Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cacna2d3 |
A |
G |
14: 29,189,909 (GRCm39) |
L109P |
probably damaging |
Het |
Caprin2 |
A |
T |
6: 148,763,964 (GRCm39) |
S568T |
possibly damaging |
Het |
Catip |
A |
G |
1: 74,403,744 (GRCm39) |
T154A |
probably null |
Het |
Ccdc187 |
A |
G |
2: 26,177,980 (GRCm39) |
S270P |
possibly damaging |
Het |
Ccdc88a |
A |
G |
11: 29,324,559 (GRCm39) |
Y39C |
probably damaging |
Het |
Chrdl2 |
A |
T |
7: 99,676,787 (GRCm39) |
H203L |
possibly damaging |
Het |
Chrnb2 |
A |
G |
3: 89,670,552 (GRCm39) |
V62A |
probably damaging |
Het |
Cklf |
T |
A |
8: 104,984,055 (GRCm39) |
S73T |
possibly damaging |
Het |
Clk1 |
A |
G |
1: 58,456,166 (GRCm39) |
|
probably null |
Het |
Ctdp1 |
T |
C |
18: 80,492,716 (GRCm39) |
D593G |
probably damaging |
Het |
Ctsc |
A |
T |
7: 87,958,988 (GRCm39) |
I423F |
probably damaging |
Het |
D130043K22Rik |
T |
A |
13: 25,073,825 (GRCm39) |
V968E |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,696,140 (GRCm39) |
S166G |
possibly damaging |
Het |
Dnah2 |
G |
T |
11: 69,327,117 (GRCm39) |
|
probably benign |
Het |
Dnajb11 |
G |
T |
16: 22,687,888 (GRCm39) |
R206L |
probably benign |
Het |
Dsel |
A |
T |
1: 111,786,908 (GRCm39) |
|
probably benign |
Het |
Ehd2 |
T |
C |
7: 15,684,396 (GRCm39) |
S468G |
possibly damaging |
Het |
Ehmt2 |
T |
A |
17: 35,125,787 (GRCm39) |
V640E |
possibly damaging |
Het |
Elmo2 |
T |
A |
2: 165,140,573 (GRCm39) |
E299D |
probably benign |
Het |
Eps8l1 |
T |
C |
7: 4,473,886 (GRCm39) |
L231P |
probably damaging |
Het |
Esd |
A |
G |
14: 74,978,686 (GRCm39) |
T83A |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,293,020 (GRCm39) |
F529L |
probably benign |
Het |
Hnrnpu |
G |
A |
1: 178,158,339 (GRCm39) |
|
probably benign |
Het |
Hpx |
G |
T |
7: 105,249,278 (GRCm39) |
A7E |
possibly damaging |
Het |
Ighv6-5 |
C |
T |
12: 114,380,320 (GRCm39) |
V85M |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,338,240 (GRCm39) |
V2503I |
probably damaging |
Het |
Itprid1 |
A |
G |
6: 55,875,114 (GRCm39) |
T355A |
probably benign |
Het |
Matr3 |
G |
T |
18: 35,705,710 (GRCm39) |
G212C |
probably damaging |
Het |
Mrpl35 |
A |
T |
6: 71,793,263 (GRCm39) |
Y129* |
probably null |
Het |
Myh2 |
T |
C |
11: 67,071,710 (GRCm39) |
I509T |
possibly damaging |
Het |
Nat8l |
G |
T |
5: 34,158,288 (GRCm39) |
A233S |
probably damaging |
Het |
Nipbl |
A |
C |
15: 8,361,936 (GRCm39) |
L1447W |
probably damaging |
Het |
Paf1 |
T |
A |
7: 28,094,481 (GRCm39) |
C31S |
possibly damaging |
Het |
Parp4 |
A |
C |
14: 56,840,313 (GRCm39) |
T573P |
probably benign |
Het |
Phf12 |
A |
T |
11: 77,913,846 (GRCm39) |
|
probably benign |
Het |
Pi4k2b |
A |
G |
5: 52,905,765 (GRCm39) |
E102G |
probably benign |
Het |
Pou2f1 |
A |
G |
1: 165,762,382 (GRCm39) |
C7R |
probably benign |
Het |
Prpsap2 |
T |
C |
11: 61,631,815 (GRCm39) |
R181G |
probably benign |
Het |
Psd |
A |
G |
19: 46,311,561 (GRCm39) |
|
probably benign |
Het |
Ptgds |
T |
C |
2: 25,359,622 (GRCm39) |
T22A |
probably benign |
Het |
Rab21 |
A |
T |
10: 115,151,097 (GRCm39) |
|
probably null |
