Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
A |
8: 60,998,290 (GRCm39) |
S431T |
probably benign |
Het |
Acot7 |
T |
G |
4: 152,302,272 (GRCm39) |
V128G |
probably damaging |
Het |
Actn3 |
T |
C |
19: 4,914,691 (GRCm39) |
D508G |
probably benign |
Het |
Adam18 |
T |
C |
8: 25,137,878 (GRCm39) |
I321V |
probably benign |
Het |
Ak1 |
T |
C |
2: 32,523,490 (GRCm39) |
V186A |
probably benign |
Het |
Aldh3a2 |
A |
G |
11: 61,139,756 (GRCm39) |
F459L |
probably benign |
Het |
Atp11a |
T |
C |
8: 12,875,721 (GRCm39) |
L256P |
probably benign |
Het |
Bcan |
T |
C |
3: 87,903,999 (GRCm39) |
E162G |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,959,033 (GRCm39) |
Q3850R |
probably damaging |
Het |
Btf3l4 |
T |
G |
4: 108,689,084 (GRCm39) |
|
probably benign |
Het |
Btla |
A |
G |
16: 45,059,430 (GRCm39) |
T45A |
probably benign |
Het |
Cad |
T |
G |
5: 31,226,908 (GRCm39) |
S1222A |
probably damaging |
Het |
Cbarp |
A |
G |
10: 79,972,976 (GRCm39) |
V39A |
possibly damaging |
Het |
Cct2 |
A |
C |
10: 116,894,090 (GRCm39) |
D221E |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,177,991 (GRCm39) |
D3621G |
probably damaging |
Het |
Col20a1 |
G |
T |
2: 180,643,131 (GRCm39) |
R867L |
possibly damaging |
Het |
Cops3 |
A |
G |
11: 59,718,802 (GRCm39) |
V164A |
probably benign |
Het |
Crygf |
A |
G |
1: 65,967,148 (GRCm39) |
R91G |
probably damaging |
Het |
Csmd2 |
T |
A |
4: 128,440,477 (GRCm39) |
S3181T |
|
Het |
Cyb5r1 |
G |
T |
1: 134,333,696 (GRCm39) |
|
probably benign |
Het |
Dennd6b |
T |
A |
15: 89,070,383 (GRCm39) |
I429F |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,475,816 (GRCm39) |
T864A |
probably benign |
Het |
Eea1 |
A |
T |
10: 95,859,853 (GRCm39) |
D713V |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,829,160 (GRCm39) |
C9Y |
probably damaging |
Het |
Gga2 |
A |
C |
7: 121,597,002 (GRCm39) |
D371E |
probably benign |
Het |
Gtpbp6 |
A |
T |
5: 110,255,186 (GRCm39) |
V2E |
unknown |
Het |
Hectd4 |
A |
T |
5: 121,461,994 (GRCm39) |
M954L |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,610,248 (GRCm39) |
C1474R |
probably damaging |
Het |
Igkv1-99 |
G |
T |
6: 68,519,370 (GRCm39) |
G109V |
|
Het |
Izumo3 |
T |
C |
4: 92,033,310 (GRCm39) |
|
probably null |
Het |
Kremen1 |
T |
C |
11: 5,144,981 (GRCm39) |
D465G |
probably benign |
Het |
Ksr1 |
T |
C |
11: 79,036,882 (GRCm39) |
E75G |
probably benign |
Het |
Mmp17 |
G |
T |
5: 129,675,773 (GRCm39) |
E311* |
probably null |
Het |
Mmrn1 |
T |
A |
6: 60,965,271 (GRCm39) |
F1101I |
probably damaging |
Het |
Muc13 |
G |
A |
16: 33,633,287 (GRCm39) |
|
probably benign |
Het |
Myl4 |
T |
A |
11: 104,475,403 (GRCm39) |
M147K |
probably damaging |
Het |
Myo1a |
T |
A |
10: 127,546,856 (GRCm39) |
N334K |
probably benign |
Het |
Myo3b |
T |
C |
2: 70,083,338 (GRCm39) |
S664P |
probably benign |
Het |
Nptxr |
T |
C |
15: 79,678,655 (GRCm39) |
N211D |
probably damaging |
Het |
Ntf5 |
A |
G |
7: 45,065,485 (GRCm39) |
T206A |
probably benign |
Het |
Obscn |
T |
A |
11: 58,945,229 (GRCm39) |
E4596D |
probably benign |
Het |
Or4d10c |
T |
C |
19: 12,065,469 (GRCm39) |
E229G |
probably benign |
Het |
Or4f14d |
T |
C |
2: 111,960,427 (GRCm39) |
H243R |
probably damaging |
Het |
Or5ak20 |
T |
A |
2: 85,184,078 (GRCm39) |
Q64L |
probably damaging |
Het |
Or5ak25 |
T |
A |
2: 85,268,981 (GRCm39) |
I174F |
probably damaging |
Het |
Or7e169 |
A |
T |
9: 19,757,462 (GRCm39) |
I151N |
possibly damaging |
Het |
Paip2 |
A |
G |
18: 35,749,273 (GRCm39) |
N114D |
possibly damaging |
Het |
Pcnx1 |
T |
C |
12: 82,039,925 (GRCm39) |
S2071P |
possibly damaging |
Het |
Pcsk2 |
A |
G |
2: 143,637,870 (GRCm39) |
T369A |
probably damaging |
Het |
Ppp1r12b |
A |
C |
1: 134,818,492 (GRCm39) |
|
probably benign |
Het |
Ppp1r35 |
T |
A |
5: 137,777,731 (GRCm39) |
D132E |
possibly damaging |
Het |
Pramel7 |
A |
T |
2: 87,320,405 (GRCm39) |
V296E |
probably benign |
Het |
Prh1 |
C |
T |
6: 132,548,948 (GRCm39) |
P152S |
unknown |
Het |
Pygl |
T |
C |
12: 70,242,390 (GRCm39) |
T689A |
probably damaging |
Het |
Rasgef1b |
T |
C |
5: 99,369,269 (GRCm39) |
S450G |
probably benign |
Het |
Rtn4ip1 |
G |
