Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7a |
C |
A |
4: 56,744,116 (GRCm39) |
Y214* |
probably null |
Het |
Adnp2 |
A |
G |
18: 80,172,960 (GRCm39) |
V483A |
probably benign |
Het |
Aif1 |
C |
T |
17: 35,390,472 (GRCm39) |
V93M |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,439,705 (GRCm39) |
S563P |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,752,581 (GRCm39) |
N378K |
probably damaging |
Het |
Ano4 |
C |
T |
10: 88,828,732 (GRCm39) |
|
probably null |
Het |
Asxl3 |
G |
A |
18: 22,658,497 (GRCm39) |
C2169Y |
probably damaging |
Het |
Atp2b1 |
T |
C |
10: 98,852,821 (GRCm39) |
C101R |
probably damaging |
Het |
Bcs1l |
C |
T |
1: 74,629,844 (GRCm39) |
R224C |
probably damaging |
Het |
Car2 |
T |
C |
3: 14,951,710 (GRCm39) |
|
probably benign |
Het |
Cbln1 |
T |
C |
8: 88,198,657 (GRCm39) |
N71S |
probably benign |
Het |
Cdh8 |
T |
A |
8: 99,950,579 (GRCm39) |
T224S |
probably benign |
Het |
Cdin1 |
A |
G |
2: 115,462,462 (GRCm39) |
I65V |
probably benign |
Het |
Cep131 |
G |
A |
11: 119,956,218 (GRCm39) |
R1014W |
probably damaging |
Het |
Cfap61 |
T |
C |
2: 145,887,363 (GRCm39) |
S603P |
possibly damaging |
Het |
Chd8 |
G |
T |
14: 52,464,125 (GRCm39) |
L659I |
probably benign |
Het |
Ckap5 |
G |
A |
2: 91,387,920 (GRCm39) |
G255D |
probably benign |
Het |
Clec18a |
C |
A |
8: 111,807,572 (GRCm39) |
W126L |
probably benign |
Het |
Cux1 |
T |
A |
5: 136,596,085 (GRCm39) |
N4Y |
probably damaging |
Het |
Dgcr8 |
A |
T |
16: 18,101,693 (GRCm39) |
Y196* |
probably null |
Het |
Dnah14 |
A |
T |
1: 181,468,970 (GRCm39) |
I1267F |
probably benign |
Het |
Dock7 |
T |
C |
4: 98,949,529 (GRCm39) |
N438D |
probably benign |
Het |
Dock8 |
A |
T |
19: 25,160,386 (GRCm39) |
H1763L |
possibly damaging |
Het |
Elp1 |
T |
C |
4: 56,771,555 (GRCm39) |
D914G |
possibly damaging |
Het |
Fpr-rs6 |
A |
T |
17: 20,403,100 (GRCm39) |
M87K |
possibly damaging |
Het |
Gabrg1 |
A |
G |
5: 70,911,610 (GRCm39) |
S339P |
probably benign |
Het |
Gm10801 |
AAGT |
AAGTAGT |
2: 98,494,148 (GRCm39) |
|
probably null |
Het |
Gm12695 |
A |
G |
4: 96,651,058 (GRCm39) |
S132P |
probably damaging |
Het |
Gm3443 |
T |
A |
19: 21,533,128 (GRCm39) |
C31S |
probably damaging |
Het |
Gzmf |
A |
T |
14: 56,444,452 (GRCm39) |
F40L |
probably benign |
Het |
Herc1 |
TCCC |
TCC |
9: 66,408,470 (GRCm39) |
|
probably null |
Het |
Lrguk |
A |
G |
6: 34,072,522 (GRCm39) |
E604G |
probably benign |
Het |
Marveld3 |
C |
A |
8: 110,674,732 (GRCm39) |
K361N |
probably benign |
Het |
Mgat4b |
A |
T |
11: 50,121,525 (GRCm39) |
Y47F |
probably damaging |
Het |
Mmel1 |
G |
T |
4: 154,976,885 (GRCm39) |
E520* |
probably null |
Het |
Msantd5f6 |
A |
T |
4: 73,321,843 (GRCm39) |
M64K |
possibly damaging |
Het |
Muc21 |
T |
C |
17: 35,934,057 (GRCm39) |
|
probably benign |
Het |
Myod1 |
A |
G |
7: 46,027,741 (GRCm39) |
T294A |
probably benign |
Het |
Nfix |
A |
T |
8: 85,454,276 (GRCm39) |
S219T |
probably damaging |
Het |
Nr4a2 |
A |
G |
2: 57,001,920 (GRCm39) |
F115L |
probably benign |
Het |
Numa1 |
A |
C |
7: 101,641,845 (GRCm39) |
M98L |
probably benign |
Het |
Or5b105 |
T |
C |
19: 13,080,567 (GRCm39) |
I28V |
probably benign |
Het |
P3h1 |
C |
T |
4: 119,095,151 (GRCm39) |
L303F |
possibly damaging |
Het |
Pias4 |
G |
A |
10: 80,993,080 (GRCm39) |
T5I |
probably damaging |
Het |
Pik3ip1 |
A |
G |
11: 3,282,124 (GRCm39) |
N68S |
probably benign |
Het |
