Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy5 |
A |
G |
16: 35,099,607 (GRCm39) |
E719G |
probably damaging |
Het |
Ankdd1a |
A |
G |
9: 65,424,220 (GRCm39) |
M31T |
possibly damaging |
Het |
Atp13a5 |
T |
C |
16: 29,070,154 (GRCm39) |
K911E |
possibly damaging |
Het |
Bpifb3 |
G |
T |
2: 153,766,728 (GRCm39) |
L210F |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,728,334 (GRCm39) |
Y211C |
probably damaging |
Het |
Carm1 |
C |
A |
9: 21,494,373 (GRCm39) |
P297T |
probably damaging |
Het |
Cdh19 |
A |
T |
1: 110,852,787 (GRCm39) |
Y383N |
probably benign |
Het |
Cfap221 |
T |
C |
1: 119,860,583 (GRCm39) |
H681R |
probably damaging |
Het |
Cmya5 |
A |
C |
13: 93,210,972 (GRCm39) |
S3274A |
possibly damaging |
Het |
Cndp2 |
T |
A |
18: 84,693,203 (GRCm39) |
K186* |
probably null |
Het |
Ctdp1 |
G |
T |
18: 80,494,470 (GRCm39) |
F310L |
probably damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,019,853 (GRCm39) |
I264F |
probably damaging |
Het |
Dhx40 |
A |
T |
11: 86,664,649 (GRCm39) |
F628I |
probably damaging |
Het |
Disc1 |
T |
A |
8: 125,862,128 (GRCm39) |
M500K |
possibly damaging |
Het |
Dnah5 |
A |
C |
15: 28,349,970 (GRCm39) |
D2551A |
possibly damaging |
Het |
Esyt1 |
A |
G |
10: 128,352,543 (GRCm39) |
|
probably null |
Het |
Fam78a |
T |
C |
2: 31,972,843 (GRCm39) |
S26G |
probably damaging |
Het |
Fn1 |
G |
A |
1: 71,687,003 (GRCm39) |
|
probably null |
Het |
Gbx1 |
T |
C |
5: 24,709,916 (GRCm39) |
T310A |
probably benign |
Het |
Ggh |
T |
A |
4: 20,042,219 (GRCm39) |
C16S |
unknown |
Het |
Gm11595 |
T |
A |
11: 99,663,600 (GRCm39) |
T27S |
unknown |
Het |
Gm17334 |
T |
A |
11: 53,663,564 (GRCm39) |
|
probably benign |
Het |
Gsk3b |
A |
G |
16: 38,014,311 (GRCm39) |
I256M |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,620,711 (GRCm39) |
S1166R |
probably benign |
Het |
Hyou1 |
T |
C |
9: 44,293,322 (GRCm39) |
|
probably null |
Het |
Jup |
G |
T |
11: 100,265,167 (GRCm39) |
R637S |
probably benign |
Het |
Lama2 |
T |
A |
10: 26,929,027 (GRCm39) |
I2087F |
possibly damaging |
Het |
Lamc1 |
T |
G |
1: 153,097,417 (GRCm39) |
K1542N |
probably benign |
Het |
Lgals4 |
G |
T |
7: 28,540,117 (GRCm39) |
|
|
Het |
Lrrc8d |
A |
G |
5: 105,959,626 (GRCm39) |
D12G |
probably damaging |
Het |
Lrwd1 |
C |
T |
5: 136,161,888 (GRCm39) |
V207M |
possibly damaging |
Het |
Mbd1 |
T |
A |
18: 74,406,762 (GRCm39) |
|
probably null |
Het |
Msi1 |
T |
A |
5: 115,588,984 (GRCm39) |
I333N |
probably damaging |
Het |
Neo1 |
C |
T |
9: 58,814,354 (GRCm39) |
V871I |
probably benign |
Het |
Nr2c1 |
T |
C |
10: 94,024,078 (GRCm39) |
C428R |
probably damaging |
Het |
Ntm |
A |
G |
9: 29,322,978 (GRCm39) |
L14P |
probably damaging |
Het |
Nxpe4 |
A |
T |
9: 48,304,145 (GRCm39) |
K77N |
probably damaging |
Het |
Or1p1c |
A |
C |
11: 74,160,235 (GRCm39) |
T7P |
possibly damaging |
Het |
Or4c119 |
T |
A |
2: 88,987,505 (GRCm39) |
S5C |
probably damaging |
Het |
Or4f17-ps1 |
T |
A |
2: 111,358,001 (GRCm39) |
M132K |
probably damaging |
Het |
Or8g30 |
T |
C |
9: 39,230,074 (GRCm39) |
T279A |
possibly damaging |
Het |
Or8k18 |
G |
A |
2: 86,085,702 (GRCm39) |
L112F |
probably benign |
Het |
Pappa |
T |
A |
4: 65,074,701 (GRCm39) |
D418E |
probably damaging |
Het |
Pde4d |
G |
A |
13: 109,738,320 (GRCm39) |
|
probably null |
Het |
Pip |
A |
G |
6: 41,828,391 (GRCm39) |
N75S |
possibly damaging |
Het |
Plcl1 |
G |
C |
1: 55,736,411 (GRCm39) |
R584P |
probably benign |
Het |
Pnp |
A |
T |
14: 51,188,471 (GRCm39) |
D237V |
