Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
C |
T |
17: 57,754,891 (GRCm39) |
A663V |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,602,699 (GRCm39) |
|
probably benign |
Het |
B4galt6 |
T |
C |
18: 20,833,804 (GRCm39) |
I194V |
probably benign |
Het |
Caprin1 |
T |
C |
2: 103,609,714 (GRCm39) |
Y188C |
probably damaging |
Het |
Ccdc85a |
A |
G |
11: 28,526,672 (GRCm39) |
F284S |
possibly damaging |
Het |
Ccdc88b |
A |
T |
19: 6,832,717 (GRCm39) |
|
probably benign |
Het |
Cox18 |
C |
T |
5: 90,365,384 (GRCm39) |
V272I |
possibly damaging |
Het |
Dars1 |
A |
T |
1: 128,299,898 (GRCm39) |
M362K |
probably benign |
Het |
Ddi1 |
A |
T |
9: 6,265,760 (GRCm39) |
M203K |
probably benign |
Het |
Dlg4 |
G |
A |
11: 69,933,093 (GRCm39) |
G500R |
probably damaging |
Het |
Ebf3 |
G |
A |
7: 136,807,919 (GRCm39) |
P375S |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,084,537 (GRCm39) |
L842M |
possibly damaging |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gm5581 |
T |
C |
6: 131,144,909 (GRCm39) |
|
noncoding transcript |
Het |
Mapk10 |
A |
T |
5: 103,186,534 (GRCm39) |
D29E |
probably benign |
Het |
Mib2 |
C |
T |
4: 155,745,628 (GRCm39) |
R61H |
probably damaging |
Het |
Mki67 |
A |
G |
7: 135,303,697 (GRCm39) |
S724P |
probably benign |
Het |
Mtor |
T |
C |
4: 148,622,758 (GRCm39) |
I1946T |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,260,995 (GRCm39) |
L1873P |
probably damaging |
Het |
Myom1 |
C |
T |
17: 71,415,310 (GRCm39) |
Q1226* |
probably null |
Het |
Neb |
A |
G |
2: 52,095,668 (GRCm39) |
L4858P |
probably damaging |
Het |
Or51f5 |
A |
T |
7: 102,424,114 (GRCm39) |
I128F |
probably damaging |
Het |
Or5p76 |
T |
C |
7: 108,122,492 (GRCm39) |
I222V |
probably benign |
Het |
Pcdhb14 |
C |
T |
18: 37,583,086 (GRCm39) |
H731Y |
probably benign |
Het |
Prdm16 |
T |
C |
4: 154,412,744 (GRCm39) |
N1087S |
probably benign |
Het |
Prdm2 |
C |
T |
4: 142,861,157 (GRCm39) |
G711D |
probably damaging |
Het |
Proser1 |
G |
A |
3: 53,386,365 (GRCm39) |
G749D |
probably damaging |
Het |
Ptch1 |
A |
T |
13: 63,713,166 (GRCm39) |
|
probably benign |
Het |
Pus10 |
A |
T |
11: 23,657,548 (GRCm39) |
K233* |
probably null |
Het |
Rasa2 |
A |
G |
9: 96,426,372 (GRCm39) |
Y825H |
probably benign |
Het |
Tbcd |
T |
C |
11: 121,494,104 (GRCm39) |
F969S |
probably damaging |
Het |
Tbp |
T |
A |
17: 15,724,878 (GRCm39) |
S133T |
probably damaging |
Het |
Tnks |
C |
T |
8: 35,310,137 (GRCm39) |
G1062D |
probably damaging |
Het |
Tnrc6b |
T |
A |
15: 80,764,372 (GRCm39) |
S625T |
probably damaging |
Het |
Triobp |
T |
C |
15: 78,850,562 (GRCm39) |
S239P |
probably benign |
Het |
Ubiad1 |
T |
C |
4: 148,528,564 (GRCm39) |
D115G |
probably benign |
Het |
Uckl1 |
A |
G |
2: 181,211,381 (GRCm39) |
S483P |
probably damaging |
Het |
Vill |
A |
G |
9: 118,887,509 (GRCm39) |
D91G |
probably benign |
Het |
Wdr62 |
C |
A |
7: 29,970,207 (GRCm39) |
C200F |
probably damaging |
Het |
Zfp341 |
G |
A |
2: 154,483,969 (GRCm39) |
C586Y |
possibly damaging |
Het |
Zfp687 |
G |
A |
3: 94,918,575 (GRCm39) |
T399I |
possibly damaging |
Het |
Zp1 |
G |
T |
19: 10,894,078 (GRCm39) |
|
probably benign |
Het |
Zzz3 |
T |
A |
3: 152,157,720 (GRCm39) |
D263E |
probably benign |
Het |
|
Other mutations in Or5m9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02370:Or5m9b
|
APN |
2 |
85,905,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R0269:Or5m9b
|
UTSW |
2 |
85,905,485 (GRCm39) |
missense |
probably benign |
0.03 |
R0409:Or5m9b
|
UTSW |
2 |
85,905,646 (GRCm39) |
nonsense |
probably null |
|
R0412:Or5m9b
|
UTSW |
2 |
85,905,435 (GRCm39) |
missense |
probably benign |
0.16 |
R0617:Or5m9b
|
UTSW |
2 |
85,905,485 (GRCm39) |
missense |
probably benign |
0.03 |
R0846:Or5m9b
|
UTSW |
2 |
85,905,510 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1251:Or5m9b
|
UTSW |
2 |
85,905,164 (GRCm39) |
missense |
probably benign |
0.20 |
R1646:Or5m9b
|
UTSW |
2 |
85,905,960 (GRCm39) |
missense |
probably damaging |
0.98 |
R1670:Or5m9b
|
UTSW |
2 |
85,905,594 (GRCm39) |
missense |
probably benign |
|
R1775:Or5m9b
|
UTSW |
2 |
85,905,104 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1968:Or5m9b
|
UTSW |
2 |
85,905,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Or5m9b
|
UTSW |
2 |
85,905,675 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4639:Or5m9b
|
UTSW |
2 |
85,905,923 (GRCm39) |
missense |
probably benign |
0.24 |
R4957:Or5m9b
|
UTSW |
2 |
85,905,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Or5m9b
|
UTSW |
2 |
85,905,882 (GRCm39) |
missense |
probably benign |
0.28 |
R5862:Or5m9b
|
UTSW |
2 |
85,905,990 (GRCm39) |
missense |
probably benign |
0.00 |
R6235:Or5m9b
|
UTSW |
2 |
85,905,510 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6355:Or5m9b
|
UTSW |
2 |
85,905,216 (GRCm39) |
missense |
probably benign |
0.04 |
R6943:Or5m9b
|
UTSW |
2 |
85,905,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R8033:Or5m9b
|
UTSW |
2 |
85,905,219 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8796:Or5m9b
|
UTSW |
2 |
85,905,518 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8861:Or5m9b
|
UTSW |
2 |
85,905,960 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1088:Or5m9b
|
UTSW |
2 |
85,905,667 (GRCm39) |
missense |
possibly damaging |
0.66 |
Z1177:Or5m9b
|
UTSW |
2 |
85,905,768 (GRCm39) |
nonsense |
probably null |
|
|