Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028K03Rik |
A |
G |
5: 107,696,067 (GRCm39) |
R168G |
probably benign |
Het |
2810004N23Rik |
C |
T |
8: 125,566,668 (GRCm39) |
G251R |
possibly damaging |
Het |
3425401B19Rik |
A |
G |
14: 32,384,919 (GRCm39) |
S349P |
possibly damaging |
Het |
Ackr4 |
A |
G |
9: 103,976,650 (GRCm39) |
V99A |
probably benign |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Asxl3 |
A |
G |
18: 22,656,577 (GRCm39) |
Q1529R |
possibly damaging |
Het |
Atg12 |
T |
C |
18: 46,874,477 (GRCm39) |
E46G |
probably benign |
Het |
Cdcp2 |
A |
G |
4: 106,964,389 (GRCm39) |
|
probably benign |
Het |
Clasrp |
A |
G |
7: 19,318,089 (GRCm39) |
|
probably benign |
Het |
Clip2 |
A |
G |
5: 134,545,005 (GRCm39) |
V383A |
probably benign |
Het |
Cntln |
C |
T |
4: 84,923,290 (GRCm39) |
|
probably benign |
Het |
Colgalt2 |
G |
T |
1: 152,384,312 (GRCm39) |
A551S |
possibly damaging |
Het |
Csmd2 |
A |
C |
4: 128,380,798 (GRCm39) |
Y2118S |
possibly damaging |
Het |
Dip2c |
T |
A |
13: 9,613,244 (GRCm39) |
V415E |
probably damaging |
Het |
Dpy19l2 |
C |
T |
9: 24,469,391 (GRCm39) |
R755Q |
probably benign |
Het |
Dsn1 |
A |
T |
2: 156,840,633 (GRCm39) |
|
probably benign |
Het |
Dtd2 |
T |
C |
12: 52,051,742 (GRCm39) |
|
probably benign |
Het |
Dync1i1 |
A |
G |
6: 6,027,399 (GRCm39) |
T602A |
probably benign |
Het |
Ercc6 |
A |
C |
14: 32,248,799 (GRCm39) |
D450A |
probably damaging |
Het |
Fgf12 |
A |
T |
16: 28,008,380 (GRCm39) |
V104D |
probably benign |
Het |
Frem1 |
A |
T |
4: 82,888,870 (GRCm39) |
|
probably null |
Het |
Gcgr |
G |
T |
11: 120,426,982 (GRCm39) |
W88L |
probably damaging |
Het |
Glb1 |
ACCC |
ACC |
9: 114,250,812 (GRCm39) |
|
probably null |
Het |
Hapln1 |
A |
G |
13: 89,732,835 (GRCm39) |
|
probably benign |
Het |
Hmgn3 |
T |
C |
9: 82,994,301 (GRCm39) |
E40G |
probably damaging |
Het |
Hsdl1 |
G |
A |
8: 120,292,450 (GRCm39) |
A255V |
probably damaging |
Het |
Hyls1 |
T |
C |
9: 35,472,499 (GRCm39) |
K306E |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,649,122 (GRCm39) |
|
probably benign |
Het |
Kif14 |
C |
A |
1: 136,396,885 (GRCm39) |
A397E |
probably damaging |
Het |
Lcmt2 |
A |
T |
2: 120,969,825 (GRCm39) |
|
probably null |
Het |
Lifr |
T |
C |
15: 7,207,061 (GRCm39) |
L524P |
probably damaging |
Het |
Ly6g6f |
T |
C |
17: 35,301,828 (GRCm39) |
K209E |
possibly damaging |
Het |
Macf1 |
G |
A |
4: 123,365,113 (GRCm39) |
T1651I |
probably benign |
Het |
Mapk4 |
T |
C |
18: 74,103,392 (GRCm39) |
D39G |
probably damaging |
Het |
Mbl1 |
A |
G |
14: 40,880,522 (GRCm39) |
M137V |
probably damaging |
Het |
Mcm10 |
G |
A |
2: 5,013,356 (GRCm39) |
S92L |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,828,383 (GRCm39) |
K265R |
possibly damaging |
Het |
Mxra7 |
A |
G |
11: 116,701,612 (GRCm39) |
|
probably null |
Het |
Neu3 |
G |
A |
7: 99,472,524 (GRCm39) |
|
probably benign |
Het |
Nsd1 |
A |
G |
13: 55,460,648 (GRCm39) |
T2395A |
probably benign |
Het |
Or1j1 |
T |
A |
2: 36,702,627 (GRCm39) |
H159L |
probably damaging |
Het |
Or5m9 |
A |
T |
2: 85,877,411 (GRCm39) |
Y195F |
probably benign |
Het |
Or6s1 |
T |
A |
14: 51,308,614 (GRCm39) |
I79F |
probably damaging |
Het |
Or7g34 |
A |
T |
9: 19,478,245 (GRCm39) |
I145N |
probably benign |
Het |
Osgepl1 |
T |
C |
1: 53,360,255 (GRCm39) |
V327A |
probably damaging |
Het |
Pcdhb21 |
T |
C |
18: 37,649,085 (GRCm39) |
V738A |
possibly damaging |
Het |
Plekha8 |
A |
T |
6: 54,599,092 (GRCm39) |
|
probably benign |
Het |
Ptprq |
A |
C |
10: 107,374,781 (GRCm39) |
|
probably benign |
Het |
Pus10 |
T |
A |
11: 23,661,201 (GRCm39) |
F263Y |
probably benign |
Het |
Rad54b |
A |
T |
4: 11,599,809 (GRCm39) |
I338F |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,585,498 (GRCm39) |
F756L |
probably damaging |
Het |
Scn11a |
A |
G |
9: 119,619,185 (GRCm39) |
L719P |
probably damaging |
Het |
Slc2a2 |
G |
A |
3: 28,772,965 (GRCm39) |
V253I |
possibly damaging |
Het |
Slc39a4 |
A |
T |
15: 76,499,338 (GRCm39) |
N192K |
probably benign |
Het |
Soat1 |
T |
A |
1: 156,268,816 (GRCm39) |
I245F |
probably damaging |
Het |
Sorcs2 |
G |
A |
5: 36,188,534 (GRCm39) |
A858V |
probably benign |
Het |
Tcim |
T |
C |
8: 24,928,651 (GRCm39) |
T88A |
possibly damaging |
Het |
Tecta |
G |
A |
9: 42,259,188 (GRCm39) |
|
probably benign |
Het |
Tgm5 |
C |
A |
2: 120,879,376 (GRCm39) |
L553F |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,952,669 (GRCm39) |
V1555A |
probably benign |
Het |
Tmem214 |
A |
C |
5: 31,027,012 (GRCm39) |
