Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610507B11Rik |
T |
C |
11: 78,268,377 (GRCm38) |
V467A |
possibly damaging |
Het |
4933405L10Rik |
G |
A |
8: 105,709,780 (GRCm38) |
V194I |
probably benign |
Het |
Acsm1 |
A |
T |
7: 119,636,455 (GRCm38) |
I133F |
probably damaging |
Het |
Adamts9 |
T |
A |
6: 92,798,005 (GRCm38) |
T1676S |
probably benign |
Het |
Adcy4 |
T |
C |
14: 55,772,288 (GRCm38) |
D769G |
probably benign |
Het |
Aif1 |
T |
C |
17: 35,171,109 (GRCm38) |
*148W |
probably null |
Het |
Akna |
C |
T |
4: 63,392,126 (GRCm38) |
|
probably benign |
Het |
Arhgap32 |
G |
A |
9: 32,245,255 (GRCm38) |
|
probably null |
Het |
Atpaf1 |
G |
A |
4: 115,785,252 (GRCm38) |
E92K |
possibly damaging |
Het |
C1s1 |
T |
C |
6: 124,533,354 (GRCm38) |
E378G |
probably benign |
Het |
Caprin1 |
T |
A |
2: 103,769,569 (GRCm38) |
Q108L |
probably damaging |
Het |
Car13 |
A |
T |
3: 14,656,239 (GRCm38) |
H154L |
probably benign |
Het |
Cdon |
C |
A |
9: 35,470,130 (GRCm38) |
N605K |
probably damaging |
Het |
Ceacam10 |
G |
A |
7: 24,781,014 (GRCm38) |
G70E |
probably damaging |
Het |
Cfap221 |
G |
A |
1: 119,954,200 (GRCm38) |
T286M |
probably benign |
Het |
Cfap61 |
T |
C |
2: 145,949,944 (GRCm38) |
F107S |
possibly damaging |
Het |
Coil |
C |
A |
11: 88,981,623 (GRCm38) |
T270N |
probably benign |
Het |
Crocc2 |
T |
G |
1: 93,224,214 (GRCm38) |
|
probably benign |
Het |
Crot |
T |
C |
5: 8,969,959 (GRCm38) |
E461G |
probably damaging |
Het |
D130052B06Rik |
G |
T |
11: 33,623,391 (GRCm38) |
R41L |
unknown |
Het |
D630045J12Rik |
T |
C |
6: 38,196,736 (GRCm38) |
S166G |
possibly damaging |
Het |
Dennd4a |
T |
G |
9: 64,862,391 (GRCm38) |
V460G |
probably damaging |
Het |
Depdc7 |
A |
T |
2: 104,727,323 (GRCm38) |
|
probably benign |
Het |
Dgkb |
G |
A |
12: 38,190,135 (GRCm38) |
|
probably null |
Het |
Dhx57 |
T |
G |
17: 80,274,797 (GRCm38) |
S407R |
probably benign |
Het |
Dnase2a |
G |
T |
8: 84,909,763 (GRCm38) |
|
probably benign |
Het |
Dqx1 |
T |
G |
6: 83,059,005 (GRCm38) |
M106R |
probably benign |
Het |
Eno1b |
T |
C |
18: 48,047,739 (GRCm38) |
I328T |
probably benign |
Het |
Ephx2 |
T |
G |
14: 66,108,063 (GRCm38) |
I151L |
probably benign |
Het |
Gdf3 |
C |
T |
6: 122,607,135 (GRCm38) |
G91D |
probably damaging |
Het |
Gm14124 |
G |
A |
2: 150,268,053 (GRCm38) |
G221D |
probably damaging |
Het |
Gpc5 |
T |
A |
14: 115,428,208 (GRCm38) |
N481K |
possibly damaging |
Het |
Gsdme |
T |
A |
6: 50,221,107 (GRCm38) |
H291L |
probably benign |
Het |
H2-Bl |
A |
G |
17: 36,083,722 (GRCm38) |
I103T |
possibly damaging |
Het |
Hif3a |
G |
A |
7: 17,052,021 (GRCm38) |
|
probably benign |
Het |
Hmox2 |
A |
T |
16: 4,765,763 (GRCm38) |
I232L |
probably benign |
Het |
Itgb2 |
A |
G |
10: 77,561,189 (GRCm38) |
