,868,602 (GRCm39) |
splice site |
probably benign |
|
R0940:Tgm3
|
UTSW |
2 |
129,854,326 (GRCm39) |
missense |
probably benign |
0.00 |
R1354:Tgm3
|
UTSW |
2 |
129,883,818 (GRCm39) |
missense |
probably benign |
|
R1642:Tgm3
|
UTSW |
2 |
129,889,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Tgm3
|
UTSW |
2 |
129,883,688 (GRCm39) |
nonsense |
probably null |
|
R1715:Tgm3
|
UTSW |
2 |
129,868,734 (GRCm39) |
critical splice donor site |
probably null |
|
R1944:Tgm3
|
UTSW |
2 |
129,871,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R2104:Tgm3
|
UTSW |
2 |
129,879,403 (GRCm39) |
missense |
probably benign |
0.39 |
R3416:Tgm3
|
UTSW |
2 |
129,889,692 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3417:Tgm3
|
UTSW |
2 |
129,889,692 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4231:Tgm3
|
UTSW |
2 |
129,886,509 (GRCm39) |
nonsense |
probably null |
|
R4296:Tgm3
|
UTSW |
2 |
129,880,333 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4794:Tgm3
|
UTSW |
2 |
129,883,875 (GRCm39) |
missense |
probably benign |
0.00 |
R4948:Tgm3
|
UTSW |
2 |
129,890,240 (GRCm39) |
missense |
probably benign |
0.00 |
R5034:Tgm3
|
UTSW |
2 |
129,879,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5144:Tgm3
|
UTSW |
2 |
129,890,202 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5786:Tgm3
|
UTSW |
2 |
129,868,704 (GRCm39) |
nonsense |
probably null |
|
R6030:Tgm3
|
UTSW |
2 |
129,883,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Tgm3
|
UTSW |
2 |
129,883,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Tgm3
|
UTSW |
2 |
129,867,221 (GRCm39) |
nonsense |
probably null |
|
R6219:Tgm3
|
UTSW |
2 |
129,880,530 (GRCm39) |
critical splice donor site |
probably null |
|
R6901:Tgm3
|
UTSW |
2 |
129,883,890 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6969:Tgm3
|
UTSW |
2 |
129,883,949 (GRCm39) |
missense |
probably benign |
0.06 |
R6980:Tgm3
|
UTSW |
2 |
129,868,697 (GRCm39) |
missense |
probably benign |
0.17 |
R7282:Tgm3
|
UTSW |
2 |
129,866,481 (GRCm39) |
missense |
probably benign |
0.00 |
R7317:Tgm3
|
UTSW |
2 |
129,890,211 (GRCm39) |
missense |
probably benign |
0.09 |
R7513:Tgm3
|
UTSW |
2 |
129,866,324 (GRCm39) |
missense |
probably benign |
0.00 |
R7517:Tgm3
|
UTSW |
2 |
129,883,684 (GRCm39) |
missense |
probably benign |
0.01 |
R7793:Tgm3
|
UTSW |
2 |
129,854,330 (GRCm39) |
critical splice donor site |
probably null |
|
R7822:Tgm3
|
UTSW |
2 |
129,883,819 (GRCm39) |
missense |
probably benign |
0.00 |
R7955:Tgm3
|
UTSW |
2 |
129,880,400 (GRCm39) |
missense |
probably benign |
|
R8747:Tgm3
|
UTSW |
2 |
129,886,452 (GRCm39) |
missense |
probably benign |
0.03 |
R8805:Tgm3
|
UTSW |
2 |
129,889,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Tgm3
|
UTSW |
2 |
129,880,403 (GRCm39) |
missense |
probably benign |
0.00 |
R9029:Tgm3
|
UTSW |
2 |
129,871,680 (GRCm39) |
missense |
probably benign |
0.00 |
R9208:Tgm3
|
UTSW |
2 |
129,865,618 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9423:Tgm3
|
UTSW |
2 |
129,880,527 (GRCm39) |
missense |
probably benign |
0.01 |
R9713:Tgm3
|
UTSW |
2 |
129,867,229 (GRCm39) |
missense |
possibly damaging |
0.74 |
X0065:Tgm3
|
UTSW |
2 |
129,866,430 (GRCm39) |
missense |
probably benign |
0.05 |
|