Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513I03Rik |
G |
T |
10: 120,614,511 (GRCm39) |
|
probably benign |
Het |
4930407I10Rik |
T |
A |
15: 81,947,267 (GRCm39) |
I388K |
probably benign |
Het |
4930407I10Rik |
T |
A |
15: 81,950,504 (GRCm39) |
V1467D |
probably damaging |
Het |
Abi2 |
T |
A |
1: 60,492,884 (GRCm39) |
N182K |
probably benign |
Het |
Adam25 |
A |
T |
8: 41,207,829 (GRCm39) |
H365L |
probably damaging |
Het |
Ankfy1 |
T |
A |
11: 72,603,030 (GRCm39) |
Y20N |
probably damaging |
Het |
Aqp11 |
C |
T |
7: 97,387,068 (GRCm39) |
V43M |
probably benign |
Het |
Arhgef10l |
A |
T |
4: 140,279,843 (GRCm39) |
L503Q |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,093,150 (GRCm39) |
I977N |
possibly damaging |
Het |
Cacna1b |
A |
G |
2: 24,648,343 (GRCm39) |
Y161H |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,579,198 (GRCm39) |
D1480G |
probably damaging |
Het |
Clk3 |
A |
G |
9: 57,659,449 (GRCm39) |
M533T |
probably damaging |
Het |
Cnbd1 |
A |
G |
4: 18,860,504 (GRCm39) |
I414T |
possibly damaging |
Het |
Commd3 |
A |
T |
2: 18,679,514 (GRCm39) |
|
probably null |
Het |
Crybg1 |
G |
T |
10: 43,873,902 (GRCm39) |
Q1069K |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,984,685 (GRCm39) |
F3128I |
probably damaging |
Het |
Dnmt3b |
C |
T |
2: 153,514,192 (GRCm39) |
P382S |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,379,224 (GRCm39) |
|
probably null |
Het |
Dpysl3 |
C |
T |
18: 43,466,941 (GRCm39) |
|
probably null |
Het |
Ebf2 |
T |
A |
14: 67,475,989 (GRCm39) |
|
probably benign |
Het |
F830045P16Rik |
T |
C |
2: 129,305,624 (GRCm39) |
E250G |
possibly damaging |
Het |
Fbp2 |
A |
T |
13: 63,001,862 (GRCm39) |
F118I |
probably damaging |
Het |
Fetub |
T |
C |
16: 22,747,836 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
A |
T |
1: 174,436,015 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
C |
5: 73,179,621 (GRCm39) |
I2929V |
probably benign |
Het |
Gm11232 |
T |
A |
4: 71,675,112 (GRCm39) |
Q130L |
possibly damaging |
Het |
Gm9637 |
G |
T |
14: 19,402,570 (GRCm38) |
|
noncoding transcript |
Het |
Gna15 |
A |
G |
10: 81,348,239 (GRCm39) |
|
probably null |
Het |
Gtf3c5 |
T |
C |
2: 28,462,198 (GRCm39) |
|
probably benign |
Het |
Irs2 |
G |
A |
8: 11,055,723 (GRCm39) |
T903I |
possibly damaging |
Het |
Itga2 |
G |
A |
13: 115,007,032 (GRCm39) |
S432L |
possibly damaging |
Het |
Izumo1 |
A |
G |
7: 45,276,621 (GRCm39) |
T395A |
probably benign |
Het |
Kcnd2 |
G |
A |
6: 21,727,225 (GRCm39) |
V593M |
possibly damaging |
Het |
Kprp |
T |
C |
3: 92,731,989 (GRCm39) |
S354G |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,694,443 (GRCm39) |
K151E |
probably damaging |
Het |
Letm2 |
A |
T |
8: 26,077,464 (GRCm39) |
|
probably benign |
Het |
Lipe |
A |
G |
7: 25,097,874 (GRCm39) |
V23A |
possibly damaging |
Het |
Mcc |
C |
G |
18: 44,652,583 (GRCm39) |
|
probably benign |
Het |
Mef2c |
A |
G |
13: 83,800,992 (GRCm39) |
N231D |
possibly damaging |
Het |
Mtdh |
T |
A |
15: 34,134,426 (GRCm39) |
|
probably benign |
Het |
Mthfd1 |
G |
A |
12: 76,344,363 (GRCm39) |
|
probably benign |
Het |
Nbeal1 |
C |
A |
1: 60,286,876 (GRCm39) |
N899K |
probably benign |
Het |
Noc3l |
T |
C |
19: 38,803,253 (GRCm39) |
S129G |
probably benign |
Het |
Odad2 |
T |
A |
18: 7,129,593 (GRCm39) |
|
probably benign |
Het |
Or10ak14 |
T |
C |
4: 118,611,100 (GRCm39) |
I212V |
probably benign |
