Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,644,122 (GRCm39) |
V940E |
probably damaging |
Het |
Adgrg7 |
A |
T |
16: 56,550,748 (GRCm39) |
|
probably null |
Het |
Alox12e |
T |
C |
11: 70,209,050 (GRCm39) |
I399V |
possibly damaging |
Het |
Apoa5 |
C |
A |
9: 46,180,607 (GRCm39) |
Q42K |
probably damaging |
Het |
Arfgap1 |
A |
G |
2: 180,620,215 (GRCm39) |
Y243C |
possibly damaging |
Het |
Arhgap12 |
A |
G |
18: 6,037,016 (GRCm39) |
|
probably null |
Het |
Arl16 |
G |
A |
11: 120,357,431 (GRCm39) |
|
probably benign |
Het |
Atp8b5 |
A |
G |
4: 43,370,577 (GRCm39) |
D951G |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,942,955 (GRCm39) |
L80Q |
probably damaging |
Het |
Celsr1 |
C |
T |
15: 85,822,176 (GRCm39) |
V1714I |
probably benign |
Het |
Celsr1 |
C |
T |
15: 85,914,550 (GRCm39) |
R1141H |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,252,775 (GRCm39) |
L351P |
probably damaging |
Het |
Dlc1 |
T |
A |
8: 37,405,829 (GRCm39) |
|
probably benign |
Het |
Dpy30 |
G |
T |
17: 74,622,906 (GRCm39) |
D25E |
probably benign |
Het |
Drosha |
T |
C |
15: 12,935,152 (GRCm39) |
W998R |
probably damaging |
Het |
Fibp |
A |
G |
19: 5,513,644 (GRCm39) |
D220G |
possibly damaging |
Het |
Grm3 |
C |
T |
5: 9,561,927 (GRCm39) |
C641Y |
probably damaging |
Het |
Gulo |
A |
T |
14: 66,245,570 (GRCm39) |
V8D |
probably benign |
Het |
Ifrd1 |
A |
T |
12: 40,263,095 (GRCm39) |
C164S |
possibly damaging |
Het |
Jam2 |
G |
A |
16: 84,606,295 (GRCm39) |
S103N |
probably benign |
Het |
Krtap17-1 |
T |
C |
11: 99,884,444 (GRCm39) |
T108A |
unknown |
Het |
Man2a2 |
A |
G |
7: 80,010,669 (GRCm39) |
F774S |
probably benign |
Het |
Map1b |
G |
A |
13: 99,566,839 (GRCm39) |
R1961W |
unknown |
Het |
Mib2 |
A |
G |
4: 155,740,508 (GRCm39) |
|
probably benign |
Het |
Mr1 |
A |
T |
1: 155,012,534 (GRCm39) |
F127I |
probably damaging |
Het |
Mrgprb2 |
A |
G |
7: 48,202,554 (GRCm39) |
I57T |
probably benign |
Het |
Ncan |
G |
T |
8: 70,550,731 (GRCm39) |
Y1154* |
probably null |
Het |
Nfx1 |
T |
A |
4: 40,977,285 (GRCm39) |
S320T |
probably benign |
Het |
Nlrp4f |
A |
G |
13: 65,335,369 (GRCm39) |
L740P |
probably damaging |
Het |
Nprl2 |
T |
C |
9: 107,422,277 (GRCm39) |
|
probably benign |
Het |
Opn1sw |
A |
G |
6: 29,379,754 (GRCm39) |
|
probably null |
Het |
Palld |
A |
G |
8: 61,986,386 (GRCm39) |
|
probably null |
Het |
Phf14 |
T |
A |
6: 11,933,726 (GRCm39) |
M196K |
possibly damaging |
Het |
Rnf145 |
T |
C |
11: 44,433,549 (GRCm39) |
|
probably null |
Het |
Sbf2 |
A |
T |
7: 109,977,303 (GRCm39) |
C610* |
probably null |
Het |
Sec24a |
C |
T |
11: 51,646,964 (GRCm39) |
A13T |
probably benign |
Het |
Smim8 |
TCTCCTC |
TCTC |
4: 34,769,010 (GRCm39) |
|
probably benign |
Het |
Sox8 |
A |
C |
17: 25,786,443 (GRCm39) |
L420R |
probably damaging |
Het |
Sry |
C |
G |
Y: 2,662,612 (GRCm39) |
Q349H |
unknown |
Het |
Sspo |
A |
G |
6: 48,441,530 (GRCm39) |
D1889G |
probably benign |
Het |
Sspo |
A |
T |
6: 48,468,418 (GRCm39) |
H4382L |
possibly damaging |
Het |
Tmem65 |
T |
C |
15: 58,662,037 (GRCm39) |
I141V |
probably damaging |
Het |
Tpr |
A |
T |
1: 150,301,400 (GRCm39) |
T1329S |
probably benign |
Het |
Trim17 |
C |
T |
11: 58,859,388 (GRCm39) |
R201W |
