Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,384,571 (GRCm39) |
T465A |
probably benign |
Het |
A430110L20Rik |
T |
G |
1: 181,054,987 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl4fm1 |
A |
T |
4: 144,248,990 (GRCm39) |
H119L |
probably damaging |
Het |
Abcb10 |
C |
T |
8: 124,689,746 (GRCm39) |
R439Q |
probably benign |
Het |
Abcb8 |
T |
C |
5: 24,605,788 (GRCm39) |
S199P |
probably damaging |
Het |
Adam8 |
C |
A |
7: 139,566,355 (GRCm39) |
C556F |
probably damaging |
Het |
Akap11 |
T |
C |
14: 78,750,819 (GRCm39) |
T523A |
probably benign |
Het |
Aldh3b1 |
T |
C |
19: 3,968,999 (GRCm39) |
|
probably benign |
Het |
Arhgap30 |
T |
A |
1: 171,231,372 (GRCm39) |
W230R |
possibly damaging |
Het |
Atp8b4 |
A |
G |
2: 126,301,614 (GRCm39) |
I82T |
possibly damaging |
Het |
Bptf |
A |
T |
11: 106,963,645 (GRCm39) |
L1850I |
probably damaging |
Het |
C4b |
C |
A |
17: 34,952,135 (GRCm39) |
V1237L |
probably benign |
Het |
Calu |
C |
A |
6: 29,374,550 (GRCm39) |
|
probably benign |
Het |
Cit |
C |
A |
5: 116,117,504 (GRCm39) |
L1227M |
possibly damaging |
Het |
Col4a1 |
C |
T |
8: 11,292,782 (GRCm39) |
|
probably null |
Het |
Cp |
T |
C |
3: 20,029,012 (GRCm39) |
|
probably benign |
Het |
Cpd |
T |
C |
11: 76,731,273 (GRCm39) |
D311G |
possibly damaging |
Het |
Ctc1 |
T |
A |
11: 68,924,363 (GRCm39) |
S972T |
probably damaging |
Het |
Dnah17 |
A |
G |
11: 117,943,500 (GRCm39) |
F3201L |
possibly damaging |
Het |
Dop1b |
C |
A |
16: 93,607,035 (GRCm39) |
R2113S |
probably benign |
Het |
Dym |
T |
A |
18: 75,332,333 (GRCm39) |
D520E |
probably damaging |
Het |
Eif5a |
G |
T |
11: 69,808,305 (GRCm39) |
T64K |
probably benign |
Het |
Flt3 |
A |
T |
5: 147,306,389 (GRCm39) |
|
probably benign |
Het |
Ints6 |
A |
T |
14: 62,945,084 (GRCm39) |
Y415* |
probably null |
Het |
Itga1 |
A |
G |
13: 115,114,130 (GRCm39) |
|
probably benign |
Het |
Itgae |
A |
G |
11: 73,021,825 (GRCm39) |
H902R |
possibly damaging |
Het |
Itprid1 |
T |
C |
6: 55,953,432 (GRCm39) |
I916T |
probably damaging |
Het |
Kdm5a |
T |
C |
6: 120,366,581 (GRCm39) |
I406T |
probably benign |
Het |
Lmx1a |
C |
T |
1: 167,618,973 (GRCm39) |
Q111* |
probably null |
Het |
Lrrc25 |
T |
C |
8: 71,070,896 (GRCm39) |
Y226H |
probably benign |
Het |
Mcam |
T |
A |
9: 44,051,483 (GRCm39) |
N447K |
possibly damaging |
Het |
Mcm10 |
A |
T |
2: 5,008,897 (GRCm39) |
D357E |
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,089,251 (GRCm39) |
T769A |
probably benign |
Het |
Ofcc1 |
G |
C |
13: 40,360,172 (GRCm39) |
Q286E |
probably benign |
Het |
Or56b35 |
A |
T |
7: 104,963,861 (GRCm39) |
I217F |
probably benign |
Het |
Parp3 |
T |
A |
9: 106,353,011 (GRCm39) |
N55I |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,825,953 (GRCm39) |
|
probably null |
Het |
Pilrb1 |
G |
A |
5: 137,853,260 (GRCm39) |
T181I |
probably benign |
Het |
Ppm1n |
A |
G |
7: 19,012,281 (GRCm39) |
V317A |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 142,905,921 (GRCm39) |
F55L |
probably damaging |
Het |
Psd2 |
C |
T |
18: 36,112,697 (GRCm39) |
R131C |
probably damaging |
Het |
Ralgps1 |
A |
T |
2: 33,031,027 (GRCm39) |
C570S |
possibly damaging |
Het |
Scaf8 |
T |
C |
17: 3,228,530 (GRCm39) |
S443P |
unknown |
Het |
Setd5 |
A |
G |
6: 113,088,442 (GRCm39) |
K190R |
probably damaging |
Het |
Spsb4 |
T |
A |
9: 96,878,161 (GRCm39) |
H54L |
probably damaging |
Het |
St7l |
T |
A |
3: 104,778,229 (GRCm39) |
L122* |
probably null |
Het |
Stom |
C |
T |
2: 35,211,646 (GRCm39) |
R125H |
probably damaging |
Het |
Tigd4 |
T |
A |
