Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
A |
6: 91,919,517 (GRCm39) |
D725E |
probably damaging |
Het |
Bco1 |
T |
A |
8: 117,840,273 (GRCm39) |
Y264N |
probably damaging |
Het |
Cd109 |
G |
A |
9: 78,572,828 (GRCm39) |
|
probably null |
Het |
Cdc45 |
T |
C |
16: 18,613,454 (GRCm39) |
|
probably null |
Het |
Ckap5 |
A |
G |
2: 91,398,564 (GRCm39) |
E578G |
probably benign |
Het |
Cracr2b |
T |
A |
7: 141,044,749 (GRCm39) |
L193Q |
probably damaging |
Het |
Dmxl2 |
G |
A |
9: 54,301,011 (GRCm39) |
L2367F |
probably damaging |
Het |
Dop1b |
T |
G |
16: 93,563,110 (GRCm39) |
D871E |
probably damaging |
Het |
Emc1 |
T |
C |
4: 139,093,842 (GRCm39) |
Y651H |
probably benign |
Het |
Enox1 |
T |
C |
14: 77,745,627 (GRCm39) |
S41P |
possibly damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,839,384 (GRCm39) |
Y399C |
probably damaging |
Het |
Foxa1 |
A |
G |
12: 57,589,686 (GRCm39) |
L178P |
probably damaging |
Het |
Gm57859 |
C |
A |
11: 113,579,801 (GRCm39) |
H399N |
possibly damaging |
Het |
Grm7 |
T |
A |
6: 111,223,258 (GRCm39) |
Y433N |
probably benign |
Het |
Gsta5 |
T |
A |
9: 78,211,737 (GRCm39) |
Y166* |
probably null |
Het |
Gtf3c2 |
G |
A |
5: 31,315,555 (GRCm39) |
R813C |
probably damaging |
Het |
H4c9 |
T |
A |
13: 22,225,247 (GRCm39) |
T83S |
probably benign |
Het |
Hacd3 |
T |
C |
9: 64,912,909 (GRCm39) |
E117G |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,522,535 (GRCm39) |
T3455M |
probably benign |
Het |
Itga6 |
A |
G |
2: 71,664,053 (GRCm39) |
I61V |
possibly damaging |
Het |
Jaml |
T |
C |
9: 45,000,071 (GRCm39) |
L81P |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,499,874 (GRCm39) |
F782S |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,339,275 (GRCm39) |
H742R |
probably benign |
Het |
Macrod2 |
G |
T |
2: 140,242,895 (GRCm39) |
M1I |
probably null |
Het |
Mcf2l |
G |
A |
8: 13,063,849 (GRCm39) |
W1020* |
probably null |
Het |
Msgn1 |
A |
G |
12: 11,258,924 (GRCm39) |
L9P |
probably damaging |
Het |
Ngdn |
C |
A |
14: 55,259,556 (GRCm39) |
S202R |
probably benign |
Het |
Notch1 |
C |
T |
2: 26,375,454 (GRCm39) |
G50R |
possibly damaging |
Het |
Or14c46 |
A |
T |
7: 85,918,009 (GRCm39) |
D329E |
probably benign |
Het |
Or1a1b |
A |
T |
11: 74,097,466 (GRCm39) |
I192N |
probably damaging |
Het |
Or2d2b |
A |
T |
7: 106,705,714 (GRCm39) |
M118K |
probably damaging |
Het |
Or5d14 |
A |
T |
2: 87,880,646 (GRCm39) |
C107* |
probably null |
Het |
Osbpl10 |
A |
G |
9: 114,938,555 (GRCm39) |
S211G |
probably benign |
Het |
Pcdhb13 |
A |
T |
18: 37,576,474 (GRCm39) |
D284V |
possibly damaging |
Het |
Pde6c |
T |
C |
19: 38,128,677 (GRCm39) |
S214P |
possibly damaging |
Het |
Pofut1 |
C |
T |
2: 153,101,536 (GRCm39) |
H192Y |
probably damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,960 (GRCm39) |
D391G |
possibly damaging |
Het |
Prc1 |
G |
A |
7: 79,954,544 (GRCm39) |
S165N |
probably benign |
Het |
Prex1 |
A |
G |
2: 166,414,883 (GRCm39) |
V304A |
probably benign |
Het |
Ptpru |
T |
C |
4: 131,513,065 (GRCm39) |
I881V |
probably benign |
Het |
Radil |
A |
G |
5: 142,472,870 (GRCm39) |
S847P |
probably benign |
Het |
Rimklb |
A |
G |
6: 122,433,371 (GRCm39) |
S317P |
probably damaging |
Het |
Sdhc |
A |
T |
1: 170,966,271 (GRCm39) |
L78* |
probably null |
Het |
Skint6 |
T |
A |
4: 112,696,510 (GRCm39) |
I1042F |
possibly damaging |
Het |
Slc1a6 |
T |
A |
10: 78,637,741 (GRCm39) |
D422E |
probably damaging |
Het |
Slc29a1 |
A |
T |
17: 45,900,854 (GRCm39) |
H71Q |
probably damaging |
Het |
