Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,448,729 (GRCm39) |
L147Q |
probably damaging |
Het |
Aadacl4fm5 |
T |
C |
4: 144,504,329 (GRCm39) |
N274S |
probably damaging |
Het |
Abcb1a |
A |
G |
5: 8,724,791 (GRCm39) |
T75A |
possibly damaging |
Het |
Acvr1 |
A |
T |
2: 58,337,597 (GRCm39) |
L495* |
probably null |
Het |
Add1 |
T |
C |
5: 34,767,961 (GRCm39) |
I240T |
probably benign |
Het |
Adgra2 |
C |
A |
8: 27,611,306 (GRCm39) |
S870* |
probably null |
Het |
Amer3 |
G |
A |
1: 34,618,408 (GRCm39) |
|
probably benign |
Het |
Baz2b |
A |
T |
2: 59,792,670 (GRCm39) |
V486D |
probably benign |
Het |
Bcorl1 |
T |
A |
X: 47,494,821 (GRCm39) |
D1697E |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,411,338 (GRCm39) |
D282G |
possibly damaging |
Het |
Cep112 |
A |
G |
11: 108,362,880 (GRCm39) |
D200G |
probably damaging |
Het |
Clec4a4 |
C |
T |
6: 122,967,401 (GRCm39) |
P26S |
probably benign |
Het |
Crygf |
A |
C |
1: 65,967,197 (GRCm39) |
R102S |
possibly damaging |
Het |
Cyp2b19 |
A |
T |
7: 26,466,585 (GRCm39) |
E404D |
probably benign |
Het |
Dcdc2a |
A |
G |
13: 25,245,237 (GRCm39) |
I105V |
probably benign |
Het |
Dus4l |
T |
C |
12: 31,690,938 (GRCm39) |
M238V |
probably damaging |
Het |
Eprs1 |
G |
A |
1: 185,114,031 (GRCm39) |
M326I |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,114,661 (GRCm39) |
T1010A |
probably benign |
Het |
Fam124b |
T |
C |
1: 80,178,148 (GRCm39) |
T284A |
possibly damaging |
Het |
Glb1l2 |
A |
G |
9: 26,680,420 (GRCm39) |
|
probably benign |
Het |
Gm16223 |
T |
A |
5: 42,225,298 (GRCm39) |
|
probably null |
Het |
Gm4952 |
T |
A |
19: 12,604,278 (GRCm39) |
M230K |
probably damaging |
Het |
Gm5828 |
C |
A |
1: 16,839,583 (GRCm39) |
|
noncoding transcript |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Ifna16 |
T |
A |
4: 88,594,979 (GRCm39) |
T39S |
possibly damaging |
Het |
Kcnc3 |
G |
A |
7: 44,245,027 (GRCm39) |
G439D |
probably damaging |
Het |
Kif1c |
T |
C |
11: 70,596,555 (GRCm39) |
S257P |
probably damaging |
Het |
Kng1 |
A |
G |
16: 22,898,510 (GRCm39) |
K456E |
probably damaging |
Het |
Lpxn |
T |
C |
19: 12,801,414 (GRCm39) |
L142P |
probably damaging |
Het |
Lratd1 |
C |
T |
12: 14,199,864 (GRCm39) |
V288M |
probably damaging |
Het |
Med23 |
A |
G |
10: 24,768,565 (GRCm39) |
|
probably benign |
Het |
Mks1 |
A |
T |
11: 87,751,937 (GRCm39) |
D369V |
probably benign |
Het |
Myo1d |
A |
T |
11: 80,576,734 (GRCm39) |
Y114N |
probably damaging |
Het |
Npas2 |
A |
G |
1: 39,350,935 (GRCm39) |
D126G |
possibly damaging |
Het |
Oga |
A |
G |
19: 45,765,370 (GRCm39) |
S146P |
probably damaging |
Het |
Onecut2 |
T |
C |
18: 64,474,651 (GRCm39) |
F401L |
possibly damaging |
Het |
Or10n1 |
T |
C |
9: 39,524,992 (GRCm39) |
I43T |
probably damaging |
Het |
Or10v1 |
A |
G |
19: 11,873,978 (GRCm39) |
T198A |
probably benign |
Het |
Parp11 |
T |
A |
6: 127,451,256 (GRCm39) |
F102Y |
possibly damaging |
Het |
Pcnx1 |
C |
T |
12: 81,965,572 (GRCm39) |
H580Y |
probably damaging |
Het |
Pde3b |
A |
G |
7: 114,130,001 (GRCm39) |
H852R |
probably damaging |
Het |
Pira1 |
G |
A |
7: 3,742,639 (GRCm39) |
T23I |
possibly damaging |
Het |
Pou2af1 |
A |
G |
9: 51,144,508 (GRCm39) |
T141A |
probably benign |
Het |
Rgs22 |
A |
C |
15: 36,013,246 (GRCm39) |
V1190G |
probably benign |
Het |
Rnf112 |
T |
C |
11: 61,341,236 (GRCm39) |
S450G |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,987,378 (GRCm39) |
I893N |
probably damaging |
Het |
Rps3a1 |
A |
G |
3: 86,045,834 (GRCm39) |
V210A |
probably benign |
Het |
Runx2 |
C |
T |
17: 45,046,224 (GRCm39) |
