Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,820 (GRCm39) |
Y1670H |
probably damaging |
Het |
Abca12 |
T |
C |
1: 71,346,212 (GRCm39) |
K886R |
possibly damaging |
Het |
Adcy3 |
G |
A |
12: 4,250,992 (GRCm39) |
E584K |
probably benign |
Het |
Ano3 |
A |
T |
2: 110,693,205 (GRCm39) |
V131D |
probably benign |
Het |
Arhgdig |
C |
T |
17: 26,418,337 (GRCm39) |
W215* |
probably null |
Het |
Cad |
G |
T |
5: 31,224,956 (GRCm39) |
W953L |
possibly damaging |
Het |
Calhm2 |
T |
C |
19: 47,124,080 (GRCm39) |
Y88C |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,156,468 (GRCm39) |
D1681E |
probably benign |
Het |
Cenpl |
T |
A |
1: 160,910,482 (GRCm39) |
L143H |
possibly damaging |
Het |
Cherp |
T |
C |
8: 73,222,230 (GRCm39) |
K270E |
|
Het |
Cmss1 |
A |
G |
16: 57,131,718 (GRCm39) |
I136T |
probably benign |
Het |
Col23a1 |
T |
C |
11: 51,456,050 (GRCm39) |
|
probably null |
Het |
Crnn |
C |
A |
3: 93,055,689 (GRCm39) |
D158E |
probably damaging |
Het |
Dnmt3a |
A |
T |
12: 3,922,844 (GRCm39) |
Q149L |
probably benign |
Het |
Dst |
T |
A |
1: 34,228,963 (GRCm39) |
N2185K |
probably benign |
Het |
Eif1ad18 |
G |
T |
12: 88,050,597 (GRCm39) |
C44F |
probably benign |
Het |
Elp2 |
T |
A |
18: 24,737,126 (GRCm39) |
N25K |
probably benign |
Het |
Ephb4 |
A |
T |
5: 137,370,308 (GRCm39) |
D845V |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,201,627 (GRCm39) |
T561A |
probably damaging |
Het |
F3 |
G |
T |
3: 121,525,235 (GRCm39) |
V159L |
probably damaging |
Het |
Fam81a |
A |
T |
9: 70,017,560 (GRCm39) |
D128E |
probably damaging |
Het |
Flot1 |
T |
G |
17: 36,135,835 (GRCm39) |
H155Q |
probably benign |
Het |
Fut9 |
T |
A |
4: 25,620,507 (GRCm39) |
K102N |
probably damaging |
Het |
Gm6309 |
T |
C |
5: 146,107,100 (GRCm39) |
Q82R |
possibly damaging |
Het |
H13 |
A |
G |
2: 152,522,992 (GRCm39) |
N102D |
probably damaging |
Het |
Lamc2 |
C |
G |
1: 153,006,518 (GRCm39) |
A878P |
possibly damaging |
Het |
Lepr |
C |
T |
4: 101,609,394 (GRCm39) |
T327I |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,285,152 (GRCm39) |
|
probably null |
Het |
Ly86 |
A |
G |
13: 37,560,986 (GRCm39) |
K116E |
probably damaging |
Het |
Mapk8ip2 |
T |
A |
15: 89,343,201 (GRCm39) |
F648I |
possibly damaging |
Het |
Muc16 |
G |
A |
9: 18,566,876 (GRCm39) |
T1881I |
unknown |
Het |
Myh13 |
T |
G |
11: 67,245,566 (GRCm39) |
S1069A |
probably benign |
Het |
Myh4 |
T |
A |
11: 67,151,054 (GRCm39) |
I1903N |
possibly damaging |
Het |
Myo18b |
A |
T |
5: 112,965,545 (GRCm39) |
L1341* |
probably null |
Het |
Naa25 |
G |
T |
5: 121,555,552 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Ncapg |
C |
T |
5: 45,827,372 (GRCm39) |
A3V |
possibly damaging |
Het |
Ncln |
T |
C |
10: 81,324,086 (GRCm39) |
H481R |
probably benign |
Het |
Nek4 |
C |
A |
14: 30,704,305 (GRCm39) |
Q607K |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,796,462 (GRCm39) |
Y1182C |
probably damaging |
Het |
Npnt |
T |
C |
3: 132,615,692 (GRCm39) |
N165S |
probably benign |
Het |
Or2l5 |
C |
G |
16: 19,333,649 (GRCm39) |
V246L |
probably damaging |
Het |
Or8b8 |
A |
G |
9: 37,808,859 (GRCm39) |
H53R |
probably benign |
Het |
Or8k30 |
T |
C |
2: 86,338,872 (GRCm39) |
L23P |
probably damaging |
Het |
Otulin |
T |
C |
15: 27,608,856 (GRCm39) |
Y229C |
probably damaging |
Het |
Palld |
A |
T |
8: 61,985,051 (GRCm39) |
D1071E |
unknown |
Het |
Pcdhb20 |
T |
C |
18: 37,638,142 (GRCm39) |
S223P |
probably damaging |
Het |
Pcdhga6 |
T |
A |
18: 37,840,781 (GRCm39) |
I167N |
probably damaging |
Het |
Pcdhgb4 |
A |
G |
18: 37,854,843 (GRCm39) |
N413D |
probably benign |
Het |
Pcdhgb8 |
T |
A |
18: 37,896,050 (GRCm39) |
Y373* |
probably null |
