Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
A |
T |
6: 146,854,606 (GRCm39) |
F145L |
probably benign |
Het |
Abcc9 |
T |
C |
6: 142,551,645 (GRCm39) |
D1221G |
possibly damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,584,864 (GRCm39) |
K935E |
probably benign |
Het |
Ago4 |
A |
T |
4: 126,409,655 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,130,575 (GRCm39) |
D421G |
probably benign |
Het |
Armh4 |
T |
A |
14: 50,011,444 (GRCm39) |
M88L |
probably benign |
Het |
Atl2 |
T |
C |
17: 80,157,588 (GRCm39) |
*413W |
probably null |
Het |
B4galt7 |
C |
A |
13: 55,756,152 (GRCm39) |
|
probably null |
Het |
Bltp3b |
A |
G |
10: 89,651,917 (GRCm39) |
N247S |
probably benign |
Het |
C8g |
A |
T |
2: 25,389,425 (GRCm39) |
S147T |
probably damaging |
Het |
Clstn3 |
A |
T |
6: 124,426,792 (GRCm39) |
Y510N |
possibly damaging |
Het |
Cnot2 |
A |
G |
10: 116,373,301 (GRCm39) |
V34A |
possibly damaging |
Het |
Cyb5d2 |
A |
T |
11: 72,686,606 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,421,144 (GRCm39) |
I3827T |
probably damaging |
Het |
Dnah7a |
G |
T |
1: 53,464,376 (GRCm39) |
Q3672K |
probably benign |
Het |
Dock1 |
A |
T |
7: 134,717,021 (GRCm39) |
Y1219F |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,478,518 (GRCm39) |
E2521D |
probably benign |
Het |
Gm10719 |
G |
T |
9: 3,019,043 (GRCm39) |
W96L |
probably damaging |
Het |
H2-M2 |
G |
A |
17: 37,792,399 (GRCm39) |
H291Y |
probably damaging |
Het |
Hmgcl |
T |
C |
4: 135,686,035 (GRCm39) |
Y167H |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,502,400 (GRCm39) |
D73V |
possibly damaging |
Het |
Incenp |
A |
T |
19: 9,861,142 (GRCm39) |
M480K |
unknown |
Het |
Irag1 |
G |
T |
7: 110,522,984 (GRCm39) |
A359D |
probably benign |
Het |
Kdm6a |
A |
G |
X: 18,117,114 (GRCm39) |
T266A |
probably benign |
Het |
Lipf |
A |
G |
19: 33,942,965 (GRCm39) |
N91S |
probably benign |
Het |
M1ap |
A |
T |
6: 82,980,756 (GRCm39) |
N214I |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,838 (GRCm39) |
V969A |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,057,005 (GRCm39) |
C826R |
probably damaging |
Het |
Msx1 |
C |
A |
5: 37,981,365 (GRCm39) |
A105S |
probably benign |
Het |
Otogl |
A |
T |
10: 107,626,510 (GRCm39) |
D1451E |
probably benign |
Het |
Otop2 |
G |
A |
11: 115,220,201 (GRCm39) |
G347D |
probably damaging |
Het |
Ppp1r13l |
A |
T |
7: 19,103,978 (GRCm39) |
H153L |
probably benign |
Het |
Pramel21 |
A |
G |
4: 143,342,559 (GRCm39) |
D222G |
possibly damaging |
Het |
Pramel29 |
T |
C |
4: 143,935,265 (GRCm39) |
K161E |
possibly damaging |
Het |
Proz |
A |
G |
8: 13,114,621 (GRCm39) |
Y85C |
probably damaging |
Het |
Prss50 |
A |
G |
9: 110,687,480 (GRCm39) |
D141G |
probably benign |
Het |
Rad54l2 |
T |
A |
9: 106,597,613 (GRCm39) |
Q131L |
probably benign |
Het |
Sdha |
A |
G |
13: 74,472,077 (GRCm39) |
|
probably benign |
Het |
Sema3d |
T |
A |
5: 12,635,091 (GRCm39) |
I719N |
probably benign |
Het |
Slc18b1 |
A |
T |
10: 23,681,879 (GRCm39) |
I148L |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,330,852 (GRCm39) |
D2086Y |
probably damaging |
Het |
Tchh |
T |
C |
3: 93,354,298 (GRCm39) |
L1246P |
unknown |
Het |
Tmprss11d |
T |
C |
5: 86,457,177 (GRCm39) |
I161V |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,725,172 (GRCm39) |
