Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
G |
A |
4: 86,117,582 (GRCm39) |
G182S |
probably damaging |
Het |
Akr1b7 |
A |
T |
6: 34,392,385 (GRCm39) |
N66I |
probably benign |
Het |
Arrdc3 |
T |
A |
13: 81,031,893 (GRCm39) |
I42N |
probably damaging |
Het |
Atp6v0d2 |
G |
T |
4: 19,878,325 (GRCm39) |
A316E |
probably damaging |
Het |
Atp8a2 |
A |
G |
14: 60,094,497 (GRCm39) |
V847A |
possibly damaging |
Het |
Ccdc171 |
A |
G |
4: 83,713,479 (GRCm39) |
N1173D |
possibly damaging |
Het |
Crb2 |
A |
C |
2: 37,676,475 (GRCm39) |
D152A |
probably damaging |
Het |
Ecm1 |
T |
C |
3: 95,641,557 (GRCm39) |
E559G |
probably damaging |
Het |
Ephb1 |
A |
G |
9: 102,071,971 (GRCm39) |
|
probably null |
Het |
Fndc11 |
C |
A |
2: 180,863,884 (GRCm39) |
R230S |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,911,037 (GRCm39) |
|
probably null |
Het |
Fyco1 |
G |
A |
9: 123,658,896 (GRCm39) |
Q427* |
probably null |
Het |
Gm17541 |
A |
G |
12: 4,739,619 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
C |
T |
11: 48,779,330 (GRCm39) |
V809M |
probably damaging |
Het |
Gm7293 |
A |
G |
9: 51,534,043 (GRCm39) |
|
noncoding transcript |
Het |
Ift52 |
T |
C |
2: 162,865,289 (GRCm39) |
S47P |
probably benign |
Het |
Iqcf6 |
A |
G |
9: 106,504,510 (GRCm39) |
D58G |
probably benign |
Het |
Itm2b |
T |
C |
14: 73,600,488 (GRCm39) |
|
probably benign |
Het |
Jakmip1 |
T |
C |
5: 37,278,331 (GRCm39) |
I536T |
probably damaging |
Het |
Kcnh1 |
T |
G |
1: 191,873,323 (GRCm39) |
M3R |
possibly damaging |
Het |
Kcnh5 |
G |
T |
12: 74,944,322 (GRCm39) |
P976T |
probably damaging |
Het |
Layn |
G |
A |
9: 50,968,591 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
T |
A |
11: 103,347,317 (GRCm39) |
Q3126L |
probably damaging |
Het |
Meioc |
A |
T |
11: 102,565,092 (GRCm39) |
D180V |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,401,954 (GRCm39) |
C3066S |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,311,418 (GRCm39) |
|
probably null |
Het |
Negr1 |
T |
C |
3: 156,721,810 (GRCm39) |
|
probably benign |
Het |
Nek1 |
T |
A |
8: 61,557,226 (GRCm39) |
N940K |
probably benign |
Het |
Nfkbib |
A |
T |
7: 28,465,667 (GRCm39) |
|
probably null |
Het |
Nol4 |
T |
A |
18: 23,054,975 (GRCm39) |
T152S |
probably damaging |
Het |
Oas3 |
G |
T |
5: 120,907,300 (GRCm39) |
R446S |
probably benign |
Het |
Oosp3 |
C |
T |
19: 11,676,784 (GRCm39) |
L48F |
probably damaging |
Het |
Or2r3 |
A |
G |
6: 42,449,025 (GRCm39) |
V29A |
probably benign |
Het |
Pik3ap1 |
C |
A |
19: 41,291,032 (GRCm39) |
W500L |
probably benign |
Het |
Ppih |
A |
G |
4: 119,168,779 (GRCm39) |
|
probably benign |
Het |
Ro60 |
G |
T |
1: 143,636,084 (GRCm39) |
|
probably benign |
Het |
Slc7a15 |
T |
C |
12: 8,585,508 (GRCm39) |
|
probably null |
Het |
Srl |
T |
C |
16: 4,315,150 (GRCm39) |
E164G |
probably benign |
Het |
Tbx10 |
C |
A |
19: 4,048,186 (GRCm39) |
T237K |
probably damaging |
Het |
Vwa5b2 |
T |
C |
16: 20,415,843 (GRCm39) |
V392A |
probably damaging |
Het |
Wfdc5 |
A |
T |
2: 164,024,483 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,342,306 (GRCm39) |
F1516L |
possibly damaging |
Het |
Znfx1 |
A |
G |
2: 166,897,683 (GRCm39) |
C414R |
probably damaging |
Het |
|
Other mutations in Or2w25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Or2w25
|
APN |
11 |
59,504,147 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01835:Or2w25
|
APN |
11 |
59,504,165 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03195:Or2w25
|
APN |
11 |
59,504,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Or2w25
|
UTSW |
11 |
59,504,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R0831:Or2w25
|
UTSW |
11 |
59,504,480 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1924:Or2w25
|
UTSW |
11 |
59,503,949 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2184:Or2w25
|
UTSW |
11 |
59,503,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Or2w25
|
UTSW |
11 |
59,504,712 (GRCm39) |
missense |
probably benign |
|
R6986:Or2w25
|
UTSW |
11 |
59,504,924 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7405:Or2w25
|
UTSW |
11 |
59,504,899 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7755:Or2w25
|
UTSW |
11 |
59,504,467 (GRCm39) |
missense |
probably damaging |
0.97 |
R7851:Or2w25
|
UTSW |
11 |
59,504,789 (GRCm39) |
missense |
probably benign |
0.33 |
R9437:Or2w25
|
UTSW |
11 |
59,504,195 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9545:Or2w25
|
UTSW |
11 |
59,504,275 (GRCm39) |
missense |
probably benign |
0.27 |
R9562:Or2w25
|
UTSW |
11 |
59,504,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Or2w25
|
UTSW |
11 |
59,504,339 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or2w25
|
UTSW |
11 |
59,504,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|