Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
T |
A |
6: 92,804,997 (GRCm39) |
|
probably benign |
Het |
Ace2 |
T |
A |
X: 162,946,996 (GRCm39) |
V293D |
probably damaging |
Het |
Adgrg6 |
T |
C |
10: 14,317,185 (GRCm39) |
Y545C |
probably damaging |
Het |
Arhgap40 |
A |
G |
2: 158,376,742 (GRCm39) |
T293A |
probably damaging |
Het |
Arhgef19 |
A |
G |
4: 140,973,707 (GRCm39) |
T65A |
probably damaging |
Het |
Brf1 |
A |
G |
12: 112,956,682 (GRCm39) |
|
probably null |
Het |
Cbfb |
T |
C |
8: 105,905,252 (GRCm39) |
S65P |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,576 (GRCm39) |
S604P |
possibly damaging |
Het |
Ckmt1 |
T |
C |
2: 121,191,643 (GRCm39) |
V271A |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Csmd2 |
T |
C |
4: 128,371,263 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,038,559 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
A |
G |
18: 20,410,007 (GRCm39) |
T492A |
probably benign |
Het |
Fam3a |
G |
A |
X: 73,430,241 (GRCm39) |
T156I |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,229,087 (GRCm39) |
C708S |
probably damaging |
Het |
Fgf5 |
G |
A |
5: 98,409,831 (GRCm39) |
G127R |
probably damaging |
Het |
Fhip1a |
T |
G |
3: 85,637,939 (GRCm39) |
K120T |
probably damaging |
Het |
Fn3k |
A |
T |
11: 121,325,909 (GRCm39) |
Y32F |
probably benign |
Het |
Frem3 |
T |
C |
8: 81,338,118 (GRCm39) |
I137T |
probably benign |
Het |
Hc |
T |
C |
2: 34,903,531 (GRCm39) |
D1041G |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,655,708 (GRCm39) |
|
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,309,553 (GRCm39) |
A598T |
probably benign |
Het |
Ifngr1 |
T |
C |
10: 19,483,007 (GRCm39) |
S254P |
probably benign |
Het |
Kel |
T |
C |
6: 41,674,408 (GRCm39) |
S341G |
probably benign |
Het |
Klra6 |
A |
C |
6: 129,990,439 (GRCm39) |
M224R |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,183,522 (GRCm39) |
|
probably null |
Het |
Mpeg1 |
C |
T |
19: 12,440,660 (GRCm39) |
T706I |
probably benign |
Het |
Mrpl41 |
T |
C |
2: 24,864,429 (GRCm39) |
D81G |
possibly damaging |
Het |
Or5al7 |
G |
T |
2: 85,993,181 (GRCm39) |
F37L |
probably benign |
Het |
Palld |
T |
C |
8: 61,978,148 (GRCm39) |
R881G |
probably damaging |
Het |
Pdha2 |
A |
T |
3: 140,916,662 (GRCm39) |
V282E |
probably damaging |
Het |
Pga5 |
C |
T |
19: 10,654,065 (GRCm39) |
R46Q |
probably benign |
Het |
Plekhg2 |
T |
C |
7: 28,068,122 (GRCm39) |
Y189C |
probably damaging |
Het |
Rnf43 |
A |
G |
11: 87,622,479 (GRCm39) |
T527A |
probably benign |
Het |
Rplp0 |
G |
A |
5: 115,699,174 (GRCm39) |
R73Q |
probably benign |
Het |
Smco3 |
A |
G |
6: 136,808,197 (GRCm39) |
*226R |
probably null |
Het |
Sugp2 |
T |
C |
8: 70,712,324 (GRCm39) |
|
probably benign |
Het |
Tsga10 |
T |
C |
1: 37,846,098 (GRCm39) |
I343V |
probably benign |
Het |
Ube2q2 |
A |
G |
9: 55,075,502 (GRCm39) |
K104E |
probably damaging |
Het |
Ube3a |
C |
T |
7: 58,925,506 (GRCm39) |
|
probably benign |
Het |
Usp11 |
T |
C |
X: 20,585,381 (GRCm39) |
I785T |
probably damaging |
Het |
Vmn2r22 |
A |
T |
6: 123,626,026 (GRCm39) |
C137S |
probably damaging |
Het |
Zfp946 |
T |
C |
17: 22,672,469 (GRCm39) |
S23P |
probably damaging |
Het |
Zfyve1 |
A |
G |
12: 83,594,694 (GRCm39) |
V766A |
probably damaging |
Het |
|
Other mutations in Zfp281 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Zfp281
|
APN |
1 |
136,555,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01408:Zfp281
|
APN |
1 |
136,553,853 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03233:Zfp281
|
APN |
1 |
136,554,567 (GRCm39) |
missense |
possibly damaging |
0.82 |
PIT4486001:Zfp281
|
UTSW |
1 |
136,554,741 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1514:Zfp281
|
UTSW |
1 |
136,554,435 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R1785:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R2049:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R2142:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R4086:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4087:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Zfp281
|
UTSW |
1 |
136,553,448 (GRCm39) |
missense |
probably benign |
|
R5380:Zfp281
|
UTSW |
1 |
136,553,676 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6033:Zfp281
|
UTSW |
1 |
136,554,464 (GRCm39) |
missense |
probably benign |
0.14 |
R6033:Zfp281
|
UTSW |
1 |
136,554,464 (GRCm39) |
missense |
probably benign |
0.14 |
R6056:Zfp281
|
UTSW |
1 |
136,553,178 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6213:Zfp281
|
UTSW |
1 |
136,553,250 (GRCm39) |
missense |
probably benign |
0.01 |
R7402:Zfp281
|
UTSW |
1 |
136,553,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R7503:Zfp281
|
UTSW |
1 |
136,554,678 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7969:Zfp281
|
UTSW |
1 |
136,553,772 (GRCm39) |
missense |
probably benign |
0.06 |
R8343:Zfp281
|
UTSW |
1 |
136,555,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Zfp281
|
UTSW |
1 |
136,553,334 (GRCm39) |
missense |
probably benign |
0.00 |
R9199:Zfp281
|
UTSW |
1 |
136,553,643 (GRCm39) |
missense |
probably benign |
|
R9461:Zfp281
|
UTSW |
1 |
136,554,500 (GRCm39) |
missense |
probably benign |
0.28 |
R9487:Zfp281
|
UTSW |
1 |
136,555,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R9532:Zfp281
|
UTSW |
1 |
136,554,894 (GRCm39) |
missense |
probably benign |
|
R9541:Zfp281
|
UTSW |
1 |
136,555,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|