Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb6 |
T |
C |
1: 75,151,479 (GRCm39) |
|
probably null |
Het |
Abcc9 |
G |
A |
6: 142,571,371 (GRCm39) |
|
probably benign |
Het |
Acss2 |
T |
C |
2: 155,416,575 (GRCm39) |
|
probably benign |
Het |
Atp8b4 |
G |
A |
2: 126,217,725 (GRCm39) |
T597I |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,961,015 (GRCm39) |
N796I |
probably benign |
Het |
Caskin2 |
T |
C |
11: 115,690,905 (GRCm39) |
|
probably null |
Het |
Cdhr2 |
A |
G |
13: 54,884,349 (GRCm39) |
N1295D |
probably benign |
Het |
Cog3 |
G |
A |
14: 75,962,239 (GRCm39) |
T534M |
probably benign |
Het |
Cpne1 |
A |
G |
2: 155,919,561 (GRCm39) |
S303P |
probably damaging |
Het |
Cs |
G |
A |
10: 128,187,086 (GRCm39) |
G74S |
possibly damaging |
Het |
Cyb5r4 |
G |
T |
9: 86,929,533 (GRCm39) |
S229I |
probably damaging |
Het |
Ddr1 |
C |
T |
17: 35,997,400 (GRCm39) |
A531T |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,018,810 (GRCm39) |
V529M |
probably damaging |
Het |
Edaradd |
C |
A |
13: 12,493,161 (GRCm39) |
R177L |
possibly damaging |
Het |
Esf1 |
T |
C |
2: 140,006,148 (GRCm39) |
D333G |
possibly damaging |
Het |
Fam8a1 |
T |
A |
13: 46,827,814 (GRCm39) |
L334H |
probably damaging |
Het |
Fbxl18 |
A |
G |
5: 142,871,558 (GRCm39) |
I559T |
probably damaging |
Het |
Fcrl2 |
A |
C |
3: 87,164,851 (GRCm39) |
V225G |
probably benign |
Het |
Ido1 |
C |
T |
8: 25,077,819 (GRCm39) |
V83M |
probably damaging |
Het |
Iffo1 |
T |
G |
6: 125,130,030 (GRCm39) |
C419G |
probably damaging |
Het |
Igfals |
A |
T |
17: 25,100,439 (GRCm39) |
Y510F |
probably benign |
Het |
Ipo9 |
A |
T |
1: 135,313,210 (GRCm39) |
Y1006* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,065,785 (GRCm39) |
S1737T |
probably benign |
Het |
Klhl32 |
C |
T |
4: 24,800,805 (GRCm39) |
|
probably null |
Het |
Klk1b11 |
T |
A |
7: 43,427,810 (GRCm39) |
C173S |
probably damaging |
Het |
Klk1b24 |
A |
T |
7: 43,840,889 (GRCm39) |
M106L |
probably benign |
Het |
Lamp1 |
G |
A |
8: 13,221,388 (GRCm39) |
|
probably null |
Het |
Mapk4 |
A |
T |
18: 74,103,365 (GRCm39) |
V48E |
probably damaging |
Het |
Marchf6 |
A |
T |
15: 31,486,082 (GRCm39) |
D395E |
probably damaging |
Het |
Mdp1 |
A |
G |
14: 55,896,465 (GRCm39) |
F157S |
probably damaging |
Het |
Mettl21e |
A |
T |
1: 44,250,255 (GRCm39) |
F50L |
probably damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,077,153 (GRCm39) |
I35T |
probably benign |
Het |
Natd1 |
T |
C |
11: 60,796,892 (GRCm39) |
Y91C |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,633,476 (GRCm39) |
Y2294N |
probably damaging |
Het |
Nrcam |
A |
G |
12: 44,610,841 (GRCm39) |
T520A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,117,061 (GRCm39) |
T324A |
probably benign |
Het |
Or10a2 |
G |
A |
7: 106,673,394 (GRCm39) |
A120T |
probably damaging |
Het |
Or4k51 |
T |
A |
2: 111,585,326 (GRCm39) |
I244N |
probably damaging |
Het |
Or52a5 |
A |
C |
7: 103,427,182 (GRCm39) |
D123E |
probably damaging |
Het |
Pam |
C |
T |
1: 97,792,123 (GRCm39) |
V433I |
probably benign |
Het |
Pck1 |
T |
A |
2: 173,000,353 (GRCm39) |
Y595N |
probably damaging |
Het |
Per2 |
C |
T |
1: 91,373,223 (GRCm39) |
|
probably null |
Het |
Piezo2 |
G |
C |
18: 63,278,162 (GRCm39) |
F247L |
possibly damaging |
Het |
Pkdcc |
A |
G |
17: 83,523,337 (GRCm39) |
Y148C |
probably damaging |
Het |
Plod2 |
A |
G |
9: 92,475,876 (GRCm39) |
T320A |
probably benign |
Het |
Ppip5k1 |
G |
A |
2: 121,147,157 (GRCm39) |
R1155C |
probably benign |
Het |
Ppp1r15b |
C |
T |
1: 133,059,382 (GRCm39) |
|
probably benign |
Het |
Prkn |
C |
T |
17: 11,456,536 (GRCm39) |
A119V |
probably damaging |
Het |
Ptprz1 |
G |
T |
6: 22,986,133 (GRCm39) |
C311F |
probably damaging |
Het |
Rab11fip3 |
A |
T |
