Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012H06Rik |
C |
T |
17: 15,163,769 (GRCm39) |
|
probably benign |
Het |
9330182O14Rik |
C |
T |
15: 40,005,500 (GRCm39) |
|
probably benign |
Het |
Adamts19 |
C |
A |
18: 59,101,834 (GRCm39) |
P635T |
probably damaging |
Het |
Adgrf1 |
T |
C |
17: 43,625,362 (GRCm39) |
W857R |
possibly damaging |
Het |
Ak9 |
T |
G |
10: 41,298,968 (GRCm39) |
Y1556* |
probably null |
Het |
Ang2 |
T |
C |
14: 51,433,326 (GRCm39) |
I19V |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,496,253 (GRCm39) |
T834S |
probably damaging |
Het |
As3mt |
A |
T |
19: 46,708,420 (GRCm39) |
I236F |
probably benign |
Het |
Asns |
A |
T |
6: 7,689,268 (GRCm39) |
I78N |
probably damaging |
Het |
Bet1 |
G |
A |
6: 4,082,471 (GRCm39) |
T44M |
probably damaging |
Het |
Cabyr |
T |
C |
18: 12,884,407 (GRCm39) |
V298A |
possibly damaging |
Het |
Cacna1c |
A |
G |
6: 118,589,598 (GRCm39) |
V1601A |
|
Het |
Ccni |
A |
T |
5: 93,350,201 (GRCm39) |
M26K |
probably damaging |
Het |
Cdhr2 |
T |
C |
13: 54,867,679 (GRCm39) |
I503T |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,792,851 (GRCm39) |
K1754R |
unknown |
Het |
Cfap69 |
A |
G |
5: 5,676,041 (GRCm39) |
V218A |
possibly damaging |
Het |
Clcn3 |
A |
G |
8: 61,372,518 (GRCm39) |
L741P |
probably damaging |
Het |
Cntnap1 |
T |
C |
11: 101,068,828 (GRCm39) |
F124L |
possibly damaging |
Het |
Col20a1 |
G |
A |
2: 180,641,577 (GRCm39) |
G673D |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,487,628 (GRCm39) |
I977V |
probably benign |
Het |
Cyp3a59 |
A |
T |
5: 146,031,190 (GRCm39) |
I118F |
probably damaging |
Het |
Dgcr8 |
A |
T |
16: 18,098,283 (GRCm39) |
D369E |
probably benign |
Het |
Dhtkd1 |
T |
C |
2: 5,919,651 (GRCm39) |
T577A |
probably benign |
Het |
Dock2 |
A |
T |
11: 34,204,417 (GRCm39) |
M1375K |
probably benign |
Het |
Fa2h |
G |
A |
8: 112,074,659 (GRCm39) |
H315Y |
probably damaging |
Het |
Foxd2 |
G |
A |
4: 114,765,684 (GRCm39) |
P112L |
unknown |
Het |
Gin1 |
A |
G |
1: 97,712,897 (GRCm39) |
I317V |
probably benign |
Het |
Gpr180 |
G |
A |
14: 118,391,302 (GRCm39) |
G235R |
probably damaging |
Het |
H2-T3 |
T |
A |
17: 36,500,744 (GRCm39) |
Y33F |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Il12rb1 |
G |
A |
8: 71,263,874 (GRCm39) |
W145* |
probably null |
Het |
Il6ra |
A |
G |
3: 89,785,219 (GRCm39) |
V330A |
probably benign |
Het |
Impdh2 |
T |
C |
9: 108,438,847 (GRCm39) |
S67P |
possibly damaging |
Het |
Ltbp3 |
T |
A |
19: 5,792,521 (GRCm39) |
S85T |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,956,458 (GRCm39) |
|
probably null |
Het |
Mettl4 |
T |
A |
17: 95,034,806 (GRCm39) |
I430F |
probably damaging |
Het |
Mmd |
T |
A |
11: 90,167,579 (GRCm39) |
F203I |
probably damaging |
Het |
Nlgn1 |
T |
C |
3: 25,494,035 (GRCm39) |
T305A |
possibly damaging |
Het |
Ntn1 |
A |
G |
11: 68,168,356 (GRCm39) |
V367A |
probably damaging |
Het |
Or5b107 |
G |
A |
19: 13,142,888 (GRCm39) |
C170Y |
possibly damaging |
Het |
Pcdh12 |
T |
C |
18: 38,415,022 (GRCm39) |
H701R |
possibly damaging |
Het |
Pcgf3 |
G |
A |
5: 108,621,773 (GRCm39) |
|
probably null |
Het |
Pik3c2g |
G |
A |
6: 139,913,517 (GRCm39) |
V972M |
unknown |
Het |
Pink1 |
A |
G |
4: 138,041,323 (GRCm39) |
C563R |
possibly damaging |
Het |
Prol1 |
A |
T |
5: 88,466,426 (GRCm39) |
N3I |
probably benign |
Het |
Ptpro |
T |
G |
6: 137,363,288 (GRCm39) |
I474S |
probably damaging |
Het |
Rabgef1 |
A |
G |
5: 130,241,781 (GRCm39) |
E395G |
probably benign |
Het |
