Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd13 |
T |
C |
8: 10,037,900 (GRCm39) |
Y166H |
possibly damaging |
Het |
Abi3bp |
G |
A |
16: 56,353,332 (GRCm39) |
|
probably null |
Het |
Actrt3 |
T |
C |
3: 30,652,624 (GRCm39) |
T157A |
probably benign |
Het |
Adam26b |
T |
C |
8: 43,974,798 (GRCm39) |
K68R |
probably benign |
Het |
Adgrg7 |
A |
G |
16: 56,568,282 (GRCm39) |
|
probably null |
Het |
Ano6 |
T |
C |
15: 95,860,143 (GRCm39) |
I755T |
possibly damaging |
Het |
Basp1 |
T |
C |
15: 25,364,953 (GRCm39) |
N15D |
unknown |
Het |
Bod1l |
T |
C |
5: 41,966,055 (GRCm39) |
N2670S |
probably benign |
Het |
Btbd3 |
T |
A |
2: 138,125,656 (GRCm39) |
I280N |
probably damaging |
Het |
Cdh16 |
T |
A |
8: 105,344,488 (GRCm39) |
Y17F |
probably damaging |
Het |
Clmp |
G |
T |
9: 40,693,703 (GRCm39) |
G307W |
possibly damaging |
Het |
Clrn2 |
C |
A |
5: 45,617,503 (GRCm39) |
Q125K |
probably benign |
Het |
Ctnna3 |
C |
T |
10: 63,656,248 (GRCm39) |
A276V |
possibly damaging |
Het |
Dram2 |
A |
T |
3: 106,480,972 (GRCm39) |
T172S |
possibly damaging |
Het |
Dync2h1 |
G |
A |
9: 7,118,822 (GRCm39) |
|
probably benign |
Het |
Ezr |
T |
C |
17: 7,009,888 (GRCm39) |
|
probably benign |
Het |
Gbe1 |
T |
A |
16: 70,275,257 (GRCm39) |
D352E |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,198,743 (GRCm39) |
|
probably null |
Het |
Gpr18 |
T |
A |
14: 122,149,789 (GRCm39) |
M79L |
probably benign |
Het |
Gss |
T |
C |
2: 155,413,479 (GRCm39) |
Y196C |
probably damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,600,398 (GRCm39) |
S444P |
probably damaging |
Het |
Hecw1 |
C |
T |
13: 14,452,878 (GRCm39) |
R712K |
probably damaging |
Het |
Helz2 |
T |
G |
2: 180,874,674 (GRCm39) |
D1940A |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,491,051 (GRCm39) |
V4166E |
possibly damaging |
Het |
Klkb1 |
T |
C |
8: 45,729,428 (GRCm39) |
Y297C |
probably damaging |
Het |
Krt75 |
T |
A |
15: 101,473,364 (GRCm39) |
I537F |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,202,584 (GRCm39) |
T1176S |
probably damaging |
Het |
Nid2 |
T |
C |
14: 19,818,745 (GRCm39) |
L413P |
probably benign |
Het |
Or10ag57 |
T |
A |
2: 87,218,187 (GRCm39) |
M46K |
possibly damaging |
Het |
Or10ag57 |
G |
T |
2: 87,218,182 (GRCm39) |
L44F |
probably benign |
Het |
Or5t7 |
A |
G |
2: 86,507,425 (GRCm39) |
V84A |
probably benign |
Het |
Piwil1 |
A |
G |
5: 128,820,890 (GRCm39) |
N272D |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 45,009,481 (GRCm39) |
|
probably null |
Het |
Prkg1 |
A |
G |
19: 30,602,089 (GRCm39) |
V389A |
probably damaging |
Het |
Sema3a |
C |
A |
5: 13,611,767 (GRCm39) |
S344R |
probably damaging |
Het |
Serpina3j |
T |
C |
12: 104,284,750 (GRCm39) |
L309P |
probably damaging |
Het |
Slc15a1 |
A |
G |
14: 121,708,688 (GRCm39) |
|
