Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp4 |
G |
T |
7: 43,906,210 (GRCm39) |
Y88* |
probably null |
Het |
Aftph |
T |
C |
11: 20,676,994 (GRCm39) |
D205G |
probably damaging |
Het |
Arhgap31 |
T |
C |
16: 38,423,793 (GRCm39) |
I758V |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,591,513 (GRCm39) |
|
probably null |
Het |
Auts2 |
T |
C |
5: 131,469,056 (GRCm39) |
T754A |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,966,216 (GRCm39) |
M4048V |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,024,870 (GRCm39) |
|
probably null |
Het |
Cmpk1 |
C |
T |
4: 114,822,121 (GRCm39) |
A143T |
probably benign |
Het |
Cwc22 |
A |
G |
2: 77,757,640 (GRCm39) |
S163P |
probably damaging |
Het |
Dnaaf11 |
T |
A |
15: 66,321,326 (GRCm39) |
M272L |
probably benign |
Het |
Faf1 |
T |
A |
4: 109,534,278 (GRCm39) |
|
probably benign |
Het |
Focad |
T |
A |
4: 88,289,043 (GRCm39) |
I1279N |
unknown |
Het |
Gp5 |
T |
C |
16: 30,127,459 (GRCm39) |
D405G |
possibly damaging |
Het |
Guf1 |
C |
A |
5: 69,718,501 (GRCm39) |
N213K |
probably damaging |
Het |
Hacd4 |
T |
C |
4: 88,341,285 (GRCm39) |
T145A |
probably damaging |
Het |
Itga11 |
T |
C |
9: 62,681,399 (GRCm39) |
M1005T |
probably benign |
Het |
Mast4 |
T |
A |
13: 102,910,781 (GRCm39) |
T621S |
probably damaging |
Het |
Mme |
T |
C |
3: 63,247,534 (GRCm39) |
M273T |
possibly damaging |
Het |
Mos |
A |
G |
4: 3,871,816 (GRCm39) |
|
probably benign |
Het |
Msln |
C |
T |
17: 25,969,004 (GRCm39) |
|
probably null |
Het |
Mtg1 |
A |
T |
7: 139,730,149 (GRCm39) |
Q315L |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,105,354 (GRCm39) |
E1048G |
probably damaging |
Het |
Ndufa9 |
C |
T |
6: 126,821,777 (GRCm39) |
G66D |
probably damaging |
Het |
Nr1i2 |
T |
C |
16: 38,086,333 (GRCm39) |
K44R |
probably benign |
Het |
Nup155 |
T |
A |
15: 8,165,272 (GRCm39) |
M636K |
probably benign |
Het |
Or12d12 |
A |
T |
17: 37,610,673 (GRCm39) |
F213L |
probably benign |
Het |
Or5b96 |
T |
A |
19: 12,867,513 (GRCm39) |
T143S |
probably benign |
Het |
Pde4b |
A |
T |
4: 102,458,832 (GRCm39) |
Q496L |
probably damaging |
Het |
Plekha6 |
T |
C |
1: 133,187,869 (GRCm39) |
V130A |
probably benign |
Het |
Prag1 |
A |
G |
8: 36,569,834 (GRCm39) |
N139S |
probably benign |
Het |
Rbpj-ps3 |
T |
C |
6: 46,507,694 (GRCm39) |
T19A |
probably benign |
Het |
Scai |
A |
G |
2: 38,984,803 (GRCm39) |
|
probably benign |
Het |
Slc12a7 |
A |
G |
13: 73,947,733 (GRCm39) |
T617A |
probably benign |
Het |
Slc15a2 |
T |
C |
16: 36,576,592 (GRCm39) |
M481V |
probably benign |
Het |
Snx5 |
A |
G |
2: 144,112,325 (GRCm39) |
L8P |
probably benign |
Het |
Spg11 |
C |
T |
2: 121,945,152 (GRCm39) |
A123T |
probably damaging |
Het |
Supt6 |
T |
A |
11: 78,113,013 (GRCm39) |
I977F |
probably damaging |
Het |
Tjp3 |
T |
C |
10: 81,114,490 (GRCm39) |
D442G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,068,200 (GRCm39) |
N275K |
probably benign |
Het |
Vmn2r50 |
A |
G |
7: 9,771,364 (GRCm39) |
F779S |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,345,482 (GRCm39) |
R2574S |
probably benign |
Het |
Zbp1 |
T |
C |
2: 173,054,038 (GRCm39) |
E161G |
possibly damaging |
Het |
|
Other mutations in Cstf2t |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01731:Cstf2t
|
APN |
19 |
31,061,738 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02466:Cstf2t
|
APN |
19 |
31,061,277 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0064:Cstf2t
|
UTSW |
19 |
31,060,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R0099:Cstf2t
|
UTSW |
19 |
31,061,231 (GRCm39) |
missense |
probably benign |
0.00 |
R0197:Cstf2t
|
UTSW |
19 |
31,062,026 (GRCm39) |
missense |
probably benign |
0.01 |
R0423:Cstf2t
|
UTSW |
19 |
31,061,676 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0883:Cstf2t
|
UTSW |
19 |
31,062,026 (GRCm39) |
missense |
probably benign |
0.01 |
R1753:Cstf2t
|
UTSW |
19 |
31,061,085 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2206:Cstf2t
|
UTSW |
19 |
31,061,175 (GRCm39) |
missense |
probably benign |
0.00 |
R2291:Cstf2t
|
UTSW |
19 |
31,062,264 (GRCm39) |
missense |
probably benign |
0.36 |
R3753:Cstf2t
|
UTSW |
19 |
31,060,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4523:Cstf2t
|
UTSW |
19 |
31,060,482 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4991:Cstf2t
|
UTSW |
19 |
31,061,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R5134:Cstf2t
|
UTSW |
19 |
31,061,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Cstf2t
|
UTSW |
19 |
31,060,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R6081:Cstf2t
|
UTSW |
19 |
31,060,523 (GRCm39) |
missense |
probably benign |
0.10 |
R6573:Cstf2t
|
UTSW |
19 |
31,061,180 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Cstf2t
|
UTSW |
19 |
31,060,593 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7648:Cstf2t
|
UTSW |
19 |
31,060,992 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8317:Cstf2t
|
UTSW |
19 |
31,061,648 (GRCm39) |
missense |
probably benign |
0.09 |
|