Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519F16Rik |
A |
G |
X: 103,183,262 (GRCm38) |
|
probably benign |
Het |
Aldob |
C |
A |
4: 49,541,220 (GRCm38) |
V151L |
probably damaging |
Het |
Cacna1i |
G |
A |
15: 80,355,645 (GRCm38) |
M298I |
probably benign |
Het |
Capn3 |
A |
G |
2: 120,491,901 (GRCm38) |
N414S |
possibly damaging |
Het |
Ccdc186 |
G |
A |
19: 56,797,500 (GRCm38) |
T701M |
probably damaging |
Het |
Ccdc190 |
A |
T |
1: 169,933,740 (GRCm38) |
H137L |
probably benign |
Het |
Clhc1 |
G |
A |
11: 29,561,389 (GRCm38) |
D278N |
probably benign |
Het |
Cntnap3 |
T |
C |
13: 64,794,352 (GRCm38) |
Y188C |
probably damaging |
Het |
Dnah1 |
A |
C |
14: 31,278,138 (GRCm38) |
V2466G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,851,710 (GRCm38) |
T4457A |
probably damaging |
Het |
Gm13078 |
T |
A |
4: 143,727,015 (GRCm38) |
M231K |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,349,106 (GRCm38) |
Q3388R |
probably benign |
Het |
Hecw1 |
T |
A |
13: 14,318,972 (GRCm38) |
D316V |
probably damaging |
Het |
Il1rap |
T |
C |
16: 26,698,839 (GRCm38) |
V263A |
probably benign |
Het |
Il6 |
G |
A |
5: 30,014,841 (GRCm38) |
G72S |
probably benign |
Het |
Katnal2 |
T |
C |
18: 77,017,493 (GRCm38) |
Y86C |
probably damaging |
Het |
Kdm7a |
G |
T |
6: 39,144,398 (GRCm38) |
S874R |
possibly damaging |
Het |
Mybpc2 |
T |
C |
7: 44,522,317 (GRCm38) |
|
probably null |
Het |
Nphs1 |
T |
G |
7: 30,460,685 (GRCm38) |
S130A |
possibly damaging |
Het |
Ntrk3 |
C |
T |
7: 78,450,953 (GRCm38) |
V444I |
probably benign |
Het |
Numbl |
T |
C |
7: 27,268,810 (GRCm38) |
V144A |
possibly damaging |
Het |
Olfr952 |
T |
A |
9: 39,426,657 (GRCm38) |
Y138F |
probably benign |
Het |
P2rx1 |
T |
C |
11: 73,013,000 (GRCm38) |
|
probably null |
Het |
Pcdhb3 |
G |
A |
18: 37,302,948 (GRCm38) |
V656I |
probably benign |
Het |
Pole |
A |
G |
5: 110,323,572 (GRCm38) |
Y1394C |
probably benign |
Het |
Rbm47 |
A |
G |
5: 66,026,738 (GRCm38) |
V174A |
possibly damaging |
Het |
Rhox4f |
T |
C |
X: 37,604,395 (GRCm38) |
|
probably benign |
Het |
Serpina12 |
T |
C |
12: 104,032,528 (GRCm38) |
Y317C |
probably damaging |
Het |
Slc12a5 |
T |
A |
2: 164,979,304 (GRCm38) |
I236N |
probably damaging |
Het |
Slc4a4 |
G |
A |
5: 88,954,798 (GRCm38) |
G32R |
probably damaging |
Het |
Slco1a4 |
T |
C |
6: 141,807,182 (GRCm38) |
|
probably null |
Het |
Sorcs3 |
A |
T |
19: 48,767,103 (GRCm38) |
N894I |
probably damaging |
Het |
Stk38l |
A |
G |
6: 146,775,402 (GRCm38) |
E393G |
probably benign |
Het |
Synpo |
A |
G |
18: 60,603,419 (GRCm38) |
I485T |
possibly damaging |
Het |
Tenm3 |
T |
A |
8: 48,256,841 (GRCm38) |
M1687L |
probably benign |
Het |
Ttc39c |
T |
C |
18: 12,684,895 (GRCm38) |
|
probably benign |
Het |
Unc13d |
T |
C |
11: 116,070,467 (GRCm38) |
E378G |
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 |
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 |
R0396:Vmn2r118
|
UTSW |
17 |
55,608,643 (GRCm38) |
missense |
probably benign |
0.00 |
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 |
|
|