Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts18 |
T |
C |
8: 114,469,833 (GRCm39) |
Y623C |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,585,676 (GRCm39) |
E4596G |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,641,329 (GRCm39) |
C3267S |
probably damaging |
Het |
Ankrd40 |
T |
G |
11: 94,225,641 (GRCm39) |
V224G |
probably benign |
Het |
Ap3s2 |
C |
T |
7: 79,570,390 (GRCm39) |
|
probably benign |
Het |
Apip |
T |
A |
2: 102,922,870 (GRCm39) |
D229E |
possibly damaging |
Het |
Atp2b4 |
C |
T |
1: 133,634,725 (GRCm39) |
R1168H |
probably benign |
Het |
Bcan |
T |
C |
3: 87,902,791 (GRCm39) |
K329R |
possibly damaging |
Het |
Camk1g |
T |
C |
1: 193,032,628 (GRCm39) |
D261G |
possibly damaging |
Het |
Ccdc30 |
T |
A |
4: 119,188,796 (GRCm39) |
Q490L |
probably damaging |
Het |
Ccdc83 |
A |
G |
7: 89,896,261 (GRCm39) |
W103R |
probably damaging |
Het |
Ctsl |
T |
A |
13: 64,514,437 (GRCm39) |
R69* |
probably null |
Het |
Dchs1 |
C |
T |
7: 105,408,000 (GRCm39) |
R1944H |
probably damaging |
Het |
Fgb |
T |
C |
3: 82,951,098 (GRCm39) |
Y305C |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,929,199 (GRCm39) |
Y3868N |
possibly damaging |
Het |
Gal3st2 |
T |
A |
1: 93,801,424 (GRCm39) |
S27T |
probably benign |
Het |
Galnt13 |
A |
G |
2: 54,745,244 (GRCm39) |
D228G |
probably damaging |
Het |
Gk5 |
A |
T |
9: 96,037,523 (GRCm39) |
T346S |
probably benign |
Het |
Gnrhr |
T |
C |
5: 86,333,172 (GRCm39) |
I233V |
probably damaging |
Het |
Greb1 |
T |
C |
12: 16,738,568 (GRCm39) |
Y1465C |
probably damaging |
Het |
H6pd |
A |
G |
4: 150,080,815 (GRCm39) |
L10P |
probably damaging |
Het |
Hspg2 |
G |
A |
4: 137,242,618 (GRCm39) |
G611E |
probably damaging |
Het |
Ighv7-4 |
A |
T |
12: 114,186,489 (GRCm39) |
D94E |
probably damaging |
Het |
Lamb3 |
T |
C |
1: 192,986,890 (GRCm39) |
Y59H |
probably benign |
Het |
Msantd1 |
C |
T |
5: 35,078,765 (GRCm39) |
T100I |
probably damaging |
Het |
Msx3 |
T |
A |
7: 139,628,659 (GRCm39) |
|
probably benign |
Het |
Mttp |
C |
A |
3: 137,812,999 (GRCm39) |
A559S |
probably damaging |
Het |
Myh1 |
C |
G |
11: 67,092,719 (GRCm39) |
D4E |
probably damaging |
Het |
Or2ah1 |
A |
G |
2: 85,654,134 (GRCm39) |
K273R |
probably damaging |
Het |
Or4c116 |
G |
T |
2: 88,942,640 (GRCm39) |
T72N |
possibly damaging |
Het |
Or4k45 |
C |
T |
2: 111,395,252 (GRCm39) |
C179Y |
probably damaging |
Het |
Pcdhac1 |
T |
C |
18: 37,223,381 (GRCm39) |
Y65H |
probably damaging |
Het |
Pcdhga8 |
A |
T |
18: 37,860,315 (GRCm39) |
Y457F |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,194,846 (GRCm39) |
L184P |
possibly damaging |
Het |
Pja2 |
A |
T |
17: 64,596,962 (GRCm39) |
M514K |
probably damaging |
Het |
Plcxd2 |
T |
C |
16: 45,792,488 (GRCm39) |
N284D |
probably damaging |
Het |
Polr3d |
A |
T |
14: 70,678,577 (GRCm39) |
M129K |
probably benign |
Het |
Ppp1r42 |
T |
G |
1: 10,069,732 (GRCm39) |
E110A |
probably damaging |
Het |
Prdm2 |
G |
A |
4: 142,859,471 (GRCm39) |
T1273M |
possibly damaging |
Het |
Prelid2 |
A |
G |
18: 42,045,514 (GRCm39) |
I132T |
possibly damaging |
