Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aoah |
A |
G |
13: 21,184,213 (GRCm39) |
S426G |
probably benign |
Het |
Arap3 |
T |
C |
18: 38,114,355 (GRCm39) |
|
probably benign |
Het |
Arhgap45 |
T |
A |
10: 79,866,585 (GRCm39) |
N1029K |
probably damaging |
Het |
Arhgef10l |
A |
T |
4: 140,311,242 (GRCm39) |
M1K |
probably null |
Het |
Bloc1s6 |
T |
C |
2: 122,584,638 (GRCm39) |
L71P |
probably damaging |
Het |
Ccer1 |
G |
T |
10: 97,529,439 (GRCm39) |
R34M |
unknown |
Het |
Cd44 |
T |
C |
2: 102,675,759 (GRCm39) |
|
probably benign |
Het |
Col17a1 |
T |
C |
19: 47,669,814 (GRCm39) |
|
probably null |
Het |
Cspp1 |
A |
G |
1: 10,117,662 (GRCm39) |
E38G |
possibly damaging |
Het |
Dock10 |
A |
T |
1: 80,584,013 (GRCm39) |
|
probably benign |
Het |
Dsg3 |
A |
T |
18: 20,660,689 (GRCm39) |
M343L |
probably benign |
Het |
Eif3l |
G |
A |
15: 78,961,251 (GRCm39) |
|
probably benign |
Het |
Fcrl1 |
T |
C |
3: 87,292,398 (GRCm39) |
L150P |
probably benign |
Het |
Flg2 |
T |
G |
3: 93,109,801 (GRCm39) |
S610A |
unknown |
Het |
Grin3b |
C |
T |
10: 79,809,615 (GRCm39) |
R374C |
probably damaging |
Het |
H2-Oa |
A |
T |
17: 34,313,377 (GRCm39) |
I143F |
probably damaging |
Het |
Itgae |
C |
T |
11: 73,022,556 (GRCm39) |
P924S |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,058,602 (GRCm39) |
D2521V |
probably damaging |
Het |
Itprid2 |
T |
A |
2: 79,475,445 (GRCm39) |
M468K |
probably damaging |
Het |
Laptm4a |
G |
A |
12: 8,981,719 (GRCm39) |
G143D |
probably benign |
Het |
Lrp6 |
T |
C |
6: 134,456,726 (GRCm39) |
Y846C |
probably damaging |
Het |
Mcm10 |
A |
T |
2: 4,999,407 (GRCm39) |
S749T |
probably damaging |
Het |
Nemf |
T |
C |
12: 69,378,679 (GRCm39) |
N548D |
probably damaging |
Het |
Nlrp4e |
T |
A |
7: 23,020,251 (GRCm39) |
L246Q |
probably damaging |
Het |
Nsun6 |
A |
T |
2: 15,001,157 (GRCm39) |
C466* |
probably null |
Het |
Olfm2 |
T |
C |
9: 20,580,019 (GRCm39) |
D252G |
probably damaging |
Het |
Or14j9 |
T |
A |
17: 37,874,681 (GRCm39) |
I174F |
probably damaging |
Het |
Or2h1 |
G |
A |
17: 37,404,311 (GRCm39) |
L152F |
probably benign |
Het |
Or9i14 |
T |
C |
19: 13,792,292 (GRCm39) |
I221V |
probably damaging |
Het |
Pcdhb14 |
C |
T |
18: 37,582,057 (GRCm39) |
R388C |
possibly damaging |
Het |
Piwil1 |
C |
T |
5: 128,828,136 (GRCm39) |
T712I |
probably benign |
Het |
Piwil4 |
G |
T |
9: 14,637,183 (GRCm39) |
T377K |
probably damaging |
Het |
Prg3 |
T |
C |
2: 84,823,370 (GRCm39) |
F182L |
probably damaging |
Het |
Ptgds |
T |
C |
2: 25,359,622 (GRCm39) |
T22A |
probably benign |
Het |
Retsat |
T |
C |
6: 72,575,666 (GRCm39) |
V19A |
probably damaging |
Het |
Rpl21-ps4 |
A |
T |
14: 11,227,760 (GRCm38) |
|
noncoding transcript |
Het |
Sh3glb2 |
A |
G |
2: 30,235,363 (GRCm39) |
V370A |
probably damaging |
Het |
Skint4 |
G |
T |
4: 112,022,883 (GRCm39) |
W459C |
possibly damaging |
Het |
Slco1a1 |
T |
A |
6: 141,857,611 (GRCm39) |
R573S |
probably benign |
Het |
Smgc |
T |
C |
15: 91,744,876 (GRCm39) |
S694P |
probably damaging |
Het |
Spaca6 |
A |
G |
17: 18,058,401 (GRCm39) |
Y7C |
probably damaging |
Het |
Spn |
T |
C |
7: 126,736,178 (GRCm39) |
T110A |
probably benign |
Het |
Tepsin |
C |
T |
11: 119,982,703 (GRCm39) |
V456I |
probably benign |
Het |
