Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
T |
11: 119,937,689 (GRCm39) |
|
probably benign |
Het |
Abca15 |
T |
C |
7: 119,965,133 (GRCm39) |
|
probably benign |
Het |
App |
T |
C |
16: 84,879,719 (GRCm39) |
Q138R |
probably benign |
Het |
Asah2 |
T |
A |
19: 31,986,814 (GRCm39) |
I529F |
probably benign |
Het |
Atp8b3 |
A |
G |
10: 80,356,128 (GRCm39) |
S1195P |
probably benign |
Het |
Brca1 |
A |
G |
11: 101,415,149 (GRCm39) |
M134T |
probably benign |
Het |
Cacna1s |
T |
C |
1: 135,996,732 (GRCm39) |
L111P |
probably damaging |
Het |
Capns2 |
A |
T |
8: 93,628,215 (GRCm39) |
N35Y |
probably benign |
Het |
Ccne1 |
A |
G |
7: 37,798,415 (GRCm39) |
|
probably null |
Het |
Cfap91 |
G |
T |
16: 38,153,181 (GRCm39) |
|
probably benign |
Het |
Csf1r |
G |
T |
18: 61,257,540 (GRCm39) |
|
probably benign |
Het |
Dipk2b |
T |
A |
X: 18,313,930 (GRCm39) |
I131F |
possibly damaging |
Het |
Dlg3 |
A |
T |
X: 99,817,007 (GRCm39) |
Y326F |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 31,013,770 (GRCm39) |
V3837A |
probably damaging |
Het |
Dock10 |
A |
G |
1: 80,562,711 (GRCm39) |
|
probably null |
Het |
Emg1 |
A |
G |
6: 124,681,620 (GRCm39) |
V208A |
probably benign |
Het |
Eml6 |
T |
A |
11: 29,727,282 (GRCm39) |
D1280V |
probably damaging |
Het |
Ep400 |
T |
C |
5: 110,868,691 (GRCm39) |
D911G |
unknown |
Het |
Fam171a1 |
T |
C |
2: 3,224,623 (GRCm39) |
|
probably null |
Het |
Fcgbp |
T |
C |
7: 27,806,395 (GRCm39) |
V2121A |
possibly damaging |
Het |
Fggy |
G |
A |
4: 95,511,714 (GRCm39) |
|
probably benign |
Het |
Fignl1 |
G |
T |
11: 11,752,845 (GRCm39) |
T70K |
possibly damaging |
Het |
Fndc3b |
T |
C |
3: 27,674,801 (GRCm39) |
E47G |
probably damaging |
Het |
Frmd4a |
A |
G |
2: 4,539,385 (GRCm39) |
K189E |
possibly damaging |
Het |
Hpse |
T |
A |
5: 100,839,199 (GRCm39) |
Y383F |
probably damaging |
Het |
Ip6k2 |
T |
C |
9: 108,681,798 (GRCm39) |
L197P |
probably damaging |
Het |
Klf1 |
A |
C |
8: 85,631,561 (GRCm39) |
H375P |
probably damaging |
Het |
Krtap6-5 |
T |
A |
16: 88,844,734 (GRCm39) |
|
probably benign |
Het |
Lacc1 |
A |
T |
14: 77,267,055 (GRCm39) |
S403T |
probably damaging |
Het |
Lama3 |
A |
G |
18: 12,689,807 (GRCm39) |
I2850V |
possibly damaging |
Het |
Lats2 |
C |
T |
14: 57,929,052 (GRCm39) |
R941Q |
probably damaging |
Het |
Lgals3bp |
A |
T |
11: 118,284,290 (GRCm39) |
Y430N |
probably benign |
Het |
Lrig3 |
A |
T |
10: 125,850,743 (GRCm39) |
H1103L |
probably benign |
Het |
Lrrc40 |
G |
A |
3: 157,742,365 (GRCm39) |
M1I |
probably null |
Het |
Magee2 |
A |
T |
X: 103,900,399 (GRCm39) |
V84D |
possibly damaging |
Het |
Msantd2 |
G |
A |
9: 37,434,602 (GRCm39) |
V281I |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,394,076 (GRCm39) |
V340A |
probably damaging |
Het |
Myh6 |
A |
T |
14: 55,181,775 (GRCm39) |
M1842K |
probably benign |
Het |
Mylk4 |
T |
C |
13: 32,906,130 (GRCm39) |
D145G |
possibly damaging |
Het |
Nfkbid |
C |
T |
7: 30,124,689 (GRCm39) |
Q160* |
probably null |
Het |
Or2y1d |
A |
T |
11: 49,321,859 (GRCm39) |
K185N |
probably damaging |
Het |
Or5w1b |
T |
A |
2: 87,475,630 (GRCm39) |
Y279F |
probably damaging |
Het |
Or7e168 |
C |
T |
9: 19,720,343 (GRCm39) |
S243F |
probably damaging |
Het |
Or8c11 |
A |
T |
9: 38,289,542 (GRCm39) |
T122S |
probably damaging |
Het |
Or9q2 |
T |
G |
19: 13,772,693 (GRCm39) |
Q94P |
possibly damaging |
Het |
Pdgfrb |
A |
C |
18: 61,213,404 (GRCm39) |
Q916P |
probably damaging |
Het |
Pex14 |
T |
C |
4: 149,050,743 (GRCm39) |
Q174R |
probably benign |
Het |
Pogz |
T |
C |
3: 94,786,321 (GRCm39) |
S970P |
probably damaging |
Het |
Potegl |
T |
C |
