Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
C |
A |
18: 65,440,544 (GRCm39) |
C283F |
probably benign |
Het |
Anapc1 |
T |
C |
2: 128,459,651 (GRCm39) |
R1803G |
probably benign |
Het |
Anapc4 |
T |
C |
5: 53,012,979 (GRCm39) |
V423A |
probably benign |
Het |
Arfgef3 |
A |
G |
10: 18,465,483 (GRCm39) |
I2120T |
possibly damaging |
Het |
Btaf1 |
T |
A |
19: 36,968,143 (GRCm39) |
H1109Q |
probably benign |
Het |
Cfap418 |
A |
G |
4: 10,882,462 (GRCm39) |
T124A |
probably benign |
Het |
Cfap70 |
G |
A |
14: 20,454,232 (GRCm39) |
P851S |
probably benign |
Het |
Clcf1 |
T |
A |
19: 4,272,252 (GRCm39) |
L103Q |
probably damaging |
Het |
Col11a2 |
T |
A |
17: 34,278,124 (GRCm39) |
V1032E |
possibly damaging |
Het |
Cyp2c38 |
T |
G |
19: 39,393,113 (GRCm39) |
D318A |
probably benign |
Het |
Dbpht2 |
A |
G |
12: 74,345,774 (GRCm39) |
|
noncoding transcript |
Het |
Dhx34 |
A |
C |
7: 15,935,883 (GRCm39) |
V893G |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,815,828 (GRCm39) |
C3854S |
possibly damaging |
Het |
Htr1a |
T |
C |
13: 105,581,344 (GRCm39) |
Y195H |
probably damaging |
Het |
Insr |
A |
G |
8: 3,208,769 (GRCm39) |
S1231P |
probably damaging |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Kpna4 |
A |
T |
3: 68,993,161 (GRCm39) |
|
probably benign |
Het |
Or52d13 |
A |
G |
7: 103,110,019 (GRCm39) |
I132T |
probably damaging |
Het |
Or52e8 |
A |
T |
7: 104,624,519 (GRCm39) |
Y228* |
probably null |
Het |
Or5m3 |
A |
G |
2: 85,838,984 (GRCm39) |
Y288C |
possibly damaging |
Het |
Osbpl7 |
G |
A |
11: 96,946,927 (GRCm39) |
R239H |
possibly damaging |
Het |
Prkce |
G |
A |
17: 86,937,588 (GRCm39) |
V674I |
probably benign |
Het |
Prkrip1 |
T |
C |
5: 136,226,685 (GRCm39) |
M52V |
possibly damaging |
Het |
Sash1 |
A |
G |
10: 8,605,843 (GRCm39) |
M849T |
probably benign |
Het |
Scaf8 |
T |
C |
17: 3,247,395 (GRCm39) |
L906S |
probably damaging |
Het |
Sfmbt2 |
T |
C |
2: 10,582,382 (GRCm39) |
L676P |
probably benign |
Het |
Sgsm1 |
C |
T |
5: 113,406,708 (GRCm39) |
V923I |
probably damaging |
Het |
Slc38a3 |
A |
T |
9: 107,533,158 (GRCm39) |
L305Q |
probably damaging |
Het |
Slc44a5 |
A |
G |
3: 153,949,223 (GRCm39) |
Y232C |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,979,259 (GRCm39) |
|
probably benign |
Het |
Synm |
T |
C |
7: 67,385,095 (GRCm39) |
I414V |
probably damaging |
Het |
Timm21 |
G |
C |
18: 84,967,387 (GRCm39) |
L130V |
probably damaging |
Het |
Trpc7 |
C |
T |
13: 56,970,462 (GRCm39) |
|
probably benign |
Het |
Trpm7 |
G |
A |
2: 126,673,158 (GRCm39) |
R532C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,777,086 (GRCm39) |
K1485* |
probably null |
Het |
Txn2 |
T |
C |
15: 77,811,949 (GRCm39) |
D69G |
probably damaging |
Het |
U2af2 |
C |
T |
7: 5,072,433 (GRCm39) |
|
probably benign |
Het |
Ubn1 |
T |
C |
16: 4,882,255 (GRCm39) |
Y239H |
probably damaging |
Het |
Ubtf |
A |
G |
11: 102,200,603 (GRCm39) |
|
probably benign |
Het |
Usp49 |
T |
A |
17: 47,983,376 (GRCm39) |
V127D |
probably benign |
Het |
Washc2 |
C |
T |
6: 116,185,225 (GRCm39) |
R20W |
probably damaging |
Het |
Zscan10 |
T |
C |
17: 23,828,981 (GRCm39) |
S476P |
probably damaging |
Het |
|
Other mutations in Tbc1d12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00594:Tbc1d12
|
APN |
19 |
38,884,487 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01583:Tbc1d12
|
APN |
19 |
38,871,176 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01667:Tbc1d12
|
APN |
19 |
38,902,744 (GRCm39) |
splice site |
probably benign |
|
IGL02207:Tbc1d12
|
APN |
19 |
38,905,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03348:Tbc1d12
|
APN |
19 |
38,905,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0844:Tbc1d12
|
UTSW |
19 |
38,825,515 (GRCm39) |
missense |
probably benign |
0.02 |
R1440:Tbc1d12
|
UTSW |
19 |
38,902,796 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1845:Tbc1d12
|
UTSW |
19 |
38,899,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R2374:Tbc1d12
|
UTSW |
19 |
38,825,614 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3499:Tbc1d12
|
UTSW |
19 |
38,884,478 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4704:Tbc1d12
|
UTSW |
19 |
38,889,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Tbc1d12
|
UTSW |
19 |
38,854,169 (GRCm39) |
nonsense |
probably null |
|
R5089:Tbc1d12
|
UTSW |
19 |
38,905,232 (GRCm39) |
nonsense |
probably null |
|
R5781:Tbc1d12
|
UTSW |
19 |
38,871,127 (GRCm39) |
missense |
probably benign |
0.00 |
R7237:Tbc1d12
|
UTSW |
19 |
38,887,346 (GRCm39) |
missense |
probably benign |
0.10 |
R7978:Tbc1d12
|
UTSW |
19 |
38,905,285 (GRCm39) |
missense |
probably benign |
0.01 |
R8283:Tbc1d12
|
UTSW |
19 |
38,825,353 (GRCm39) |
missense |
probably benign |
0.43 |
R8304:Tbc1d12
|
UTSW |
19 |
38,825,824 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8376:Tbc1d12
|
UTSW |
19 |
38,889,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8931:Tbc1d12
|
UTSW |
19 |
38,854,098 (GRCm39) |
missense |
probably benign |
|
R8944:Tbc1d12
|
UTSW |
19 |
38,899,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R9206:Tbc1d12
|
UTSW |
19 |
38,825,442 (GRCm39) |
missense |
probably benign |
0.08 |
R9252:Tbc1d12
|
UTSW |
19 |
38,899,477 (GRCm39) |
missense |
probably benign |
0.42 |
R9258:Tbc1d12
|
UTSW |
19 |
38,889,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9430:Tbc1d12
|
UTSW |
19 |
38,884,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R9434:Tbc1d12
|
UTSW |
19 |
38,902,461 (GRCm39) |
missense |
probably benign |
0.05 |
RF010:Tbc1d12
|
UTSW |
19 |
38,825,384 (GRCm39) |
small deletion |
probably benign |
|
RF011:Tbc1d12
|
UTSW |
19 |
38,825,401 (GRCm39) |
small deletion |
probably benign |
|
RF039:Tbc1d12
|
UTSW |
19 |
38,825,401 (GRCm39) |
small deletion |
probably benign |
|
|