Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam15 |
G |
A |
3: 89,343,567 (GRCm38) |
Q581* |
probably null |
Het |
Agl |
A |
G |
3: 116,793,774 (GRCm38) |
V44A |
probably damaging |
Het |
Alpk3 |
T |
A |
7: 81,092,260 (GRCm38) |
D608E |
possibly damaging |
Het |
Aspm |
C |
A |
1: 139,455,227 (GRCm38) |
|
probably benign |
Het |
Bbs2 |
T |
C |
8: 94,068,367 (GRCm38) |
N692S |
probably benign |
Het |
Bend4 |
A |
G |
5: 67,417,818 (GRCm38) |
I240T |
probably benign |
Het |
Casp8 |
G |
T |
1: 58,833,736 (GRCm38) |
R277L |
possibly damaging |
Het |
Ccdc61 |
A |
T |
7: 18,900,940 (GRCm38) |
I123N |
probably damaging |
Het |
Ccr9 |
T |
G |
9: 123,779,434 (GRCm38) |
I60M |
probably benign |
Het |
Cd163 |
T |
A |
6: 124,326,572 (GRCm38) |
W1066R |
probably benign |
Het |
Cd226 |
A |
T |
18: 89,207,183 (GRCm38) |
H68L |
probably benign |
Het |
Cdkn3 |
T |
A |
14: 46,767,217 (GRCm38) |
C79S |
probably null |
Het |
Cnnm1 |
A |
T |
19: 43,469,723 (GRCm38) |
E658V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,956,029 (GRCm38) |
R304G |
probably damaging |
Het |
Cpt1a |
T |
A |
19: 3,365,760 (GRCm38) |
V286E |
possibly damaging |
Het |
Creg2 |
C |
A |
1: 39,624,954 (GRCm38) |
R212L |
probably benign |
Het |
Cyp26a1 |
T |
G |
19: 37,699,962 (GRCm38) |
S311A |
probably damaging |
Het |
Cyp2b10 |
T |
C |
7: 25,926,223 (GRCm38) |
Y484H |
probably benign |
Het |
Cyp3a44 |
T |
A |
5: 145,788,467 (GRCm38) |
Y308F |
possibly damaging |
Het |
Dlg5 |
A |
G |
14: 24,164,089 (GRCm38) |
V744A |
probably benign |
Het |
Dlgap2 |
T |
A |
8: 14,727,128 (GRCm38) |
Y124* |
probably null |
Het |
Dnah3 |
T |
C |
7: 119,922,880 (GRCm38) |
D4030G |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,458,584 (GRCm38) |
T4456A |
possibly damaging |
Het |
Dtx2 |
T |
A |
5: 136,023,699 (GRCm38) |
V347D |
probably benign |
Het |
Gigyf2 |
C |
T |
1: 87,407,167 (GRCm38) |
T294M |
probably damaging |
Het |
Gli3 |
C |
G |
13: 15,726,162 (GRCm38) |
S1378* |
probably null |
Het |
Gm884 |
A |
G |
11: 103,542,120 (GRCm38) |
S1232P |
possibly damaging |
Het |
Gnao1 |
G |
A |
8: 93,966,999 (GRCm38) |
D337N |
probably benign |
Het |
Gp2 |
T |
A |
7: 119,449,129 (GRCm38) |
Q422L |
probably benign |
Het |
Ifit1 |
T |
A |
19: 34,648,469 (GRCm38) |
M335K |
possibly damaging |
Het |
Ism1 |
T |
C |
2: 139,678,757 (GRCm38) |
S30P |
probably benign |
Het |
Itgax |
A |
G |
7: 128,140,447 (GRCm38) |
D677G |
probably damaging |
Het |
Kansl1l |
G |
A |
1: 66,725,922 (GRCm38) |
A442V |
probably damaging |
Het |
Kif13a |
T |
C |
13: 46,771,524 (GRCm38) |
I311M |
probably damaging |
Het |
Lsm14b |
T |
A |
2: 180,031,425 (GRCm38) |
S84R |
probably benign |
Het |
Lzts3 |
A |
G |
2: 130,636,288 (GRCm38) |
Y297H |
probably damaging |
Het |
Map4k3 |
A |
G |
17: 80,644,762 (GRCm38) |
I205T |
probably damaging |
Het |
Matn2 |
A |
T |
15: 34,410,165 (GRCm38) |
N501I |
probably damaging |
Het |
Mctp2 |
T |
C |
7: 72,103,177 (GRCm38) |
E776G |
probably damaging |
Het |
Mex3d |
A |
T |
10: 80,382,587 (GRCm38) |
N265K |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,203,833 (GRCm38) |
T1534A |
probably benign |
Het |
Ncoa7 |
T |
C |
10: 30,704,636 (GRCm38) |
M35V |
probably damaging |
Het |
Nek4 |
G |
A |
14: 30,957,079 (GRCm38) |
|
probably null |
Het |
Ngrn |
T |
C |
7: 80,261,933 (GRCm38) |
|
probably null |
Het |
Nlrp1a |
T |
A |
11: 71,123,020 (GRCm38) |
Q468L |
probably benign |
Het |
Olfr743 |
T |
A |
14: 50,534,198 (GRCm38) |
M262K |
probably damaging |
Het |
Phtf2 |
T |
C |
5: 20,775,934 (GRCm38) |
D433G |
probably damaging |
Het |
Prdm13 |
G |
A |
4: 21,683,852 (GRCm38) |
Q140* |
probably null |
Het |
Prtg |
G |
A |
9: 72,892,254 (GRCm38) |
G778E |
probably benign |
Het |
Pum3 |
T |
C |
19: 27,420,051 (GRCm38) |
E308G |
probably damaging |
Het |
Pwp1 |
T |
G |
10: 85,882,886 (GRCm38) |
F306V |
probably damaging |
Het |
Rab24 |
A |
T |
13: 55,321,576 (GRCm38) |
Y27N |
probably damaging |
Het |
