Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adrb2 |
T |
C |
18: 62,312,127 (GRCm39) |
I233V |
probably damaging |
Het |
Alox5 |
T |
A |
6: 116,437,924 (GRCm39) |
Y21F |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,739,798 (GRCm39) |
T1942A |
probably benign |
Het |
Aoc1l1 |
T |
C |
6: 48,953,064 (GRCm39) |
S330P |
probably damaging |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
Bckdk |
C |
T |
7: 127,505,591 (GRCm39) |
A238V |
probably benign |
Het |
Casp1 |
A |
G |
9: 5,299,333 (GRCm39) |
T21A |
probably benign |
Het |
Ccdc39 |
T |
C |
3: 33,880,671 (GRCm39) |
H432R |
probably benign |
Het |
Cttnbp2 |
A |
C |
6: 18,405,248 (GRCm39) |
C574G |
probably damaging |
Het |
Cyp1a1 |
T |
C |
9: 57,607,432 (GRCm39) |
V20A |
probably benign |
Het |
Dhx38 |
C |
T |
8: 110,279,763 (GRCm39) |
V976I |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,126,467 (GRCm39) |
S1287P |
possibly damaging |
Het |
Dnttip2 |
T |
C |
3: 122,070,146 (GRCm39) |
S454P |
probably damaging |
Het |
Drp2 |
A |
T |
X: 133,335,884 (GRCm39) |
|
probably benign |
Het |
Flcn |
C |
T |
11: 59,694,610 (GRCm39) |
V121I |
possibly damaging |
Het |
Fmo1 |
G |
C |
1: 162,661,217 (GRCm39) |
Y355* |
probably null |
Het |
Git2 |
T |
A |
5: 114,902,727 (GRCm39) |
H138L |
probably damaging |
Het |
Gpr162 |
G |
A |
6: 124,838,658 (GRCm39) |
|
probably benign |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,797,638 (GRCm39) |
I881T |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,646,747 (GRCm39) |
C1754S |
probably damaging |
Het |
Mpp3 |
A |
T |
11: 101,914,246 (GRCm39) |
D116E |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,036,747 (GRCm39) |
D985G |
probably damaging |
Het |
Necap1 |
T |
C |
6: 122,864,337 (GRCm39) |
V273A |
probably damaging |
Het |
Nlrc5 |
T |
C |
8: 95,203,192 (GRCm39) |
S431P |
probably damaging |
Het |
Nutm2 |
A |
T |
13: 50,623,920 (GRCm39) |
T206S |
probably benign |
Het |
Or2d3 |
GAACAACAACAA |
GAACAACAA |
7: 106,490,567 (GRCm39) |
|
probably benign |
Het |
Or8g19 |
G |
A |
9: 39,055,725 (GRCm39) |
A110T |
probably damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,564 (GRCm39) |
S235P |
probably damaging |
Het |
Podnl1 |
G |
A |
8: 84,853,897 (GRCm39) |
R89H |
probably benign |
Het |
Prpf38b |
T |
C |
3: 108,818,487 (GRCm39) |
Y91C |
probably damaging |
Het |
Radil |
C |
T |
5: 142,480,560 (GRCm39) |
A632T |
probably benign |
Het |
Rpap2 |
G |
A |
5: 107,749,661 (GRCm39) |
V62I |
possibly damaging |
Het |
Sdf2 |
C |
T |
11: 78,141,863 (GRCm39) |
T66I |
probably damaging |
Het |
Specc1 |
T |
C |
11: 62,009,356 (GRCm39) |
S371P |
probably damaging |
Het |
Suco |
T |
C |
1: 161,674,799 (GRCm39) |
E416G |
probably damaging |
Het |
Sys1 |
T |
C |
2: 164,303,315 (GRCm39) |
W10R |
probably damaging |
Het |
Tars3 |
C |
T |
7: 65,332,567 (GRCm39) |
T556M |
probably damaging |
Het |
Tcirg1 |
C |
T |
19: 3,949,069 (GRCm39) |
D407N |
probably damaging |
Het |
Tefm |
G |
T |
11: 80,031,156 (GRCm39) |
L27I |
probably benign |
Het |
Tenm2 |
A |
G |
11: 35,918,225 (GRCm39) |
I1845T |
probably benign |
Het |
Tfam |
A |
T |
10: 71,069,233 (GRCm39) |
I119N |
probably damaging |
Het |
Tle1 |
ACAGGTTTCTTCAGGTTTCTT |
ACAGGTTTCTT |
4: 72,036,400 (GRCm39) |
|
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,804,889 (GRCm39) |
I947T |
probably damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,611,202 (GRCm39) |
T1205A |
probably benign |
Het |
Vmn2r25 |
T |
C |
6: 123,805,496 (GRCm39) |
R454G |
probably damaging |
Het |
Xylb |
T |
C |
9: 119,217,781 (GRCm39) |
V477A |
probably benign |
Het |
|
Other mutations in Or5p79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Or5p79
|
APN |
7 |
108,221,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01979:Or5p79
|
APN |
7 |
108,221,648 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02373:Or5p79
|
APN |
7 |
108,221,310 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02754:Or5p79
|
APN |
7 |
108,221,880 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03008:Or5p79
|
APN |
7 |
108,221,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R0305:Or5p79
|
UTSW |
7 |
108,221,792 (GRCm39) |
missense |
probably benign |
0.01 |
R0584:Or5p79
|
UTSW |
7 |
108,221,622 (GRCm39) |
missense |
probably benign |
0.00 |
R0611:Or5p79
|
UTSW |
7 |
108,221,494 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0947:Or5p79
|
UTSW |
7 |
108,221,879 (GRCm39) |
missense |
probably benign |
0.02 |
R1488:Or5p79
|
UTSW |
7 |
108,221,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:Or5p79
|
UTSW |
7 |
108,221,817 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3763:Or5p79
|
UTSW |
7 |
108,221,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4369:Or5p79
|
UTSW |
7 |
108,221,096 (GRCm39) |
missense |
probably benign |
0.27 |
R4371:Or5p79
|
UTSW |
7 |
108,221,096 (GRCm39) |
missense |
probably benign |
0.27 |
R4609:Or5p79
|
UTSW |
7 |
108,221,711 (GRCm39) |
missense |
probably benign |
0.35 |
R5389:Or5p79
|
UTSW |
7 |
108,221,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R6499:Or5p79
|
UTSW |
7 |
108,221,713 (GRCm39) |
missense |
probably benign |
0.02 |
R6684:Or5p79
|
UTSW |
7 |
108,221,141 (GRCm39) |
missense |
probably damaging |
0.98 |
R7531:Or5p79
|
UTSW |
7 |
108,221,269 (GRCm39) |
missense |
probably benign |
0.06 |
R7555:Or5p79
|
UTSW |
7 |
108,221,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7893:Or5p79
|
UTSW |
7 |
108,221,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Or5p79
|
UTSW |
7 |
108,221,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Or5p79
|
UTSW |
7 |
108,221,027 (GRCm39) |
missense |
probably benign |
0.00 |
R8904:Or5p79
|
UTSW |
7 |
108,221,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R9635:Or5p79
|
UTSW |
7 |
108,221,654 (GRCm39) |
missense |
probably benign |
0.00 |
R9795:Or5p79
|
UTSW |
7 |
108,221,869 (GRCm39) |
missense |
probably benign |
0.39 |
|