Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot6 |
A |
T |
12: 84,153,215 (GRCm39) |
|
probably null |
Het |
Adamtsl3 |
A |
T |
7: 82,247,330 (GRCm39) |
N1429Y |
probably benign |
Het |
Adk |
T |
C |
14: 21,153,892 (GRCm39) |
S32P |
possibly damaging |
Het |
Akap13 |
A |
T |
7: 75,376,786 (GRCm39) |
M2005L |
probably benign |
Het |
Atp10a |
A |
T |
7: 58,478,058 (GRCm39) |
D1367V |
probably benign |
Het |
Bckdhb |
A |
G |
9: 83,870,915 (GRCm39) |
I142V |
probably benign |
Het |
Brap |
C |
T |
5: 121,817,358 (GRCm39) |
Q322* |
probably null |
Het |
Carmil3 |
A |
T |
14: 55,734,305 (GRCm39) |
N401I |
probably damaging |
Het |
Cdan1 |
A |
T |
2: 120,558,921 (GRCm39) |
S426T |
possibly damaging |
Het |
Cdc27 |
C |
A |
11: 104,408,317 (GRCm39) |
S531I |
probably benign |
Het |
Cela3a |
A |
T |
4: 137,131,185 (GRCm39) |
Y184* |
probably null |
Het |
Cep63 |
T |
C |
9: 102,490,576 (GRCm39) |
K178R |
probably benign |
Het |
Cfb |
G |
A |
17: 35,076,290 (GRCm39) |
Q152* |
probably null |
Het |
Cnpy2 |
G |
A |
10: 128,162,044 (GRCm39) |
V106I |
probably benign |
Het |
Cntn1 |
GCTGTCTTC |
GC |
15: 92,237,404 (GRCm39) |
|
probably null |
Het |
Ctc1 |
G |
A |
11: 68,917,045 (GRCm39) |
G67D |
probably damaging |
Het |
Cwc27 |
G |
T |
13: 104,940,772 (GRCm39) |
P196T |
probably benign |
Het |
Cwc27 |
C |
A |
13: 104,940,776 (GRCm39) |
L194F |
possibly damaging |
Het |
Cyp2d12 |
T |
G |
15: 82,439,378 (GRCm39) |
S11A |
possibly damaging |
Het |
Ddx55 |
T |
A |
5: 124,697,184 (GRCm39) |
|
probably null |
Het |
Dedd2 |
G |
T |
7: 24,918,331 (GRCm39) |
R75S |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,147,530 (GRCm39) |
S3904F |
possibly damaging |
Het |
Fibp |
G |
A |
19: 5,513,215 (GRCm39) |
V177I |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,810,284 (GRCm39) |
E2201V |
probably benign |
Het |
Gbp11 |
C |
T |
5: 105,472,928 (GRCm39) |
D499N |
probably benign |
Het |
Gfm1 |
A |
G |
3: 67,339,032 (GRCm39) |
E45G |
probably damaging |
Het |
H2-D1 |
A |
G |
17: 35,482,487 (GRCm39) |
Y69C |
probably damaging |
Het |
Hcar1 |
A |
G |
5: 124,017,109 (GRCm39) |
F194S |
probably damaging |
Het |
Heatr4 |
A |
T |
12: 84,024,707 (GRCm39) |
|
probably null |
Het |
Kcnd2 |
G |
A |
6: 21,216,695 (GRCm39) |
C133Y |
probably damaging |
Het |
Kcnq1 |
A |
T |
7: 142,979,711 (GRCm39) |
Q619L |
probably benign |
Het |
Kctd12 |
T |
A |
14: 103,218,901 (GRCm39) |
R326W |
probably damaging |
Het |
Kel |
A |
G |
6: 41,666,472 (GRCm39) |
|
probably null |
Het |
Lipk |
A |
T |
19: 34,024,197 (GRCm39) |
I332F |
probably benign |
Het |
Lrrc37 |
T |
A |
11: 103,506,947 (GRCm39) |
|
probably benign |
Het |
Masp2 |
A |
G |
4: 148,696,516 (GRCm39) |
D371G |
possibly damaging |
Het |
Met |
A |
G |
6: 17,571,809 (GRCm39) |
E1376G |
probably benign |
Het |
Mup5 |
A |
T |
4: 61,752,015 (GRCm39) |
I78K |
probably benign |
Het |
Mynn |
A |
T |
3: 30,670,790 (GRCm39) |
D526V |
probably damaging |