Rnf215 |
T |
C |
11: 4,135,898 (GRCm38) |
F126L |
probably benign |
Het |
Samd13 |
A |
T |
3: 146,680,696 (GRCm38) |
|
probably benign |
Het |
Serac1 |
T |
A |
17: 6,065,049 (GRCm38) |
H213L |
probably benign |
Het |
Slc45a3 |
A |
G |
1: 131,978,073 (GRCm38) |
E278G |
probably damaging |
Het |
Slit3 |
C |
T |
11: 35,700,236 (GRCm38) |
R1292C |
probably damaging |
Het |
Slx4 |
A |
T |
16: 4,000,951 (GRCm38) |
|
probably null |
Het |
Smarca4 |
C |
A |
9: 21,647,430 (GRCm38) |
T631K |
probably benign |
Het |
Snx16 |
C |
T |
3: 10,434,481 (GRCm38) |
R163Q |
possibly damaging |
Het |
Stk40 |
T |
C |
4: 126,128,895 (GRCm38) |
V140A |
probably damaging |
Het |
Tcf12 |
A |
T |
9: 71,868,240 (GRCm38) |
D409E |
probably damaging |
Het |
Tgfbr2 |
G |
T |
9: 116,110,255 (GRCm38) |
T168K |
possibly damaging |
Het |
Ticam1 |
G |
T |
17: 56,271,703 (GRCm38) |
H131N |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,829,888 (GRCm38) |
R7458I |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,713,511 (GRCm38) |
E31298* |
probably null |
Het |
Usp7 |
A |
G |
16: 8,712,102 (GRCm38) |
V133A |
possibly damaging |
Het |
Wbp1l |
C |
T |
19: 46,654,180 (GRCm38) |
R191* |
probably null |
Het |
Wdfy4 |
T |
C |
14: 33,106,011 (GRCm38) |
E1118G |
probably damaging |
Het |
Zfp81 |
G |
C |
17: 33,336,845 (GRCm38) |
P3A |
probably damaging |
Het |
Znhit6 |
A |
G |
3: 145,576,933 (GRCm38) |
K21R |
possibly damaging |
Het |
|
Other mutations in Olfr1450 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01978:Olfr1450
|
APN |
19 |
12,954,042 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02378:Olfr1450
|
APN |
19 |
12,954,383 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02405:Olfr1450
|
APN |
19 |
12,954,459 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02493:Olfr1450
|
APN |
19 |
12,953,774 (GRCm38) |
missense |
probably benign |
0.12 |
IGL02496:Olfr1450
|
APN |
19 |
12,954,192 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL02866:Olfr1450
|
APN |
19 |
12,954,355 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02886:Olfr1450
|
APN |
19 |
12,954,518 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03223:Olfr1450
|
APN |
19 |
12,953,904 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03286:Olfr1450
|
APN |
19 |
12,954,168 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03396:Olfr1450
|
APN |
19 |
12,953,820 (GRCm38) |
missense |
probably damaging |
1.00 |
R0106:Olfr1450
|
UTSW |
19 |
12,954,356 (GRCm38) |
missense |
probably benign |
0.10 |
R0106:Olfr1450
|
UTSW |
19 |
12,954,356 (GRCm38) |
missense |
probably benign |
0.10 |
R0544:Olfr1450
|
UTSW |
19 |
12,953,702 (GRCm38) |
missense |
possibly damaging |
0.79 |
R1660:Olfr1450
|
UTSW |
19 |
12,953,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R2020:Olfr1450
|
UTSW |
19 |
12,954,332 (GRCm38) |
missense |
possibly damaging |
0.61 |
R4292:Olfr1450
|
UTSW |
19 |
12,954,156 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4647:Olfr1450
|
UTSW |
19 |
12,954,077 (GRCm38) |
missense |
probably benign |
0.00 |
R6398:Olfr1450
|
UTSW |
19 |
12,954,317 (GRCm38) |
missense |
probably damaging |
1.00 |
R6681:Olfr1450
|
UTSW |
19 |
12,954,459 (GRCm38) |
missense |
probably damaging |
1.00 |
R7129:Olfr1450
|
UTSW |
19 |
12,954,114 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7399:Olfr1450
|
UTSW |
19 |
12,954,447 (GRCm38) |
missense |
probably damaging |
1.00 |
R7561:Olfr1450
|
UTSW |
19 |
12,954,039 (GRCm38) |
missense |
probably benign |
0.00 |
R7692:Olfr1450
|
UTSW |
19 |
12,953,642 (GRCm38) |
missense |
possibly damaging |
0.59 |
R8094:Olfr1450
|
UTSW |
19 |
12,954,002 (GRCm38) |
missense |
probably benign |
0.00 |
R8258:Olfr1450
|
UTSW |
19 |
12,954,363 (GRCm38) |
missense |
possibly damaging |
0.58 |
R8259:Olfr1450
|
UTSW |
19 |
12,954,363 (GRCm38) |
missense |
possibly damaging |
0.58 |
R9522:Olfr1450
|
UTSW |
19 |
12,954,013 (GRCm38) |
nonsense |
probably null |
|
|