Rpgrip1l |
G |
T |
8: 91,987,391 (GRCm39) |
H889N |
possibly damaging |
Het |
Sapcd2 |
T |
A |
2: 25,262,925 (GRCm39) |
C161* |
probably null |
Het |
Sbsn |
GAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCA |
GAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCA |
7: 30,452,391 (GRCm39) |
|
probably benign |
Het |
Spen |
A |
G |
4: 141,196,275 (GRCm39) |
L3625P |
probably damaging |
Het |
Stil |
T |
C |
4: 114,878,701 (GRCm39) |
I379T |
probably benign |
Het |
Stim1 |
A |
G |
7: 102,078,014 (GRCm39) |
D172G |
|
Het |
Timm50 |
A |
G |
7: 28,010,350 (GRCm39) |
L68P |
probably damaging |
Het |
Tlr9 |
C |
T |
9: 106,100,723 (GRCm39) |
R5* |
probably null |
Het |
Top1mt |
A |
T |
15: 75,547,874 (GRCm39) |
Y71N |
probably damaging |
Het |
Trpv4 |
A |
G |
5: 114,771,285 (GRCm39) |
Y415H |
possibly damaging |
Het |
Try10 |
C |
T |
6: 41,331,041 (GRCm39) |
|
probably benign |
Het |
Uhrf2 |
A |
G |
19: 30,063,780 (GRCm39) |
E581G |
probably damaging |
Het |
Usp17lb |
G |
A |
7: 104,490,495 (GRCm39) |
T144I |
possibly damaging |
Het |
Vmn1r64 |
T |
C |
7: 5,886,859 (GRCm39) |
N228S |
probably benign |
Het |
Vwa1 |
G |
A |
4: 155,857,336 (GRCm39) |
P154L |
probably damaging |
Het |
|
Other mutations in Or2w1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01689:Or2w1b
|
APN |
13 |
21,300,243 (GRCm39) |
missense |
probably damaging |
0.97 |
R0631:Or2w1b
|
UTSW |
13 |
21,300,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R0960:Or2w1b
|
UTSW |
13 |
21,300,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1499:Or2w1b
|
UTSW |
13 |
21,300,303 (GRCm39) |
missense |
probably benign |
0.32 |
R1549:Or2w1b
|
UTSW |
13 |
21,300,288 (GRCm39) |
missense |
probably benign |
0.01 |
R1698:Or2w1b
|
UTSW |
13 |
21,300,735 (GRCm39) |
missense |
probably benign |
0.11 |
R1711:Or2w1b
|
UTSW |
13 |
21,300,476 (GRCm39) |
missense |
probably benign |
0.01 |
R2404:Or2w1b
|
UTSW |
13 |
21,300,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R2471:Or2w1b
|
UTSW |
13 |
21,300,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3844:Or2w1b
|
UTSW |
13 |
21,300,233 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3977:Or2w1b
|
UTSW |
13 |
21,300,031 (GRCm39) |
missense |
probably benign |
0.03 |
R3979:Or2w1b
|
UTSW |
13 |
21,300,031 (GRCm39) |
missense |
probably benign |
0.03 |
R4804:Or2w1b
|
UTSW |
13 |
21,300,175 (GRCm39) |
nonsense |
probably null |
|
R4914:Or2w1b
|
UTSW |
13 |
21,300,567 (GRCm39) |
missense |
probably benign |
0.12 |
R5210:Or2w1b
|
UTSW |
13 |
21,300,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R5359:Or2w1b
|
UTSW |
13 |
21,300,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Or2w1b
|
UTSW |
13 |
21,300,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Or2w1b
|
UTSW |
13 |
21,300,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Or2w1b
|
UTSW |
13 |
21,300,227 (GRCm39) |
missense |
probably benign |
0.02 |
R7396:Or2w1b
|
UTSW |
13 |
21,300,477 (GRCm39) |
missense |
probably benign |
0.02 |
R7476:Or2w1b
|
UTSW |
13 |
21,300,191 (GRCm39) |
missense |
probably benign |
0.04 |
R7612:Or2w1b
|
UTSW |
13 |
21,300,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R8257:Or2w1b
|
UTSW |
13 |
21,300,543 (GRCm39) |
missense |
probably benign |
0.11 |
R9388:Or2w1b
|
UTSW |
13 |
21,300,774 (GRCm39) |
missense |
probably damaging |
0.96 |
V8831:Or2w1b
|
UTSW |
13 |
21,300,173 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Or2w1b
|
UTSW |
13 |
21,300,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|