Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agl |
T |
A |
3: 116,582,198 (GRCm39) |
I275F |
probably damaging |
Het |
Avil |
G |
A |
10: 126,856,415 (GRCm39) |
E815K |
possibly damaging |
Het |
Car9 |
T |
A |
4: 43,510,252 (GRCm39) |
I278N |
probably damaging |
Het |
Cast |
T |
A |
13: 74,875,408 (GRCm39) |
K480* |
probably null |
Het |
Cenpj |
A |
G |
14: 56,790,931 (GRCm39) |
F373L |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,204,366 (GRCm39) |
|
probably null |
Het |
Diaph3 |
G |
A |
14: 87,156,288 (GRCm39) |
T675I |
possibly damaging |
Het |
Dip2b |
A |
T |
15: 100,069,101 (GRCm39) |
|
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,988,427 (GRCm39) |
D3425G |
probably damaging |
Het |
Dolk |
A |
G |
2: 30,175,926 (GRCm39) |
Y40H |
probably benign |
Het |
Drosha |
T |
C |
15: 12,866,736 (GRCm39) |
|
probably benign |
Het |
Dusp15 |
A |
G |
2: 152,790,956 (GRCm39) |
|
probably null |
Het |
Edrf1 |
T |
C |
7: 133,258,831 (GRCm39) |
F770L |
probably benign |
Het |
Gabra1 |
T |
C |
11: 42,024,586 (GRCm39) |
K363R |
possibly damaging |
Het |
Glipr1l1 |
A |
C |
10: 111,912,074 (GRCm39) |
T203P |
probably benign |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
H2-Q10 |
T |
C |
17: 35,784,168 (GRCm39) |
S270P |
probably damaging |
Het |
Hipk2 |
A |
T |
6: 38,795,330 (GRCm39) |
M313K |
probably benign |
Het |
Htt |
T |
A |
5: 35,034,174 (GRCm39) |
I1920N |
probably damaging |
Het |
Lsr |
A |
T |
7: 30,661,657 (GRCm39) |
V210E |
possibly damaging |
Het |
Mbtd1 |
A |
T |
11: 93,812,238 (GRCm39) |
I181L |
probably null |
Het |
Mettl16 |
A |
T |
11: 74,696,097 (GRCm39) |
T273S |
possibly damaging |
Het |
Mlst8 |
T |
C |
17: 24,696,961 (GRCm39) |
N74D |
probably benign |
Het |
Nek9 |
A |
G |
12: 85,383,174 (GRCm39) |
I102T |
probably damaging |
Het |
Nme7 |
C |
T |
1: 164,172,850 (GRCm39) |
A187V |
probably damaging |
Het |
Nphp1 |
A |
T |
2: 127,611,564 (GRCm39) |
W261R |
probably damaging |
Het |
Or12e13 |
G |
T |
2: 87,664,207 (GRCm39) |
G275* |
probably null |
Het |
Or2h2 |
A |
G |
17: 37,396,760 (GRCm39) |
L99P |
probably damaging |
Het |
Orc6 |
A |
G |
8: 86,034,272 (GRCm39) |
D165G |
probably damaging |
Het |
Ovca2 |
A |
G |
11: 75,069,133 (GRCm39) |
S89P |
probably benign |
Het |
Pcdhb12 |
T |
G |
18: 37,570,263 (GRCm39) |
S470A |
probably benign |
Het |
Phactr2 |
T |
C |
10: 13,122,932 (GRCm39) |
T397A |
probably benign |
Het |
Pms2 |
T |
C |
5: 143,860,337 (GRCm39) |
L50P |
probably damaging |
Het |
Prr36 |
G |
A |
8: 4,265,243 (GRCm39) |
P169L |
probably damaging |
Het |
Serpinb11 |
C |
A |
1: 107,305,387 (GRCm39) |
S254R |
probably benign |
Het |
Serpinb11 |
C |
A |
1: 107,305,388 (GRCm39) |
Q255K |
probably benign |
Het |
Skap2 |
T |
C |
6: 51,851,556 (GRCm39) |
T79A |
probably damaging |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Tbx19 |
A |
T |
1: 164,967,767 (GRCm39) |
S327T |
possibly damaging |
Het |
Themis3 |
A |
G |
17: 66,866,622 (GRCm39) |
L206P |
possibly damaging |
Het |
Tmem132c |
T |
A |
5: 127,540,093 (GRCm39) |
L373Q |
possibly damaging |
Het |
Unc13c |
G |
T |
9: 73,600,648 (GRCm39) |
N1365K |
probably benign |
Het |
Vmn2r106 |
A |
T |
17: 20,497,730 (GRCm39) |
M503K |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r33 |
A |
G |
7: 7,566,776 (GRCm39) |
I112T |
probably benign |
Het |
Vps13a |
A |
C |
19: 16,641,139 (GRCm39) |
W2328G |
probably damaging |
Het |
|
Other mutations in Or4f14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Or4f14
|
APN |
2 |
111,742,381 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01310:Or4f14
|
APN |
2 |
111,742,652 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02433:Or4f14
|
APN |
2 |
111,742,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03302:Or4f14
|
APN |
2 |
111,743,167 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0544:Or4f14
|
UTSW |
2 |
111,742,905 (GRCm39) |
nonsense |
probably null |
|
R0674:Or4f14
|
UTSW |
2 |
111,743,018 (GRCm39) |
missense |
probably benign |
0.41 |
R1118:Or4f14
|
UTSW |
2 |
111,743,222 (GRCm39) |
missense |
probably benign |
0.02 |
R1764:Or4f14
|
UTSW |
2 |
111,742,526 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2915:Or4f14
|
UTSW |
2 |
111,743,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R3976:Or4f14
|
UTSW |
2 |
111,742,951 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4855:Or4f14
|
UTSW |
2 |
111,742,444 (GRCm39) |
missense |
probably benign |
0.41 |
R6475:Or4f14
|
UTSW |
2 |
111,743,204 (GRCm39) |
nonsense |
probably null |
|
R6513:Or4f14
|
UTSW |
2 |
111,743,228 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6536:Or4f14
|
UTSW |
2 |
111,743,119 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6748:Or4f14
|
UTSW |
2 |
111,742,702 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6843:Or4f14
|
UTSW |
2 |
111,743,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Or4f14
|
UTSW |
2 |
111,742,601 (GRCm39) |
missense |
probably benign |
0.16 |
R7169:Or4f14
|
UTSW |
2 |
111,742,939 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7230:Or4f14
|
UTSW |
2 |
111,742,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Or4f14
|
UTSW |
2 |
111,742,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Or4f14
|
UTSW |
2 |
111,742,637 (GRCm39) |
missense |
probably benign |
0.00 |
R7753:Or4f14
|
UTSW |
2 |
111,742,927 (GRCm39) |
missense |
probably benign |
0.06 |
R7761:Or4f14
|
UTSW |
2 |
111,743,222 (GRCm39) |
missense |
probably benign |
0.02 |
R8330:Or4f14
|
UTSW |
2 |
111,742,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8497:Or4f14
|
UTSW |
2 |
111,742,964 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8942:Or4f14
|
UTSW |
2 |
111,743,207 (GRCm39) |
missense |
probably benign |
0.05 |
R9603:Or4f14
|
UTSW |
2 |
111,743,128 (GRCm39) |
missense |
possibly damaging |
0.69 |
|