Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
G |
5: 8,863,693 (GRCm39) |
V216G |
probably damaging |
Het |
Abcb5 |
T |
C |
12: 118,875,265 (GRCm39) |
R636G |
probably benign |
Het |
Ago1 |
G |
T |
4: 126,354,215 (GRCm39) |
F198L |
possibly damaging |
Het |
Ankrd42 |
C |
T |
7: 92,268,755 (GRCm39) |
|
probably null |
Het |
Anxa11 |
T |
A |
14: 25,875,176 (GRCm39) |
F274I |
probably damaging |
Het |
Ascc1 |
T |
C |
10: 59,849,475 (GRCm39) |
L122P |
probably damaging |
Het |
Bptf |
T |
C |
11: 106,971,649 (GRCm39) |
S953G |
probably damaging |
Het |
Chml |
T |
A |
1: 175,515,727 (GRCm39) |
N65Y |
probably damaging |
Het |
Clcc1 |
A |
G |
3: 108,578,284 (GRCm39) |
K262E |
probably damaging |
Het |
Clhc1 |
T |
G |
11: 29,519,346 (GRCm39) |
D384E |
probably damaging |
Het |
Cnot2 |
G |
A |
10: 116,373,128 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
T |
C |
11: 101,073,730 (GRCm39) |
V627A |
probably damaging |
Het |
Col6a4 |
A |
G |
9: 105,949,370 (GRCm39) |
V755A |
probably damaging |
Het |
Cyp4f18 |
T |
A |
8: 72,743,738 (GRCm39) |
I406F |
probably benign |
Het |
Dclre1a |
T |
C |
19: 56,533,451 (GRCm39) |
E381G |
possibly damaging |
Het |
Dnah1 |
A |
G |
14: 30,990,861 (GRCm39) |
Y3153H |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 31,013,633 (GRCm39) |
D3791E |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,975,975 (GRCm39) |
E1358G |
possibly damaging |
Het |
Eef1g |
G |
A |
19: 8,945,656 (GRCm39) |
R30H |
probably benign |
Het |
Egln3 |
A |
T |
12: 54,230,738 (GRCm39) |
I181N |
probably benign |
Het |
Entpd6 |
A |
G |
2: 150,605,519 (GRCm39) |
T250A |
probably damaging |
Het |
Epb41l5 |
C |
T |
1: 119,536,859 (GRCm39) |
R344Q |
probably damaging |
Het |
Fam20b |
T |
C |
1: 156,515,091 (GRCm39) |
D258G |
probably benign |
Het |
Fbxw18 |
A |
T |
9: 109,531,655 (GRCm39) |
D21E |
probably damaging |
Het |
Fbxw21 |
T |
C |
9: 108,986,603 (GRCm39) |
E92G |
probably damaging |
Het |
Fzd6 |
T |
A |
15: 38,889,212 (GRCm39) |
M110K |
possibly damaging |
Het |
Golgb1 |
C |
T |
16: 36,732,475 (GRCm39) |
P574L |
probably benign |
Het |
Gpr153 |
A |
G |
4: 152,363,820 (GRCm39) |
E80G |
probably damaging |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
Kcnt1 |
T |
C |
2: 25,767,840 (GRCm39) |
|
probably benign |
Het |
Kcnt2 |
T |
G |
1: 140,511,803 (GRCm39) |
V962G |
probably benign |
Het |
Malt1 |
T |
C |
18: 65,570,991 (GRCm39) |
V109A |
probably benign |
Het |
Marchf7 |
A |
G |
2: 60,064,587 (GRCm39) |
I288V |
probably benign |
Het |
Mief1 |
C |
T |
15: 80,133,644 (GRCm39) |
R234C |
probably damaging |
Het |
Morc3 |
A |
G |
16: 93,667,460 (GRCm39) |
S613G |
probably benign |
Het |
Myt1 |
A |
G |
2: 181,439,387 (GRCm39) |
E345G |
possibly damaging |
Het |
Napb |
T |
C |
2: 148,548,889 (GRCm39) |
T133A |
probably benign |
Het |
Nwd1 |
T |
C |
8: 73,380,162 (GRCm39) |
V16A |
possibly damaging |
Het |
Oas1f |
G |
A |
5: 120,986,247 (GRCm39) |
E67K |
probably benign |
Het |
Obscn |
T |
C |
