Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,310,135 (GRCm38) |
|
probably null |
Het |
Abcb1a |
T |
A |
5: 8,715,016 (GRCm38) |
C669S |
probably benign |
Het |
Abcc3 |
A |
G |
11: 94,365,087 (GRCm38) |
L524P |
probably damaging |
Het |
Akap5 |
A |
T |
12: 76,329,971 (GRCm38) |
K726* |
probably null |
Het |
Aldh16a1 |
T |
C |
7: 45,142,017 (GRCm38) |
E778G |
probably damaging |
Het |
Ankle2 |
G |
A |
5: 110,252,744 (GRCm38) |
V649M |
possibly damaging |
Het |
Apon |
A |
G |
10: 128,254,963 (GRCm38) |
N170S |
probably benign |
Het |
Baiap2l1 |
T |
C |
5: 144,280,954 (GRCm38) |
Y274C |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,814,936 (GRCm38) |
N425K |
possibly damaging |
Het |
Camsap1 |
A |
G |
2: 25,930,016 (GRCm38) |
C1487R |
probably damaging |
Het |
Cd4 |
A |
C |
6: 124,867,688 (GRCm38) |
V378G |
probably damaging |
Het |
Cenpa |
C |
A |
5: 30,667,036 (GRCm38) |
P3Q |
unknown |
Het |
Cfap44 |
T |
C |
16: 44,404,781 (GRCm38) |
|
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,917,358 (GRCm38) |
M1021L |
probably benign |
Het |
Ddx39 |
G |
T |
8: 83,722,484 (GRCm38) |
M300I |
probably benign |
Het |
Dgkh |
T |
C |
14: 78,595,161 (GRCm38) |
R819G |
probably damaging |
Het |
Dlc1 |
A |
T |
8: 36,938,632 (GRCm38) |
M1K |
probably null |
Het |
Dnah9 |
A |
G |
11: 66,005,146 (GRCm38) |
W2468R |
probably benign |
Het |
Ebag9 |
A |
T |
15: 44,640,310 (GRCm38) |
K177I |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,151,184 (GRCm38) |
I249V |
probably damaging |
Het |
Fam171b |
T |
C |
2: 83,880,021 (GRCm38) |
V679A |
probably damaging |
Het |
Gabbr2 |
G |
A |
4: 46,674,533 (GRCm38) |
T818I |
probably damaging |
Het |
Gcn1l1 |
T |
C |
5: 115,614,118 (GRCm38) |
S2098P |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,473,923 (GRCm38) |
I609T |
probably damaging |
Het |
Gm12355 |
A |
G |
11: 98,625,361 (GRCm38) |
V62A |
possibly damaging |
Het |
Gm5916 |
T |
G |
9: 36,120,724 (GRCm38) |
H88P |
probably benign |
Het |
Gm6205 |
T |
C |
5: 94,683,896 (GRCm38) |
V254A |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,879,311 (GRCm38) |
S586P |
probably benign |
Het |
Gzmg |
T |
A |
14: 56,157,257 (GRCm38) |
T185S |
probably benign |
Het |
Hipk3 |
T |
A |
2: 104,446,591 (GRCm38) |
D381V |
probably damaging |
Het |
Hnrnpul2 |
C |
A |
19: 8,830,955 (GRCm38) |
N681K |
probably benign |
Het |
Hpdl |
C |
A |
4: 116,821,175 (GRCm38) |
G30C |
probably damaging |
Het |
Iws1 |
G |
A |
18: 32,080,160 (GRCm38) |
E214K |
possibly damaging |
Het |
Krt82 |
C |
A |
15: 101,541,825 (GRCm38) |
V479L |
probably benign |
Het |
Lama4 |
G |
A |
10: 39,048,128 (GRCm38) |
|
probably null |
Het |
Lamc1 |
C |
A |
1: 153,221,688 (GRCm38) |
E1537* |
probably null |
Het |
Mab21l3 |
G |
A |
3: 101,823,278 (GRCm38) |
T215M |
probably benign |
Het |
Magi3 |
C |
A |
3: 104,015,757 (GRCm38) |
