Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
G |
T |
3: 137,772,149 (GRCm39) |
G446V |
possibly damaging |
Het |
Aadac |
T |
G |
3: 59,946,984 (GRCm39) |
N227K |
probably benign |
Het |
Acap1 |
C |
T |
11: 69,780,133 (GRCm39) |
G74R |
probably benign |
Het |
Adrm1 |
A |
G |
2: 179,813,981 (GRCm39) |
|
probably benign |
Het |
Appl1 |
G |
C |
14: 26,645,737 (GRCm39) |
S691* |
probably null |
Het |
Atp2a2 |
T |
C |
5: 122,595,245 (GRCm39) |
D1035G |
probably benign |
Het |
AW551984 |
A |
G |
9: 39,504,169 (GRCm39) |
I599T |
probably benign |
Het |
Col23a1 |
C |
A |
11: 51,458,776 (GRCm39) |
D304E |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,338,674 (GRCm39) |
R478G |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,464,412 (GRCm39) |
N3660D |
probably benign |
Het |
Drosha |
T |
A |
15: 12,929,797 (GRCm39) |
Y1331N |
possibly damaging |
Het |
E2f6 |
T |
G |
12: 16,874,685 (GRCm39) |
S256A |
probably benign |
Het |
Evc |
A |
G |
5: 37,483,927 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,817,403 (GRCm39) |
I4379F |
probably benign |
Het |
Galnt2 |
T |
C |
8: 125,050,412 (GRCm39) |
C91R |
probably damaging |
Het |
Gm3095 |
G |
T |
14: 15,170,371 (GRCm39) |
M73I |
probably benign |
Het |
Gpr179 |
T |
A |
11: 97,234,641 (GRCm39) |
Q480L |
probably damaging |
Het |
Gucy2g |
T |
A |
19: 55,226,359 (GRCm39) |
I186F |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,631,042 (GRCm39) |
I919F |
probably benign |
Het |
Kdm3a |
A |
C |
6: 71,588,920 (GRCm39) |
V363G |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,749,990 (GRCm39) |
|
probably benign |
Het |
Lama5 |
C |
T |
2: 179,831,142 (GRCm39) |
R1839H |
probably damaging |
Het |
Lpo |
T |
C |
11: 87,707,389 (GRCm39) |
D208G |
probably damaging |
Het |
Lpp |
A |
G |
16: 24,663,956 (GRCm39) |
D411G |
possibly damaging |
Het |
Marco |
T |
C |
1: 120,432,464 (GRCm39) |
S8G |
possibly damaging |
Het |
Mthfr |
T |
C |
4: 148,128,940 (GRCm39) |
F171S |
probably damaging |
Het |
Nlrx1 |
A |
T |
9: 44,175,183 (GRCm39) |
S198T |
probably damaging |
Het |
Nol10 |
C |
A |
12: 17,466,138 (GRCm39) |
S511* |
probably null |
Het |
Nup153 |
T |
C |
13: 46,836,485 (GRCm39) |
T1375A |
probably benign |
Het |
Obscn |
A |
G |
11: 58,998,697 (GRCm39) |
S1367P |
probably damaging |
Het |
Or4x6 |
A |
G |
2: 89,949,183 (GRCm39) |
V253A |
probably benign |
Het |
Pcdha7 |
G |
A |
18: 37,108,303 (GRCm39) |
V443M |
probably damaging |
Het |
Plekha1 |
G |
T |
7: 130,511,331 (GRCm39) |
R305I |
probably damaging |
Het |
Psmb2 |
T |
A |
4: 126,578,002 (GRCm39) |
I60N |
probably damaging |
Het |
Rad17 |
C |
A |
13: 100,767,612 (GRCm39) |
G330C |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,200,446 (GRCm39) |
S80P |
probably damaging |
Het |
Srgap2 |
T |
A |
1: 131,228,128 (GRCm39) |
|
probably null |
Het |
Taf8 |
C |
A |
17: 47,805,407 (GRCm39) |
R164L |
possibly damaging |
Het |
Tmem87a |
C |
A |
2: 120,227,911 (GRCm39) |
D79Y |
probably damaging |
Het |
Tmtc4 |
G |
A |
14: 123,170,291 (GRCm39) |
R574W |
probably benign |
Het |
Tprn |
G |
A |
2: 25,153,369 (GRCm39) |
A224T |
probably benign |
Het |
Usf3 |
A |
G |
16: 44,037,733 (GRCm39) |
T738A |
probably benign |
Het |
Vmn2r54 |
A |
C |
7: 12,366,343 (GRCm39) |
V197G |
probably benign |
Het |
Zbtb40 |
G |
T |
4: 136,714,642 (GRCm39) |
P1049Q |
probably damaging |
Het |
Zfp551 |
A |
T |
7: 12,149,488 (GRCm39) |
S640R |
possibly damaging |
Het |
Zfp932 |
T |
A |
5: 110,157,713 (GRCm39) |
C470* |
probably null |
Het |
Zmat4 |
T |
C |
8: 24,238,508 (GRCm39) |
V30A |
probably damaging |
Het |
|
Other mutations in Zkscan8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01726:Zkscan8
|
APN |
13 |
21,704,973 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01987:Zkscan8
|
APN |
13 |
21,710,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0129:Zkscan8
|
UTSW |
13 |
21,706,441 (GRCm39) |
missense |
probably benign |
0.35 |
R0371:Zkscan8
|
UTSW |
13 |
21,710,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Zkscan8
|
UTSW |
13 |
21,710,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Zkscan8
|
UTSW |
13 |
21,710,765 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1688:Zkscan8
|
UTSW |
13 |
21,704,324 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1908:Zkscan8
|
UTSW |
13 |
21,709,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R1912:Zkscan8
|
UTSW |
13 |
21,704,927 (GRCm39) |
nonsense |
probably null |
|
R2117:Zkscan8
|
UTSW |
13 |
21,704,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R2155:Zkscan8
|
UTSW |
13 |
21,704,759 (GRCm39) |
nonsense |
probably null |
|
R2214:Zkscan8
|
UTSW |
13 |
21,705,082 (GRCm39) |
missense |
probably benign |
0.43 |
R2274:Zkscan8
|
UTSW |
13 |
21,705,966 (GRCm39) |
missense |
probably benign |
0.02 |
R3624:Zkscan8
|
UTSW |
13 |
21,704,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R5528:Zkscan8
|
UTSW |
13 |
21,704,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6492:Zkscan8
|
UTSW |
13 |
21,709,397 (GRCm39) |
missense |
probably benign |
0.25 |
R6533:Zkscan8
|
UTSW |
13 |
21,704,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Zkscan8
|
UTSW |
13 |
21,709,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Zkscan8
|
UTSW |
13 |
21,704,598 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7877:Zkscan8
|
UTSW |
13 |
21,704,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9342:Zkscan8
|
UTSW |
13 |
21,710,702 (GRCm39) |
missense |
probably benign |
0.05 |
R9609:Zkscan8
|
UTSW |
13 |
21,709,434 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9623:Zkscan8
|
UTSW |
13 |
21,704,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|