11: 58,929,756 (GRCm39) |
K5153R |
probably damaging |
Het |
Or2w3b |
T |
A |
11: 58,623,068 (GRCm39) |
S308C |
possibly damaging |
Het |
Or5a3 |
G |
T |
19: 12,400,628 (GRCm39) |
M318I |
probably benign |
Het |
Or5g26 |
C |
T |
2: 85,494,195 (GRCm39) |
M194I |
probably benign |
Het |
Or6d12 |
T |
C |
6: 116,492,791 (GRCm39) |
F18L |
possibly damaging |
Het |
Pdcd2 |
T |
C |
17: 15,745,632 (GRCm39) |
N185S |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,569,320 (GRCm39) |
W349R |
probably damaging |
Het |
Prpf39 |
T |
A |
12: 65,089,454 (GRCm39) |
V64E |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,624,857 (GRCm39) |
W54R |
probably null |
Het |
Rbms3 |
G |
T |
9: 116,939,173 (GRCm39) |
P29Q |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,940,822 (GRCm39) |
L679P |
probably benign |
Het |
Samd4 |
T |
A |
14: 47,254,092 (GRCm39) |
D84E |
possibly damaging |
Het |
Scarf1 |
T |
C |
11: 75,413,032 (GRCm39) |
V426A |
probably benign |
Het |
Slc12a1 |
A |
G |
2: 125,002,454 (GRCm39) |
N145D |
probably damaging |
Het |
Slc2a6 |
A |
T |
2: 26,916,076 (GRCm39) |
M99K |
probably damaging |
Het |
Slc34a2 |
A |
T |
5: 53,222,225 (GRCm39) |
I306L |
probably benign |
Het |
Slx4ip |
A |
G |
2: 136,910,195 (GRCm39) |
K397E |
probably damaging |
Het |
Smr3a |
C |
T |
5: 88,155,949 (GRCm39) |
|
probably benign |
Het |
Spata31h1 |
A |
C |
10: 82,132,056 (GRCm39) |
I318R |
probably benign |
Het |
Spef2 |
T |
C |
15: 9,592,835 (GRCm39) |
E1502G |
probably damaging |
Het |
Sri |
A |
T |
5: 8,113,365 (GRCm39) |
T119S |
probably benign |
Het |
Synrg |
T |
A |
11: 83,915,912 (GRCm39) |
L1085H |
probably damaging |
Het |
Taf7 |
A |
T |
18: 37,775,910 (GRCm39) |
L219H |
probably damaging |
Het |
Tmco3 |
T |
A |
8: 13,353,729 (GRCm39) |
V347E |
probably damaging |
Het |
Tmem8b |
A |
T |
4: 43,674,465 (GRCm39) |
I250F |
probably damaging |
Het |
Tom1l2 |
A |
G |
11: 60,139,817 (GRCm39) |
V239A |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 63,893,181 (GRCm39) |
M1011K |
probably damaging |
Het |
Tspan9 |
A |
T |
6: 127,942,769 (GRCm39) |
Y153N |
probably benign |
Het |
Ttll11 |
T |
C |
2: 35,642,306 (GRCm39) |
H675R |
probably benign |
Het |
Unc50 |
C |
T |
1: 37,471,743 (GRCm39) |
T131M |
probably damaging |
Het |
Vgf |
T |
A |
5: 137,061,206 (GRCm39) |
I456N |
probably damaging |
Het |
Vmn1r223 |
A |
G |
13: 23,433,483 (GRCm39) |
I26V |
unknown |
Het |
Vmn1r39 |
T |
C |
6: 66,782,205 (GRCm39) |
M1V |
probably null |
Het |
Vmn2r14 |
T |
C |
5: 109,363,925 (GRCm39) |
T664A |
probably benign |
Het |
Vmn2r14 |
G |
A |
5: 109,364,140 (GRCm39) |
T592I |
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,817,891 (GRCm39) |
F489L |
probably benign |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,697,393 (GRCm39) |
F817L |
possibly 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 |
R0519:Vmn2r111
|
UTSW |
17 |
22,792,102 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
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 |
|