Het |
Plxna2 |
G |
T |
1: 194,331,830 (GRCm39) |
V419L |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,959,434 (GRCm39) |
|
probably null |
Het |
Rsrc2 |
A |
G |
5: 123,877,630 (GRCm39) |
|
probably benign |
Het |
Scaper |
C |
T |
9: 55,819,395 (GRCm39) |
D107N |
unknown |
Het |
Scgb2b3 |
T |
A |
7: 31,059,573 (GRCm39) |
Y67F |
probably benign |
Het |
Scn5a |
G |
A |
9: 119,315,437 (GRCm39) |
T1757I |
probably damaging |
Het |
Sgo2b |
G |
A |
8: 64,381,218 (GRCm39) |
P538L |
probably damaging |
Het |
Slc9a3 |
A |
G |
13: 74,298,797 (GRCm39) |
K72R |
probably damaging |
Het |
Smchd1 |
T |
A |
17: 71,685,202 (GRCm39) |
T1409S |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,867,030 (GRCm39) |
|
probably null |
Het |
Sult2b1 |
T |
C |
7: 45,383,056 (GRCm39) |
E242G |
probably damaging |
Het |
Tcaf1 |
A |
T |
6: 42,663,687 (GRCm39) |
H64Q |
probably damaging |
Het |
Tle6 |
T |
C |
10: 81,435,910 (GRCm39) |
T2A |
possibly damaging |
Het |
Tmem115 |
T |
C |
9: 107,412,285 (GRCm39) |
V203A |
probably benign |
Het |
Tmem45b |
G |
A |
9: 31,340,337 (GRCm39) |
T108I |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,153,079 (GRCm39) |
D331E |
probably damaging |
Het |
Txndc9 |
T |
C |
1: 38,029,377 (GRCm39) |
Y157C |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r27 |
C |
A |
6: 124,168,711 (GRCm39) |
R806S |
probably benign |
Het |
Vmn2r59 |
G |
A |
7: 41,695,188 (GRCm39) |
A408V |
probably damaging |
Het |
Ythdc1 |
T |
C |
5: 86,964,467 (GRCm39) |
V92A |
probably benign |
Het |
|
Other mutations in Or4p22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01286:Or4p22
|
APN |
2 |
88,317,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Or4p22
|
APN |
2 |
88,317,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01790:Or4p22
|
APN |
2 |
88,317,270 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02070:Or4p22
|
APN |
2 |
88,317,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02247:Or4p22
|
APN |
2 |
88,317,771 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02932:Or4p22
|
APN |
2 |
88,317,519 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02997:Or4p22
|
APN |
2 |
88,317,732 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03161:Or4p22
|
APN |
2 |
88,317,792 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4531001:Or4p22
|
UTSW |
2 |
88,317,601 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3713:Or4p22
|
UTSW |
2 |
88,317,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R3715:Or4p22
|
UTSW |
2 |
88,317,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Or4p22
|
UTSW |
2 |
88,317,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Or4p22
|
UTSW |
2 |
88,317,709 (GRCm39) |
missense |
probably benign |
0.05 |
R5096:Or4p22
|
UTSW |
2 |
88,317,646 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5661:Or4p22
|
UTSW |
2 |
88,317,441 (GRCm39) |
missense |
probably damaging |
0.98 |
R5851:Or4p22
|
UTSW |
2 |
88,317,204 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6458:Or4p22
|
UTSW |
2 |
88,317,562 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7073:Or4p22
|
UTSW |
2 |
88,317,651 (GRCm39) |
missense |
probably benign |
0.00 |
R7102:Or4p22
|
UTSW |
2 |
88,317,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Or4p22
|
UTSW |
2 |
88,317,973 (GRCm39) |
missense |
probably damaging |
0.97 |
R8827:Or4p22
|
UTSW |
2 |
88,317,165 (GRCm39) |
missense |
probably damaging |
0.96 |
R9324:Or4p22
|
UTSW |
2 |
88,317,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R9645:Or4p22
|
UTSW |
2 |
88,317,373 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0063:Or4p22
|
UTSW |
2 |
88,317,834 (GRCm39) |
missense |
probably benign |
0.23 |
|