A114T |
possibly damaging |
Het |
Sardh |
A |
G |
2: 27,087,702 (GRCm39) |
V723A |
possibly damaging |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Secisbp2 |
A |
G |
13: 51,836,131 (GRCm39) |
S742G |
possibly damaging |
Het |
Selenow |
G |
T |
7: 15,654,223 (GRCm39) |
|
probably benign |
Het |
Slc30a4 |
A |
G |
2: 122,531,334 (GRCm39) |
V226A |
probably damaging |
Het |
Sntb2 |
A |
G |
8: 107,718,164 (GRCm39) |
N291D |
probably damaging |
Het |
Sorbs2 |
A |
G |
8: 46,222,866 (GRCm39) |
T190A |
probably damaging |
Het |
Spata31e5 |
T |
A |
1: 28,817,829 (GRCm39) |
T68S |
possibly damaging |
Het |
Specc1 |
T |
A |
11: 62,047,358 (GRCm39) |
L909H |
probably damaging |
Het |
Sprr1b |
T |
C |
3: 92,344,414 (GRCm39) |
*154W |
probably null |
Het |
Taar4 |
T |
A |
10: 23,836,510 (GRCm39) |
M40K |
possibly damaging |
Het |
Ubr2 |
A |
T |
17: 47,311,749 (GRCm39) |
L34H |
probably damaging |
Het |
Ubxn6 |
T |
C |
17: 56,376,003 (GRCm39) |
K386R |
probably benign |
Het |
Vmn2r112 |
A |
T |
17: 22,821,825 (GRCm39) |
T168S |
probably benign |
Het |
Xirp2 |
A |
T |
2: 67,344,667 (GRCm39) |
R2303* |
probably null |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp13 |
G |
T |
17: 23,795,386 (GRCm39) |
T395K |
probably damaging |
Het |
Zfp281 |
A |
G |
1: 136,554,435 (GRCm39) |
N471S |
probably benign |
Het |
|
Other mutations in Or4f61 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Or4f61
|
APN |
2 |
111,922,439 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01701:Or4f61
|
APN |
2 |
111,922,851 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02085:Or4f61
|
APN |
2 |
111,922,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02156:Or4f61
|
APN |
2 |
111,922,361 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02266:Or4f61
|
APN |
2 |
111,922,588 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02396:Or4f61
|
APN |
2 |
111,922,812 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02602:Or4f61
|
APN |
2 |
111,922,906 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03130:Or4f61
|
APN |
2 |
111,922,166 (GRCm39) |
missense |
probably benign |
|
R0452:Or4f61
|
UTSW |
2 |
111,922,981 (GRCm39) |
nonsense |
probably null |
|
R1498:Or4f61
|
UTSW |
2 |
111,922,938 (GRCm39) |
missense |
probably benign |
0.40 |
R1852:Or4f61
|
UTSW |
2 |
111,922,192 (GRCm39) |
missense |
probably benign |
0.03 |
R2118:Or4f61
|
UTSW |
2 |
111,922,675 (GRCm39) |
missense |
probably benign |
0.02 |
R2219:Or4f61
|
UTSW |
2 |
111,922,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R2357:Or4f61
|
UTSW |
2 |
111,922,743 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3743:Or4f61
|
UTSW |
2 |
111,922,965 (GRCm39) |
missense |
probably benign |
0.33 |
R4692:Or4f61
|
UTSW |
2 |
111,923,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Or4f61
|
UTSW |
2 |
111,922,452 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5150:Or4f61
|
UTSW |
2 |
111,922,880 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5230:Or4f61
|
UTSW |
2 |
111,922,734 (GRCm39) |
missense |
probably benign |
0.12 |
R5991:Or4f61
|
UTSW |
2 |
111,922,960 (GRCm39) |
missense |
probably benign |
0.30 |
R7894:Or4f61
|
UTSW |
2 |
111,922,822 (GRCm39) |
missense |
probably benign |
|
R8991:Or4f61
|
UTSW |
2 |
111,922,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Or4f61
|
UTSW |
2 |
111,922,410 (GRCm39) |
missense |
probably benign |
0.12 |
R9595:Or4f61
|
UTSW |
2 |
111,922,375 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Or4f61
|
UTSW |
2 |
111,922,929 (GRCm39) |
missense |
possibly damaging |
0.88 |
|