Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA467197 |
T |
C |
2: 122,482,622 (GRCm39) |
L62P |
probably damaging |
Het |
Amotl2 |
T |
G |
9: 102,607,291 (GRCm39) |
S700A |
probably damaging |
Het |
Ccdc7a |
A |
G |
8: 129,549,942 (GRCm39) |
S1259P |
possibly damaging |
Het |
Cenpj |
C |
T |
14: 56,790,355 (GRCm39) |
E565K |
probably damaging |
Het |
Clmp |
C |
T |
9: 40,692,549 (GRCm39) |
R273* |
probably null |
Het |
Cops7b |
A |
T |
1: 86,528,846 (GRCm39) |
Q191L |
probably benign |
Het |
Cyp2c23 |
A |
G |
19: 44,002,054 (GRCm39) |
F312L |
probably benign |
Het |
Dgkd |
G |
A |
1: 87,843,266 (GRCm39) |
C169Y |
probably damaging |
Het |
Dlec1 |
A |
T |
9: 118,956,498 (GRCm39) |
N724I |
probably benign |
Het |
Dmxl1 |
T |
C |
18: 50,090,406 (GRCm39) |
V2831A |
probably damaging |
Het |
Dnah5 |
G |
T |
15: 28,229,719 (GRCm39) |
G118W |
probably damaging |
Het |
Dnah6 |
G |
T |
6: 73,104,937 (GRCm39) |
T1884K |
probably damaging |
Het |
Dnai4 |
T |
C |
4: 102,947,697 (GRCm39) |
E193G |
possibly damaging |
Het |
Efnb2 |
T |
A |
8: 8,670,731 (GRCm39) |
S290C |
probably damaging |
Het |
Eif1ad6 |
A |
G |
12: 87,668,593 (GRCm39) |
D75G |
probably damaging |
Het |
Eif2ak4 |
C |
A |
2: 118,278,806 (GRCm39) |
T990K |
probably damaging |
Het |
Erich3 |
A |
G |
3: 154,468,827 (GRCm39) |
D1093G |
unknown |
Het |
H2-DMa |
T |
C |
17: 34,354,734 (GRCm39) |
|
probably benign |
Het |
Habp2 |
G |
A |
19: 56,295,216 (GRCm39) |
D36N |
probably benign |
Het |
Kcnk13 |
G |
T |
12: 100,027,647 (GRCm39) |
G241W |
probably damaging |
Het |
Kdm6b |
GGGTGGTGGTGGTGGTGG |
GGGTGGTGGTGGTGGTGGTGG |
11: 69,297,655 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
TGG |
TGGGGG |
11: 69,297,658 (GRCm39) |
|
probably benign |
Het |
Klk1b5 |
G |
T |
7: 43,496,549 (GRCm39) |
M160I |
probably benign |
Het |
Lonp2 |
A |
G |
8: 87,358,073 (GRCm39) |
Y98C |
probably damaging |
Het |
Marcksl1 |
C |
T |
4: 129,408,999 (GRCm39) |
P193S |
probably benign |
Het |
Nup133 |
AAGAGA |
AAGA |
8: 124,638,627 (GRCm39) |
900 |
probably null |
Het |
Nxf7 |
G |
A |
X: 134,484,515 (GRCm39) |
R513C |
possibly damaging |
Het |
Or13a19 |
C |
A |
7: 139,902,793 (GRCm39) |
Y60* |
probably null |
Het |
Or4a73 |
A |
T |
2: 89,420,730 (GRCm39) |
M243K |
probably benign |
Het |
Or52e5 |
T |
A |
7: 104,719,518 (GRCm39) |
Y281* |
probably null |
Het |
Or7g32 |
T |
G |
9: 19,389,477 (GRCm39) |
D23A |
possibly damaging |
Het |
Otof |
T |
A |
5: 30,540,242 (GRCm39) |
M965L |
probably benign |
Het |
Parp12 |
A |
G |
6: 39,073,508 (GRCm39) |
F439S |
probably damaging |
Het |
Pde1a |
G |
A |
2: 79,959,261 (GRCm39) |
|
probably benign |
Het |
Pramel22 |
T |
A |
4: 143,380,913 (GRCm39) |
N370I |
probably damaging |
Het |
Prrc2c |
T |
C |
1: 162,532,812 (GRCm39) |
N1268D |
unknown |
Het |
Pter |
T |
C |
2: 12,985,114 (GRCm39) |
V148A |
probably benign |
Het |
Rb1 |
A |
G |
14: 73,500,027 (GRCm39) |
M540T |
probably damaging |
Het |
Rnasel |
T |
A |
