Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
C |
8: 111,767,284 (GRCm39) |
V130A |
probably benign |
Het |
Acte1 |
C |
T |
7: 143,451,203 (GRCm39) |
|
probably null |
Het |
Adamts12 |
A |
C |
15: 11,331,877 (GRCm39) |
K1465T |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,166,306 (GRCm39) |
V223A |
|
Het |
Adamtsl3 |
T |
A |
7: 82,251,487 (GRCm39) |
I1494N |
possibly damaging |
Het |
Ank3 |
T |
C |
10: 69,826,148 (GRCm39) |
Y1606H |
|
Het |
Arhgap32 |
A |
G |
9: 32,093,150 (GRCm39) |
I168V |
probably benign |
Het |
Atxn7l2 |
G |
A |
3: 108,110,617 (GRCm39) |
R675C |
probably damaging |
Het |
Brcc3dc |
A |
G |
10: 108,535,520 (GRCm39) |
M145T |
probably damaging |
Het |
Bst2 |
A |
T |
8: 71,989,990 (GRCm39) |
W28R |
probably damaging |
Het |
Cadps |
T |
A |
14: 12,488,975 (GRCm38) |
T861S |
probably benign |
Het |
Ceacam11 |
A |
G |
7: 17,709,243 (GRCm39) |
Y147C |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,740,588 (GRCm39) |
N1187K |
probably damaging |
Het |
Dcaf7 |
T |
C |
11: 105,937,604 (GRCm39) |
W76R |
probably damaging |
Het |
Ephb1 |
G |
A |
9: 101,918,222 (GRCm39) |
T429I |
probably damaging |
Het |
Flg |
A |
T |
3: 93,197,734 (GRCm39) |
Q21L |
unknown |
Het |
Flrt2 |
T |
C |
12: 95,747,333 (GRCm39) |
V557A |
probably benign |
Het |
Gdpgp1 |
T |
C |
7: 79,888,581 (GRCm39) |
V204A |
probably damaging |
Het |
Gmcl1 |
G |
T |
6: 86,698,408 (GRCm39) |
A163E |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Jph2 |
T |
C |
2: 163,181,206 (GRCm39) |
K653E |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,486,382 (GRCm39) |
S4724G |
probably damaging |
Het |
Llgl2 |
T |
C |
11: 115,741,619 (GRCm39) |
V583A |
possibly damaging |
Het |
Met |
T |
C |
6: 17,562,236 (GRCm39) |
V1199A |
probably damaging |
Het |
Mmp25 |
A |
G |
17: 23,863,768 (GRCm39) |
W21R |
probably benign |
Het |
Nsun4 |
A |
T |
4: 115,909,040 (GRCm39) |
C507S |
probably benign |
Het |
Or1j19 |
T |
A |
2: 36,676,618 (GRCm39) |
M27K |
probably benign |
Het |
Pard6g |
T |
C |
18: 80,160,658 (GRCm39) |
V257A |
possibly damaging |
Het |
Pcdh1 |
A |
G |
18: 38,332,049 (GRCm39) |
V457A |
probably damaging |
Het |
Pcnx1 |
C |
T |
12: 81,965,593 (GRCm39) |
R59* |
probably null |
Het |
Pdzd2 |
G |
A |
15: 12,373,592 (GRCm39) |
S2181L |
probably benign |
Het |
Plpp6 |
T |
A |
19: 28,941,891 (GRCm39) |
M164K |
possibly damaging |
Het |
Rhobtb2 |
C |
A |
14: 70,038,080 (GRCm39) |
R60L |
probably damaging |
Het |
Rsph10b |
A |
C |
5: 143,922,348 (GRCm39) |
I845L |
probably benign |
Het |
Sdf4 |
C |
T |
4: 156,094,295 (GRCm39) |
A325V |
probably damaging |
Het |
Slc4a3 |
A |
G |
1: 75,528,448 (GRCm39) |
D481G |
possibly damaging |
Het |
Smo |
A |
G |
6: 29,755,522 (GRCm39) |
Y398C |
probably damaging |
Het |
Sox18 |
A |
G |
2: 181,313,293 (GRCm39) |
Y8H |
possibly damaging |
Het |
Sycp1 |
A |
T |
3: 102,758,918 (GRCm39) |
S780T |
probably benign |
Het |
Tdg |
T |
A |
10: 82,480,353 (GRCm39) |
V239E |
probably damaging |
Het |
Tenm2 |
T |
C |
11: 35,899,137 (GRCm39) |
T2675A |
probably benign |
Het |
Thrap3 |
C |
A |
4: 126,080,273 (GRCm39) |
R31L |
unknown |
Het |
Tinagl1 |
T |
A |
4: 130,063,123 (GRCm39) |
I149F |
probably damaging |
Het |
Tnc |
A |
G |
4: 63,927,000 (GRCm39) |
V842A |
probably benign |
Het |
Ube4a |
T |
C |
9: 44,846,781 (GRCm39) |
I773V |
probably benign |
Het |
Vmn1r229 |
T |
C |
17: 21,035,268 (GRCm39) |
V171A |
probably benign |
Het |
Zc3hav1 |
T |
C |
6: 38,306,114 (GRCm39) |
E646G |
probably damaging |
Het |
Zfp341 |
A |
T |
2: 154,469,820 (GRCm39) |
M168L |
probably benign |
Het |
Zfp874a |
A |
C |
13: 67,597,563 (GRCm39) |
D13E |
possibly damaging |
Het |
|
Other mutations in Tpm3-rs7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02568:Tpm3-rs7
|
APN |
14 |
113,552,370 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02966:Tpm3-rs7
|
APN |
14 |
113,552,810 (GRCm39) |
nonsense |
probably null |
|
R1414:Tpm3-rs7
|
UTSW |
14 |
113,552,274 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1789:Tpm3-rs7
|
UTSW |
14 |
113,552,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R1823:Tpm3-rs7
|
UTSW |
14 |
113,552,595 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5770:Tpm3-rs7
|
UTSW |
14 |
113,552,807 (GRCm39) |
missense |
probably benign |
0.00 |
R6612:Tpm3-rs7
|
UTSW |
14 |
113,552,268 (GRCm39) |
missense |
probably benign |
0.01 |
R6815:Tpm3-rs7
|
UTSW |
14 |
113,552,292 (GRCm39) |
missense |
probably benign |
0.09 |
R6818:Tpm3-rs7
|
UTSW |
14 |
113,552,448 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8921:Tpm3-rs7
|
UTSW |
14 |
113,552,493 (GRCm39) |
missense |
probably benign |
0.42 |
R8985:Tpm3-rs7
|
UTSW |
14 |
113,552,756 (GRCm39) |
missense |
probably benign |
0.44 |
R9386:Tpm3-rs7
|
UTSW |
14 |
113,552,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Tpm3-rs7
|
UTSW |
14 |
113,552,109 (GRCm39) |
start codon destroyed |
probably null |
0.62 |
|