Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Adam30 |
G |
A |
3: 98,070,222 (GRCm39) |
S685N |
probably benign |
Het |
Adamts12 |
T |
C |
15: 11,071,843 (GRCm39) |
V129A |
probably benign |
Het |
Agxt2 |
T |
C |
15: 10,373,837 (GRCm39) |
F81S |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,749,409 (GRCm39) |
I186N |
probably damaging |
Het |
Amz1 |
A |
T |
5: 140,737,691 (GRCm39) |
|
probably null |
Het |
Anapc5 |
G |
A |
5: 122,926,481 (GRCm39) |
A619V |
possibly damaging |
Het |
Aoc1l3 |
C |
A |
6: 48,967,173 (GRCm39) |
P707H |
probably damaging |
Het |
Bbox1 |
T |
C |
2: 110,095,956 (GRCm39) |
D336G |
probably damaging |
Het |
Bivm |
A |
G |
1: 44,165,942 (GRCm39) |
T131A |
probably benign |
Het |
Bpi |
A |
T |
2: 158,109,660 (GRCm39) |
I203F |
probably benign |
Het |
Cd151 |
A |
C |
7: 141,050,569 (GRCm39) |
T241P |
probably damaging |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,148,171 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dclre1b |
A |
C |
3: 103,711,192 (GRCm39) |
S240A |
probably benign |
Het |
Ddc |
A |
C |
11: 11,796,634 (GRCm39) |
|
probably null |
Het |
Dkk1 |
T |
C |
19: 30,524,650 (GRCm39) |
R252G |
probably damaging |
Het |
Dmrtc2 |
T |
A |
7: 24,573,738 (GRCm39) |
M191K |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,699,824 (GRCm39) |
S1771P |
possibly damaging |
Het |
Emx1 |
T |
C |
6: 85,165,353 (GRCm39) |
|
probably benign |
Het |
Fah |
T |
C |
7: 84,250,344 (GRCm39) |
M1V |
probably null |
Het |
Fmo6 |
A |
T |
1: 162,753,710 (GRCm39) |
M144K |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,868,589 (GRCm39) |
V1445A |
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Gfm2 |
A |
G |
13: 97,301,708 (GRCm39) |
|
probably null |
Het |
Ghrhr |
T |
A |
6: 55,365,254 (GRCm39) |
L416* |
probably null |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gm19965 |
T |
A |
1: 116,748,550 (GRCm39) |
|
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,511,888 (GRCm39) |
L37P |
probably damaging |
Het |
Hoxa9 |
A |
G |
6: 52,202,693 (GRCm39) |
I131T |
probably damaging |
Het |
Htra4 |
T |
C |
8: 25,520,635 (GRCm39) |
D342G |
possibly damaging |
Het |
Idh1 |
G |
T |
1: 65,200,319 (GRCm39) |
N348K |
probably benign |
Het |
Impdh2 |
T |
C |
9: 108,439,028 (GRCm39) |
F99S |
probably benign |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Kazn |
A |
T |
4: 141,886,349 (GRCm39) |
|
probably benign |
Het |
Kcnq3 |
T |
A |
15: 65,871,891 (GRCm39) |
T593S |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,122,977 (GRCm39) |
|
probably benign |
Het |
Magi3 |
A |
G |
3: 103,968,946 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
G |
1: 127,751,617 (GRCm39) |
V578A |
probably benign |
Het |
Meox2 |
T |
C |
12: 37,159,151 (GRCm39) |
C108R |
possibly damaging |
Het |
Nlrp9c |
C |
A |
7: 26,079,860 (GRCm39) |
C722F |
probably damaging |
Het |
Or2a5 |
T |
C |
6: 42,874,285 (GRCm39) |
V300A |
probably benign |
Het |
Pde10a |
C |
T |
17: 9,139,378 (GRCm39) |
|
probably benign |
Het |
Ppfia4 |
A |
G |
1: 134,260,021 (GRCm39) |
|
probably benign |
Het |
Psg18 |
T |
C |
7: 18,088,742 (GRCm39) |
M1V |
probably null |
Het |
Qtrt1 |
A |
G |
9: 21,323,782 (GRCm39) |
T136A |
probably benign |
Het |
Retsat |
T |
C |
6: 72,580,634 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Sfswap |
