Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
A |
5: 114,364,928 (GRCm39) |
I1536N |
probably damaging |
Het |
Actr1b |
A |
G |
1: 36,741,162 (GRCm39) |
S140P |
probably damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Anapc7 |
A |
T |
5: 122,566,366 (GRCm39) |
T92S |
probably benign |
Het |
Ash2l |
G |
A |
8: 26,307,642 (GRCm39) |
T585M |
possibly damaging |
Het |
Asxl1 |
T |
C |
2: 153,243,931 (GRCm39) |
F1495L |
probably damaging |
Het |
Atp5pf |
T |
C |
16: 84,625,328 (GRCm39) |
|
probably null |
Het |
Bcl2a1c |
A |
G |
9: 114,159,465 (GRCm39) |
N81S |
probably benign |
Het |
Bfsp2 |
A |
C |
9: 103,309,856 (GRCm39) |
|
probably null |
Het |
Casq1 |
A |
G |
1: 172,047,068 (GRCm39) |
Y64H |
probably damaging |
Het |
Ceacam16 |
A |
G |
7: 19,590,262 (GRCm39) |
V227A |
probably damaging |
Het |
Cers6 |
T |
A |
2: 68,898,969 (GRCm39) |
|
probably null |
Het |
Chrnb1 |
A |
G |
11: 69,686,671 (GRCm39) |
|
probably benign |
Het |
Clpb |
G |
A |
7: 101,313,204 (GRCm39) |
V63I |
probably benign |
Het |
Dnah11 |
G |
T |
12: 118,074,687 (GRCm39) |
D1388E |
probably benign |
Het |
Dst |
T |
C |
1: 34,195,938 (GRCm39) |
L405P |
probably damaging |
Het |
Dstyk |
A |
G |
1: 132,362,149 (GRCm39) |
E193G |
probably damaging |
Het |
Dusp2 |
A |
T |
2: 127,179,208 (GRCm39) |
S188C |
probably damaging |
Het |
Ep400 |
T |
C |
5: 110,877,697 (GRCm39) |
I810V |
unknown |
Het |
Faim2 |
C |
T |
15: 99,419,132 (GRCm39) |
G79D |
probably benign |
Het |
Fpgt |
A |
T |
3: 154,793,040 (GRCm39) |
I329K |
probably damaging |
Het |
Fut8 |
A |
G |
12: 77,411,771 (GRCm39) |
T78A |
probably benign |
Het |
Gm15130 |
A |
G |
2: 110,965,714 (GRCm39) |
|
probably benign |
Het |
Gm17087 |
A |
C |
17: 8,785,529 (GRCm39) |
I58R |
probably benign |
Het |
Grk2 |
T |
C |
19: 4,337,925 (GRCm39) |
D485G |
possibly damaging |
Het |
Hax1 |
GTCATCATCATCATCATC |
GTCATCATCATCATCATCATC |
3: 89,905,247 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,439,568 (GRCm39) |
S5539P |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,310,335 (GRCm39) |
V3310M |
probably damaging |
Het |
Impdh1 |
A |
T |
6: 29,207,161 (GRCm39) |
L61Q |
probably damaging |
Het |
Inhbb |
A |
T |
1: 119,345,806 (GRCm39) |
V161D |
possibly damaging |
Het |
Kansl2 |
C |
T |
15: 98,427,306 (GRCm39) |
V192M |
probably damaging |
Het |
Krt1c |
T |
C |
15: 101,724,747 (GRCm39) |
K288E |
probably damaging |
Het |
Lyar |
A |
G |
5: 38,385,290 (GRCm39) |
K110R |
probably damaging |
Het |
Lyrm9 |
C |
A |
11: 78,726,961 (GRCm39) |
H35N |
probably damaging |
Het |
Mab21l1 |
A |
G |
3: 55,690,533 (GRCm39) |
D40G |
probably benign |
Het |
Maml2 |
A |
C |
9: 13,532,915 (GRCm39) |
|
probably benign |
Het |
Mbd5 |
A |
G |
2: 49,162,401 (GRCm39) |
H69R |
probably benign |
Het |
Morc2b |
G |
T |
17: 33,356,446 (GRCm39) |
A442E |
probably damaging |
Het |
Moxd2 |
A |
T |
6: 40,855,744 (GRCm39) |
L615Q |
probably damaging |
Het |
Msh2 |
G |
A |
17: 88,016,011 (GRCm39) |
G548S |
probably damaging |
Het |
Napg |
G |
A |
18: 63,128,054 (GRCm39) |
S279N |
possibly damaging |
Het |
Ncor1 |
A |
T |
11: 62,240,136 (GRCm39) |
|
probably null |
Het |
Nkiras2 |
G |
T |
11: 100,516,866 (GRCm39) |
R128L |
probably damaging |
Het |
Npy4r |
T |
C |
14: 33,868,664 (GRCm39) |
D208G |
probably benign |
Het |
Or52e2 |
A |
G |
7: 102,804,081 (GRCm39) |
V291A |
possibly damaging |
Het |
Or8b42 |
G |
T |
9: 38,341,627 (GRCm39) |
L16F |
probably damaging |
Het |
Pcdhgb2 |
A |
G |
18: 37,823,560 (GRCm39) |
T184A |
probably benign |
Het |
Plxna4 |
T |
C |
6: 32,228,000 (GRCm39) |
|
probably null |
Het |
Pnldc1 |
C |
T |
17: 13,113,260 (GRCm39) |
E328K |
probably benign |
Het |
Pon1 |
T |
A |
6: 5,185,334 (GRCm39) |
L55F |
probably damaging |
Het |
Pramel51 |
T |
C |
12: 88,142,683 (GRCm39) |
I312V |
probably benign |
Het |