V1215F |
possibly damaging |
Het |
Mical2 |
T |
A |
7: 112,303,590 (GRCm38) |
C89* |
probably null |
Het |
Mitf |
T |
A |
6: 98,017,874 (GRCm38) |
V427D |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,768,728 (GRCm38) |
V753A |
|
Het |
Myo16 |
G |
A |
8: 10,442,233 (GRCm38) |
R725H |
unknown |
Het |
Ncapg2 |
T |
A |
12: 116,438,667 (GRCm38) |
D706E |
probably damaging |
Het |
Ndst1 |
T |
C |
18: 60,691,196 (GRCm38) |
D803G |
probably benign |
Het |
Neb |
A |
T |
2: 52,206,103 (GRCm38) |
V5065D |
probably damaging |
Het |
Npm3 |
G |
A |
19: 45,749,502 (GRCm38) |
R19* |
probably null |
Het |
Ntrk3 |
A |
C |
7: 78,247,218 (GRCm38) |
N690K |
possibly damaging |
Het |
Olfr850 |
T |
C |
9: 19,477,870 (GRCm38) |
I127V |
probably benign |
Het |
Olfr985 |
C |
A |
9: 40,127,590 (GRCm38) |
V124L |
possibly damaging |
Het |
P3h2 |
G |
A |
16: 26,105,436 (GRCm38) |
A83V |
probably benign |
Het |
Pdia2 |
A |
G |
17: 26,196,936 (GRCm38) |
S362P |
probably damaging |
Het |
Pmp22 |
T |
C |
11: 63,134,491 (GRCm38) |
V50A |
probably benign |
Het |
Pmp22 |
C |
T |
11: 63,134,442 (GRCm38) |
H34Y |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,327,268 (GRCm38) |
D283G |
probably damaging |
Het |
Prss55 |
T |
A |
14: 64,077,082 (GRCm38) |
Q213L |
probably null |
Het |
Rgsl1 |
C |
T |
1: 153,793,867 (GRCm38) |
E258K |
possibly damaging |
Het |
Ripor2 |
T |
C |
13: 24,713,649 (GRCm38) |
F777L |
probably benign |
Het |
Rsf1 |
GGC |
GGCGGCGGCCGC |
7: 97,579,933 (GRCm38) |
|
probably benign |
Het |
Sgce |
G |
A |
6: 4,711,362 (GRCm38) |
R173C |
probably benign |
Het |
Sncaip |
T |
G |
18: 52,906,939 (GRCm38) |
M735R |
probably benign |
Het |
Snrpd2 |
T |
A |
7: 19,152,580 (GRCm38) |
I96N |
probably damaging |
Het |
Spryd3 |
T |
G |
15: 102,130,675 (GRCm38) |
D121A |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,495,289 (GRCm38) |
C149R |
probably damaging |
Het |
Tbc1d10b |
A |
T |
7: 127,207,933 (GRCm38) |
M144K |
probably benign |
Het |
Tbc1d31 |
T |
A |
15: 57,916,089 (GRCm38) |
I66N |
probably damaging |
Het |
Tssk1 |
A |
G |
16: 17,894,593 (GRCm38) |
T81A |
possibly damaging |
Het |
Ttc28 |
A |
G |
5: 111,102,036 (GRCm38) |
Y284C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,743,411 (GRCm38) |
T25713A |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,351,259 (GRCm38) |
W311R |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 79,194,604 (GRCm38) |
T755S |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,081,219 (GRCm38) |
C828R |
probably damaging |
Het |
Wwox |
T |
C |
8: 114,712,238 (GRCm38) |
F348S |
probably damaging |
Het |
Zeb2 |
T |
A |
2: 45,110,028 (GRCm38) |
R65W |
possibly damaging |
Het |
Zfp712 |
T |
A |
13: 67,040,573 (GRCm38) |
H630L |
probably damaging |
Het |
Zfp764 |
G |
T |
7: 127,405,436 (GRCm38) |
H174Q |
probably damaging |
Het |