Y686C |
probably damaging |
Het |
Jmjd1c |
A |
G |
10: 67,219,523 (GRCm38) |
T528A |
possibly damaging |
Het |
Kdr |
T |
C |
5: 75,960,728 (GRCm38) |
I541V |
possibly damaging |
Het |
Khdrbs2 |
C |
A |
1: 32,519,973 (GRCm38) |
V343L |
probably damaging |
Het |
Kif16b |
C |
T |
2: 142,853,659 (GRCm38) |
R175H |
probably damaging |
Het |
Klri2 |
T |
G |
6: 129,740,288 (GRCm38) |
E44A |
possibly damaging |
Het |
Kmt2b |
G |
T |
7: 30,576,755 (GRCm38) |
T1773K |
probably damaging |
Het |
Lair1 |
A |
G |
7: 4,010,786 (GRCm38) |
L154P |
probably damaging |
Het |
Larp1b |
G |
A |
3: 40,970,561 (GRCm38) |
V158M |
probably damaging |
Het |
Lgi3 |
T |
A |
14: 70,534,840 (GRCm38) |
I275N |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,295,179 (GRCm38) |
N246D |
probably damaging |
Het |
Lrrc45 |
T |
A |
11: 120,714,907 (GRCm38) |
|
probably benign |
Het |
Mdh2 |
G |
T |
5: 135,789,679 (GRCm38) |
V263L |
probably benign |
Het |
Myom1 |
T |
A |
17: 71,034,693 (GRCm38) |
V149E |
probably damaging |
Het |
Nanos1 |
A |
T |
19: 60,757,041 (GRCm38) |
D259V |
probably damaging |
Het |
Nedd4l |
T |
A |
18: 65,161,654 (GRCm38) |
|
probably benign |
Het |
Npas3 |
A |
G |
12: 53,831,745 (GRCm38) |
Y150C |
probably damaging |
Het |
Olfr1066 |
T |
C |
2: 86,456,019 (GRCm38) |
N84S |
possibly damaging |
Het |
Olfr1129 |
T |
A |
2: 87,575,567 (GRCm38) |
V161D |
possibly damaging |
Het |
Olfr1392 |
A |
T |
11: 49,293,338 (GRCm38) |
I6F |
probably benign |
Het |
Olfr479 |
A |
T |
7: 108,055,963 (GRCm38) |
H327L |
probably benign |
Het |
Olfr672 |
G |
A |
7: 104,996,706 (GRCm38) |
A66V |
probably damaging |
Het |
Olfr93 |
C |
T |
17: 37,151,555 (GRCm38) |
C139Y |
probably damaging |
Het |
Pde4c |
A |
G |
8: 70,750,076 (GRCm38) |
N637S |
probably benign |
Het |
Pds5b |
T |
A |
5: 150,779,275 (GRCm38) |
V824D |
possibly damaging |
Het |
Pole2 |
A |
T |
12: 69,222,386 (GRCm38) |
|
probably benign |
Het |
Ppig |
C |
T |
2: 69,735,976 (GRCm38) |
|
probably benign |
Het |
Prep |
A |
G |
10: 45,092,676 (GRCm38) |
Y90C |
probably damaging |
Het |
Proca1 |
A |
T |
11: 78,194,905 (GRCm38) |
R11S |
probably damaging |
Het |
Prph |
T |
A |
15: 99,056,991 (GRCm38) |
W313R |
probably benign |
Het |
Prune2 |
C |
T |
19: 17,123,080 (GRCm38) |
P1983S |
probably benign |
Het |
Ptbp2 |
G |
A |
3: 119,724,198 (GRCm38) |
|
probably benign |
Het |
Rsph6a |
C |
T |
7: 19,074,106 (GRCm38) |
P398L |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,829,967 (GRCm38) |
I1379V |
probably benign |
Het |
Sf3b1 |
C |
T |
1: 55,019,271 (GRCm38) |
G53E |
probably damaging |
Het |
Slc9a3 |
T |
C |
13: 74,157,784 (GRCm38) |
|
probably null |
Het |
Smarcal1 |
A |
T |
1: 72,626,473 (GRCm38) |
H710L |
probably benign |
Het |
Soat2 |
GAGAAG |
GAG |
