Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
A |
5: 64,055,948 (GRCm39) |
L228* |
probably null |
Het |
Acsf2 |
T |
C |
11: 94,460,802 (GRCm39) |
D368G |
probably benign |
Het |
Adat2 |
T |
A |
10: 13,438,452 (GRCm39) |
N177K |
probably damaging |
Het |
Adgrf5 |
G |
T |
17: 43,760,795 (GRCm39) |
R830M |
probably damaging |
Het |
Apoh |
G |
A |
11: 108,286,792 (GRCm39) |
W72* |
probably null |
Het |
Bcl2l12 |
G |
T |
7: 44,642,301 (GRCm39) |
P195Q |
probably damaging |
Het |
Cacna1b |
T |
C |
2: 24,596,282 (GRCm39) |
M470V |
probably benign |
Het |
Ccdc188 |
A |
T |
16: 18,036,268 (GRCm39) |
R79* |
probably null |
Het |
Cd34 |
T |
A |
1: 194,641,501 (GRCm39) |
M309K |
probably damaging |
Het |
Clec4a2 |
A |
T |
6: 123,101,942 (GRCm39) |
K32N |
possibly damaging |
Het |
Csmd3 |
G |
T |
15: 47,845,299 (GRCm39) |
P88H |
|
Het |
Def6 |
A |
G |
17: 28,438,755 (GRCm39) |
S154G |
probably benign |
Het |
Dot1l |
T |
C |
10: 80,620,613 (GRCm39) |
L530P |
probably damaging |
Het |
Fam13a |
A |
G |
6: 58,951,014 (GRCm39) |
|
probably null |
Het |
Fat3 |
G |
A |
9: 16,286,871 (GRCm39) |
A884V |
possibly damaging |
Het |
Frem3 |
C |
A |
8: 81,339,134 (GRCm39) |
H476N |
probably benign |
Het |
Gm3404 |
T |
C |
5: 146,463,031 (GRCm39) |
V71A |
probably benign |
Het |
Hnf4g |
T |
G |
3: 3,703,273 (GRCm39) |
S53R |
probably benign |
Het |
Ighv13-2 |
T |
C |
12: 114,321,796 (GRCm39) |
N15D |
probably benign |
Het |
Jak1 |
T |
C |
4: 101,034,926 (GRCm39) |
K339E |
possibly damaging |
Het |
Klhl35 |
C |
G |
7: 99,117,702 (GRCm39) |
P82R |
probably benign |
Het |
Klhl40 |
T |
A |
9: 121,607,743 (GRCm39) |
V301E |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,901,089 (GRCm39) |
N930I |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,603,217 (GRCm39) |
|
probably null |
Het |
Mapk7 |
T |
C |
11: 61,382,498 (GRCm39) |
D68G |
probably damaging |
Het |
Myo3b |
A |
G |
2: 70,086,908 (GRCm39) |
H852R |
probably damaging |
Het |
Or51a6 |
A |
T |
7: 102,604,633 (GRCm39) |
H58Q |
probably benign |
Het |
Pkd2 |
A |
G |
5: 104,637,256 (GRCm39) |
D623G |
probably damaging |
Het |
Rfxank |
T |
C |
8: 70,588,198 (GRCm39) |
T118A |
probably benign |
Het |
Rxrb |
T |
A |
17: 34,252,020 (GRCm39) |
|
probably null |
Het |
Sec14l3 |
G |
A |
11: 4,025,486 (GRCm39) |
V337M |
probably damaging |
Het |
Sema3e |
A |
G |
5: 14,212,217 (GRCm39) |
T98A |
probably benign |
Het |
Ska1 |
A |
T |
18: 74,333,010 (GRCm39) |
M136K |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 83,000,297 (GRCm39) |
D240G |
probably benign |
Het |
Snph |
T |
C |
2: 151,436,331 (GRCm39) |
Y199C |
probably damaging |
Het |
Sorl1 |
A |
T |
9: 41,943,077 (GRCm39) |
I933N |
possibly damaging |
Het |
Spag16 |
C |
A |
1: 69,883,495 (GRCm39) |
H75N |
probably benign |
Het |
Spice1 |
C |
T |
16: 44,199,671 (GRCm39) |
R708C |
probably benign |
Het |
Tet3 |
C |
A |
6: 83,381,136 (GRCm39) |
S344I |
possibly damaging |
Het |
Trav5-4 |
A |
G |
14: 53,941,816 (GRCm39) |
E63G |
possibly damaging |
Het |
Trp73 |
G |
A |
4: 154,148,403 (GRCm39) |
P337L |
probably benign |
Het |
Ttn |
A |
G |
2: 76,778,359 (GRCm39) |
F1343L |
unknown |
Het |
Vipas39 |
T |
C |
12: 87,292,985 (GRCm39) |
H320R |
probably benign |