|
Other mutations in Olfr855 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Olfr855
|
APN |
9 |
19,585,320 (GRCm38) |
missense |
possibly damaging |
0.74 |
IGL01405:Olfr855
|
APN |
9 |
19,585,205 (GRCm38) |
missense |
probably benign |
0.23 |
IGL01775:Olfr855
|
APN |
9 |
19,584,705 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01920:Olfr855
|
APN |
9 |
19,585,022 (GRCm38) |
missense |
probably benign |
0.01 |
R0501:Olfr855
|
UTSW |
9 |
19,584,618 (GRCm38) |
missense |
probably damaging |
1.00 |
R0600:Olfr855
|
UTSW |
9 |
19,585,304 (GRCm38) |
missense |
possibly damaging |
0.47 |
R0667:Olfr855
|
UTSW |
9 |
19,585,447 (GRCm38) |
missense |
probably benign |
|
R1769:Olfr855
|
UTSW |
9 |
19,585,386 (GRCm38) |
missense |
probably damaging |
0.98 |
R3117:Olfr855
|
UTSW |
9 |
19,584,941 (GRCm38) |
missense |
probably damaging |
0.99 |
R4002:Olfr855
|
UTSW |
9 |
19,584,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R4003:Olfr855
|
UTSW |
9 |
19,584,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R4043:Olfr855
|
UTSW |
9 |
19,584,995 (GRCm38) |
missense |
probably benign |
0.16 |
R4243:Olfr855
|
UTSW |
9 |
19,584,558 (GRCm38) |
missense |
probably damaging |
1.00 |
R4672:Olfr855
|
UTSW |
9 |
19,585,430 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4673:Olfr855
|
UTSW |
9 |
19,585,430 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4959:Olfr855
|
UTSW |
9 |
19,585,208 (GRCm38) |
missense |
probably benign |
|
R4973:Olfr855
|
UTSW |
9 |
19,585,208 (GRCm38) |
missense |
probably benign |
|
R5223:Olfr855
|
UTSW |
9 |
19,585,026 (GRCm38) |
missense |
probably benign |
0.16 |
R5681:Olfr855
|
UTSW |
9 |
19,584,899 (GRCm38) |
missense |
probably damaging |
1.00 |
R6005:Olfr855
|
UTSW |
9 |
19,584,885 (GRCm38) |
missense |
probably benign |
0.45 |
R6017:Olfr855
|
UTSW |
9 |
19,585,434 (GRCm38) |
missense |
probably benign |
0.00 |
R6145:Olfr855
|
UTSW |
9 |
19,584,888 (GRCm38) |
missense |
probably benign |
0.02 |
R6615:Olfr855
|
UTSW |
9 |
19,584,989 (GRCm38) |
missense |
probably benign |
0.05 |
R6771:Olfr855
|
UTSW |
9 |
19,585,379 (GRCm38) |
missense |
probably benign |
0.16 |
R6969:Olfr855
|
UTSW |
9 |
19,584,590 (GRCm38) |
missense |
possibly damaging |
0.77 |
R7239:Olfr855
|
UTSW |
9 |
19,585,191 (GRCm38) |
missense |
probably damaging |
1.00 |
R7313:Olfr855
|
UTSW |
9 |
19,584,642 (GRCm38) |
missense |
probably damaging |
1.00 |
R7361:Olfr855
|
UTSW |
9 |
19,584,560 (GRCm38) |
missense |
probably benign |
0.00 |
R8112:Olfr855
|
UTSW |
9 |
19,584,724 (GRCm38) |
missense |
probably benign |
0.44 |
R8470:Olfr855
|
UTSW |
9 |
19,584,969 (GRCm38) |
missense |
probably damaging |
0.99 |
R9155:Olfr855
|
UTSW |
9 |
19,585,083 (GRCm38) |
missense |
probably benign |
0.00 |
R9422:Olfr855
|
UTSW |
9 |
19,584,672 (GRCm38) |
missense |
probably damaging |
1.00 |
|