Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox8 |
G |
T |
11: 69,087,864 (GRCm39) |
Q147K |
probably benign |
Het |
Ankib1 |
T |
A |
5: 3,784,152 (GRCm39) |
M275L |
possibly damaging |
Het |
Asb2 |
G |
A |
12: 103,287,922 (GRCm39) |
P546S |
possibly damaging |
Het |
B9d1 |
T |
C |
11: 61,398,449 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,557,257 (GRCm39) |
D1957G |
possibly damaging |
Het |
Cryzl2 |
T |
C |
1: 157,299,970 (GRCm39) |
V44A |
possibly damaging |
Het |
Fbxw19 |
A |
C |
9: 109,312,347 (GRCm39) |
|
probably benign |
Het |
Gabrb3 |
T |
C |
7: 57,466,163 (GRCm39) |
F326L |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm11168 |
T |
C |
9: 3,005,204 (GRCm39) |
C16R |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Gm7808 |
T |
A |
9: 19,839,542 (GRCm39) |
|
probably benign |
Het |
Gpam |
T |
C |
19: 55,071,806 (GRCm39) |
I312V |
probably benign |
Het |
H2-M10.5 |
A |
G |
17: 37,084,708 (GRCm39) |
Y144C |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,952,424 (GRCm39) |
S247P |
possibly damaging |
Het |
Hs3st4 |
T |
G |
7: 123,996,536 (GRCm39) |
C401G |
probably damaging |
Het |
Klhl2 |
A |
G |
8: 65,212,858 (GRCm39) |
V227A |
probably damaging |
Het |
Lct |
T |
C |
1: 128,222,003 (GRCm39) |
N1512S |
probably damaging |
Het |
Lipm |
T |
A |
19: 34,093,911 (GRCm39) |
L276Q |
possibly damaging |
Het |
Lmf2 |
T |
A |
15: 89,236,621 (GRCm39) |
H515L |
probably damaging |
Het |
Mccc1 |
G |
A |
3: 36,030,041 (GRCm39) |
S423L |
probably damaging |
Het |
Mettl21e |
G |
A |
1: 44,250,193 (GRCm39) |
S71L |
probably null |
Het |
Muc16 |
T |
A |
9: 18,406,839 (GRCm39) |
H251L |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,059,852 (GRCm39) |
|
probably benign |
Het |
Ntf5 |
T |
C |
7: 45,065,450 (GRCm39) |
I194T |
probably damaging |
Het |
Or10ag58 |
T |
C |
2: 87,265,314 (GRCm39) |
I161T |
possibly damaging |
Het |
Or1o4 |
A |
G |
17: 37,590,891 (GRCm39) |
V140A |
possibly damaging |
Het |
Or4x11 |
T |
C |
2: 89,867,478 (GRCm39) |
S72P |
probably damaging |
Het |
Or9m1 |
A |
T |
2: 87,733,675 (GRCm39) |
L115* |
probably null |
Het |
Pigv |
T |
C |
4: 133,392,428 (GRCm39) |
I247M |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,383,356 (GRCm39) |
N392D |
probably benign |
Het |
Postn |
A |
G |
3: 54,290,901 (GRCm39) |
|
probably null |
Het |
Prl2c5 |
G |
A |
13: 13,360,402 (GRCm39) |
S23N |
probably benign |
Het |
Prpf40b |
T |
C |
15: 99,204,413 (GRCm39) |
C220R |
possibly damaging |
Het |
Pzp |
A |
G |
6: 128,472,261 (GRCm39) |
S843P |
probably damaging |
Het |
Rpl23 |
C |
A |
11: 97,669,177 (GRCm39) |
R85L |
probably benign |
Het |
Shcbp1 |
A |
G |
8: 4,799,721 (GRCm39) |
S252P |
probably damaging |
Het |
Slc26a7 |
C |
T |
4: 14,519,388 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,063,571 (GRCm39) |
E2285G |
probably damaging |
Het |
Telo2 |
G |
T |
17: 25,320,332 (GRCm39) |
T784K |
probably benign |
Het |
Tnfrsf19 |
C |
T |
14: 61,234,093 (GRCm39) |
V136M |
probably damaging |
Het |
Trpm5 |
T |
A |
7: 142,628,234 (GRCm39) |
I22F |
probably damaging |
Het |
Trpv6 |
G |
T |
6: 41,603,801 (GRCm39) |
|
probably benign |
Het |
Vmn1r173 |
T |
G |
7: 23,401,877 (GRCm39) |
H37Q |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Xpo6 |
T |
A |
7: 125,773,365 (GRCm39) |
H20L |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,010,613 (GRCm39) |
Y860H |
probably damaging |
Het |
|
Other mutations in Or2w6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02025:Or2w6
|
APN |
13 |
21,843,433 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02275:Or2w6
|
APN |
13 |
21,843,170 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02831:Or2w6
|
APN |
13 |
21,843,074 (GRCm39) |
missense |
probably benign |
|
IGL02932:Or2w6
|
APN |
13 |
21,843,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Or2w6
|
UTSW |
13 |
21,842,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Or2w6
|
UTSW |
13 |
21,843,316 (GRCm39) |
missense |
probably damaging |
0.96 |
R1669:Or2w6
|
UTSW |
13 |
21,843,456 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2006:Or2w6
|
UTSW |
13 |
21,842,642 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2292:Or2w6
|
UTSW |
13 |
21,843,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Or2w6
|
UTSW |
13 |
21,843,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R4919:Or2w6
|
UTSW |
13 |
21,842,794 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5339:Or2w6
|
UTSW |
13 |
21,843,404 (GRCm39) |
missense |
probably benign |
0.37 |
R5815:Or2w6
|
UTSW |
13 |
21,842,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Or2w6
|
UTSW |
13 |
21,843,244 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8273:Or2w6
|
UTSW |
13 |
21,843,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Or2w6
|
UTSW |
13 |
21,843,302 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8913:Or2w6
|
UTSW |
13 |
21,843,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R9010:Or2w6
|
UTSW |
13 |
21,842,681 (GRCm39) |
missense |
probably damaging |
0.99 |
|