Het |
Vmn2r4 |
T |
C |
3: 64,317,271 (GRCm39) |
I156V |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,345,189 (GRCm39) |
D26G |
probably damaging |
Het |
Zscan4d |
A |
T |
7: 10,898,945 (GRCm39) |
F111I |
probably damaging |
Het |
|
Other mutations in Pramel14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Pramel14
|
APN |
4 |
143,719,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01981:Pramel14
|
APN |
4 |
143,720,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02322:Pramel14
|
APN |
4 |
143,718,591 (GRCm39) |
splice site |
probably benign |
|
IGL02514:Pramel14
|
APN |
4 |
143,719,772 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02806:Pramel14
|
APN |
4 |
143,719,501 (GRCm39) |
splice site |
probably null |
|
IGL02888:Pramel14
|
APN |
4 |
143,720,669 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03032:Pramel14
|
APN |
4 |
143,719,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Pramel14
|
UTSW |
4 |
143,720,088 (GRCm39) |
splice site |
probably benign |
|
R0363:Pramel14
|
UTSW |
4 |
143,718,221 (GRCm39) |
missense |
probably benign |
0.01 |
R0617:Pramel14
|
UTSW |
4 |
143,720,088 (GRCm39) |
splice site |
probably benign |
|
R1456:Pramel14
|
UTSW |
4 |
143,719,851 (GRCm39) |
missense |
probably benign |
|
R1475:Pramel14
|
UTSW |
4 |
143,720,882 (GRCm39) |
missense |
probably benign |
0.00 |
R1724:Pramel14
|
UTSW |
4 |
143,720,002 (GRCm39) |
missense |
probably benign |
0.00 |
R2158:Pramel14
|
UTSW |
4 |
143,720,885 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2210:Pramel14
|
UTSW |
4 |
143,720,789 (GRCm39) |
missense |
probably benign |
|
R3834:Pramel14
|
UTSW |
4 |
143,720,796 (GRCm39) |
missense |
probably benign |
0.01 |
R4438:Pramel14
|
UTSW |
4 |
143,718,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5152:Pramel14
|
UTSW |
4 |
143,720,830 (GRCm39) |
missense |
probably damaging |
0.97 |
R5832:Pramel14
|
UTSW |
4 |
143,718,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R6809:Pramel14
|
UTSW |
4 |
143,719,651 (GRCm39) |
missense |
probably benign |
0.01 |
R6986:Pramel14
|
UTSW |
4 |
143,719,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R7072:Pramel14
|
UTSW |
4 |
143,720,698 (GRCm39) |
missense |
probably damaging |
0.97 |
R7144:Pramel14
|
UTSW |
4 |
143,718,103 (GRCm39) |
missense |
probably benign |
0.43 |
R7268:Pramel14
|
UTSW |
4 |
143,720,090 (GRCm39) |
splice site |
probably null |
|
R7737:Pramel14
|
UTSW |
4 |
143,718,526 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8048:Pramel14
|
UTSW |
4 |
143,718,177 (GRCm39) |
missense |
probably benign |
0.04 |
R8074:Pramel14
|
UTSW |
4 |
143,718,424 (GRCm39) |
missense |
probably benign |
0.00 |
R8342:Pramel14
|
UTSW |
4 |
143,720,809 (GRCm39) |
missense |
probably benign |
|
R8855:Pramel14
|
UTSW |
4 |
143,720,905 (GRCm39) |
missense |
probably damaging |
0.97 |
R9105:Pramel14
|
UTSW |
4 |
143,718,595 (GRCm39) |
splice site |
probably benign |
|
R9490:Pramel14
|
UTSW |
4 |
143,719,606 (GRCm39) |
missense |
probably benign |
0.01 |
R9633:Pramel14
|
UTSW |
4 |
143,720,818 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9685:Pramel14
|
UTSW |
4 |
143,719,520 (GRCm39) |
missense |
probably benign |
0.03 |
|