probably damaging |
Het |
Trim3 |
A |
G |
7: 105,267,182 (GRCm39) |
L399P |
possibly damaging |
Het |
Trim7 |
A |
G |
11: 48,736,477 (GRCm39) |
D277G |
possibly damaging |
Het |
Vstm2b |
A |
G |
7: 40,552,107 (GRCm39) |
N153S |
possibly damaging |
Het |
Wnk2 |
G |
T |
13: 49,231,561 (GRCm39) |
Q786K |
probably damaging |
Het |
Wnk4 |
A |
G |
11: 101,154,720 (GRCm39) |
*286W |
probably null |
Het |
Xpot |
A |
T |
10: 121,450,998 (GRCm39) |
L134Q |
probably damaging |
Het |
Ylpm1 |
C |
T |
12: 85,087,660 (GRCm39) |
P1148L |
probably damaging |
Het |
Zc3h7a |
G |
A |
16: 10,982,466 (GRCm39) |
Q20* |
probably null |
Het |
Zfp599 |
C |
T |
9: 22,161,130 (GRCm39) |
C345Y |
probably damaging |
Het |
|
Other mutations in Or5bw2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Or5bw2
|
APN |
7 |
6,573,667 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01387:Or5bw2
|
APN |
7 |
6,573,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Or5bw2
|
APN |
7 |
6,573,211 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01568:Or5bw2
|
APN |
7 |
6,573,569 (GRCm39) |
missense |
possibly damaging |
0.91 |
I2288:Or5bw2
|
UTSW |
7 |
6,573,818 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Or5bw2
|
UTSW |
7 |
6,573,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Or5bw2
|
UTSW |
7 |
6,573,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Or5bw2
|
UTSW |
7 |
6,573,652 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1103:Or5bw2
|
UTSW |
7 |
6,573,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1352:Or5bw2
|
UTSW |
7 |
6,573,782 (GRCm39) |
missense |
probably benign |
0.11 |
R1503:Or5bw2
|
UTSW |
7 |
6,573,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1630:Or5bw2
|
UTSW |
7 |
6,573,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R1981:Or5bw2
|
UTSW |
7 |
6,573,557 (GRCm39) |
missense |
probably benign |
0.01 |
R2228:Or5bw2
|
UTSW |
7 |
6,573,802 (GRCm39) |
missense |
probably benign |
|
R2258:Or5bw2
|
UTSW |
7 |
6,573,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R2259:Or5bw2
|
UTSW |
7 |
6,573,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R2260:Or5bw2
|
UTSW |
7 |
6,573,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4075:Or5bw2
|
UTSW |
7 |
6,573,142 (GRCm39) |
missense |
probably benign |
0.00 |
R4750:Or5bw2
|
UTSW |
7 |
6,573,850 (GRCm39) |
missense |
probably benign |
0.34 |
R4917:Or5bw2
|
UTSW |
7 |
6,573,643 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4918:Or5bw2
|
UTSW |
7 |
6,573,643 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5571:Or5bw2
|
UTSW |
7 |
6,573,824 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6969:Or5bw2
|
UTSW |
7 |
6,573,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Or5bw2
|
UTSW |
7 |
6,573,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7286:Or5bw2
|
UTSW |
7 |
6,573,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Or5bw2
|
UTSW |
7 |
6,572,960 (GRCm39) |
start gained |
probably benign |
|
R9475:Or5bw2
|
UTSW |
7 |
6,573,818 (GRCm39) |
missense |
probably damaging |
1.00 |
V1662:Or5bw2
|
UTSW |
7 |
6,573,818 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or5bw2
|
UTSW |
7 |
6,573,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|