Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,530,301 (GRCm39) |
|
probably benign |
Het |
Ap1b1 |
T |
C |
11: 4,989,169 (GRCm39) |
L782P |
probably damaging |
Het |
Arid1a |
T |
C |
4: 133,408,765 (GRCm39) |
D1914G |
unknown |
Het |
C8a |
G |
A |
4: 104,719,808 (GRCm39) |
Q57* |
probably null |
Het |
Cachd1 |
T |
C |
4: 100,850,069 (GRCm39) |
S1144P |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,255,598 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,924,268 (GRCm39) |
Q198R |
possibly damaging |
Het |
Cpne8 |
T |
C |
15: 90,453,700 (GRCm39) |
I228V |
probably benign |
Het |
Cr2 |
A |
T |
1: 194,833,222 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,522,395 (GRCm39) |
|
probably benign |
Het |
Cyp2c23 |
A |
G |
19: 43,994,046 (GRCm39) |
V440A |
probably benign |
Het |
Dag1 |
T |
C |
9: 108,085,281 (GRCm39) |
D620G |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 50,011,449 (GRCm39) |
L1202* |
probably null |
Het |
Dnah3 |
T |
G |
7: 119,542,798 (GRCm39) |
H3538P |
probably benign |
Het |
Dock8 |
A |
T |
19: 25,067,292 (GRCm39) |
Q312L |
probably benign |
Het |
E2f7 |
T |
G |
10: 110,610,596 (GRCm39) |
V407G |
probably benign |
Het |
F13b |
T |
C |
1: 139,444,165 (GRCm39) |
S500P |
probably damaging |
Het |
F5 |
A |
G |
1: 164,039,395 (GRCm39) |
I2002V |
probably benign |
Het |
Flywch1 |
T |
A |
17: 23,979,319 (GRCm39) |
M439L |
possibly damaging |
Het |
Gcn1 |
C |
A |
5: 115,757,759 (GRCm39) |
A2488E |
probably damaging |
Het |
Gria1 |
T |
C |
11: 57,208,600 (GRCm39) |
S832P |
probably damaging |
Het |
Hnrnpr |
T |
C |
4: 136,066,724 (GRCm39) |
|
probably benign |
Het |
Hps3 |
A |
G |
3: 20,083,165 (GRCm39) |
I177T |
probably benign |
Het |
Irgm2 |
G |
A |
11: 58,111,167 (GRCm39) |
G298D |
probably benign |
Het |
Kcnk7 |
G |
A |
19: 5,756,230 (GRCm39) |
G152D |
probably damaging |
Het |
Man2a2 |
T |
C |
7: 80,012,654 (GRCm39) |
T620A |
probably benign |
Het |
Mapk12 |
A |
G |
15: 89,021,669 (GRCm39) |
|
probably benign |
Het |
Mapk6 |
T |
C |
9: 75,297,572 (GRCm39) |
Y315C |
probably damaging |
Het |
Mdga2 |
T |
A |
12: 66,769,905 (GRCm39) |
|
probably null |
Het |
Met |
T |
A |
6: 17,491,700 (GRCm39) |
I154N |
probably damaging |
Het |
Mtrex |
T |
C |
13: 113,055,095 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,328,772 (GRCm39) |
R234G |
possibly damaging |
Het |
Or4d11 |
G |
T |
19: 12,014,041 (GRCm39) |
H22N |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,145,886 (GRCm39) |
T659I |
probably benign |
Het |
Pfkm |
T |
C |
15: 98,027,187 (GRCm39) |
V620A |
possibly damaging |
Het |
Rbak |
A |
G |
5: 143,162,355 (GRCm39) |
|
probably benign |
Het |
Rbl2 |
A |
G |
8: 91,816,844 (GRCm39) |
I401M |
probably benign |
Het |
Rragc |
T |
C |
4: 123,814,852 (GRCm39) |
S183P |
probably damaging |
Het |
Septin3 |
A |
G |
15: 82,163,814 (GRCm39) |
|
probably benign |
Het |
Slc22a6 |
A |
T |
19: 8,603,578 (GRCm39) |
|
probably benign |
Het |
Spag4 |
A |
T |
2: 155,910,417 (GRCm39) |
T348S |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,054,623 (GRCm39) |
R2157G |
probably benign |
Het |
Tmem168 |
G |
A |
6: 13,582,940 (GRCm39) |
T263M |
probably damaging |
Het |
Tnik |
T |
A |
3: 28,625,007 (GRCm39) |
|
probably null |
Het |