M1L |
probably null |
Het |
Togaram1 |
T |
C |
12: 65,012,776 (GRCm39) |
|
probably benign |
Het |
Topaz1 |
C |
A |
9: 122,578,544 (GRCm39) |
L485I |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,548,626 (GRCm39) |
|
probably benign |
Het |
Ube2o |
A |
G |
11: 116,437,285 (GRCm39) |
|
probably null |
Het |
Ubr7 |
T |
A |
12: 102,734,465 (GRCm39) |
D246E |
probably benign |
Het |
Vcpkmt |
T |
C |
12: 69,629,102 (GRCm39) |
D132G |
probably benign |
Het |
Vmn2r95 |
C |
T |
17: 18,659,765 (GRCm39) |
P170S |
probably damaging |
Het |
Zbtb38 |
A |
G |
9: 96,567,826 (GRCm39) |
I1086T |
probably damaging |
Het |
Zfp444 |
G |
A |
7: 6,191,172 (GRCm39) |
A118T |
probably benign |
Het |
Zp2 |
A |
G |
7: 119,737,372 (GRCm39) |
I272T |
probably damaging |
Het |
|
Other mutations in Vmn2r111 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Vmn2r111
|
APN |
17 |
22,767,734 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01306:Vmn2r111
|
APN |
17 |
22,787,965 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01309:Vmn2r111
|
APN |
17 |
22,787,997 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01457:Vmn2r111
|
APN |
17 |
22,790,966 (GRCm39) |
nonsense |
probably null |
|
IGL01465:Vmn2r111
|
APN |
17 |
22,767,718 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01505:Vmn2r111
|
APN |
17 |
22,767,553 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01571:Vmn2r111
|
APN |
17 |
22,790,373 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01715:Vmn2r111
|
APN |
17 |
22,788,054 (GRCm39) |
splice site |
probably benign |
|
IGL01962:Vmn2r111
|
APN |
17 |
22,767,265 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02190:Vmn2r111
|
APN |
17 |
22,789,754 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02496:Vmn2r111
|
APN |
17 |
22,787,837 (GRCm39) |
missense |
probably benign |
|
IGL02519:Vmn2r111
|
APN |
17 |
22,767,320 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02616:Vmn2r111
|
APN |
17 |
22,790,031 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02641:Vmn2r111
|
APN |
17 |
22,792,205 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02690:Vmn2r111
|
APN |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02698:Vmn2r111
|
APN |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03017:Vmn2r111
|
APN |
17 |
22,789,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Vmn2r111
|
UTSW |
17 |
22,766,990 (GRCm39) |
missense |
probably benign |
|
R0064:Vmn2r111
|
UTSW |
17 |
22,791,053 (GRCm39) |
missense |
probably benign |
0.00 |
R1439:Vmn2r111
|
UTSW |
17 |
22,790,097 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
R1636:Vmn2r111
|
UTSW |
17 |
22,790,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1648:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
R1697:Vmn2r111
|
UTSW |
17 |
22,767,041 (GRCm39) |
missense |
probably benign |
0.26 |
R1996:Vmn2r111
|
UTSW |
17 |
22,767,062 (GRCm39) |
missense |
probably benign |
0.21 |
R2040:Vmn2r111
|
UTSW |
17 |
22,767,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Vmn2r111
|
UTSW |
17 |
22,778,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Vmn2r111
|
UTSW |
17 |
22,792,085 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2357:Vmn2r111
|
UTSW |
17 |
22,778,151 (GRCm39) |
splice site |
probably benign |
|
R3700:Vmn2r111
|
UTSW |
17 |
22,790,142 (GRCm39) |
nonsense |
probably null |
|
R3782:Vmn2r111
|
UTSW |
17 |
22,790,301 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4085:Vmn2r111
|
UTSW |
17 |
22,778,096 (GRCm39) |
missense |
probably benign |
0.00 |
R4323:Vmn2r111
|
UTSW |
17 |
22,792,159 (GRCm39) |
missense |
probably benign |
0.02 |
R4900:Vmn2r111
|
UTSW |
17 |
22,767,637 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5072:Vmn2r111
|
UTSW |
17 |
22,767,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R5123:Vmn2r111
|
UTSW |
17 |
22,790,124 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5181:Vmn2r111
|
UTSW |
17 |
22,790,001 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5357:Vmn2r111
|
UTSW |
17 |
22,767,083 (GRCm39) |
nonsense |
probably null |
|
R5398:Vmn2r111
|
UTSW |
17 |
22,792,252 (GRCm39) |
start codon destroyed |
probably null |
0.88 |
R5434:Vmn2r111
|
UTSW |
17 |
22,767,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R5462:Vmn2r111
|
UTSW |
17 |
22,767,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6149:Vmn2r111
|
UTSW |
17 |
22,767,796 (GRCm39) |
missense |
probably benign |
0.00 |
