Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adap1 |
C |
T |
5: 139,293,541 (GRCm39) |
V57M |
probably damaging |
Het |
Agap3 |
A |
G |
5: 24,688,369 (GRCm39) |
K23E |
possibly damaging |
Het |
Anln |
A |
T |
9: 22,249,331 (GRCm39) |
I132K |
probably damaging |
Het |
Anxa4 |
T |
C |
6: 86,737,683 (GRCm39) |
T13A |
probably benign |
Het |
Bdp1 |
A |
T |
13: 100,235,022 (GRCm39) |
Y191N |
possibly damaging |
Het |
Carm1 |
G |
A |
9: 21,498,204 (GRCm39) |
V403M |
probably damaging |
Het |
Cbx7 |
A |
G |
15: 79,807,671 (GRCm39) |
|
probably null |
Het |
Chd8 |
A |
C |
14: 52,451,757 (GRCm39) |
N16K |
possibly damaging |
Het |
Crtc3 |
A |
T |
7: 80,242,315 (GRCm39) |
D499E |
probably damaging |
Het |
Cul3 |
A |
G |
1: 80,249,432 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 104,060,631 (GRCm39) |
D1421G |
probably damaging |
Het |
Fgb |
T |
A |
3: 82,952,367 (GRCm39) |
E167D |
probably benign |
Het |
Gimap6 |
T |
A |
6: 48,679,409 (GRCm39) |
Q209L |
probably damaging |
Het |
Gm3604 |
G |
A |
13: 62,517,990 (GRCm39) |
H123Y |
possibly damaging |
Het |
Gm5884 |
A |
T |
6: 128,622,749 (GRCm39) |
|
noncoding transcript |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Obox3 |
T |
C |
7: 15,360,848 (GRCm39) |
E97G |
probably damaging |
Het |
Obsl1 |
T |
C |
1: 75,466,264 (GRCm39) |
H1488R |
probably benign |
Het |
Or6c75 |
A |
G |
10: 129,337,723 (GRCm39) |
*323W |
probably null |
Het |
Pak5 |
T |
A |
2: 135,958,855 (GRCm39) |
K78* |
probably null |
Het |
Paqr9 |
A |
G |
9: 95,442,877 (GRCm39) |
N289S |
probably damaging |
Het |
Pde3b |
G |
A |
7: 114,122,577 (GRCm39) |
R715H |
probably damaging |
Het |
Pglyrp2 |
T |
C |
17: 32,634,835 (GRCm39) |
H509R |
probably benign |
Het |
Pik3ap1 |
A |
C |
19: 41,290,881 (GRCm39) |
N550K |
probably benign |
Het |
Pon3 |
A |
G |
6: 5,221,671 (GRCm39) |
Y320H |
probably damaging |
Het |
Ptprt |
T |
A |
2: 161,608,227 (GRCm39) |
T690S |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,000,686 (GRCm39) |
D925E |
probably benign |
Het |
Rag1 |
T |
C |
2: 101,473,018 (GRCm39) |
D708G |
probably damaging |
Het |
Rbm12 |
C |
T |
2: 155,937,480 (GRCm39) |
|
probably benign |
Het |
Rbmy1b |
A |
G |
Y: 3,774,885 (GRCm39) |
I27M |
probably benign |
Het |
Rfx2 |
G |
A |
17: 57,092,354 (GRCm39) |
H315Y |
possibly damaging |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sis |
T |
C |
3: 72,820,543 (GRCm39) |
N1407S |
probably benign |
Het |
Slco1c1 |
T |
A |
6: 141,490,555 (GRCm39) |
L261Q |
probably damaging |
Het |
Sox30 |
T |
G |
11: 45,875,589 (GRCm39) |
L447R |
possibly damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Ssu72 |
A |
G |
4: 155,789,882 (GRCm39) |
N15S |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,137,574 (GRCm39) |
S455F |
probably damaging |
Het |
Stk4 |
T |
A |
2: 163,928,462 (GRCm39) |
L97Q |
probably damaging |
Het |
Sulf1 |
A |
T |
1: 12,856,869 (GRCm39) |
N40I |
probably damaging |
Het |
Sympk |
G |
A |
7: 18,782,794 (GRCm39) |
V877I |
probably benign |
Het |
Taar7b |
A |
T |
10: 23,876,204 (GRCm39) |
H123L |
probably damaging |
Het |
Teddm1b |
A |
G |
1: 153,750,362 (GRCm39) |
Y57C |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,070,935 (GRCm39) |
C2121* |
probably null |
Het |
Tnfsf11 |
T |
A |
14: 78,537,385 (GRCm39) |
R93* |
probably null |
Het |
Tspan12 |
A |
C |
6: 21,835,378 (GRCm39) |
|
probably benign |
Het |
Tyrp1 |
A |
G |
4: 80,759,012 (GRCm39) |
E295G |
probably null |
Het |
Vps4a |
T |
C |
8: 107,769,693 (GRCm39) |
I334T |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,583,462 (GRCm39) |
S1110P |
probably damaging |
Het |
Zfp507 |
A |
G |
7: 35,491,136 (GRCm39) |
S716P |
probably damaging |
Het |
|
Other mutations in Or4e1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01596:Or4e1
|
APN |
14 |
52,700,822 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02635:Or4e1
|
APN |
14 |
52,701,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Or4e1
|
UTSW |
14 |
52,700,669 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Or4e1
|
UTSW |
14 |
52,701,383 (GRCm39) |
start codon destroyed |
possibly damaging |
0.79 |
R0600:Or4e1
|
UTSW |
14 |
52,700,966 (GRCm39) |
missense |
probably benign |
0.00 |
R0612:Or4e1
|
UTSW |
14 |
52,701,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1691:Or4e1
|
UTSW |
14 |
52,701,288 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4290:Or4e1
|
UTSW |
14 |
52,701,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Or4e1
|
UTSW |
14 |
52,701,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Or4e1
|
UTSW |
14 |
52,700,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Or4e1
|
UTSW |
14 |
52,701,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Or4e1
|
UTSW |
14 |
52,701,311 (GRCm39) |
missense |
probably benign |
0.00 |
R5384:Or4e1
|
UTSW |
14 |
52,700,714 (GRCm39) |
missense |
probably benign |
0.41 |
R5663:Or4e1
|
UTSW |
14 |
52,701,052 (GRCm39) |
missense |
probably benign |
0.12 |
R5861:Or4e1
|
UTSW |
14 |
52,700,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Or4e1
|
UTSW |
14 |
52,701,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Or4e1
|
UTSW |
14 |
52,700,932 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7216:Or4e1
|
UTSW |
14 |
52,700,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Or4e1
|
UTSW |
14 |
52,700,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Or4e1
|
UTSW |
14 |
52,701,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Or4e1
|
UTSW |
14 |
52,701,358 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8942:Or4e1
|
UTSW |
14 |
52,700,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R9185:Or4e1
|
UTSW |
14 |
52,700,984 (GRCm39) |
missense |
probably benign |
0.33 |
R9218:Or4e1
|
UTSW |
14 |
52,700,788 (GRCm39) |
missense |
probably damaging |
0.97 |
R9516:Or4e1
|
UTSW |
14 |
52,700,873 (GRCm39) |
missense |
probably benign |
0.02 |
|