Tnpo2 |
T |
A |
8: 85,777,137 (GRCm39) |
V549E |
probably damaging |
Het |
Ttll7 |
A |
C |
3: 146,645,776 (GRCm39) |
K545Q |
possibly damaging |
Het |
Tubgcp5 |
T |
G |
7: 55,449,221 (GRCm39) |
D139E |
probably benign |
Het |
Vmn1r233 |
T |
A |
17: 21,214,861 (GRCm39) |
N30Y |
probably damaging |
Het |
Vmn2r25 |
T |
G |
6: 123,829,962 (GRCm39) |
D63A |
possibly damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,485 (GRCm39) |
L622Q |
probably damaging |
Het |
Vmn2r84 |
T |
C |
10: 130,222,148 (GRCm39) |
M691V |
probably benign |
Het |
Zc3hc1 |
A |
T |
6: 30,372,729 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Olfm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02097:Olfm5
|
APN |
7 |
103,803,438 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02322:Olfm5
|
APN |
7 |
103,803,608 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02324:Olfm5
|
APN |
7 |
103,803,302 (GRCm39) |
splice site |
probably null |
|
IGL02702:Olfm5
|
APN |
7 |
103,803,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Olfm5
|
UTSW |
7 |
103,810,133 (GRCm39) |
missense |
probably benign |
|
R0400:Olfm5
|
UTSW |
7 |
103,803,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0600:Olfm5
|
UTSW |
7 |
103,803,076 (GRCm39) |
nonsense |
probably null |
|
R0610:Olfm5
|
UTSW |
7 |
103,803,652 (GRCm39) |
nonsense |
probably null |
|
R0699:Olfm5
|
UTSW |
7 |
103,803,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Olfm5
|
UTSW |
7 |
103,809,619 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1978:Olfm5
|
UTSW |
7 |
103,813,948 (GRCm39) |
missense |
unknown |
|
R2391:Olfm5
|
UTSW |
7 |
103,810,041 (GRCm39) |
missense |
probably benign |
0.00 |
R3774:Olfm5
|
UTSW |
7 |
103,811,056 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4632:Olfm5
|
UTSW |
7 |
103,810,100 (GRCm39) |
missense |
probably benign |
0.00 |
R4770:Olfm5
|
UTSW |
7 |
103,809,685 (GRCm39) |
missense |
probably benign |
0.04 |
R4838:Olfm5
|
UTSW |
7 |
103,803,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Olfm5
|
UTSW |
7 |
103,809,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Olfm5
|
UTSW |
7 |
103,803,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R5930:Olfm5
|
UTSW |
7 |
103,803,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Olfm5
|
UTSW |
7 |
103,803,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Olfm5
|
UTSW |
7 |
103,809,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Olfm5
|
UTSW |
7 |
103,803,444 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7682:Olfm5
|
UTSW |
7 |
103,810,979 (GRCm39) |
missense |
probably null |
0.49 |
R7835:Olfm5
|
UTSW |
7 |
103,803,652 (GRCm39) |
nonsense |
probably null |
|
R8308:Olfm5
|
UTSW |
7 |
103,803,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Olfm5
|
UTSW |
7 |
103,803,029 (GRCm39) |
missense |
probably benign |
0.00 |
R9035:Olfm5
|
UTSW |
7 |
103,803,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Olfm5
|
UTSW |
7 |
103,802,984 (GRCm39) |
missense |
probably benign |
|
R9185:Olfm5
|
UTSW |
7 |
103,810,095 (GRCm39) |
nonsense |
probably null |
|
X0011:Olfm5
|
UTSW |
7 |
103,803,153 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1088:Olfm5
|
UTSW |
7 |
103,803,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|