Prkci |
G |
T |
3: 31,092,605 (GRCm39) |
D296Y |
probably damaging |
Het |
Prkd1 |
T |
C |
12: 50,435,038 (GRCm39) |
H563R |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,546,236 (GRCm39) |
N266S |
probably benign |
Het |
Rapgef6 |
A |
T |
11: 54,530,609 (GRCm39) |
I589F |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,145,853 (GRCm39) |
S127T |
probably benign |
Het |
Sh3tc2 |
A |
G |
18: 62,110,975 (GRCm39) |
D277G |
probably benign |
Het |
Sipa1l3 |
G |
A |
7: 29,098,949 (GRCm39) |
A440V |
probably benign |
Het |
Slc13a2 |
A |
C |
11: 78,291,358 (GRCm39) |
I372S |
probably damaging |
Het |
Slco1a7 |
T |
A |
6: 141,700,182 (GRCm39) |
T117S |
probably benign |
Het |
Spns1 |
A |
T |
7: 125,969,495 (GRCm39) |
I528N |
probably damaging |
Het |
Sult6b2 |
T |
C |
6: 142,736,021 (GRCm39) |
K191R |
probably benign |
Het |
Swt1 |
A |
G |
1: 151,278,700 (GRCm39) |
|
probably null |
Het |
Tcn2 |
A |
T |
11: 3,877,546 (GRCm39) |
L34* |
probably null |
Het |
Tmem131l |
C |
T |
3: 83,829,553 (GRCm39) |
A1035T |
possibly damaging |
Het |
Trpc4 |
A |
G |
3: 54,223,263 (GRCm39) |
E733G |
probably damaging |
Het |
Uap1l1 |
A |
T |
2: 25,254,642 (GRCm39) |
H184Q |
possibly damaging |
Het |
Vil1 |
T |
G |
1: 74,455,192 (GRCm39) |
V48G |
possibly damaging |
Het |
Vps39 |
A |
T |
2: 120,159,186 (GRCm39) |
H367Q |
probably damaging |
Het |
Wars2 |
A |
G |
3: 99,094,962 (GRCm39) |
T86A |
probably benign |
Het |
Wdr90 |
A |
G |
17: 26,064,107 (GRCm39) |
S1872P |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,065,381 (GRCm39) |
L1625P |
probably damaging |
Het |
Xaf1 |
A |
T |
11: 72,194,256 (GRCm39) |
M46L |
probably damaging |
Het |
Zfp1005 |
A |
G |
2: 150,109,855 (GRCm39) |
T182A |
unknown |
Het |
|
Other mutations in Or10ak11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Or10ak11
|
APN |
4 |
118,686,989 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03023:Or10ak11
|
APN |
4 |
118,687,449 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03387:Or10ak11
|
APN |
4 |
118,687,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0326:Or10ak11
|
UTSW |
4 |
118,687,022 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0532:Or10ak11
|
UTSW |
4 |
118,686,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Or10ak11
|
UTSW |
4 |
118,687,065 (GRCm39) |
missense |
probably benign |
0.00 |
R1906:Or10ak11
|
UTSW |
4 |
118,687,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Or10ak11
|
UTSW |
4 |
118,687,223 (GRCm39) |
missense |
probably benign |
0.00 |
R2260:Or10ak11
|
UTSW |
4 |
118,687,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Or10ak11
|
UTSW |
4 |
118,686,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Or10ak11
|
UTSW |
4 |
118,686,863 (GRCm39) |
missense |
probably benign |
0.44 |
R5444:Or10ak11
|
UTSW |
4 |
118,687,308 (GRCm39) |
missense |
probably benign |
|
R5817:Or10ak11
|
UTSW |
4 |
118,687,296 (GRCm39) |
missense |
probably damaging |
0.96 |
R5987:Or10ak11
|
UTSW |
4 |
118,687,478 (GRCm39) |
missense |
probably damaging |
0.96 |
R6031:Or10ak11
|
UTSW |
4 |
118,687,588 (GRCm39) |
splice site |
probably null |
|
R6031:Or10ak11
|
UTSW |
4 |
118,687,588 (GRCm39) |
splice site |
probably null |
|
R7255:Or10ak11
|
UTSW |
4 |
118,687,149 (GRCm39) |
missense |
probably benign |
0.17 |
R7483:Or10ak11
|
UTSW |
4 |
118,687,517 (GRCm39) |
missense |
probably damaging |
0.98 |
R8214:Or10ak11
|
UTSW |
4 |
118,687,288 (GRCm39) |
missense |
probably benign |
|
R8479:Or10ak11
|
UTSW |
4 |
118,687,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8847:Or10ak11
|
UTSW |
4 |
118,686,821 (GRCm39) |
missense |
probably damaging |
0.97 |
R9661:Or10ak11
|
UTSW |
4 |
118,687,526 (GRCm39) |
missense |
probably benign |
0.45 |
Z1176:Or10ak11
|
UTSW |
4 |
118,687,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|