Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
T |
C |
19: 55,268,933 (GRCm39) |
V198A |
possibly damaging |
Het |
Adam34l |
T |
G |
8: 44,078,949 (GRCm39) |
N425T |
probably benign |
Het |
Adgra2 |
A |
T |
8: 27,609,193 (GRCm39) |
M805L |
probably benign |
Het |
Arhgap39 |
T |
C |
15: 76,620,712 (GRCm39) |
S630G |
probably damaging |
Het |
Bcl3 |
T |
A |
7: 19,546,409 (GRCm39) |
N142I |
probably damaging |
Het |
Cfap210 |
C |
T |
2: 69,602,398 (GRCm39) |
E338K |
possibly damaging |
Het |
Chuk |
A |
T |
19: 44,085,431 (GRCm39) |
D238E |
probably benign |
Het |
Cnga4 |
T |
G |
7: 105,056,906 (GRCm39) |
Y336* |
probably null |
Het |
Cyp2j8 |
A |
T |
4: 96,395,427 (GRCm39) |
L66Q |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dst |
T |
A |
1: 34,227,253 (GRCm39) |
D1290E |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,075,235 (GRCm39) |
I583T |
probably benign |
Het |
Eif1ad13 |
A |
T |
12: 87,762,351 (GRCm39) |
R24* |
probably null |
Het |
Fbxl2 |
T |
A |
9: 113,815,516 (GRCm39) |
D249V |
probably damaging |
Het |
Fbxo30 |
A |
T |
10: 11,165,602 (GRCm39) |
Y108F |
possibly damaging |
Het |
Fibin |
G |
T |
2: 110,193,041 (GRCm39) |
H34N |
probably damaging |
Het |
Gabrr1 |
A |
G |
4: 33,161,632 (GRCm39) |
I319V |
probably benign |
Het |
Gfm1 |
G |
T |
3: 67,375,215 (GRCm39) |
L559F |
possibly damaging |
Het |
Gm5134 |
T |
A |
10: 75,821,859 (GRCm39) |
L231Q |
possibly damaging |
Het |
Grm5 |
A |
G |
7: 87,251,638 (GRCm39) |
|
probably benign |
Het |
Hbs1l |
T |
A |
10: 21,183,657 (GRCm39) |
|
probably null |
Het |
Hsf5 |
C |
G |
11: 87,508,120 (GRCm39) |
T8S |
probably benign |
Het |
Hspa4 |
C |
T |
11: 53,153,766 (GRCm39) |
E702K |
probably benign |
Het |
Inpp4b |
A |
G |
8: 82,678,813 (GRCm39) |
Q281R |
probably damaging |
Het |
Krt40 |
G |
A |
11: 99,433,920 (GRCm39) |
A22V |
possibly damaging |
Het |
Ldlrap1 |
C |
T |
4: 134,486,345 (GRCm39) |
R38Q |
possibly damaging |
Het |
Lepr |
A |
G |
4: 101,671,588 (GRCm39) |
|
probably null |
Het |
Map3k12 |
A |
G |
15: 102,412,081 (GRCm39) |
S328P |
probably damaging |
Het |
Mrpl2 |
T |
C |
17: 46,958,356 (GRCm39) |
V46A |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,568,294 (GRCm39) |
N1408K |
unknown |
Het |
Myh7 |
T |
A |
14: 55,226,753 (GRCm39) |
Q366L |
probably benign |
Het |
Nbeal2 |
A |
G |
9: 110,467,802 (GRCm39) |
V462A |
probably damaging |
Het |
Nradd |
G |
T |
9: 110,450,655 (GRCm39) |
T174N |
probably damaging |
Het |
Nup155 |
T |
C |
15: 8,138,963 (GRCm39) |
S12P |
probably benign |
Het |
Obscn |
C |
A |
11: 58,943,337 (GRCm39) |
E4832* |
probably null |
Het |
Opn3 |
G |
A |
1: 175,490,669 (GRCm39) |
R331W |
probably damaging |
Het |
Or2ag15 |
A |
T |
7: 106,340,761 (GRCm39) |
C127S |
probably damaging |
Het |
Or2w3 |
T |
A |
11: 58,556,757 (GRCm39) |
V124E |
possibly damaging |
Het |
Or4a66 |
G |
T |
2: 88,531,161 (GRCm39) |
H171N |
probably benign |
Het |
Or52ae9 |
T |
A |
7: 103,389,661 (GRCm39) |
H262L |
probably damaging |
Het |
Or5b120 |
G |
A |
19: 13,480,427 (GRCm39) |
C240Y |
probably damaging |
Het |
Phip |
A |
G |
9: 82,785,234 (GRCm39) |
V827A |
probably benign |
Het |
Phldb1 |
G |
A |
9: 44,607,414 (GRCm39) |
R1264W |
probably damaging |
Het |
Pibf1 |
T |
G |
14: 99,424,014 (GRCm39) |
I529S |
probably benign |
Het |
Pkp1 |
T |
A |
1: 135,814,599 (GRCm39) |
I241F |
probably benign |
Het |
Pla2g4f |
G |
T |
2: 120,132,702 (GRCm39) |
D711E |
possibly damaging |
Het |
Pold1 |
A |
G |
7: 44,190,266 (GRCm39) |
|
probably null |
Het |
Pold2 |
T |
C |
11: 5,823,691 (GRCm39) |