Pkdrej |
T |
C |
15: 85,702,850 (GRCm39) |
T1029A |
probably benign |
Het |
Recql |
A |
T |
6: 142,310,278 (GRCm39) |
D517E |
probably benign |
Het |
Sall2 |
G |
T |
14: 52,552,078 (GRCm39) |
H372Q |
probably damaging |
Het |
Scn8a |
A |
C |
15: 100,930,096 (GRCm39) |
I1436L |
probably benign |
Het |
Slc4a5 |
T |
C |
6: 83,273,729 (GRCm39) |
|
probably null |
Het |
Stox2 |
A |
C |
8: 47,639,500 (GRCm39) |
F898C |
probably damaging |
Het |
Sumo2 |
A |
T |
11: 115,414,601 (GRCm39) |
|
probably null |
Het |
Sycp2 |
C |
T |
2: 178,025,345 (GRCm39) |
E366K |
possibly damaging |
Het |
Tanc1 |
A |
G |
2: 59,622,150 (GRCm39) |
K423R |
probably benign |
Het |
Tbx21 |
T |
A |
11: 97,005,872 (GRCm39) |
Q31L |
possibly damaging |
Het |
Tfap2a |
T |
A |
13: 40,882,230 (GRCm39) |
N25I |
probably damaging |
Het |
Tfdp1 |
C |
T |
8: 13,420,485 (GRCm39) |
R105W |
probably damaging |
Het |
Trav18 |
G |
A |
14: 54,069,122 (GRCm39) |
V55I |
probably benign |
Het |
Trgc1 |
A |
T |
13: 19,400,646 (GRCm39) |
D125V |
unknown |
Het |
Trim55 |
A |
G |
3: 19,726,938 (GRCm39) |
D335G |
probably benign |
Het |
Trim71 |
T |
A |
9: 114,341,772 (GRCm39) |
T837S |
probably benign |
Het |
Vmn2r17 |
A |
T |
5: 109,575,695 (GRCm39) |
T189S |
probably benign |
Het |
Xaf1 |
A |
G |
11: 72,197,461 (GRCm39) |
T146A |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,343,679 (GRCm39) |
V686A |
possibly damaging |
Het |
Zfp65 |
T |
C |
13: 67,856,130 (GRCm39) |
H383R |
probably damaging |
Het |
Zfp932 |
A |
G |
5: 110,157,606 (GRCm39) |
T435A |
probably damaging |
Het |
Zfp947 |
C |
T |
17: 22,364,750 (GRCm39) |
G308D |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,662,771 (GRCm39) |
V417E |
probably damaging |
Het |
|
Other mutations in Vmn1r56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02102:Vmn1r56
|
APN |
7 |
5,199,335 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02173:Vmn1r56
|
APN |
7 |
5,199,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02545:Vmn1r56
|
APN |
7 |
5,199,113 (GRCm39) |
missense |
probably benign |
0.06 |
R0142:Vmn1r56
|
UTSW |
7 |
5,199,372 (GRCm39) |
missense |
probably benign |
0.17 |
R0599:Vmn1r56
|
UTSW |
7 |
5,199,429 (GRCm39) |
missense |
probably benign |
|
R2110:Vmn1r56
|
UTSW |
7 |
5,199,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R3019:Vmn1r56
|
UTSW |
7 |
5,199,061 (GRCm39) |
missense |
probably benign |
|
R4883:Vmn1r56
|
UTSW |
7 |
5,199,443 (GRCm39) |
missense |
probably damaging |
0.98 |
R5655:Vmn1r56
|
UTSW |
7 |
5,198,700 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5728:Vmn1r56
|
UTSW |
7 |
5,199,122 (GRCm39) |
missense |
probably benign |
0.42 |
R6083:Vmn1r56
|
UTSW |
7 |
5,199,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:Vmn1r56
|
UTSW |
7 |
5,199,575 (GRCm39) |
missense |
probably benign |
0.02 |
R7031:Vmn1r56
|
UTSW |
7 |
5,199,261 (GRCm39) |
nonsense |
probably null |
|
R7584:Vmn1r56
|
UTSW |
7 |
5,198,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Vmn1r56
|
UTSW |
7 |
5,199,516 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8472:Vmn1r56
|
UTSW |
7 |
5,198,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Vmn1r56
|
UTSW |
7 |
5,198,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R8813:Vmn1r56
|
UTSW |
7 |
5,198,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Vmn1r56
|
UTSW |
7 |
5,199,389 (GRCm39) |
missense |
probably damaging |
0.99 |
|