15: 102,150,707 (GRCm38) |
|
probably benign |
Het |
Sptan1 |
T |
C |
2: 29,991,033 (GRCm38) |
V438A |
probably damaging |
Het |
Sstr4 |
T |
A |
2: 148,396,261 (GRCm38) |
V264D |
probably damaging |
Het |
Susd2 |
A |
G |
10: 75,639,911 (GRCm38) |
L418P |
probably damaging |
Het |
Synj1 |
A |
G |
16: 90,938,640 (GRCm38) |
V1475A |
probably benign |
Het |
Szt2 |
G |
A |
4: 118,376,347 (GRCm38) |
|
probably benign |
Het |
Tbc1d4 |
T |
C |
14: 101,458,063 (GRCm38) |
|
probably null |
Het |
Tesk1 |
A |
G |
4: 43,446,000 (GRCm38) |
E311G |
probably damaging |
Het |
Tmed5 |
A |
T |
5: 108,126,016 (GRCm38) |
V119E |
probably damaging |
Het |
Tmem260 |
T |
C |
14: 48,486,867 (GRCm38) |
S201P |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,671,733 (GRCm38) |
Y350C |
probably damaging |
Het |
Tpte |
T |
C |
8: 22,335,608 (GRCm38) |
|
probably benign |
Het |
Trim37 |
A |
T |
11: 87,146,968 (GRCm38) |
D161V |
probably damaging |
Het |
Trrap |
C |
A |
5: 144,814,556 (GRCm38) |
Q1640K |
probably damaging |
Het |
Tspoap1 |
T |
C |
11: 87,776,346 (GRCm38) |
|
probably benign |
Het |
Ttk |
T |
A |
9: 83,847,260 (GRCm38) |
|
probably benign |
Het |
Vmn1r172 |
A |
G |
7: 23,660,532 (GRCm38) |
S281G |
probably benign |
Het |
Vmn1r177 |
A |
G |
7: 23,865,597 (GRCm38) |
S285P |
probably damaging |
Het |
Vmn1r231 |
C |
T |
17: 20,890,399 (GRCm38) |
V85I |
probably damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,522,120 (GRCm38) |
P252Q |
possibly damaging |
Het |
Vmn2r12 |
T |
C |
5: 109,092,899 (GRCm38) |
K116R |
probably benign |
Het |
Vmn2r28 |
T |
A |
7: 5,488,514 (GRCm38) |
I245L |
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,180,651 (GRCm38) |
|
probably benign |
Het |
Xrcc3 |
A |
T |
12: 111,809,957 (GRCm38) |
H67Q |
probably benign |
Het |
Zbbx |
A |
T |
3: 75,078,495 (GRCm38) |
S417T |
possibly damaging |
Het |
Zc3h13 |
A |
G |
14: 75,323,482 (GRCm38) |
D504G |
unknown |
Het |
Zfp217 |
C |
T |
2: 170,115,462 (GRCm38) |
A539T |
probably benign |
Het |
Zyg11b |
A |
T |
4: 108,255,308 (GRCm38) |
F388I |
probably damaging |
Het |
|
Other mutations in Vmn2r118 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Vmn2r118
|
APN |
17 |
55,592,708 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00976:Vmn2r118
|
APN |
17 |
55,593,204 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01419:Vmn2r118
|
APN |
17 |
55,593,000 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01796:Vmn2r118
|
APN |
17 |
55,608,585 (GRCm38) |
missense |
probably benign |
0.30 |
IGL01799:Vmn2r118
|
APN |
17 |
55,592,990 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02002:Vmn2r118
|
APN |
17 |
55,592,619 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02075:Vmn2r118
|
APN |
17 |
55,610,517 (GRCm38) |