2: 23,102,667 (GRCm39) |
|
probably benign |
Het |
Rabggta |
A |
G |
14: 55,955,952 (GRCm39) |
V165A |
possibly damaging |
Het |
Rdh10 |
G |
A |
1: 16,176,438 (GRCm39) |
W66* |
probably null |
Het |
Ripor2 |
T |
A |
13: 24,879,549 (GRCm39) |
|
probably benign |
Het |
Slc35g1 |
T |
A |
19: 38,391,678 (GRCm39) |
M320K |
possibly damaging |
Het |
Slc9a7 |
A |
G |
X: 20,068,963 (GRCm39) |
Y197H |
probably damaging |
Het |
Smn1 |
T |
C |
13: 100,272,192 (GRCm39) |
|
probably benign |
Het |
Spam1 |
G |
A |
6: 24,796,696 (GRCm39) |
G216S |
probably damaging |
Het |
Spata31 |
A |
T |
13: 65,068,194 (GRCm39) |
N114I |
probably damaging |
Het |
Sptbn1 |
A |
T |
11: 30,069,491 (GRCm39) |
V1615D |
possibly damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Thoc2 |
T |
A |
X: 40,914,355 (GRCm39) |
Q1005H |
possibly damaging |
Het |
Thra |
G |
A |
11: 98,652,742 (GRCm39) |
R189Q |
probably damaging |
Het |
Trappc11 |
A |
T |
8: 47,983,685 (GRCm39) |
|
probably null |
Het |
Vps13d |
G |
T |
4: 144,882,934 (GRCm39) |
H886Q |
probably damaging |
Het |
Zfp157 |
G |
A |
5: 138,445,859 (GRCm39) |
W71* |
probably null |
Het |
|
Other mutations in Or11h6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Or11h6
|
APN |
14 |
50,880,625 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02316:Or11h6
|
APN |
14 |
50,879,744 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02471:Or11h6
|
APN |
14 |
50,880,214 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02486:Or11h6
|
APN |
14 |
50,880,089 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02517:Or11h6
|
APN |
14 |
50,880,658 (GRCm39) |
missense |
probably benign |
0.01 |
R0453:Or11h6
|
UTSW |
14 |
50,880,461 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0727:Or11h6
|
UTSW |
14 |
50,880,460 (GRCm39) |
missense |
probably damaging |
0.98 |
R0746:Or11h6
|
UTSW |
14 |
50,880,232 (GRCm39) |
splice site |
probably null |
|
R1638:Or11h6
|
UTSW |
14 |
50,880,565 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1688:Or11h6
|
UTSW |
14 |
50,880,705 (GRCm39) |
missense |
probably benign |
0.04 |
R1991:Or11h6
|
UTSW |
14 |
50,880,323 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2245:Or11h6
|
UTSW |
14 |
50,880,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R3758:Or11h6
|
UTSW |
14 |
50,880,493 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4084:Or11h6
|
UTSW |
14 |
50,880,305 (GRCm39) |
missense |
probably damaging |
0.98 |
R5033:Or11h6
|
UTSW |
14 |
50,880,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Or11h6
|
UTSW |
14 |
50,880,710 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5302:Or11h6
|
UTSW |
14 |
50,879,776 (GRCm39) |
splice site |
probably null |
|
R5645:Or11h6
|
UTSW |
14 |
50,880,524 (GRCm39) |
missense |
probably benign |
0.00 |
R5731:Or11h6
|
UTSW |
14 |
50,880,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R6917:Or11h6
|
UTSW |
14 |
50,880,680 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7408:Or11h6
|
UTSW |
14 |
50,879,852 (GRCm39) |
missense |
probably benign |
0.16 |
R7716:Or11h6
|
UTSW |
14 |
50,879,815 (GRCm39) |
missense |
probably benign |
0.17 |
R7728:Or11h6
|
UTSW |
14 |
50,879,849 (GRCm39) |
missense |
probably benign |
0.00 |
R8208:Or11h6
|
UTSW |
14 |
50,880,088 (GRCm39) |
missense |
probably benign |
0.28 |
R8447:Or11h6
|
UTSW |
14 |
50,880,008 (GRCm39) |
missense |
probably benign |
0.00 |
R8726:Or11h6
|
UTSW |
14 |
50,880,703 (GRCm39) |
missense |
probably benign |
0.00 |
R8748:Or11h6
|
UTSW |
14 |
50,880,211 (GRCm39) |
missense |
probably benign |
0.19 |
R9279:Or11h6
|
UTSW |
14 |
50,880,493 (GRCm39) |
missense |
possibly damaging |
0.96 |
|