R6207:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6281:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6282:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6283:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6307:Vmn2r111
|
UTSW |
17 |
22,792,070 (GRCm39) |
missense |
probably benign |
0.00 |
R6323:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6325:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6367:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6368:Vmn2r111
|
UTSW |
17 |
22,790,889 (GRCm39) |
missense |
probably benign |
0.38 |
R6369:Vmn2r111
|
UTSW |
17 |
22,767,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6490:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6546:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6547:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6557:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6654:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6655:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6657:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6659:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6660:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6664:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6798:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6799:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6801:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6893:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6895:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6897:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6922:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6923:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6944:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6945:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7017:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7018:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7024:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7031:Vmn2r111
|
UTSW |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Vmn2r111
|
UTSW |
17 |
22,767,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R7053:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7054:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7055:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7056:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7145:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7146:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7246:Vmn2r111
|
UTSW |
17 |
22,767,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7260:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7327:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7401:Vmn2r111
|
UTSW |
17 |
22,790,067 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7514:Vmn2r111
|
UTSW |
17 |
22,767,380 (GRCm39) |
missense |
probably benign |
0.05 |
R7651:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7781:Vmn2r111
|
UTSW |
17 |
22,789,714 (GRCm39) |
missense |
probably benign |
0.17 |
R7816:Vmn2r111
|
UTSW |
17 |
22,792,083 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7838:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8078:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8080:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8117:Vmn2r111
|
UTSW |
17 |
22,790,469 (GRCm39) |
missense |
probably benign |
0.12 |
R8171:Vmn2r111
|
UTSW |
17 |
22,792,073 (GRCm39) |
missense |
probably benign |
0.10 |
R8195:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8197:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8411:Vmn2r111
|
UTSW |
17 |
22,767,562 (GRCm39) |
missense |
probably benign |
0.03 |
R8539:Vmn2r111
|
UTSW |
17 |
22,790,274 (GRCm39) |
missense |
probably benign |
0.23 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Vmn2r111
|
UTSW |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
R8557:Vmn2r111
|
UTSW |
17 |
22,790,910 (GRCm39) |
nonsense |
probably null |
|
R8720:Vmn2r111
|
UTSW |
17 |
22,792,194 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8729:Vmn2r111
|
UTSW |
17 |
22,767,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Vmn2r111
|
UTSW |
17 |
22,767,011 (GRCm39) |
missense |
probably benign |
0.00 |
R9184:Vmn2r111
|
UTSW |
17 |
22,790,822 (GRCm39) |
missense |
probably benign |
|
R9374:Vmn2r111
|
UTSW |
17 |
22,787,859 (GRCm39) |
missense |
probably benign |
0.17 |
R9452:Vmn2r111
|
UTSW |
17 |
22,778,132 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Vmn2r111
|
UTSW |
17 |
22,767,676 (GRCm39) |
missense |
probably damaging |
0.98 |
|