S287G |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,331,567 (GRCm39) |
|
probably benign |
Het |
Prl8a1 |
T |
C |
13: 27,759,557 (GRCm39) |
E160G |
possibly damaging |
Het |
Rfc4 |
C |
T |
16: 22,932,840 (GRCm39) |
|
probably benign |
Het |
Robo3 |
T |
G |
9: 37,332,225 (GRCm39) |
Y891S |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Rsph14 |
G |
A |
10: 74,797,520 (GRCm39) |
R156W |
probably benign |
Het |
Sec61a1 |
T |
C |
6: 88,482,150 (GRCm39) |
Y457C |
probably benign |
Het |
Sec63 |
T |
A |
10: 42,704,861 (GRCm39) |
|
probably null |
Het |
Spen |
T |
C |
4: 141,244,333 (GRCm39) |
E234G |
unknown |
Het |
Sphkap |
T |
A |
1: 83,258,200 (GRCm39) |
E181V |
probably damaging |
Het |
Stau2 |
C |
T |
1: 16,445,035 (GRCm39) |
A298T |
probably benign |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tbc1d23 |
T |
C |
16: 56,990,796 (GRCm39) |
I661V |
probably benign |
Het |
Thoc6 |
A |
C |
17: 23,889,295 (GRCm39) |
|
probably null |
Het |
Trpv1 |
T |
A |
11: 73,141,636 (GRCm39) |
M553K |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,641,579 (GRCm39) |
I11760V |
probably benign |
Het |
Vmn1r61 |
G |
A |
7: 5,613,850 (GRCm39) |
H155Y |
probably damaging |
Het |
Vmn2r41 |
A |
G |
7: 8,153,214 (GRCm39) |
|
probably null |
Het |
Vmn2r74 |
A |
G |
7: 85,607,498 (GRCm39) |
I75T |
possibly damaging |
Het |
Wwp2 |
C |
A |
8: 108,232,977 (GRCm39) |
T205K |
probably benign |
Het |
Zfp1003 |
A |
T |
2: 177,546,195 (GRCm39) |
T40S |
probably benign |
Het |
Zfp747 |
C |
T |
7: 126,973,306 (GRCm39) |
G288D |
probably damaging |
Het |
Zfp871 |
CCACAC |
CC |
17: 32,994,494 (GRCm39) |
|
probably null |
Het |
Zfp953 |
G |
A |
13: 67,491,161 (GRCm39) |
L264F |
possibly damaging |
Het |
|
Other mutations in Or6b2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Or6b2
|
APN |
1 |
92,407,746 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00980:Or6b2
|
APN |
1 |
92,407,402 (GRCm39) |
splice site |
probably null |
|
IGL01540:Or6b2
|
APN |
1 |
92,408,202 (GRCm39) |
missense |
probably damaging |
0.96 |
BB007:Or6b2
|
UTSW |
1 |
92,407,570 (GRCm39) |
missense |
probably benign |
0.01 |
BB017:Or6b2
|
UTSW |
1 |
92,407,570 (GRCm39) |
missense |
probably benign |
0.01 |
R1146:Or6b2
|
UTSW |
1 |
92,407,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Or6b2
|
UTSW |
1 |
92,407,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Or6b2
|
UTSW |
1 |
92,407,705 (GRCm39) |
missense |
probably benign |
0.01 |
R5207:Or6b2
|
UTSW |
1 |
92,407,594 (GRCm39) |
missense |
probably benign |
|
R5287:Or6b2
|
UTSW |
1 |
92,408,019 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5403:Or6b2
|
UTSW |
1 |
92,408,019 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6074:Or6b2
|
UTSW |
1 |
92,407,497 (GRCm39) |
missense |
probably benign |
0.45 |
R6355:Or6b2
|
UTSW |
1 |
92,407,702 (GRCm39) |
missense |
probably benign |
0.21 |
R6378:Or6b2
|
UTSW |
1 |
92,408,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Or6b2
|
UTSW |
1 |
92,408,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7930:Or6b2
|
UTSW |
1 |
92,407,570 (GRCm39) |
missense |
probably benign |
0.01 |
R8280:Or6b2
|
UTSW |
1 |
92,407,729 (GRCm39) |
missense |
noncoding transcript |
|
R8351:Or6b2
|
UTSW |
1 |
92,407,660 (GRCm39) |
missense |
probably benign |
0.09 |
R8437:Or6b2
|
UTSW |
1 |
92,408,187 (GRCm39) |
missense |
probably benign |
0.00 |
R8451:Or6b2
|
UTSW |
1 |
92,407,660 (GRCm39) |
missense |
probably benign |
0.09 |
X0065:Or6b2
|
UTSW |
1 |
92,407,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|