Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
G |
7: 120,102,694 (GRCm39) |
Y864* |
probably null |
Het |
Abhd2 |
T |
C |
7: 78,998,032 (GRCm39) |
M188T |
probably benign |
Het |
Adamtsl3 |
T |
A |
7: 82,206,054 (GRCm39) |
|
probably null |
Het |
Ankrd36 |
G |
T |
11: 5,637,348 (GRCm39) |
V1306L |
probably benign |
Het |
Ankrd50 |
C |
A |
3: 38,538,831 (GRCm39) |
|
probably benign |
Het |
Btbd2 |
T |
C |
10: 80,482,226 (GRCm39) |
D258G |
probably damaging |
Het |
Cabin1 |
C |
T |
10: 75,568,277 (GRCm39) |
R75K |
possibly damaging |
Het |
Carmil3 |
A |
G |
14: 55,735,348 (GRCm39) |
N507S |
probably benign |
Het |
Cntn1 |
A |
G |
15: 92,143,970 (GRCm39) |
E311G |
probably damaging |
Het |
Csnk1a1 |
T |
C |
18: 61,718,387 (GRCm39) |
M371T |
unknown |
Het |
Dnah1 |
A |
T |
14: 31,006,739 (GRCm39) |
V2192E |
possibly damaging |
Het |
Entrep3 |
T |
A |
3: 89,092,278 (GRCm39) |
I199N |
probably damaging |
Het |
Grip2 |
A |
C |
6: 91,742,031 (GRCm39) |
|
probably null |
Het |
Gxylt2 |
G |
T |
6: 100,760,146 (GRCm39) |
W227L |
probably damaging |
Het |
Ighv6-5 |
G |
T |
12: 114,380,626 (GRCm39) |
|
probably benign |
Het |
Jak1 |
T |
A |
4: 101,031,408 (GRCm39) |
|
probably null |
Het |
Jakmip1 |
A |
G |
5: 37,328,345 (GRCm39) |
D393G |
possibly damaging |
Het |
Klf10 |
A |
T |
15: 38,297,080 (GRCm39) |
V320E |
probably damaging |
Het |
Krt87 |
A |
T |
15: 101,336,426 (GRCm39) |
C76S |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,106,701 (GRCm39) |
D1261G |
possibly damaging |
Het |
Myo18b |
A |
C |
5: 112,905,319 (GRCm39) |
|
probably null |
Het |
Or4c124 |
T |
A |
2: 89,155,723 (GRCm39) |
D267V |
probably damaging |
Het |
Oxct2a |
A |
C |
4: 123,217,150 (GRCm39) |
L77R |
probably damaging |
Het |
P2rx2 |
A |
T |
5: 110,489,950 (GRCm39) |
C172S |
probably damaging |
Het |
P3h3 |
A |
G |
6: 124,832,969 (GRCm39) |
Y195H |
probably damaging |
Het |
Pex11b |
T |
C |
3: 96,544,107 (GRCm39) |
|
probably null |
Het |
Ppm1j |
T |
A |
3: 104,691,059 (GRCm39) |
Y274* |
probably null |
Het |
Scn9a |
A |
T |
2: 66,370,893 (GRCm39) |
D562E |
possibly damaging |
Het |
Slc14a2 |
A |
G |
18: 78,203,156 (GRCm39) |
V557A |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,042,221 (GRCm39) |
I500T |
probably damaging |
Het |
Sult2a3 |
C |
T |
7: 13,806,981 (GRCm39) |
V234I |
probably benign |
Het |
Tktl2 |
A |
G |
8: 66,965,651 (GRCm39) |
D403G |
probably benign |
Het |
Tmprss13 |
G |
A |
9: 45,244,858 (GRCm39) |
W212* |
probably null |
Het |
Tspoap1 |
T |
G |
11: 87,654,451 (GRCm39) |
S244A |
probably benign |
Het |
Upb1 |
A |
C |
10: 75,260,368 (GRCm39) |
T136P |
probably benign |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,662,188 (GRCm39) |
T136A |
probably benign |
Het |
Zfp354a |
A |
G |
11: 50,960,751 (GRCm39) |
T320A |
probably benign |
Het |
Zfyve16 |
A |
G |
13: 92,641,070 (GRCm39) |
Y1225H |
probably damaging |
Het |
|
Other mutations in Tcp10c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4618001:Tcp10c
|
UTSW |
17 |
13,576,772 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2397:Tcp10c
|
UTSW |
17 |
13,590,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Tcp10c
|
UTSW |
17 |
13,588,453 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7095:Tcp10c
|
UTSW |
17 |
13,576,196 (GRCm39) |
missense |
probably benign |
0.23 |
R7151:Tcp10c
|
UTSW |
17 |
13,576,166 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7286:Tcp10c
|
UTSW |
17 |
13,582,438 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7423:Tcp10c
|
UTSW |
17 |
13,581,503 (GRCm39) |
splice site |
probably null |
|
R7544:Tcp10c
|
UTSW |
17 |
13,581,260 (GRCm39) |
missense |
probably damaging |
0.98 |
R9109:Tcp10c
|
UTSW |
17 |
13,576,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Tcp10c
|
UTSW |
17 |
13,584,463 (GRCm39) |
missense |
probably benign |
0.03 |
R9444:Tcp10c
|
UTSW |
17 |
13,581,503 (GRCm39) |
splice site |
probably null |
|
|