Het |
Sergef |
G |
A |
7: 46,282,091 (GRCm39) |
|
probably null |
Het |
Slc24a2 |
C |
A |
4: 87,145,119 (GRCm39) |
|
probably null |
Het |
Stxbp3 |
A |
T |
3: 108,734,916 (GRCm39) |
D24E |
possibly damaging |
Het |
Tas2r123 |
A |
T |
6: 132,824,801 (GRCm39) |
M233L |
probably damaging |
Het |
Thsd7a |
G |
A |
6: 12,555,630 (GRCm39) |
H85Y |
possibly damaging |
Het |
Tlr2 |
T |
A |
3: 83,745,603 (GRCm39) |
E160V |
probably benign |
Het |
Tmem171 |
A |
T |
13: 98,828,678 (GRCm39) |
C157* |
probably null |
Het |
Trpm3 |
T |
C |
19: 22,903,392 (GRCm39) |
Y1051H |
probably damaging |
Het |
Vmn2r28 |
A |
G |
7: 5,491,408 (GRCm39) |
F280L |
probably benign |
Het |
Xpo7 |
A |
T |
14: 70,914,253 (GRCm39) |
Y748N |
probably damaging |
Het |
Zan |
T |
C |
5: 137,436,782 (GRCm39) |
S2024G |
unknown |
Het |
Zfhx2 |
A |
T |
14: 55,301,539 (GRCm39) |
Y2148* |
probably null |
Het |
Zscan4-ps1 |
T |
C |
7: 10,799,906 (GRCm39) |
T328A |
probably benign |
Het |
|
Other mutations in Or52e19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00814:Or52e19
|
APN |
7 |
102,959,014 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01917:Or52e19
|
APN |
7 |
102,959,564 (GRCm39) |
nonsense |
probably null |
|
G1patch:Or52e19
|
UTSW |
7 |
102,959,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Or52e19
|
UTSW |
7 |
102,959,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:Or52e19
|
UTSW |
7 |
102,959,780 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1762:Or52e19
|
UTSW |
7 |
102,959,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Or52e19
|
UTSW |
7 |
102,959,449 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1806:Or52e19
|
UTSW |
7 |
102,959,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Or52e19
|
UTSW |
7 |
102,959,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R2365:Or52e19
|
UTSW |
7 |
102,959,380 (GRCm39) |
missense |
probably benign |
0.00 |
R3827:Or52e19
|
UTSW |
7 |
102,959,009 (GRCm39) |
missense |
probably benign |
0.12 |
R4241:Or52e19
|
UTSW |
7 |
102,959,868 (GRCm39) |
makesense |
probably null |
|
R4619:Or52e19
|
UTSW |
7 |
102,959,165 (GRCm39) |
missense |
probably benign |
0.04 |
R4620:Or52e19
|
UTSW |
7 |
102,959,165 (GRCm39) |
missense |
probably benign |
0.04 |
R6279:Or52e19
|
UTSW |
7 |
102,959,636 (GRCm39) |
missense |
probably benign |
|
R6300:Or52e19
|
UTSW |
7 |
102,959,636 (GRCm39) |
missense |
probably benign |
|
R6505:Or52e19
|
UTSW |
7 |
102,959,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7175:Or52e19
|
UTSW |
7 |
102,959,054 (GRCm39) |
missense |
probably benign |
0.22 |
R7708:Or52e19
|
UTSW |
7 |
102,959,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:Or52e19
|
UTSW |
7 |
102,959,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Or52e19
|
UTSW |
7 |
102,959,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Or52e19
|
UTSW |
7 |
102,958,927 (GRCm39) |
start gained |
probably benign |
|
R9489:Or52e19
|
UTSW |
7 |
102,959,452 (GRCm39) |
missense |
probably benign |
0.00 |
R9799:Or52e19
|
UTSW |
7 |
102,959,065 (GRCm39) |
missense |
probably damaging |
1.00 |
|