probably null |
Het |
Sp8 |
G |
T |
12: 118,812,759 (GRCm39) |
A205S |
probably benign |
Het |
Speer4a1 |
T |
A |
5: 26,240,045 (GRCm39) |
Q235L |
possibly damaging |
Het |
St6gal1 |
A |
G |
16: 23,140,305 (GRCm39) |
T159A |
probably benign |
Het |
Tbrg1 |
G |
T |
9: 37,565,596 (GRCm39) |
P119T |
possibly damaging |
Het |
Tmem59l |
T |
C |
8: 70,939,874 (GRCm39) |
T32A |
probably damaging |
Het |
Trmt13 |
G |
A |
3: 116,376,561 (GRCm39) |
R277* |
probably null |
Het |
Zfp316 |
A |
G |
5: 143,248,631 (GRCm39) |
F205S |
unknown |
Het |
Zfp418 |
G |
T |
7: 7,184,448 (GRCm39) |
W137L |
possibly damaging |
Het |
Zp3r |
A |
T |
1: 130,526,603 (GRCm39) |
V200D |
possibly damaging |
Het |
|
Other mutations in Or4c11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01410:Or4c11
|
APN |
2 |
88,695,864 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01415:Or4c11
|
APN |
2 |
88,695,864 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4812001:Or4c11
|
UTSW |
2 |
88,695,314 (GRCm39) |
missense |
probably benign |
0.27 |
R0437:Or4c11
|
UTSW |
2 |
88,695,229 (GRCm39) |
missense |
probably benign |
0.01 |
R0561:Or4c11
|
UTSW |
2 |
88,695,024 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0669:Or4c11
|
UTSW |
2 |
88,695,272 (GRCm39) |
missense |
probably benign |
|
R0835:Or4c11
|
UTSW |
2 |
88,695,345 (GRCm39) |
missense |
probably benign |
|
R0987:Or4c11
|
UTSW |
2 |
88,695,527 (GRCm39) |
missense |
probably benign |
0.00 |
R1271:Or4c11
|
UTSW |
2 |
88,695,475 (GRCm39) |
nonsense |
probably null |
|
R1386:Or4c11
|
UTSW |
2 |
88,695,697 (GRCm39) |
missense |
probably benign |
0.14 |
R1618:Or4c11
|
UTSW |
2 |
88,695,871 (GRCm39) |
splice site |
probably null |
|
R1935:Or4c11
|
UTSW |
2 |
88,695,524 (GRCm39) |
missense |
probably benign |
|
R2098:Or4c11
|
UTSW |
2 |
88,695,215 (GRCm39) |
missense |
probably benign |
0.43 |
R2112:Or4c11
|
UTSW |
2 |
88,695,545 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2157:Or4c11
|
UTSW |
2 |
88,695,213 (GRCm39) |
missense |
probably benign |
|
R2912:Or4c11
|
UTSW |
2 |
88,695,458 (GRCm39) |
missense |
probably benign |
0.17 |
R2913:Or4c11
|
UTSW |
2 |
88,695,458 (GRCm39) |
missense |
probably benign |
0.17 |
R4583:Or4c11
|
UTSW |
2 |
88,695,838 (GRCm39) |
missense |
probably benign |
0.07 |
R4631:Or4c11
|
UTSW |
2 |
88,695,174 (GRCm39) |
missense |
probably benign |
0.00 |
R7707:Or4c11
|
UTSW |
2 |
88,695,153 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8559:Or4c11
|
UTSW |
2 |
88,695,527 (GRCm39) |
missense |
probably benign |
0.00 |
R9163:Or4c11
|
UTSW |
2 |
88,695,795 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9164:Or4c11
|
UTSW |
2 |
88,695,795 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9468:Or4c11
|
UTSW |
2 |
88,695,795 (GRCm39) |
missense |
possibly damaging |
0.63 |
|