Tex261 |
C |
T |
6: 83,748,249 (GRCm39) |
R171Q |
possibly damaging |
Het |
Tmem184a |
A |
T |
5: 139,798,755 (GRCm39) |
F65I |
probably damaging |
Het |
Tpm3 |
G |
A |
3: 89,995,052 (GRCm39) |
|
probably null |
Het |
Tubgcp2 |
T |
A |
7: 139,580,940 (GRCm39) |
H671L |
probably benign |
Het |
Unc13b |
T |
G |
4: 43,237,110 (GRCm39) |
D3393E |
possibly damaging |
Het |
Vcan |
T |
A |
13: 89,853,125 (GRCm39) |
M612L |
probably benign |
Het |
Vmn1r180 |
C |
A |
7: 23,652,077 (GRCm39) |
S80* |
probably null |
Het |
Vmn1r64 |
C |
T |
7: 5,887,070 (GRCm39) |
V158I |
probably benign |
Het |
Vps13d |
C |
T |
4: 144,894,072 (GRCm39) |
V496I |
possibly damaging |
Het |
Wee2 |
T |
G |
6: 40,429,589 (GRCm39) |
|
probably null |
Het |
Zfp804b |
T |
C |
5: 6,820,039 (GRCm39) |
N972S |
probably benign |
Het |
|
Other mutations in Or10j5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Or10j5
|
APN |
1 |
172,785,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00336:Or10j5
|
APN |
1 |
172,785,045 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01155:Or10j5
|
APN |
1 |
172,784,491 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01549:Or10j5
|
APN |
1 |
172,784,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Or10j5
|
APN |
1 |
172,784,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03071:Or10j5
|
APN |
1 |
172,784,502 (GRCm39) |
missense |
probably benign |
0.01 |
R0449:Or10j5
|
UTSW |
1 |
172,784,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Or10j5
|
UTSW |
1 |
172,784,908 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1726:Or10j5
|
UTSW |
1 |
172,784,658 (GRCm39) |
missense |
probably benign |
0.00 |
R1735:Or10j5
|
UTSW |
1 |
172,784,374 (GRCm39) |
missense |
probably benign |
|
R1928:Or10j5
|
UTSW |
1 |
172,784,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Or10j5
|
UTSW |
1 |
172,785,205 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4359:Or10j5
|
UTSW |
1 |
172,784,647 (GRCm39) |
missense |
probably benign |
|
R4434:Or10j5
|
UTSW |
1 |
172,785,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Or10j5
|
UTSW |
1 |
172,785,157 (GRCm39) |
missense |
probably benign |
|
R4874:Or10j5
|
UTSW |
1 |
172,785,166 (GRCm39) |
missense |
probably benign |
0.00 |
R5063:Or10j5
|
UTSW |
1 |
172,785,009 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5988:Or10j5
|
UTSW |
1 |
172,784,723 (GRCm39) |
nonsense |
probably null |
|
R6074:Or10j5
|
UTSW |
1 |
172,784,945 (GRCm39) |
missense |
probably benign |
0.10 |
R7021:Or10j5
|
UTSW |
1 |
172,784,494 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Or10j5
|
UTSW |
1 |
172,784,673 (GRCm39) |
missense |
probably damaging |
0.96 |
R7527:Or10j5
|
UTSW |
1 |
172,784,511 (GRCm39) |
missense |
probably benign |
0.00 |
R8271:Or10j5
|
UTSW |
1 |
172,784,744 (GRCm39) |
nonsense |
probably null |
|
R8890:Or10j5
|
UTSW |
1 |
172,785,045 (GRCm39) |
missense |
probably benign |
0.30 |
R8906:Or10j5
|
UTSW |
1 |
172,784,186 (GRCm39) |
start gained |
probably benign |
|
R9048:Or10j5
|
UTSW |
1 |
172,784,929 (GRCm39) |
missense |
probably benign |
|
R9583:Or10j5
|
UTSW |
1 |
172,784,893 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or10j5
|
UTSW |
1 |
172,784,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|