G |
A |
5: 129,584,207 (GRCm39) |
|
probably null |
Het |
Slc16a7 |
A |
T |
10: 125,067,241 (GRCm39) |
L133I |
possibly damaging |
Het |
Spmip4 |
T |
A |
6: 50,566,121 (GRCm39) |
K118M |
probably damaging |
Het |
Srbd1 |
C |
T |
17: 86,405,940 (GRCm39) |
C620Y |
probably null |
Het |
Trip10 |
T |
A |
17: 57,560,363 (GRCm39) |
L100Q |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Vangl2 |
G |
T |
1: 171,832,353 (GRCm39) |
T501N |
probably damaging |
Het |
Vdr |
A |
T |
15: 97,767,214 (GRCm39) |
Y185N |
probably benign |
Het |
Vmn1r123 |
C |
T |
7: 20,896,257 (GRCm39) |
P50S |
probably damaging |
Het |
Vmn1r158 |
T |
A |
7: 22,489,870 (GRCm39) |
H113L |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,240,720 (GRCm39) |
I131N |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Xrcc6 |
A |
G |
15: 81,915,364 (GRCm39) |
D94G |
probably damaging |
Het |
Zbtb32 |
T |
A |
7: 30,290,692 (GRCm39) |
E201V |
possibly damaging |
Het |
Zfp185 |
A |
T |
X: 72,042,929 (GRCm39) |
E138D |
possibly damaging |
Het |
Zmynd11 |
T |
A |
13: 9,739,585 (GRCm39) |
H437L |
probably damaging |
Het |
|
Other mutations in Slc30a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00803:Slc30a3
|
APN |
5 |
31,245,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01411:Slc30a3
|
APN |
5 |
31,247,424 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02678:Slc30a3
|
APN |
5 |
31,245,676 (GRCm39) |
nonsense |
probably null |
|
R0606:Slc30a3
|
UTSW |
5 |
31,246,067 (GRCm39) |
missense |
probably benign |
0.02 |
R1184:Slc30a3
|
UTSW |
5 |
31,247,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Slc30a3
|
UTSW |
5 |
31,245,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Slc30a3
|
UTSW |
5 |
31,244,165 (GRCm39) |
nonsense |
probably null |
|
R2432:Slc30a3
|
UTSW |
5 |
31,246,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Slc30a3
|
UTSW |
5 |
31,252,422 (GRCm39) |
intron |
probably benign |
|
R4011:Slc30a3
|
UTSW |
5 |
31,244,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Slc30a3
|
UTSW |
5 |
31,250,638 (GRCm39) |
missense |
probably benign |
|
R4956:Slc30a3
|
UTSW |
5 |
31,244,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5469:Slc30a3
|
UTSW |
5 |
31,246,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Slc30a3
|
UTSW |
5 |
31,246,083 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6799:Slc30a3
|
UTSW |
5 |
31,246,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Slc30a3
|
UTSW |
5 |
31,247,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Slc30a3
|
UTSW |
5 |
31,244,169 (GRCm39) |
missense |
probably benign |
|
R7195:Slc30a3
|
UTSW |
5 |
31,246,139 (GRCm39) |
missense |
probably benign |
0.04 |
R7260:Slc30a3
|
UTSW |
5 |
31,245,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R8057:Slc30a3
|
UTSW |
5 |
31,247,395 (GRCm39) |
splice site |
probably benign |
|
R8836:Slc30a3
|
UTSW |
5 |
31,250,668 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8855:Slc30a3
|
UTSW |
5 |
31,245,325 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8866:Slc30a3
|
UTSW |
5 |
31,245,325 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9193:Slc30a3
|
UTSW |
5 |
31,246,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R9456:Slc30a3
|
UTSW |
5 |
31,246,889 (GRCm39) |
frame shift |
probably null |
|
|