D268G |
probably damaging |
Het |
Trpm8 |
G |
A |
1: 88,289,727 (GRCm39) |
R895H |
probably damaging |
Het |
Txndc2 |
A |
G |
17: 65,945,079 (GRCm39) |
I366T |
possibly damaging |
Het |
Ugt2a3 |
T |
C |
5: 87,484,725 (GRCm39) |
I100V |
probably benign |
Het |
Upp1 |
C |
A |
11: 9,081,709 (GRCm39) |
P82Q |
probably damaging |
Het |
Vim |
A |
G |
2: 13,584,827 (GRCm39) |
|
probably null |
Het |
Vmn2r12 |
A |
T |
5: 109,240,058 (GRCm39) |
N168K |
possibly damaging |
Het |
Zdhhc14 |
G |
T |
17: 5,802,983 (GRCm39) |
C362F |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,863 (GRCm39) |
V727A |
probably damaging |
Het |
Zswim5 |
G |
A |
4: 116,735,177 (GRCm39) |
G174D |
unknown |
Het |
|
Other mutations in Or5ac23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02475:Or5ac23
|
APN |
16 |
59,149,088 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03236:Or5ac23
|
APN |
16 |
59,149,200 (GRCm39) |
missense |
probably damaging |
0.97 |
R0054:Or5ac23
|
UTSW |
16 |
59,149,428 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0054:Or5ac23
|
UTSW |
16 |
59,149,428 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0167:Or5ac23
|
UTSW |
16 |
59,149,337 (GRCm39) |
nonsense |
probably null |
|
R0178:Or5ac23
|
UTSW |
16 |
59,149,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Or5ac23
|
UTSW |
16 |
59,149,585 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0577:Or5ac23
|
UTSW |
16 |
59,149,061 (GRCm39) |
missense |
probably benign |
0.01 |
R0597:Or5ac23
|
UTSW |
16 |
59,149,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Or5ac23
|
UTSW |
16 |
59,149,546 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1670:Or5ac23
|
UTSW |
16 |
59,149,607 (GRCm39) |
missense |
probably benign |
0.03 |
R1702:Or5ac23
|
UTSW |
16 |
59,149,504 (GRCm39) |
missense |
probably benign |
0.12 |
R1995:Or5ac23
|
UTSW |
16 |
59,149,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Or5ac23
|
UTSW |
16 |
59,149,738 (GRCm39) |
missense |
probably damaging |
0.99 |
R4400:Or5ac23
|
UTSW |
16 |
59,148,961 (GRCm39) |
missense |
probably benign |
|
R4666:Or5ac23
|
UTSW |
16 |
59,149,573 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4795:Or5ac23
|
UTSW |
16 |
59,149,213 (GRCm39) |
missense |
probably benign |
0.09 |
R5327:Or5ac23
|
UTSW |
16 |
59,149,461 (GRCm39) |
missense |
probably benign |
0.01 |
R5471:Or5ac23
|
UTSW |
16 |
59,148,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R5770:Or5ac23
|
UTSW |
16 |
59,149,514 (GRCm39) |
nonsense |
probably null |
|
R6195:Or5ac23
|
UTSW |
16 |
59,149,785 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6702:Or5ac23
|
UTSW |
16 |
59,148,961 (GRCm39) |
missense |
probably benign |
|
R7686:Or5ac23
|
UTSW |
16 |
59,149,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7911:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7912:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7913:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7998:Or5ac23
|
UTSW |
16 |
59,149,633 (GRCm39) |
missense |
probably benign |
0.09 |
R8772:Or5ac23
|
UTSW |
16 |
59,149,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Or5ac23
|
UTSW |
16 |
59,149,765 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Or5ac23
|
UTSW |
16 |
59,149,713 (GRCm39) |
missense |
probably benign |
0.09 |
|