missense |
probably benign |
0.18 |
IGL02172:Vmn2r118
|
APN |
17 |
55,624,598 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02529:Vmn2r118
|
APN |
17 |
55,610,870 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL02712:Vmn2r118
|
APN |
17 |
55,592,655 (GRCm38) |
missense |
probably benign |
0.21 |
IGL03096:Vmn2r118
|
APN |
17 |
55,607,996 (GRCm38) |
missense |
probably damaging |
1.00 |
R0306:Vmn2r118
|
UTSW |
17 |
55,608,616 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0329:Vmn2r118
|
UTSW |
17 |
55,610,717 (GRCm38) |
missense |
probably damaging |
1.00 |
R0330:Vmn2r118
|
UTSW |
17 |
55,610,717 (GRCm38) |
missense |
probably damaging |
1.00 |
R0411:Vmn2r118
|
UTSW |
17 |
55,611,021 (GRCm38) |
splice site |
probably benign |
|
R0513:Vmn2r118
|
UTSW |
17 |
55,610,970 (GRCm38) |
nonsense |
probably null |
|
R0627:Vmn2r118
|
UTSW |
17 |
55,610,772 (GRCm38) |
missense |
probably benign |
0.01 |
R0638:Vmn2r118
|
UTSW |
17 |
55,608,466 (GRCm38) |
missense |
probably benign |
0.03 |
R1328:Vmn2r118
|
UTSW |
17 |
55,608,620 (GRCm38) |
missense |
probably benign |
0.01 |
R1366:Vmn2r118
|
UTSW |
17 |
55,593,237 (GRCm38) |
nonsense |
probably null |
|
R1465:Vmn2r118
|
UTSW |
17 |
55,610,935 (GRCm38) |
missense |
probably benign |
0.33 |
R1465:Vmn2r118
|
UTSW |
17 |
55,610,935 (GRCm38) |
missense |
probably benign |
0.33 |
R1511:Vmn2r118
|
UTSW |
17 |
55,608,496 (GRCm38) |
nonsense |
probably null |
|
R1515:Vmn2r118
|
UTSW |
17 |
55,610,643 (GRCm38) |
missense |
probably benign |
0.25 |
R1550:Vmn2r118
|
UTSW |
17 |
55,608,083 (GRCm38) |
missense |
probably damaging |
1.00 |
R1779:Vmn2r118
|
UTSW |
17 |
55,611,530 (GRCm38) |
missense |
probably benign |
0.03 |
R1834:Vmn2r118
|
UTSW |
17 |
55,592,456 (GRCm38) |
missense |
probably damaging |
1.00 |
R1840:Vmn2r118
|
UTSW |
17 |
55,610,406 (GRCm38) |
nonsense |
probably null |
|
R1854:Vmn2r118
|
UTSW |
17 |
55,611,556 (GRCm38) |
missense |
possibly damaging |
0.57 |
R1967:Vmn2r118
|
UTSW |
17 |
55,592,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R1976:Vmn2r118
|
UTSW |
17 |
55,592,925 (GRCm38) |
missense |
probably damaging |
1.00 |
R2308:Vmn2r118
|
UTSW |
17 |
55,624,650 (GRCm38) |
missense |
probably benign |
0.33 |
R3700:Vmn2r118
|
UTSW |
17 |
55,608,421 (GRCm38) |
missense |
possibly damaging |
0.68 |
R4334:Vmn2r118
|
UTSW |
17 |
55,610,347 (GRCm38) |
missense |
possibly damaging |
0.58 |
R4647:Vmn2r118
|
UTSW |
17 |
55,610,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R4709:Vmn2r118
|
UTSW |
17 |
55,610,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R4805:Vmn2r118
|
UTSW |
17 |
55,592,581 (GRCm38) |
missense |
probably damaging |
1.00 |
R4858:Vmn2r118
|
UTSW |
17 |
55,592,894 (GRCm38) |
missense |
probably damaging |