T |
10: 43,783,842 (GRCm39) |
R121L |
probably damaging |
Het |
Scarf2 |
A |
T |
16: 17,620,695 (GRCm39) |
H121L |
probably damaging |
Het |
Selenbp1 |
C |
A |
3: 94,851,821 (GRCm39) |
A454E |
possibly damaging |
Het |
Slc7a9 |
A |
G |
7: 35,163,143 (GRCm39) |
I449M |
possibly damaging |
Het |
Snapc2 |
C |
T |
8: 4,305,558 (GRCm39) |
H278Y |
probably damaging |
Het |
Stambp |
C |
T |
6: 83,524,212 (GRCm39) |
|
probably null |
Het |
Syne1 |
T |
C |
10: 5,311,535 (GRCm39) |
Y550C |
probably damaging |
Het |
Tas2r113 |
T |
C |
6: 132,870,104 (GRCm39) |
V44A |
possibly damaging |
Het |
Trpv4 |
T |
C |
5: 114,772,816 (GRCm39) |
T305A |
probably benign |
Het |
Twf1 |
T |
C |
15: 94,479,136 (GRCm39) |
Y241C |
probably damaging |
Het |
Ugt2a3 |
T |
C |
5: 87,484,389 (GRCm39) |
K212E |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,676,998 (GRCm39) |
H4770L |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,247,800 (GRCm39) |
V1001A |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,751,290 (GRCm39) |
R92Q |
probably benign |
Het |
|
Other mutations in Or5b3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01064:Or5b3
|
APN |
19 |
13,388,590 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01520:Or5b3
|
APN |
19 |
13,388,114 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01671:Or5b3
|
APN |
19 |
13,388,255 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02247:Or5b3
|
APN |
19 |
13,388,831 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02297:Or5b3
|
APN |
19 |
13,388,839 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02417:Or5b3
|
APN |
19 |
13,388,259 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02442:Or5b3
|
APN |
19 |
13,388,351 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02989:Or5b3
|
APN |
19 |
13,388,850 (GRCm39) |
missense |
probably benign |
|
IGL03269:Or5b3
|
APN |
19 |
13,388,792 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02988:Or5b3
|
UTSW |
19 |
13,388,826 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0707:Or5b3
|
UTSW |
19 |
13,388,784 (GRCm39) |
missense |
probably benign |
0.22 |
R1055:Or5b3
|
UTSW |
19 |
13,388,754 (GRCm39) |
missense |
probably benign |
0.10 |
R1102:Or5b3
|
UTSW |
19 |
13,388,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Or5b3
|
UTSW |
19 |
13,388,143 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2111:Or5b3
|
UTSW |
19 |
13,388,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R4072:Or5b3
|
UTSW |
19 |
13,388,299 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4073:Or5b3
|
UTSW |
19 |
13,388,299 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4076:Or5b3
|
UTSW |
19 |
13,388,299 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4726:Or5b3
|
UTSW |
19 |
13,388,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Or5b3
|
UTSW |
19 |
13,388,219 (GRCm39) |
missense |
probably benign |
0.10 |
R5914:Or5b3
|
UTSW |
19 |
13,388,326 (GRCm39) |
missense |
probably benign |
0.31 |
R6003:Or5b3
|
UTSW |
19 |
13,388,403 (GRCm39) |
missense |
probably benign |
0.34 |
R6743:Or5b3
|
UTSW |
19 |
13,387,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Or5b3
|
UTSW |
19 |
13,388,514 (GRCm39) |
missense |
probably benign |
0.01 |
R6826:Or5b3
|
UTSW |
19 |
13,388,452 (GRCm39) |
missense |
probably benign |
0.05 |
R6970:Or5b3
|
UTSW |
19 |
13,388,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R7558:Or5b3
|
UTSW |
19 |
13,388,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R7596:Or5b3
|
UTSW |
19 |
13,388,511 (GRCm39) |
missense |
probably benign |
0.01 |
R7923:Or5b3
|
UTSW |
19 |
13,388,182 (GRCm39) |
missense |
probably benign |
0.17 |
R8014:Or5b3
|
UTSW |
19 |
13,388,175 (GRCm39) |
missense |
not run |
|
R8506:Or5b3
|
UTSW |
19 |
13,388,604 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8746:Or5b3
|
UTSW |
19 |
13,388,092 (GRCm39) |
missense |
probably benign |
0.44 |
R9112:Or5b3
|
UTSW |
19 |
13,388,475 (GRCm39) |
missense |
probably benign |
0.05 |
R9721:Or5b3
|
UTSW |
19 |
13,388,334 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Or5b3
|
UTSW |
19 |
13,388,083 (GRCm39) |
missense |
possibly damaging |
0.94 |
|