1: 153,629,641 (GRCm39) |
N52K |
probably damaging |
Het |
Rragd |
A |
T |
4: 33,012,953 (GRCm39) |
I317F |
possibly damaging |
Het |
Sla |
G |
T |
15: 66,664,127 (GRCm39) |
S81R |
probably benign |
Het |
T |
A |
G |
17: 8,653,532 (GRCm39) |
E57G |
probably benign |
Het |
Tanc1 |
T |
A |
2: 59,630,265 (GRCm39) |
F748L |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,938,136 (GRCm39) |
W3073R |
probably damaging |
Het |
Trim33 |
A |
G |
3: 103,254,052 (GRCm39) |
T967A |
probably benign |
Het |
Tro |
G |
A |
X: 149,438,555 (GRCm39) |
S34L |
unknown |
Het |
Trpm1 |
T |
A |
7: 63,851,756 (GRCm39) |
M158K |
possibly damaging |
Het |
Vmn1r205 |
A |
G |
13: 22,776,424 (GRCm39) |
L226P |
probably benign |
Het |
Vmn1r56 |
C |
T |
7: 5,198,733 (GRCm39) |
V295M |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,778,566 (GRCm39) |
D208G |
probably damaging |
Het |
Zfp11 |
T |
C |
5: 129,735,278 (GRCm39) |
D61G |
probably benign |
Het |
Zscan4e |
C |
A |
7: 11,041,540 (GRCm39) |
E139* |
probably null |
Het |
|
Other mutations in Or7g34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00930:Or7g34
|
APN |
9 |
19,478,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02072:Or7g34
|
APN |
9 |
19,478,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Or7g34
|
APN |
9 |
19,478,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02187:Or7g34
|
APN |
9 |
19,478,393 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02252:Or7g34
|
APN |
9 |
19,478,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R0519:Or7g34
|
UTSW |
9 |
19,478,245 (GRCm39) |
missense |
probably benign |
0.21 |
R0755:Or7g34
|
UTSW |
9 |
19,478,415 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0899:Or7g34
|
UTSW |
9 |
19,477,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Or7g34
|
UTSW |
9 |
19,478,492 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2115:Or7g34
|
UTSW |
9 |
19,478,618 (GRCm39) |
missense |
probably benign |
0.12 |
R4326:Or7g34
|
UTSW |
9 |
19,478,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4328:Or7g34
|
UTSW |
9 |
19,478,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4329:Or7g34
|
UTSW |
9 |
19,478,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4379:Or7g34
|
UTSW |
9 |
19,478,038 (GRCm39) |
missense |
probably benign |
0.15 |
R4381:Or7g34
|
UTSW |
9 |
19,478,038 (GRCm39) |
missense |
probably benign |
0.15 |
R5576:Or7g34
|
UTSW |
9 |
19,478,369 (GRCm39) |
missense |
probably benign |
|
R6102:Or7g34
|
UTSW |
9 |
19,478,318 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7449:Or7g34
|
UTSW |
9 |
19,478,162 (GRCm39) |
missense |
probably benign |
0.06 |
R7515:Or7g34
|
UTSW |
9 |
19,477,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Or7g34
|
UTSW |
9 |
19,478,587 (GRCm39) |
missense |
probably benign |
0.04 |
R9515:Or7g34
|
UTSW |
9 |
19,478,396 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1176:Or7g34
|
UTSW |
9 |
19,477,822 (GRCm39) |
missense |
probably damaging |
1.00 |
|