Het |
Or2aj6 |
T |
C |
16: 19,443,167 (GRCm39) |
M228V |
probably benign |
Het |
Or4c118 |
T |
C |
2: 88,974,966 (GRCm39) |
I134V |
possibly damaging |
Het |
Or8b1c |
T |
A |
9: 38,384,554 (GRCm39) |
D170E |
probably benign |
Het |
Pik3r6 |
T |
A |
11: 68,419,635 (GRCm39) |
Y149N |
probably damaging |
Het |
Pja2 |
C |
A |
17: 64,615,966 (GRCm39) |
V310L |
probably damaging |
Het |
Plcd3 |
G |
A |
11: 102,965,720 (GRCm39) |
A504V |
probably benign |
Het |
Rint1 |
G |
A |
5: 23,992,826 (GRCm39) |
|
probably benign |
Het |
Ripor3 |
A |
G |
2: 167,826,358 (GRCm39) |
|
probably benign |
Het |
Rpa2 |
C |
A |
4: 132,505,125 (GRCm39) |
N251K |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,029,090 (GRCm39) |
|
probably null |
Het |
Ryr2 |
C |
T |
13: 11,884,002 (GRCm39) |
|
probably null |
Het |
Scara3 |
T |
C |
14: 66,168,417 (GRCm39) |
N400S |
probably damaging |
Het |
Slc7a6 |
G |
T |
8: 106,916,263 (GRCm39) |
V180L |
possibly damaging |
Het |
Slc7a6 |
T |
A |
8: 106,916,264 (GRCm39) |
V180E |
probably damaging |
Het |
Slc8b1 |
T |
A |
5: 120,659,928 (GRCm39) |
|
probably null |
Het |
Slco1a4 |
G |
A |
6: 141,765,205 (GRCm39) |
Q346* |
probably null |
Het |
Stk32b |
A |
G |
5: 37,618,792 (GRCm39) |
S229P |
probably damaging |
Het |
Syde2 |
A |
G |
3: 145,704,508 (GRCm39) |
R487G |
probably benign |
Het |
Tbc1d2b |
T |
C |
9: 90,104,355 (GRCm39) |
|
probably benign |
Het |
Ticrr |
T |
C |
7: 79,317,654 (GRCm39) |
V396A |
probably benign |
Het |
Trrap |
T |
C |
5: 144,719,003 (GRCm39) |
|
probably benign |
Het |
Vps13a |
A |
T |
19: 16,646,054 (GRCm39) |
H1994Q |
probably damaging |
Het |
Wdr36 |
T |
G |
18: 32,997,802 (GRCm39) |
V820G |
possibly damaging |
Het |
Wdr83 |
G |
A |
8: 85,806,456 (GRCm39) |
T114I |
possibly damaging |
Het |
Zc3h7a |
T |
C |
16: 10,957,011 (GRCm39) |
N866S |
probably damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,252,658 (GRCm39) |
K1324E |
probably benign |
Het |
|
Other mutations in Vmn1r124 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02102:Vmn1r124
|
APN |
7 |
20,994,467 (GRCm39) |
missense |
probably benign |
0.00 |
FR4976:Vmn1r124
|
UTSW |
7 |
20,993,861 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0671:Vmn1r124
|
UTSW |
7 |
20,994,436 (GRCm39) |
missense |
probably damaging |
0.96 |
R1305:Vmn1r124
|
UTSW |
7 |
20,994,188 (GRCm39) |
missense |
probably benign |
0.01 |
R3954:Vmn1r124
|
UTSW |
7 |
20,994,448 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4628:Vmn1r124
|
UTSW |
7 |
20,994,302 (GRCm39) |
nonsense |
probably null |
|
R4830:Vmn1r124
|
UTSW |
7 |
20,993,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Vmn1r124
|
UTSW |
7 |
20,994,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5381:Vmn1r124
|
UTSW |
7 |
20,994,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5477:Vmn1r124
|
UTSW |
7 |
20,993,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Vmn1r124
|
UTSW |
7 |
20,994,104 (GRCm39) |
missense |
probably benign |
0.03 |
R6987:Vmn1r124
|
UTSW |
7 |
20,993,743 (GRCm39) |
missense |
probably benign |
0.35 |
R7151:Vmn1r124
|
UTSW |
7 |
20,994,184 (GRCm39) |
missense |
probably benign |
0.04 |
R7152:Vmn1r124
|
UTSW |
7 |
20,994,184 (GRCm39) |
missense |
probably benign |
0.04 |
R9635:Vmn1r124
|
UTSW |
7 |
20,993,720 (GRCm39) |
missense |
probably benign |
0.23 |
X0065:Vmn1r124
|
UTSW |
7 |
20,994,255 (GRCm39) |
missense |
probably benign |
0.19 |
|