Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
A |
T |
19: 31,888,519 (GRCm39) |
Y83F |
possibly damaging |
Het |
Adgre1 |
C |
G |
17: 57,715,459 (GRCm39) |
Q260E |
probably benign |
Het |
Adgrf4 |
T |
A |
17: 42,977,799 (GRCm39) |
M515L |
probably benign |
Het |
Adgrl2 |
A |
T |
3: 148,565,161 (GRCm39) |
C140S |
probably damaging |
Het |
Ago3 |
T |
A |
4: 126,270,721 (GRCm39) |
K258* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,003,002 (GRCm39) |
E573V |
possibly damaging |
Het |
Atxn7l3b |
T |
A |
10: 112,764,567 (GRCm39) |
I21F |
possibly damaging |
Het |
Bckdha |
C |
T |
7: 25,330,872 (GRCm39) |
R298H |
probably damaging |
Het |
Cacng3 |
A |
C |
7: 122,367,569 (GRCm39) |
I150L |
possibly damaging |
Het |
Ccdc18 |
A |
T |
5: 108,309,369 (GRCm39) |
K321N |
possibly damaging |
Het |
Ccl11 |
A |
T |
11: 81,952,568 (GRCm39) |
K47M |
possibly damaging |
Het |
Cdkn2a |
T |
C |
4: 89,194,987 (GRCm39) |
I142M |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,967,203 (GRCm39) |
G249R |
probably benign |
Het |
Chrna1 |
C |
A |
2: 73,400,953 (GRCm39) |
E192D |
probably benign |
Het |
Clasp1 |
A |
G |
1: 118,431,629 (GRCm39) |
N420D |
probably damaging |
Het |
Clca3a2 |
T |
A |
3: 144,511,703 (GRCm39) |
|
probably null |
Het |
Cntn2 |
T |
C |
1: 132,449,512 (GRCm39) |
Y643C |
probably damaging |
Het |
Dcun1d1 |
G |
A |
3: 35,951,703 (GRCm39) |
H204Y |
probably benign |
Het |
Dlg2 |
A |
T |
7: 92,087,222 (GRCm39) |
Q767L |
possibly damaging |
Het |
Dnah11 |
A |
G |
12: 118,049,466 (GRCm39) |
S1653P |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,342,513 (GRCm39) |
|
probably null |
Het |
Egf |
T |
C |
3: 129,548,592 (GRCm39) |
T8A |
unknown |
Het |
Eln |
G |
T |
5: 134,757,246 (GRCm39) |
T219K |
unknown |
Het |
Evc |
T |
C |
5: 37,471,872 (GRCm39) |
D536G |
possibly damaging |
Het |
Fbxo3 |
A |
G |
2: 103,881,553 (GRCm39) |
E295G |
possibly damaging |
Het |
Gp2 |
C |
T |
7: 119,042,010 (GRCm39) |
C505Y |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,669,530 (GRCm39) |
F438S |
probably damaging |
Het |
Gsk3b |
T |
C |
16: 38,011,987 (GRCm39) |
S236P |
probably benign |
Het |
Kdm5d |
A |
G |
Y: 942,477 (GRCm39) |
T1381A |
probably benign |
Het |
Klhl12 |
T |
C |
1: 134,413,460 (GRCm39) |
I315T |
possibly damaging |
Het |
Ltb |
T |
A |
17: 35,414,169 (GRCm39) |
N102K |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,420,649 (GRCm39) |
T202A |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,278,476 (GRCm39) |
D5993Y |
probably damaging |
Het |
Mak |
T |
A |
13: 41,199,679 (GRCm39) |
D320V |
probably benign |
Het |
Map2 |
G |
A |
1: 66,460,872 (GRCm39) |
R1556H |
probably damaging |
Het |
Mgat4d |
G |
T |
8: 84,094,762 (GRCm39) |
M266I |
probably benign |
Het |
Mmp24 |
G |
T |
2: 155,652,223 (GRCm39) |
R310S |
possibly damaging |
Het |
Myh6 |
A |
T |
14: 55,190,891 (GRCm39) |
L928Q |
probably damaging |
Het |
Npnt |
A |
G |
3: 132,614,217 (GRCm39) |
L179P |
probably damaging |
Het |
Or2f1b |
A |
G |
6: 42,739,499 (GRCm39) |
N171S |
probably benign |
Het |
Or8g55 |
T |
G |
9: 39,785,231 (GRCm39) |
F220C |
probably benign |
Het |
Parp4 |
A |
T |
14: 56,886,186 (GRCm39) |
Y1755F |
unknown |
Het |
Phactr1 |
A |
G |
13: 42,863,297 (GRCm39) |
E74G |
possibly damaging |
Het |
Pira12 |
T |
A |
7: 3,899,954 (GRCm39) |
E216V |
possibly damaging |
Het |
Plcg1 |
G |
A |
2: 160,589,816 (GRCm39) |
M113I |
probably benign |
Het |
Plekhh2 |
T |
G |
17: 84,879,189 (GRCm39) |
S638A |
possibly damaging |
Het |
Ppp2r3d |
T |
A |
9: 101,088,985 (GRCm39) |
H446L |
probably benign |
Het |
Prkcg |
G |
T |
7: 3,378,686 (GRCm39) |
D644Y |
probably damaging |
Het |
Rbbp8nl |
G |
T |
2: 179,921,506 (GRCm39) |
R293S |
probably benign |
Het |
Rbl2 |
A |
T |
8: 91,842,387 (GRCm39) |
H1057L |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,387,819 (GRCm39) |
H1076L |
possibly damaging |
