Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
T |
C |
11: 94,236,870 (GRCm39) |
T1456A |
probably damaging |
Het |
Acad11 |
T |
C |
9: 103,950,844 (GRCm39) |
F56S |
probably damaging |
Het |
Adamts8 |
A |
G |
9: 30,867,952 (GRCm39) |
N592S |
possibly damaging |
Het |
Amh |
A |
G |
10: 80,642,755 (GRCm39) |
D313G |
probably damaging |
Het |
Ampd2 |
T |
C |
3: 107,994,052 (GRCm39) |
|
probably benign |
Het |
Arap3 |
A |
G |
18: 38,111,653 (GRCm39) |
L1115P |
probably damaging |
Het |
Arfgap1 |
C |
A |
2: 180,622,869 (GRCm39) |
D327E |
probably benign |
Het |
Capns2 |
T |
A |
8: 93,628,252 (GRCm39) |
I47N |
possibly damaging |
Het |
Cd163 |
T |
C |
6: 124,304,862 (GRCm39) |
S1080P |
possibly damaging |
Het |
Ceacam10 |
A |
T |
7: 24,480,433 (GRCm39) |
Y68F |
possibly damaging |
Het |
Cep44 |
G |
A |
8: 56,991,652 (GRCm39) |
P317S |
probably benign |
Het |
Cfh |
A |
T |
1: 140,028,613 (GRCm39) |
Y688* |
probably null |
Het |
Chrnb1 |
A |
T |
11: 69,677,773 (GRCm39) |
S326R |
probably damaging |
Het |
Cngb1 |
C |
T |
8: 96,026,344 (GRCm39) |
V25M |
probably damaging |
Het |
Cyp2c50 |
A |
T |
19: 40,079,136 (GRCm39) |
N160Y |
possibly damaging |
Het |
Dalrd3 |
T |
C |
9: 108,448,800 (GRCm39) |
|
probably benign |
Het |
Eef1d |
C |
A |
15: 75,774,648 (GRCm39) |
S253I |
possibly damaging |
Het |
Efl1 |
G |
A |
7: 82,412,491 (GRCm39) |
C960Y |
probably damaging |
Het |
Elmo1 |
C |
G |
13: 20,784,382 (GRCm39) |
Y646* |
probably null |
Het |
Epb41l2 |
C |
A |
10: 25,382,078 (GRCm39) |
D701E |
possibly damaging |
Het |
Fbxl4 |
T |
A |
4: 22,422,699 (GRCm39) |
|
probably null |
Het |
Fhod1 |
T |
C |
8: 106,063,983 (GRCm39) |
|
probably benign |
Het |
Gm8741 |
G |
T |
17: 35,555,062 (GRCm39) |
|
noncoding transcript |
Het |
Igkv10-95 |
A |
T |
6: 68,657,606 (GRCm39) |
I21F |
probably damaging |
Het |
Il10rb |
C |
A |
16: 91,204,603 (GRCm39) |
N51K |
possibly damaging |
Het |
Krt78 |
T |
C |
15: 101,856,375 (GRCm39) |
T479A |
probably benign |
Het |
Lrig3 |
T |
C |
10: 125,849,273 (GRCm39) |
S998P |
probably benign |
Het |
Lrrc8c |
T |
A |
5: 105,755,755 (GRCm39) |
M510K |
probably benign |
Het |
Nfrkb |
G |
T |
9: 31,311,258 (GRCm39) |
C369F |
probably damaging |
Het |
Nphp1 |
T |
C |
2: 127,630,719 (GRCm39) |
E19G |
possibly damaging |
Het |
Or10a5 |
A |
C |
7: 106,635,698 (GRCm39) |
E112A |
probably damaging |
Het |
Ovol3 |
A |
T |
7: 29,934,789 (GRCm39) |
|
probably null |
Het |
Ppp1r16b |
C |
T |
2: 158,599,174 (GRCm39) |
T382I |
probably benign |
Het |
Rims2 |
T |
C |
15: 39,301,320 (GRCm39) |
|
probably null |
Het |
Sh3rf3 |
T |
C |
10: 58,919,398 (GRCm39) |
V505A |
probably benign |
Het |
Shkbp1 |
T |
C |
7: 27,042,727 (GRCm39) |
N570S |
probably benign |
Het |
Slc35f4 |
C |
T |
14: 49,556,307 (GRCm39) |
V149I |
possibly damaging |
Het |
Snx27 |
A |
G |
3: 94,469,330 (GRCm39) |
F4L |
probably benign |
Het |
Syvn1 |
C |
T |
19: 6,099,951 (GRCm39) |
|
probably benign |
Het |
Tagap1 |
G |
A |
17: 7,223,511 (GRCm39) |
S395L |
probably benign |
Het |
Tcstv2b |
C |
A |
13: 120,373,908 (GRCm39) |
L127F |
probably damaging |
Het |
Tek |
A |
G |
4: 94,751,904 (GRCm39) |
T1014A |
probably damaging |
Het |
Top2a |
A |
G |