Het |
Relb |
T |
C |
7: 19,346,582 (GRCm39) |
D330G |
probably damaging |
Het |
Rhoc |
A |
T |
3: 104,700,236 (GRCm39) |
T100S |
probably benign |
Het |
Ryr1 |
G |
T |
7: 28,802,389 (GRCm39) |
H744N |
probably damaging |
Het |
Sardh |
C |
T |
2: 27,129,458 (GRCm39) |
G280D |
probably damaging |
Het |
Scyl2 |
A |
C |
10: 89,493,729 (GRCm39) |
N346K |
possibly damaging |
Het |
Sec16b |
T |
C |
1: 157,362,970 (GRCm39) |
F267S |
probably damaging |
Het |
Slc44a5 |
T |
A |
3: 153,956,714 (GRCm39) |
M322K |
probably benign |
Het |
St8sia4 |
T |
A |
1: 95,519,508 (GRCm39) |
N327Y |
probably benign |
Het |
Tbl1xr1 |
T |
A |
3: 22,257,323 (GRCm39) |
Y395* |
probably null |
Het |
Unc13c |
A |
T |
9: 73,441,307 (GRCm39) |
S1897R |
probably benign |
Het |
Vangl2 |
A |
G |
1: 171,840,415 (GRCm39) |
S58P |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,501 (GRCm39) |
I288T |
probably benign |
Het |
Zfp809 |
A |
G |
9: 22,149,950 (GRCm39) |
Y149C |
probably damaging |
Het |
|
Other mutations in Vmn1r236 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01446:Vmn1r236
|
APN |
17 |
21,506,918 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01953:Vmn1r236
|
APN |
17 |
21,507,473 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02252:Vmn1r236
|
APN |
17 |
21,507,101 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03030:Vmn1r236
|
APN |
17 |
21,507,108 (GRCm39) |
nonsense |
probably null |
|
IGL03342:Vmn1r236
|
APN |
17 |
21,507,236 (GRCm39) |
missense |
probably benign |
0.37 |
R0569:Vmn1r236
|
UTSW |
17 |
21,507,172 (GRCm39) |
missense |
probably benign |
0.05 |
R1747:Vmn1r236
|
UTSW |
17 |
21,507,179 (GRCm39) |
missense |
probably benign |
0.31 |
R1872:Vmn1r236
|
UTSW |
17 |
21,507,673 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1876:Vmn1r236
|
UTSW |
17 |
21,506,900 (GRCm39) |
missense |
probably benign |
|
R3692:Vmn1r236
|
UTSW |
17 |
21,507,068 (GRCm39) |
missense |
probably benign |
0.09 |
R4822:Vmn1r236
|
UTSW |
17 |
21,507,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R6918:Vmn1r236
|
UTSW |
17 |
21,507,878 (GRCm39) |
missense |
probably benign |
0.37 |
R7089:Vmn1r236
|
UTSW |
17 |
21,507,204 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7895:Vmn1r236
|
UTSW |
17 |
21,507,728 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7965:Vmn1r236
|
UTSW |
17 |
21,507,696 (GRCm39) |
nonsense |
probably null |
|
R8906:Vmn1r236
|
UTSW |
17 |
21,507,356 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9300:Vmn1r236
|
UTSW |
17 |
21,506,945 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9410:Vmn1r236
|
UTSW |
17 |
21,507,756 (GRCm39) |
nonsense |
probably null |
|
R9535:Vmn1r236
|
UTSW |
17 |
21,507,418 (GRCm39) |
missense |
probably benign |
0.01 |
R9617:Vmn1r236
|
UTSW |
17 |
21,507,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Vmn1r236
|
UTSW |
17 |
21,507,043 (GRCm39) |
missense |
probably benign |
|
R9679:Vmn1r236
|
UTSW |
17 |
21,507,286 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9797:Vmn1r236
|
UTSW |
17 |
21,506,969 (GRCm39) |
missense |
probably benign |
0.00 |
|