Het |
Scn11a |
A |
C |
9: 119,611,036 (GRCm39) |
D938E |
probably benign |
Het |
Sec24b |
T |
C |
3: 129,798,650 (GRCm39) |
D573G |
probably damaging |
Het |
Serpinf1 |
T |
G |
11: 75,306,397 (GRCm39) |
Q147P |
unknown |
Het |
Skint6 |
C |
T |
4: 113,093,642 (GRCm39) |
G167D |
probably damaging |
Het |
Slc15a5 |
A |
G |
6: 138,056,898 (GRCm39) |
F6S |
probably damaging |
Het |
Smc2 |
T |
A |
4: 52,449,376 (GRCm39) |
I179K |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,677,073 (GRCm39) |
K57R |
possibly damaging |
Het |
Smpdl3b |
T |
A |
4: 132,473,990 (GRCm39) |
H25L |
probably damaging |
Het |
Srpk1 |
T |
C |
17: 28,839,398 (GRCm39) |
D35G |
unknown |
Het |
Strn |
A |
G |
17: 78,980,076 (GRCm39) |
V324A |
probably damaging |
Het |
Sult6b2 |
T |
C |
6: 142,736,022 (GRCm39) |
K191E |
probably benign |
Het |
Tmem168 |
A |
G |
6: 13,583,324 (GRCm39) |
I519T |
probably benign |
Het |
Tmem41a |
T |
C |
16: 21,756,784 (GRCm39) |
T112A |
probably benign |
Het |
Tmem67 |
A |
G |
4: 12,058,576 (GRCm39) |
I507T |
probably benign |
Het |
Tns1 |
T |
C |
1: 74,024,201 (GRCm39) |
E454G |
probably damaging |
Het |
Trim26 |
C |
A |
17: 37,168,602 (GRCm39) |
D422E |
unknown |
Het |
Triobp |
C |
A |
15: 78,842,475 (GRCm39) |
R58S |
possibly damaging |
Het |
Trp53 |
T |
C |
11: 69,478,409 (GRCm39) |
F106S |
probably damaging |
Het |
Tshz3 |
C |
A |
7: 36,470,962 (GRCm39) |
Q984K |
probably damaging |
Het |
Ttll3 |
A |
G |
6: 113,371,959 (GRCm39) |
E73G |
probably damaging |
Het |
Vmn1r194 |
A |
G |
13: 22,429,247 (GRCm39) |
N288S |
probably benign |
Het |
|
Other mutations in Or4c11c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00923:Or4c11c
|
APN |
2 |
88,661,456 (GRCm39) |
splice site |
probably null |
|
IGL02079:Or4c11c
|
APN |
2 |
88,661,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02183:Or4c11c
|
APN |
2 |
88,662,372 (GRCm39) |
missense |
probably benign |
|
IGL02813:Or4c11c
|
APN |
2 |
88,661,495 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02839:Or4c11c
|
APN |
2 |
88,661,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02895:Or4c11c
|
APN |
2 |
88,661,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0680:Or4c11c
|
UTSW |
2 |
88,662,124 (GRCm39) |
missense |
probably benign |
|
R2029:Or4c11c
|
UTSW |
2 |
88,661,749 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2095:Or4c11c
|
UTSW |
2 |
88,661,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Or4c11c
|
UTSW |
2 |
88,661,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R6216:Or4c11c
|
UTSW |
2 |
88,661,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Or4c11c
|
UTSW |
2 |
88,661,707 (GRCm39) |
missense |
probably benign |
0.22 |
R6377:Or4c11c
|
UTSW |
2 |
88,661,613 (GRCm39) |
nonsense |
probably null |
|
R6429:Or4c11c
|
UTSW |
2 |
88,661,869 (GRCm39) |
missense |
probably benign |
0.01 |
R6521:Or4c11c
|
UTSW |
2 |
88,661,700 (GRCm39) |
missense |
probably benign |
0.03 |
R7065:Or4c11c
|
UTSW |
2 |
88,661,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Or4c11c
|
UTSW |
2 |
88,662,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R7476:Or4c11c
|
UTSW |
2 |
88,661,932 (GRCm39) |
missense |
probably benign |
0.07 |
R7570:Or4c11c
|
UTSW |
2 |
88,661,472 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8303:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8306:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8307:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8308:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8386:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8387:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8809:Or4c11c
|
UTSW |
2 |
88,662,256 (GRCm39) |
missense |
probably benign |
0.01 |
R8894:Or4c11c
|
UTSW |
2 |
88,661,809 (GRCm39) |
missense |
probably benign |
0.12 |
Z1176:Or4c11c
|
UTSW |
2 |
88,661,922 (GRCm39) |
missense |
probably damaging |
0.99 |
|