0.98 |
R5384:Vmn2r118
|
UTSW |
17 |
55,611,565 (GRCm38) |
missense |
probably benign |
0.00 |
R5385:Vmn2r118
|
UTSW |
17 |
55,611,565 (GRCm38) |
missense |
probably benign |
0.00 |
R5664:Vmn2r118
|
UTSW |
17 |
55,592,765 (GRCm38) |
missense |
possibly damaging |
0.46 |
R5740:Vmn2r118
|
UTSW |
17 |
55,593,103 (GRCm38) |
missense |
probably benign |
0.00 |
R5927:Vmn2r118
|
UTSW |
17 |
55,624,494 (GRCm38) |
missense |
probably benign |
0.04 |
R6143:Vmn2r118
|
UTSW |
17 |
55,592,871 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6513:Vmn2r118
|
UTSW |
17 |
55,608,093 (GRCm38) |
missense |
probably damaging |
1.00 |
R6573:Vmn2r118
|
UTSW |
17 |
55,592,996 (GRCm38) |
missense |
probably damaging |
1.00 |
R6760:Vmn2r118
|
UTSW |
17 |
55,592,714 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6794:Vmn2r118
|
UTSW |
17 |
55,592,348 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6929:Vmn2r118
|
UTSW |
17 |
55,610,440 (GRCm38) |
missense |
probably benign |
0.01 |
R7201:Vmn2r118
|
UTSW |
17 |
55,608,496 (GRCm38) |
nonsense |
probably null |
|
R7539:Vmn2r118
|
UTSW |
17 |
55,592,853 (GRCm38) |
missense |
probably damaging |
0.98 |
R7836:Vmn2r118
|
UTSW |
17 |
55,593,242 (GRCm38) |
missense |
probably damaging |
0.99 |
R8179:Vmn2r118
|
UTSW |
17 |
55,608,484 (GRCm38) |
missense |
probably benign |
0.36 |
R8248:Vmn2r118
|
UTSW |
17 |
55,610,936 (GRCm38) |
missense |
probably benign |
0.18 |
R8347:Vmn2r118
|
UTSW |
17 |
55,610,423 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8415:Vmn2r118
|
UTSW |
17 |
55,608,057 (GRCm38) |
missense |
probably benign |
0.08 |
R8428:Vmn2r118
|
UTSW |
17 |
55,608,642 (GRCm38) |
missense |
probably benign |
0.33 |
R8917:Vmn2r118
|
UTSW |
17 |
55,610,216 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8993:Vmn2r118
|
UTSW |
17 |
55,610,835 (GRCm38) |
missense |
possibly damaging |
0.72 |
R9038:Vmn2r118
|
UTSW |
17 |
55,611,649 (GRCm38) |
missense |
probably damaging |
1.00 |
R9155:Vmn2r118
|
UTSW |
17 |
55,610,207 (GRCm38) |
missense |
probably null |
0.83 |
R9603:Vmn2r118
|
UTSW |
17 |
55,592,837 (GRCm38) |
missense |
probably damaging |
1.00 |
R9742:Vmn2r118
|
UTSW |
17 |
55,611,009 (GRCm38) |
missense |
probably damaging |
0.98 |
R9749:Vmn2r118
|
UTSW |
17 |
55,608,415 (GRCm38) |
critical splice donor site |
probably null |
|
R9792:Vmn2r118
|
UTSW |
17 |
55,592,496 (GRCm38) |
missense |
probably damaging |
0.99 |
R9793:Vmn2r118
|
UTSW |
17 |
55,592,496 (GRCm38) |
missense |
probably damaging |
0.99 |
R9795:Vmn2r118
|
UTSW |
17 |
55,592,496 (GRCm38) |
missense |
probably damaging |
0.99 |
X0022:Vmn2r118
|
UTSW |
17 |
55,593,218 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r118
|
UTSW |
17 |
55,610,655 (GRCm38) |
nonsense |
probably null |
|
|