Slfn14 |
A |
T |
11: 83,167,429 (GRCm39) |
D695E |
probably damaging |
Het |
Spg11 |
A |
T |
2: 121,917,286 (GRCm39) |
|
probably null |
Het |
Srgap2 |
A |
G |
1: 131,217,354 (GRCm39) |
V986A |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,884,476 (GRCm39) |
C172* |
probably null |
Het |
Tigd4 |
A |
G |
3: 84,502,574 (GRCm39) |
H497R |
probably benign |
Het |
Ubn2 |
G |
A |
6: 38,438,471 (GRCm39) |
G60D |
probably damaging |
Het |
Uckl1 |
C |
T |
2: 181,214,866 (GRCm39) |
|
probably null |
Het |
Vmn2r24 |
A |
T |
6: 123,793,236 (GRCm39) |
K854N |
probably benign |
Het |
Vps13d |
G |
A |
4: 144,701,763 (GRCm39) |
Q3193* |
probably null |
Het |
Wdr26 |
G |
A |
1: 181,019,433 (GRCm39) |
L315F |
probably damaging |
Het |
Zc3h8 |
C |
A |
2: 128,785,775 (GRCm39) |
E24* |
probably null |
Het |
Zfp39 |
A |
G |
11: 58,782,213 (GRCm39) |
V183A |
probably benign |
Het |
Zfp608 |
C |
A |
18: 55,121,616 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pabpc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00591:Pabpc6
|
APN |
17 |
9,887,427 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL00984:Pabpc6
|
APN |
17 |
9,887,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01123:Pabpc6
|
APN |
17 |
9,887,076 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01301:Pabpc6
|
APN |
17 |
9,886,899 (GRCm39) |
missense |
probably benign |
|
IGL02347:Pabpc6
|
APN |
17 |
9,887,993 (GRCm39) |
missense |
probably benign |
0.03 |
ANU18:Pabpc6
|
UTSW |
17 |
9,886,899 (GRCm39) |
missense |
probably benign |
|
R0022:Pabpc6
|
UTSW |
17 |
9,888,145 (GRCm39) |
missense |
probably benign |
0.19 |
R0022:Pabpc6
|
UTSW |
17 |
9,888,145 (GRCm39) |
missense |
probably benign |
0.19 |
R1593:Pabpc6
|
UTSW |
17 |
9,886,742 (GRCm39) |
missense |
probably damaging |
0.98 |
R1695:Pabpc6
|
UTSW |
17 |
9,887,003 (GRCm39) |
missense |
probably benign |
0.01 |
R3897:Pabpc6
|
UTSW |
17 |
9,888,056 (GRCm39) |
missense |
probably benign |
0.38 |
R3903:Pabpc6
|
UTSW |
17 |
9,888,083 (GRCm39) |
missense |
probably benign |
0.16 |
R4585:Pabpc6
|
UTSW |
17 |
9,888,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Pabpc6
|
UTSW |
17 |
9,887,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Pabpc6
|
UTSW |
17 |
9,888,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Pabpc6
|
UTSW |
17 |
9,886,772 (GRCm39) |
nonsense |
probably null |
|
R6488:Pabpc6
|
UTSW |
17 |
9,888,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Pabpc6
|
UTSW |
17 |
9,887,357 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7586:Pabpc6
|
UTSW |
17 |
9,887,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Pabpc6
|
UTSW |
17 |
9,888,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Pabpc6
|
UTSW |
17 |
9,887,427 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8211:Pabpc6
|
UTSW |
17 |
9,888,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R8393:Pabpc6
|
UTSW |
17 |
9,887,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Pabpc6
|
UTSW |
17 |
9,888,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R9036:Pabpc6
|
UTSW |
17 |
9,888,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Pabpc6
|
UTSW |
17 |
9,886,937 (GRCm39) |
missense |
probably benign |
|
R9148:Pabpc6
|
UTSW |
17 |
9,886,937 (GRCm39) |
missense |
probably benign |
|
R9255:Pabpc6
|
UTSW |
17 |
9,886,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Pabpc6
|
UTSW |
17 |
9,888,114 (GRCm39) |
missense |
probably damaging |
1.00 |
RF038:Pabpc6
|
UTSW |
17 |
9,887,044 (GRCm39) |
small deletion |
probably benign |
|
|