Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3 |
A |
C |
11: 95,725,213 (GRCm39) |
L159W |
probably damaging |
Het |
Abi3 |
A |
T |
11: 95,725,214 (GRCm39) |
L159M |
probably damaging |
Het |
Adam11 |
A |
C |
11: 102,664,636 (GRCm39) |
I406L |
probably benign |
Het |
Ager |
G |
T |
17: 34,819,051 (GRCm39) |
V300L |
probably damaging |
Het |
Ank3 |
C |
T |
10: 69,822,660 (GRCm39) |
S1726L |
probably benign |
Het |
Boc |
A |
G |
16: 44,311,014 (GRCm39) |
I740T |
probably damaging |
Het |
C8a |
T |
A |
4: 104,711,129 (GRCm39) |
D178V |
probably damaging |
Het |
Ces3a |
G |
A |
8: 105,777,198 (GRCm39) |
V174M |
probably damaging |
Het |
Cisd1 |
A |
T |
10: 71,172,244 (GRCm39) |
W13R |
probably damaging |
Het |
Commd8 |
A |
T |
5: 72,320,107 (GRCm39) |
D111E |
probably benign |
Het |
Ddx60 |
A |
T |
8: 62,490,104 (GRCm39) |
D1691V |
probably damaging |
Het |
Desi2 |
A |
G |
1: 178,065,479 (GRCm39) |
Y15C |
probably damaging |
Het |
Dnmt1 |
A |
G |
9: 20,864,013 (GRCm39) |
V24A |
probably damaging |
Het |
Dock10 |
G |
A |
1: 80,538,640 (GRCm39) |
T968M |
probably benign |
Het |
Dsel |
A |
T |
1: 111,787,168 (GRCm39) |
F1122L |
probably damaging |
Het |
Eml3 |
T |
C |
19: 8,910,807 (GRCm39) |
F220L |
probably damaging |
Het |
Entpd2 |
A |
C |
2: 25,290,824 (GRCm39) |
N443H |
probably damaging |
Het |
Epgn |
A |
G |
5: 91,176,222 (GRCm39) |
N36S |
probably benign |
Het |
Fsip2 |
G |
T |
2: 82,814,785 (GRCm39) |
S3506I |
possibly damaging |
Het |
Gprin3 |
T |
C |
6: 59,331,771 (GRCm39) |
S179G |
probably benign |
Het |
Grifin |
G |
T |
5: 140,549,342 (GRCm39) |
H125N |
possibly damaging |
Het |
H1f9 |
A |
G |
11: 94,858,989 (GRCm39) |
T95A |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,506,078 (GRCm39) |
V3816A |
probably damaging |
Het |
Hspa14 |
A |
G |
2: 3,499,207 (GRCm39) |
F196L |
probably benign |
Het |
Ice1 |
T |
C |
13: 70,754,620 (GRCm39) |
K489E |
probably benign |
Het |
Jmjd6 |
C |
T |
11: 116,730,682 (GRCm39) |
W117* |
probably null |
Het |
Lrit2 |
G |
T |
14: 36,794,192 (GRCm39) |
A419S |
probably benign |
Het |
Mc3r |
T |
C |
2: 172,091,092 (GRCm39) |
S105P |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,018,531 (GRCm39) |
V601A |
probably benign |
Het |
Myo1f |
A |
G |
17: 33,795,627 (GRCm39) |
D91G |
probably damaging |
Het |
Myo1f |
G |
A |
17: 33,799,259 (GRCm39) |
E255K |
possibly damaging |
Het |
Necap1 |
T |
A |
6: 122,858,503 (GRCm39) |
D115E |
probably benign |
Het |
Or4b12 |
A |
T |
2: 90,096,786 (GRCm39) |
|
probably null |
Het |
Or51b6 |
T |
A |
7: 103,555,883 (GRCm39) |
M79K |
probably damaging |
Het |
Papln |
A |
G |
12: 83,818,652 (GRCm39) |
E78G |
probably null |
Het |
Phldb3 |
T |
C |
7: 24,326,147 (GRCm39) |
|
probably null |
Het |
Pkd1l2 |
A |
G |
8: 117,724,321 (GRCm39) |
I2394T |
probably damaging |
Het |
Ppa2 |
A |
T |
3: 133,036,200 (GRCm39) |
N118I |
probably damaging |
Het |
Ppef2 |
A |
T |
5: 92,398,388 (GRCm39) |
C43* |
probably null |
Het |
Pramel51 |
A |
G |
12: 88,143,111 (GRCm39) |
L169P |
probably damaging |
Het |
Rab27a |
G |
A |
9: 72,992,321 (GRCm39) |
|
probably null |
Het |
Rabgap1l |
A |
T |
1: 160,169,683 (GRCm39) |
F47I |
probably damaging |
Het |
Rala |
A |
G |
13: 18,067,746 (GRCm39) |
I95T |
probably damaging |
Het |
Rgl2 |
A |
G |
17: 34,151,691 (GRCm39) |
D245G |
probably benign |
Het |