probably damaging |
Het |
Ppp1r12a |
T |
C |
10: 108,098,281 (GRCm39) |
W857R |
probably damaging |
Het |
Pramel13 |
T |
C |
4: 144,119,653 (GRCm39) |
T305A |
possibly damaging |
Het |
Ptchd3 |
A |
T |
11: 121,727,229 (GRCm39) |
M368L |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,501,816 (GRCm39) |
S868R |
probably damaging |
Het |
R3hdml |
A |
T |
2: 163,344,324 (GRCm39) |
S238C |
probably damaging |
Het |
Robo2 |
G |
A |
16: 73,843,697 (GRCm39) |
R173* |
probably null |
Het |
Sall3 |
A |
G |
18: 81,016,402 (GRCm39) |
S509P |
possibly damaging |
Het |
Sap130 |
T |
G |
18: 31,799,418 (GRCm39) |
H298Q |
possibly damaging |
Het |
Selenov |
C |
A |
7: 27,987,458 (GRCm39) |
G307C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,379,453 (GRCm39) |
H1089Q |
possibly damaging |
Het |
Setdb2 |
T |
C |
14: 59,656,505 (GRCm39) |
N287D |
probably damaging |
Het |
Sis |
C |
T |
3: 72,865,507 (GRCm39) |
V182I |
probably benign |
Het |
Slc32a1 |
A |
C |
2: 158,453,457 (GRCm39) |
D99A |
probably benign |
Het |
Slk |
A |
G |
19: 47,609,327 (GRCm39) |
D760G |
probably damaging |
Het |
Smg5 |
T |
A |
3: 88,258,527 (GRCm39) |
D499E |
probably benign |
Het |
Spata31e2 |
T |
A |
1: 26,723,111 (GRCm39) |
N690Y |
probably benign |
Het |
Stat3 |
T |
C |
11: 100,780,400 (GRCm39) |
T720A |
possibly damaging |
Het |
Trdn |
T |
G |
10: 33,015,110 (GRCm39) |
N21K |
probably damaging |
Het |
Trpm4 |
A |
T |
7: 44,975,992 (GRCm39) |
V118E |
possibly damaging |
Het |
Vgll3 |
A |
G |
16: 65,612,640 (GRCm39) |
Q41R |
probably damaging |
Het |
Vmn1r189 |
A |
G |
13: 22,286,525 (GRCm39) |
V104A |
probably damaging |
Het |
Zscan4c |
T |
C |
7: 10,740,856 (GRCm39) |
M125T |
probably benign |
Het |
|
Other mutations in Vmn1r46 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02271:Vmn1r46
|
APN |
6 |
89,953,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Vmn1r46
|
APN |
6 |
89,953,963 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03116:Vmn1r46
|
APN |
6 |
89,953,898 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03270:Vmn1r46
|
APN |
6 |
89,953,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Vmn1r46
|
UTSW |
6 |
89,954,044 (GRCm39) |
missense |
probably benign |
0.03 |
R0126:Vmn1r46
|
UTSW |
6 |
89,953,935 (GRCm39) |
missense |
probably benign |
|
R0681:Vmn1r46
|
UTSW |
6 |
89,953,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R1501:Vmn1r46
|
UTSW |
6 |
89,953,198 (GRCm39) |
missense |
probably benign |
0.03 |
R1717:Vmn1r46
|
UTSW |
6 |
89,953,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Vmn1r46
|
UTSW |
6 |
89,953,716 (GRCm39) |
missense |
probably benign |
0.00 |
R4323:Vmn1r46
|
UTSW |
6 |
89,953,349 (GRCm39) |
missense |
probably benign |
0.06 |
R5449:Vmn1r46
|
UTSW |
6 |
89,953,343 (GRCm39) |
missense |
probably benign |
0.18 |
R6062:Vmn1r46
|
UTSW |
6 |
89,953,241 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6385:Vmn1r46
|
UTSW |
6 |
89,953,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R7126:Vmn1r46
|
UTSW |
6 |
89,953,976 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7391:Vmn1r46
|
UTSW |
6 |
89,953,607 (GRCm39) |
missense |
probably benign |
0.23 |
R8700:Vmn1r46
|
UTSW |
6 |
89,953,325 (GRCm39) |
missense |
probably benign |
0.04 |
R8950:Vmn1r46
|
UTSW |
6 |
89,954,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R9046:Vmn1r46
|
UTSW |
6 |
89,953,585 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Vmn1r46
|
UTSW |
6 |
89,953,723 (GRCm39) |
missense |
probably damaging |
1.00 |
|