17: 26,235,038 (GRCm39) |
V44E |
probably damaging |
Het |
Rpl5 |
T |
A |
5: 108,051,514 (GRCm39) |
|
probably benign |
Het |
Rttn |
G |
A |
18: 89,066,556 (GRCm39) |
V1201I |
probably benign |
Het |
Sdk1 |
A |
G |
5: 141,921,853 (GRCm39) |
N283S |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,405,529 (GRCm39) |
N418K |
probably benign |
Het |
Shmt2 |
T |
C |
10: 127,353,668 (GRCm39) |
D499G |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,293 (GRCm39) |
L403S |
probably damaging |
Het |
Slc5a1 |
A |
G |
5: 33,303,955 (GRCm39) |
T257A |
probably benign |
Het |
Snrnp35 |
T |
C |
5: 124,628,535 (GRCm39) |
V116A |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,981,538 (GRCm39) |
F593I |
probably damaging |
Het |
Tmem171 |
C |
A |
13: 98,828,574 (GRCm39) |
R192L |
probably benign |
Het |
Trappc3l |
T |
A |
10: 33,978,703 (GRCm39) |
L169Q |
unknown |
Het |
Ube2s |
T |
C |
7: 4,811,431 (GRCm39) |
E148G |
probably damaging |
Het |
Uspl1 |
T |
C |
5: 149,146,521 (GRCm39) |
F424S |
probably damaging |
Het |
Vmn1r2 |
T |
C |
4: 3,172,261 (GRCm39) |
V60A |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,829,575 (GRCm39) |
|
probably null |
Het |
Zfp735 |
C |
T |
11: 73,602,964 (GRCm39) |
S636L |
possibly damaging |
Het |
Zswim9 |
G |
A |
7: 12,995,094 (GRCm39) |
S354F |
probably damaging |
Het |
|
Other mutations in Or5m11b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02020:Or5m11b
|
APN |
2 |
85,805,579 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02126:Or5m11b
|
APN |
2 |
85,806,517 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02584:Or5m11b
|
APN |
2 |
85,806,219 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03410:Or5m11b
|
APN |
2 |
85,805,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Or5m11b
|
UTSW |
2 |
85,806,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Or5m11b
|
UTSW |
2 |
85,806,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Or5m11b
|
UTSW |
2 |
85,806,372 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1584:Or5m11b
|
UTSW |
2 |
85,806,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R2925:Or5m11b
|
UTSW |
2 |
85,806,125 (GRCm39) |
nonsense |
probably null |
|
R2970:Or5m11b
|
UTSW |
2 |
85,806,454 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4571:Or5m11b
|
UTSW |
2 |
85,806,175 (GRCm39) |
missense |
probably damaging |
0.97 |
R5533:Or5m11b
|
UTSW |
2 |
85,805,797 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5827:Or5m11b
|
UTSW |
2 |
85,805,650 (GRCm39) |
missense |
probably benign |
0.00 |
R5967:Or5m11b
|
UTSW |
2 |
85,806,535 (GRCm39) |
missense |
probably benign |
0.01 |
R6291:Or5m11b
|
UTSW |
2 |
85,805,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R6735:Or5m11b
|
UTSW |
2 |
85,805,778 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6897:Or5m11b
|
UTSW |
2 |
85,805,700 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7053:Or5m11b
|
UTSW |
2 |
85,806,358 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7163:Or5m11b
|
UTSW |
2 |
85,805,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Or5m11b
|
UTSW |
2 |
85,805,780 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8047:Or5m11b
|
UTSW |
2 |
85,806,271 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8271:Or5m11b
|
UTSW |
2 |
85,806,085 (GRCm39) |
missense |
probably benign |
0.40 |
R8271:Or5m11b
|
UTSW |
2 |
85,805,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Or5m11b
|
UTSW |
2 |
85,806,358 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9100:Or5m11b
|
UTSW |
2 |
85,806,096 (GRCm39) |
missense |
probably benign |
0.00 |
R9190:Or5m11b
|
UTSW |
2 |
85,805,884 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9646:Or5m11b
|
UTSW |
2 |
85,806,446 (GRCm39) |
missense |
probably benign |
0.18 |
|