11: 98,892,231 (GRCm39) |
I1077T |
probably benign |
Het |
Tpo |
T |
C |
12: 30,154,015 (GRCm39) |
Y230C |
probably damaging |
Het |
Trav12-2 |
A |
G |
14: 53,854,332 (GRCm39) |
Q102R |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,733,430 (GRCm39) |
|
probably benign |
Het |
Vmn1r183 |
A |
T |
7: 23,754,973 (GRCm39) |
I259F |
probably benign |
Het |
Vmn1r228 |
T |
C |
17: 20,996,861 (GRCm39) |
E219G |
probably damaging |
Het |
Vsig8 |
G |
T |
1: 172,390,714 (GRCm39) |
G254V |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,320,246 (GRCm39) |
I1086V |
probably benign |
Het |
Zfp423 |
G |
A |
8: 88,509,601 (GRCm39) |
H123Y |
probably damaging |
Het |
Zfp811 |
A |
T |
17: 33,016,521 (GRCm39) |
C506* |
probably null |
Het |
|
Other mutations in Or4f14b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01501:Or4f14b
|
APN |
2 |
111,774,863 (GRCm39) |
makesense |
probably null |
|
IGL01947:Or4f14b
|
APN |
2 |
111,775,339 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02373:Or4f14b
|
APN |
2 |
111,775,178 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02682:Or4f14b
|
APN |
2 |
111,775,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R0714:Or4f14b
|
UTSW |
2 |
111,774,898 (GRCm39) |
missense |
probably benign |
0.01 |
R1670:Or4f14b
|
UTSW |
2 |
111,775,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Or4f14b
|
UTSW |
2 |
111,775,633 (GRCm39) |
missense |
probably benign |
0.45 |
R1733:Or4f14b
|
UTSW |
2 |
111,775,625 (GRCm39) |
missense |
probably benign |
0.13 |
R1773:Or4f14b
|
UTSW |
2 |
111,775,204 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1783:Or4f14b
|
UTSW |
2 |
111,775,633 (GRCm39) |
missense |
probably benign |
0.45 |
R2180:Or4f14b
|
UTSW |
2 |
111,775,348 (GRCm39) |
missense |
probably benign |
0.39 |
R2197:Or4f14b
|
UTSW |
2 |
111,775,658 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2207:Or4f14b
|
UTSW |
2 |
111,775,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R2377:Or4f14b
|
UTSW |
2 |
111,774,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Or4f14b
|
UTSW |
2 |
111,774,997 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4859:Or4f14b
|
UTSW |
2 |
111,775,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R4910:Or4f14b
|
UTSW |
2 |
111,775,423 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5167:Or4f14b
|
UTSW |
2 |
111,775,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R5537:Or4f14b
|
UTSW |
2 |
111,775,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Or4f14b
|
UTSW |
2 |
111,775,739 (GRCm39) |
missense |
probably null |
0.41 |
R6877:Or4f14b
|
UTSW |
2 |
111,775,184 (GRCm39) |
missense |
probably benign |
0.16 |
R7011:Or4f14b
|
UTSW |
2 |
111,775,031 (GRCm39) |
missense |
probably benign |
0.01 |
R7177:Or4f14b
|
UTSW |
2 |
111,775,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7937:Or4f14b
|
UTSW |
2 |
111,774,875 (GRCm39) |
missense |
probably benign |
0.00 |
R8792:Or4f14b
|
UTSW |
2 |
111,775,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Or4f14b
|
UTSW |
2 |
111,774,967 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9358:Or4f14b
|
UTSW |
2 |
111,775,429 (GRCm39) |
missense |
probably benign |
0.31 |
|