Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
G |
T |
6: 128,544,023 (GRCm39) |
A506D |
probably benign |
Het |
Agap1 |
G |
T |
1: 89,770,913 (GRCm39) |
V635L |
possibly damaging |
Het |
Akr1c12 |
T |
C |
13: 4,329,331 (GRCm39) |
K9E |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,606,034 (GRCm39) |
Y2561* |
probably null |
Het |
Atm |
T |
C |
9: 53,382,718 (GRCm39) |
H1957R |
probably damaging |
Het |
Bcr |
T |
C |
10: 74,996,222 (GRCm39) |
F922S |
probably benign |
Het |
Cfap44 |
T |
A |
16: 44,291,230 (GRCm39) |
|
probably benign |
Het |
Chil5 |
A |
G |
3: 105,926,906 (GRCm39) |
V243A |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,960,465 (GRCm39) |
C3317R |
probably damaging |
Het |
Dsc1 |
T |
C |
18: 20,241,942 (GRCm39) |
K133R |
probably damaging |
Het |
Ecm1 |
T |
A |
3: 95,644,989 (GRCm39) |
Q136L |
probably damaging |
Het |
Fscn3 |
C |
A |
6: 28,435,997 (GRCm39) |
A431E |
possibly damaging |
Het |
Gas7 |
C |
T |
11: 67,565,061 (GRCm39) |
|
probably benign |
Het |
Gbx2 |
A |
G |
1: 89,856,517 (GRCm39) |
V291A |
probably damaging |
Het |
Hipk3 |
G |
A |
2: 104,301,604 (GRCm39) |
T196M |
probably damaging |
Het |
Il20ra |
T |
A |
10: 19,634,789 (GRCm39) |
N343K |
probably benign |
Het |
Il24 |
C |
T |
1: 130,813,470 (GRCm39) |
W42* |
probably null |
Het |
Kif13b |
A |
T |
14: 65,005,166 (GRCm39) |
I1153F |
probably damaging |
Het |
Krt1c |
A |
T |
15: 101,719,763 (GRCm39) |
S636T |
unknown |
Het |
Or13a25 |
C |
T |
7: 140,247,463 (GRCm39) |
P81S |
probably damaging |
Het |
Or14c40 |
T |
C |
7: 86,313,737 (GRCm39) |
F289S |
probably damaging |
Het |
Or4k52 |
T |
A |
2: 111,610,955 (GRCm39) |
C97S |
probably damaging |
Het |
Or6d15 |
A |
T |
6: 116,559,505 (GRCm39) |
M134K |
probably damaging |
Het |
Osmr |
T |
C |
15: 6,845,378 (GRCm39) |
D796G |
possibly damaging |
Het |
Peli2 |
A |
T |
14: 48,477,754 (GRCm39) |
T99S |
probably benign |
Het |
Pi4k2a |
A |
T |
19: 42,101,510 (GRCm39) |
K317N |
probably benign |
Het |
Pik3r1 |
T |
G |
13: 101,894,037 (GRCm39) |
D44A |
probably benign |
Het |
Pkhd1 |
G |
T |
1: 20,678,640 (GRCm39) |
S96* |
probably null |
Het |
Plekha5 |
A |
G |
6: 140,489,904 (GRCm39) |
E9G |
probably damaging |
Het |
Plekha8 |
T |
C |
6: 54,592,254 (GRCm39) |
F71S |
probably damaging |
Het |
Polq |
G |
T |
16: 36,906,928 (GRCm39) |
L2296F |
probably damaging |
Het |
Rbm5 |
G |
A |
9: 107,631,384 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
T |
C |
2: 37,295,366 (GRCm39) |
K217E |
probably damaging |
Het |
Scrib |
A |
G |
15: 75,937,056 (GRCm39) |
L350P |
probably damaging |
Het |
Slc4a10 |
T |
A |
2: 62,098,487 (GRCm39) |
S540R |
probably damaging |
Het |
Smc3 |
G |
T |
19: 53,611,988 (GRCm39) |
V354L |
probably benign |
Het |
Smurf1 |
T |
A |
5: 144,836,199 (GRCm39) |
I105F |
probably damaging |
Het |
Stx7 |
G |
T |
10: 24,031,247 (GRCm39) |
R17L |
probably benign |
Het |
Tbca |
C |
T |
13: 94,979,203 (GRCm39) |
R74C |
probably benign |
Het |
Tmem92 |
T |
C |
11: 94,669,504 (GRCm39) |
Q153R |
possibly damaging |
Het |
Trim41 |
C |
A |
11: 48,698,307 (GRCm39) |
G553V |
probably damaging |
Het |
Trim75 |
A |
T |
8: 65,435,417 (GRCm39) |
N344K |
possibly damaging |
Het |
Tsr1 |
A |
G |
11: 74,791,075 (GRCm39) |
D218G |
probably benign |
Het |
Ubr2 |
A |
C |
17: 47,286,877 (GRCm39) |
V474G |
probably damaging |
Het |
Unc45a |
T |
G |
7: 79,982,721 (GRCm39) |
|
probably benign |
Het |
Zfp609 |
C |
T |
9: 65,610,675 (GRCm39) |
A763T |
probably benign |
Het |
|
Other mutations in Or11g24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Or11g24
|
APN |
14 |
50,662,018 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02430:Or11g24
|
APN |
14 |
50,662,608 (GRCm39) |
missense |
probably benign |
|
IGL02603:Or11g24
|
APN |
14 |
50,662,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Or11g24
|
APN |
14 |
50,662,080 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Or11g24
|
UTSW |
14 |
50,662,359 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1984:Or11g24
|
UTSW |
14 |
50,662,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3160:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3161:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4821:Or11g24
|
UTSW |
14 |
50,662,206 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4880:Or11g24
|
UTSW |
14 |
50,662,758 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5047:Or11g24
|
UTSW |
14 |
50,662,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5385:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5386:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5640:Or11g24
|
UTSW |
14 |
50,662,111 (GRCm39) |
missense |
probably benign |
0.18 |
R5809:Or11g24
|
UTSW |
14 |
50,662,905 (GRCm39) |
makesense |
probably null |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6229:Or11g24
|
UTSW |
14 |
50,662,662 (GRCm39) |
missense |
probably benign |
0.38 |
R6614:Or11g24
|
UTSW |
14 |
50,662,546 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Or11g24
|
UTSW |
14 |
50,662,722 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7443:Or11g24
|
UTSW |
14 |
50,662,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7700:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7851:Or11g24
|
UTSW |
14 |
50,662,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R8397:Or11g24
|
UTSW |
14 |
50,662,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Or11g24
|
UTSW |
14 |
50,662,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Or11g24
|
UTSW |
14 |
50,662,255 (GRCm39) |
missense |
probably benign |
0.00 |
|