3: 84,502,481 (GRCm39) |
V466E |
probably benign |
Het |
Tmc3 |
A |
C |
7: 83,257,027 (GRCm39) |
|
probably benign |
Het |
Vcl |
C |
T |
14: 21,035,692 (GRCm39) |
|
probably benign |
Het |
Vmn1r168 |
G |
A |
7: 23,240,767 (GRCm39) |
R208H |
probably benign |
Het |
Vmn2r75 |
C |
A |
7: 85,814,288 (GRCm39) |
V402L |
probably benign |
Het |
Vps13b |
A |
T |
15: 35,674,974 (GRCm39) |
H1698L |
probably damaging |
Het |
Wnt16 |
T |
G |
6: 22,297,992 (GRCm39) |
V286G |
possibly damaging |
Het |
Xirp1 |
C |
A |
9: 119,845,533 (GRCm39) |
V1117L |
probably benign |
Het |
Zfp788 |
C |
T |
7: 41,298,971 (GRCm39) |
H536Y |
probably damaging |
Het |
|
Other mutations in Or1e23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00235:Or1e23
|
APN |
11 |
73,407,236 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL00896:Or1e23
|
APN |
11 |
73,407,167 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Or1e23
|
APN |
11 |
73,407,452 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01734:Or1e23
|
APN |
11 |
73,407,462 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02267:Or1e23
|
APN |
11 |
73,407,375 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02681:Or1e23
|
APN |
11 |
73,407,356 (GRCm39) |
missense |
probably benign |
|
IGL03165:Or1e23
|
APN |
11 |
73,407,710 (GRCm39) |
nonsense |
probably null |
|
BB009:Or1e23
|
UTSW |
11 |
73,407,983 (GRCm39) |
missense |
probably damaging |
1.00 |
BB019:Or1e23
|
UTSW |
11 |
73,407,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Or1e23
|
UTSW |
11 |
73,407,941 (GRCm39) |
missense |
probably benign |
0.02 |
R0633:Or1e23
|
UTSW |
11 |
73,407,753 (GRCm39) |
missense |
probably benign |
0.23 |
R0638:Or1e23
|
UTSW |
11 |
73,407,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Or1e23
|
UTSW |
11 |
73,407,670 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1630:Or1e23
|
UTSW |
11 |
73,407,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Or1e23
|
UTSW |
11 |
73,407,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4001:Or1e23
|
UTSW |
11 |
73,407,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Or1e23
|
UTSW |
11 |
73,407,998 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5707:Or1e23
|
UTSW |
11 |
73,407,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5911:Or1e23
|
UTSW |
11 |
73,407,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R6225:Or1e23
|
UTSW |
11 |
73,407,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R6251:Or1e23
|
UTSW |
11 |
73,407,534 (GRCm39) |
missense |
probably benign |
0.00 |
R6332:Or1e23
|
UTSW |
11 |
73,408,001 (GRCm39) |
missense |
probably benign |
0.00 |
R7013:Or1e23
|
UTSW |
11 |
73,407,247 (GRCm39) |
nonsense |
probably null |
|
R7196:Or1e23
|
UTSW |
11 |
73,407,957 (GRCm39) |
missense |
probably benign |
|
R7443:Or1e23
|
UTSW |
11 |
73,407,674 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7932:Or1e23
|
UTSW |
11 |
73,407,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8201:Or1e23
|
UTSW |
11 |
73,407,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8257:Or1e23
|
UTSW |
11 |
73,407,203 (GRCm39) |
missense |
probably benign |
0.28 |
R8547:Or1e23
|
UTSW |
11 |
73,407,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9219:Or1e23
|
UTSW |
11 |
73,407,801 (GRCm39) |
missense |
probably damaging |
0.98 |
R9526:Or1e23
|
UTSW |
11 |
73,407,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9638:Or1e23
|
UTSW |
11 |
73,407,875 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Or1e23
|
UTSW |
11 |
73,407,861 (GRCm39) |
missense |
probably damaging |
1.00 |
|