Rnf34 |
A |
T |
5: 123,002,146 (GRCm39) |
T35S |
probably damaging |
Het |
Ros1 |
C |
T |
10: 52,057,894 (GRCm39) |
R51Q |
probably benign |
Het |
Samd9l |
T |
C |
6: 3,372,716 (GRCm39) |
D1515G |
possibly damaging |
Het |
Scn7a |
T |
C |
2: 66,505,870 (GRCm39) |
E1673G |
probably benign |
Het |
Slc6a20a |
A |
C |
9: 123,470,773 (GRCm39) |
|
probably null |
Het |
Tdrd5 |
A |
T |
1: 156,122,070 (GRCm39) |
S280T |
probably damaging |
Het |
Tent2 |
A |
T |
13: 93,312,246 (GRCm39) |
C180* |
probably null |
Het |
Tie1 |
T |
C |
4: 118,332,800 (GRCm39) |
I911V |
possibly damaging |
Het |
Vipas39 |
G |
A |
12: 87,298,581 (GRCm39) |
R194* |
probably null |
Het |
Ybx3 |
A |
C |
6: 131,345,451 (GRCm39) |
N307K |
possibly damaging |
Het |
Ylpm1 |
A |
T |
12: 85,088,899 (GRCm39) |
H1216L |
probably damaging |
Het |
|
Other mutations in Or4k15b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01116:Or4k15b
|
APN |
14 |
50,272,507 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01412:Or4k15b
|
APN |
14 |
50,272,770 (GRCm39) |
missense |
probably benign |
|
IGL03241:Or4k15b
|
APN |
14 |
50,272,525 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03268:Or4k15b
|
APN |
14 |
50,272,024 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03348:Or4k15b
|
APN |
14 |
50,272,212 (GRCm39) |
missense |
probably benign |
0.00 |
R0358:Or4k15b
|
UTSW |
14 |
50,272,743 (GRCm39) |
missense |
probably damaging |
0.97 |
R0577:Or4k15b
|
UTSW |
14 |
50,272,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Or4k15b
|
UTSW |
14 |
50,272,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Or4k15b
|
UTSW |
14 |
50,272,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R3421:Or4k15b
|
UTSW |
14 |
50,271,997 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3422:Or4k15b
|
UTSW |
14 |
50,271,997 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4436:Or4k15b
|
UTSW |
14 |
50,272,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Or4k15b
|
UTSW |
14 |
50,272,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4438:Or4k15b
|
UTSW |
14 |
50,272,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Or4k15b
|
UTSW |
14 |
50,272,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Or4k15b
|
UTSW |
14 |
50,272,821 (GRCm39) |
missense |
probably damaging |
0.98 |
R5253:Or4k15b
|
UTSW |
14 |
50,272,745 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5254:Or4k15b
|
UTSW |
14 |
50,272,135 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5641:Or4k15b
|
UTSW |
14 |
50,272,746 (GRCm39) |
missense |
probably benign |
0.04 |
R5906:Or4k15b
|
UTSW |
14 |
50,272,306 (GRCm39) |
missense |
probably benign |
0.05 |
R6511:Or4k15b
|
UTSW |
14 |
50,272,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Or4k15b
|
UTSW |
14 |
50,272,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7980:Or4k15b
|
UTSW |
14 |
50,272,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Or4k15b
|
UTSW |
14 |
50,272,608 (GRCm39) |
missense |
probably benign |
0.13 |
R8942:Or4k15b
|
UTSW |
14 |
50,272,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R9084:Or4k15b
|
UTSW |
14 |
50,271,916 (GRCm39) |
missense |
probably benign |
|
R9797:Or4k15b
|
UTSW |
14 |
50,272,224 (GRCm39) |
missense |
probably benign |
0.19 |
X0062:Or4k15b
|
UTSW |
14 |
50,272,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|