Het |
Naip6 |
G |
T |
13: 100,433,423 (GRCm39) |
T1138N |
possibly damaging |
Het |
Neurod1 |
G |
T |
2: 79,284,696 (GRCm39) |
P229Q |
probably damaging |
Het |
Npepps |
T |
G |
11: 97,139,085 (GRCm39) |
R162S |
probably damaging |
Het |
Ntrk3 |
T |
A |
7: 78,112,631 (GRCm39) |
Q175L |
probably damaging |
Het |
Obsl1 |
T |
C |
1: 75,480,032 (GRCm39) |
T310A |
probably damaging |
Het |
Or4g7 |
A |
T |
2: 111,309,425 (GRCm39) |
T99S |
probably benign |
Het |
Or8c9 |
A |
T |
9: 38,241,410 (GRCm39) |
I176F |
possibly damaging |
Het |
Or8j3c |
A |
T |
2: 86,253,975 (GRCm39) |
M15K |
probably benign |
Het |
Or8k32 |
A |
G |
2: 86,368,731 (GRCm39) |
I176T |
probably damaging |
Het |
Pigf |
G |
A |
17: 87,304,964 (GRCm39) |
T193I |
possibly damaging |
Het |
Pkp4 |
T |
C |
2: 59,172,525 (GRCm39) |
V904A |
possibly damaging |
Het |
Plekha6 |
C |
T |
1: 133,197,778 (GRCm39) |
T141M |
probably damaging |
Het |
Rapgef6 |
G |
A |
11: 54,582,308 (GRCm39) |
D1407N |
probably benign |
Het |
Rhobtb3 |
T |
C |
13: 76,087,741 (GRCm39) |
D82G |
probably damaging |
Het |
Rims1 |
T |
C |
1: 22,498,731 (GRCm39) |
N767S |
possibly damaging |
Het |
Ripor2 |
T |
A |
13: 24,849,451 (GRCm39) |
|
probably benign |
Het |
Sec14l4 |
T |
A |
11: 3,993,948 (GRCm39) |
I296N |
probably damaging |
Het |
Serpinb12 |
G |
T |
1: 106,884,342 (GRCm39) |
V363F |
probably damaging |
Het |
Serpinb9c |
A |
G |
13: 33,334,016 (GRCm39) |
I342T |
probably damaging |
Het |
Shmt2 |
A |
G |
10: 127,355,945 (GRCm39) |
V133A |
probably damaging |
Het |
Slc30a6 |
A |
G |
17: 74,722,661 (GRCm39) |
M243V |
probably benign |
Het |
Slfn2 |
T |
A |
11: 82,960,487 (GRCm39) |
N155K |
probably damaging |
Het |
Spata31h1 |
A |
T |
10: 82,152,298 (GRCm39) |
L23M |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 75,900,898 (GRCm39) |
D19V |
possibly damaging |
Het |
Tcl1b3 |
A |
T |
12: 105,160,736 (GRCm39) |
I116L |
probably benign |
Het |
Tcp11 |
A |
G |
17: 28,286,766 (GRCm39) |
I411T |
probably damaging |
Het |
Tctn1 |
C |
T |
5: 122,379,859 (GRCm39) |
A560T |
probably benign |
Het |
Tenm3 |
C |
A |
8: 48,682,216 (GRCm39) |
Q2471H |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,713,645 (GRCm39) |
D691G |
probably benign |
Het |
Ube3b |
C |
T |
5: 114,528,451 (GRCm39) |
P150S |
probably damaging |
Het |
Ugt2b5 |
T |
C |
5: 87,287,518 (GRCm39) |
I216M |
possibly damaging |
Het |
Unc5d |
T |
A |
8: 29,156,877 (GRCm39) |
R789S |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,147,875 (GRCm39) |
G934D |
probably damaging |
Het |
Usp6nl |
A |
T |
2: 6,399,352 (GRCm39) |
R70S |
probably damaging |
Het |
Vmn2r15 |
C |
A |
5: 109,445,302 (GRCm39) |
D41Y |
probably damaging |
Het |
Vmn2r17 |
T |
A |
5: 109,600,691 (GRCm39) |
I663N |
probably damaging |
Het |
Vnn3 |
C |
A |
10: 23,741,780 (GRCm39) |
Q362K |
possibly damaging |
Het |
Wdr72 |
A |
G |
9: 74,059,730 (GRCm39) |
D380G |
possibly damaging |
Het |
Wfdc10 |
