Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
G |
A |
8: 111,781,762 (GRCm39) |
V945M |
probably benign |
Het |
Amotl2 |
A |
G |
9: 102,601,967 (GRCm39) |
T371A |
probably damaging |
Het |
Bmpr1a |
A |
G |
14: 34,163,132 (GRCm39) |
I86T |
possibly damaging |
Het |
C9 |
A |
T |
15: 6,474,945 (GRCm39) |
M35L |
probably benign |
Het |
Cc2d1a |
G |
T |
8: 84,862,528 (GRCm39) |
P661T |
probably damaging |
Het |
Ccdc202 |
T |
A |
14: 96,119,869 (GRCm39) |
W209R |
probably damaging |
Het |
Dcdc2a |
T |
A |
13: 25,303,349 (GRCm39) |
S293R |
probably benign |
Het |
Dchs2 |
T |
A |
3: 83,261,233 (GRCm39) |
N2500K |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,697,282 (GRCm39) |
S92P |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,616,446 (GRCm39) |
I1172F |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,471,470 (GRCm39) |
S364G |
probably damaging |
Het |
Dpp6 |
A |
T |
5: 27,803,819 (GRCm39) |
N255I |
probably damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,252,748 (GRCm39) |
I440T |
probably damaging |
Het |
Fam184b |
T |
C |
5: 45,688,099 (GRCm39) |
T937A |
probably damaging |
Het |
Fam229b |
T |
A |
10: 39,009,843 (GRCm39) |
|
probably null |
Het |
Gbp11 |
A |
G |
5: 105,476,241 (GRCm39) |
|
probably null |
Het |
Gipc2 |
A |
G |
3: 151,799,885 (GRCm39) |
F282L |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
H2-T3 |
T |
A |
17: 36,500,263 (GRCm39) |
Y144F |
probably damaging |
Het |
Kel |
T |
G |
6: 41,664,907 (GRCm39) |
D7A |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,994,668 (GRCm39) |
V166A |
probably benign |
Het |
Mapt |
T |
C |
11: 104,209,081 (GRCm39) |
|
probably null |
Het |
Marchf3 |
A |
G |
18: 56,909,053 (GRCm39) |
V244A |
probably benign |
Het |
Mboat1 |
T |
C |
13: 30,422,059 (GRCm39) |
V396A |
possibly damaging |
Het |
Mphosph9 |
T |
C |
5: 124,435,621 (GRCm39) |
D604G |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,556,322 (GRCm39) |
T3324A |
unknown |
Het |
Nalf1 |
T |
A |
8: 9,820,744 (GRCm39) |
Q92L |
probably benign |
Het |
Nat10 |
T |
C |
2: 103,564,757 (GRCm39) |
I495V |
probably benign |
Het |
Or6c208 |
A |
T |
10: 129,224,166 (GRCm39) |
K221N |
probably benign |
Het |
Pfkfb2 |
T |
C |
1: 130,635,337 (GRCm39) |
N75D |
probably damaging |
Het |
Psmd3 |
T |
A |
11: 98,586,377 (GRCm39) |
L515Q |
probably damaging |
Het |
Rpgrip1l |
A |
C |
8: 92,012,941 (GRCm39) |
|
probably null |
Het |
Scube1 |
T |
C |
15: 83,606,077 (GRCm39) |
Y65C |
probably damaging |
Het |
Slc12a4 |
A |
G |
8: 106,680,484 (GRCm39) |
F211L |
probably damaging |
Het |
Socs7 |
T |
C |
11: 97,267,849 (GRCm39) |
S327P |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,685,021 (GRCm39) |
D591E |
probably damaging |
Het |
Sult2a6 |
T |
A |
7: 13,988,748 (GRCm39) |
D4V |
possibly damaging |
Het |
Tdpoz8 |
T |
C |
3: 92,981,279 (GRCm39) |
V25A |
possibly damaging |
Het |
Tdrd9 |
A |
G |
12: 112,002,788 (GRCm39) |
|
probably benign |
Het |
Tgm4 |
G |
T |
9: 122,893,768 (GRCm39) |
M155I |
possibly damaging |
Het |
Togaram2 |
T |
C |
17: 72,036,183 (GRCm39) |
V891A |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,819,243 (GRCm39) |
E235G |
probably damaging |
Het |
Usp2 |
T |
A |
9: 44,004,053 (GRCm39) |
V533E |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,837,550 (GRCm39) |
I2665F |
probably damaging |
Het |
Vmn2r84 |
C |
A |
10: 130,225,136 (GRCm39) |
C458F |
probably damaging |
Het |
|
Other mutations in Vmn2r31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01104:Vmn2r31
|
APN |
7 |
7,399,565 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01536:Vmn2r31
|
APN |
7 |
7,387,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Vmn2r31
|
APN |
7 |
7,397,510 (GRCm39) |
missense |
probably benign |
|
IGL02116:Vmn2r31
|
APN |
7 |
7,397,548 (GRCm39) |
missense |
probably damaging |
0.97 |
FR4304:Vmn2r31
|
UTSW |
7 |
7,387,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Vmn2r31
|
UTSW |
7 |
7,387,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Vmn2r31
|
UTSW |
7 |
7,387,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Vmn2r31
|
UTSW |
7 |
7,387,757 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4824:Vmn2r31
|
UTSW |
7 |
7,390,062 (GRCm39) |
critical splice donor site |
probably null |
|
R5619:Vmn2r31
|
UTSW |
7 |
7,387,529 (GRCm39) |
nonsense |
probably null |
|
R6225:Vmn2r31
|
UTSW |
7 |
7,397,638 (GRCm39) |
missense |
probably benign |
0.19 |
R6610:Vmn2r31
|
UTSW |
7 |
7,387,588 (GRCm39) |
missense |
probably damaging |
0.97 |
R7111:Vmn2r31
|
UTSW |
7 |
7,399,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R7219:Vmn2r31
|
UTSW |
7 |
7,397,397 (GRCm39) |
missense |
probably damaging |
0.97 |
R7219:Vmn2r31
|
UTSW |
7 |
7,390,105 (GRCm39) |
missense |
probably benign |
|
R7300:Vmn2r31
|
UTSW |
7 |
7,387,775 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7395:Vmn2r31
|
UTSW |
7 |
7,387,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Vmn2r31
|
UTSW |
7 |
7,387,579 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8015:Vmn2r31
|
UTSW |
7 |
7,387,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8434:Vmn2r31
|
UTSW |
7 |
7,387,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Vmn2r31
|
UTSW |
7 |
7,387,400 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8972:Vmn2r31
|
UTSW |
7 |
7,399,654 (GRCm39) |
missense |
probably benign |
0.00 |
R9034:Vmn2r31
|
UTSW |
7 |
7,397,680 (GRCm39) |
missense |
probably benign |
0.08 |
R9596:Vmn2r31
|
UTSW |
7 |
7,397,292 (GRCm39) |
missense |
probably benign |
0.01 |
R9711:Vmn2r31
|
UTSW |
7 |
7,387,085 (GRCm39) |
missense |
probably damaging |
0.99 |
R9714:Vmn2r31
|
UTSW |
7 |
7,387,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|