Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,773,874 (GRCm39) |
K1021R |
probably damaging |
Het |
2610528J11Rik |
G |
A |
4: 118,386,762 (GRCm39) |
V36M |
probably damaging |
Het |
4930402F06Rik |
T |
A |
2: 35,265,795 (GRCm39) |
R292* |
probably null |
Het |
Abcb4 |
T |
C |
5: 8,959,194 (GRCm39) |
F207S |
probably damaging |
Het |
Afap1l2 |
G |
T |
19: 56,916,872 (GRCm39) |
|
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,687,385 (GRCm39) |
H203L |
probably benign |
Het |
Cfi |
A |
C |
3: 129,642,416 (GRCm39) |
H90P |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,520,775 (GRCm39) |
S371T |
possibly damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,288,794 (GRCm39) |
M229I |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,245,897 (GRCm39) |
|
probably benign |
Het |
Dnttip2 |
G |
T |
3: 122,069,452 (GRCm39) |
M222I |
probably benign |
Het |
Dync1li2 |
A |
T |
8: 105,154,757 (GRCm39) |
Y284N |
probably benign |
Het |
Ebf1 |
T |
C |
11: 44,882,282 (GRCm39) |
Y413H |
probably benign |
Het |
Exog |
A |
G |
9: 119,281,319 (GRCm39) |
T186A |
possibly damaging |
Het |
Fam171a2 |
T |
C |
11: 102,334,939 (GRCm39) |
N66S |
possibly damaging |
Het |
Gad1 |
G |
A |
2: 70,417,583 (GRCm39) |
|
probably null |
Het |
Golgb1 |
C |
A |
16: 36,695,830 (GRCm39) |
|
probably benign |
Het |
Gprc5a |
A |
T |
6: 135,056,033 (GRCm39) |
N160I |
probably damaging |
Het |
Haus3 |
A |
G |
5: 34,323,258 (GRCm39) |
|
probably null |
Het |
Klhl20 |
A |
T |
1: 160,918,015 (GRCm39) |
C90* |
probably null |
Het |
Krt84 |
T |
A |
15: 101,437,138 (GRCm39) |
I342L |
probably damaging |
Het |
Lifr |
G |
A |
15: 7,208,373 (GRCm39) |
D584N |
probably damaging |
Het |
Lrp1b |
G |
A |
2: 41,298,997 (GRCm39) |
|
probably benign |
Het |
Lrtm1 |
T |
A |
14: 28,744,184 (GRCm39) |
|
probably benign |
Het |
Med25 |
C |
T |
7: 44,534,904 (GRCm39) |
V80I |
possibly damaging |
Het |
Mest |
A |
G |
6: 30,746,269 (GRCm39) |
I279V |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,315,532 (GRCm39) |
R81G |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,573,632 (GRCm39) |
D787G |
possibly damaging |
Het |
Naaladl1 |
C |
T |
19: 6,162,534 (GRCm39) |
P465S |
probably damaging |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Necab3 |
G |
A |
2: 154,387,232 (GRCm39) |
R302C |
probably damaging |
Het |
Nsg1 |
A |
T |
5: 38,316,254 (GRCm39) |
D32E |
probably damaging |
Het |
Nuggc |
A |
G |
14: 65,851,000 (GRCm39) |
D290G |
probably null |
Het |
Nup205 |
A |
T |
6: 35,202,715 (GRCm39) |
|
probably benign |
Het |
Or11g27 |
T |
A |
14: 50,771,088 (GRCm39) |
L73Q |
probably damaging |
Het |
Or4a77 |
T |
C |
2: 89,486,999 (GRCm39) |
N262S |
probably benign |
Het |
Or4c111 |
T |
C |
2: 88,844,015 (GRCm39) |
Y131C |
probably damaging |
Het |
Or4f57 |
G |
C |
2: 111,790,942 (GRCm39) |
Q159E |
probably damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,549 (GRCm39) |
I197N |
possibly damaging |
Het |
Otp |
T |
C |
13: 95,013,663 (GRCm39) |
V27A |
probably benign |
Het |
Phip |
A |
T |
9: 82,787,845 (GRCm39) |
|
probably null |
Het |
Pon2 |
A |
G |
6: 5,289,091 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
T |
A |
1: 134,763,637 (GRCm39) |
|
probably null |
Het |
Ppp1r15b |
A |
G |
1: 133,060,908 (GRCm39) |
N475S |
probably damaging |
Het |
Prrt3 |
A |
T |
6: 113,474,790 (GRCm39) |
L144H |
probably damaging |
Het |
Psmb7 |
A |
G |
2: 38,533,377 (GRCm39) |
V50A |
possibly damaging |
Het |
Sacs |
T |
A |
14: 61,442,017 (GRCm39) |
S1354R |
probably damaging |
Het |
Sdcbp2 |
A |
G |
2: 151,425,884 (GRCm39) |
T29A |
probably benign |
Het |
Shbg |
T |
A |
11: 69,508,415 (GRCm39) |
|
probably benign |
Het |
Shcbp1 |
A |
G |
8: 4,794,452 (GRCm39) |
I447T |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,026,676 (GRCm39) |
V48A |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,248,903 (GRCm39) |
C322S |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Trappc12 |
A |
T |
12: 28,796,751 (GRCm39) |
F260L |
probably damaging |
Het |
Trim10 |
C |
A |
17: 37,181,074 (GRCm39) |
H102N |
probably damaging |
Het |
Ube2u |
A |
G |
4: 100,407,122 (GRCm39) |
T215A |
possibly damaging |
Het |
Vcan |
T |
G |
13: 89,851,787 (GRCm39) |
T1058P |
probably benign |
Het |
|
Other mutations in Or2w6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01878:Or2w6
|
APN |
13 |
21,842,953 (GRCm39) |
missense |
possibly damaging |
0.63 |
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 |
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 |
|