G |
A |
2: 164,499,180 (GRCm39) |
E97K |
possibly damaging |
Het |
Xdh |
A |
T |
17: 74,206,007 (GRCm39) |
C1002* |
probably null |
Het |
Zscan4e |
A |
C |
7: 11,041,578 (GRCm39) |
V126G |
probably damaging |
Het |
|
Other mutations in Vmn1r181 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Vmn1r181
|
APN |
7 |
23,684,006 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02055:Vmn1r181
|
APN |
7 |
23,683,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02444:Vmn1r181
|
APN |
7 |
23,683,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Vmn1r181
|
APN |
7 |
23,684,027 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03026:Vmn1r181
|
APN |
7 |
23,684,000 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0255:Vmn1r181
|
UTSW |
7 |
23,683,759 (GRCm39) |
missense |
probably benign |
0.02 |
R1481:Vmn1r181
|
UTSW |
7 |
23,684,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R2847:Vmn1r181
|
UTSW |
7 |
23,683,943 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2848:Vmn1r181
|
UTSW |
7 |
23,683,943 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2849:Vmn1r181
|
UTSW |
7 |
23,683,943 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3441:Vmn1r181
|
UTSW |
7 |
23,684,308 (GRCm39) |
missense |
probably benign |
0.05 |
R3757:Vmn1r181
|
UTSW |
7 |
23,683,909 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3945:Vmn1r181
|
UTSW |
7 |
23,683,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R3983:Vmn1r181
|
UTSW |
7 |
23,684,234 (GRCm39) |
missense |
probably benign |
0.23 |
R4780:Vmn1r181
|
UTSW |
7 |
23,684,008 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4999:Vmn1r181
|
UTSW |
7 |
23,683,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R5463:Vmn1r181
|
UTSW |
7 |
23,683,787 (GRCm39) |
missense |
probably benign |
0.02 |
R5672:Vmn1r181
|
UTSW |
7 |
23,683,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Vmn1r181
|
UTSW |
7 |
23,683,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R6315:Vmn1r181
|
UTSW |
7 |
23,684,183 (GRCm39) |
missense |
probably benign |
0.23 |
R6316:Vmn1r181
|
UTSW |
7 |
23,684,183 (GRCm39) |
missense |
probably benign |
0.23 |
R6317:Vmn1r181
|
UTSW |
7 |
23,684,183 (GRCm39) |
missense |
probably benign |
0.23 |
R6324:Vmn1r181
|
UTSW |
7 |
23,684,183 (GRCm39) |
missense |
probably benign |
0.23 |
R6326:Vmn1r181
|
UTSW |
7 |
23,684,183 (GRCm39) |
missense |
probably benign |
0.23 |
R6988:Vmn1r181
|
UTSW |
7 |
23,684,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R7446:Vmn1r181
|
UTSW |
7 |
23,684,356 (GRCm39) |
missense |
probably benign |
0.01 |
R7972:Vmn1r181
|
UTSW |
7 |
23,683,871 (GRCm39) |
missense |
probably benign |
0.30 |
R9096:Vmn1r181
|
UTSW |
7 |
23,684,444 (GRCm39) |
missense |
probably benign |
0.00 |
R9097:Vmn1r181
|
UTSW |
7 |
23,684,444 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Vmn1r181
|
UTSW |
7 |
23,684,326 (GRCm39) |
missense |
probably benign |
0.00 |
|