Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
T |
A |
8: 41,278,975 (GRCm39) |
D455E |
not run |
Het |
Aldoc |
T |
C |
11: 78,215,553 (GRCm39) |
F79S |
possibly damaging |
Het |
Atmin |
A |
G |
8: 117,683,389 (GRCm39) |
S350G |
probably benign |
Het |
Bms1 |
A |
G |
6: 118,390,711 (GRCm39) |
F206S |
probably damaging |
Het |
Carmil1 |
T |
A |
13: 24,259,711 (GRCm39) |
I698L |
probably benign |
Het |
Cd47 |
T |
A |
16: 49,715,779 (GRCm39) |
S182T |
|
Het |
Ces2e |
G |
T |
8: 105,659,629 (GRCm39) |
|
probably null |
Het |
Cfap251 |
A |
G |
5: 123,394,229 (GRCm39) |
S373G |
not run |
Het |
Cit |
C |
A |
5: 116,090,525 (GRCm39) |
H906Q |
probably damaging |
Het |
Cit |
T |
C |
5: 116,120,294 (GRCm39) |
S1370P |
probably benign |
Het |
Dchs2 |
T |
C |
3: 83,207,745 (GRCm39) |
F1739L |
probably benign |
Het |
Dlx4 |
T |
C |
11: 95,036,156 (GRCm39) |
Y51C |
possibly damaging |
Het |
Drosha |
T |
A |
15: 12,883,276 (GRCm39) |
Y796* |
probably null |
Het |
Elf1 |
T |
A |
14: 79,773,830 (GRCm39) |
F14I |
probably benign |
Het |
Fam135b |
T |
C |
15: 71,404,827 (GRCm39) |
Q73R |
probably damaging |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gls2 |
C |
G |
10: 128,030,983 (GRCm39) |
R81G |
unknown |
Het |
Hnrnpll |
T |
C |
17: 80,358,281 (GRCm39) |
M157V |
possibly damaging |
Het |
Itgb3 |
T |
A |
11: 104,556,337 (GRCm39) |
M726K |
probably benign |
Het |
Kcna10 |
T |
G |
3: 107,101,726 (GRCm39) |
M119R |
possibly damaging |
Het |
Kcnh1 |
A |
G |
1: 191,924,250 (GRCm39) |
T155A |
probably benign |
Het |
Kctd9 |
T |
A |
14: 67,962,111 (GRCm39) |
D51E |
unknown |
Het |
Lgr6 |
T |
C |
1: 134,991,402 (GRCm39) |
I129V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,055,824 (GRCm39) |
D598V |
probably damaging |
Het |
Ltbp4 |
G |
T |
7: 27,023,593 (GRCm39) |
Q850K |
probably damaging |
Het |
Mdm1 |
A |
G |
10: 117,982,709 (GRCm39) |
R115G |
possibly damaging |
Het |
Mns1 |
A |
C |
9: 72,355,809 (GRCm39) |
|
probably null |
Het |
Mthfs |
G |
A |
9: 89,093,288 (GRCm39) |
R14Q |
probably damaging |
Het |
Muc2 |
T |
A |
7: 141,298,422 (GRCm39) |
S25T |
|
Het |
Ncapd3 |
T |
C |
9: 26,974,657 (GRCm39) |
S710P |
possibly damaging |
Het |
Nrip1 |
T |
A |
16: 76,089,841 (GRCm39) |
H572L |
possibly damaging |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Opa3 |
A |
G |
7: 18,978,910 (GRCm39) |
E125G |
probably damaging |
Het |
Or52p1 |
T |
A |
7: 104,267,460 (GRCm39) |
C191* |
probably null |
Het |
Or5ap2 |
A |
G |
2: 85,680,150 (GRCm39) |
E118G |
probably damaging |
Het |
Or5w19 |
A |
G |
2: 87,698,995 (GRCm39) |
Y220C |
probably benign |
Het |
P3h1 |
A |
G |
4: 119,094,059 (GRCm39) |
Y238C |
probably damaging |
Het |
Pappa2 |
T |
C |
1: 158,763,555 (GRCm39) |
D652G |
possibly damaging |
Het |
Pcdha11 |
T |
A |
18: 37,138,618 (GRCm39) |
N82K |
probably damaging |
Het |
Pde4b |
T |
C |
4: 102,453,212 (GRCm39) |
I293T |
probably damaging |
Het |
Prrc2c |
TTGCTGCTGCTGCTGCTGCTGCTGCTGC |
TTGCTGCTGCTGCTGCTGCTGCTGC |
1: 162,536,630 (GRCm39) |
|
probably benign |
Het |
Qki |
T |
C |
17: 10,537,732 (GRCm39) |
D24G |
possibly damaging |
Het |
Rbpjl |
A |
G |
2: 164,250,438 (GRCm39) |
K197E |
possibly damaging |
Het |
Rnf111 |
A |
T |
9: 70,365,223 (GRCm39) |
S415T |
probably benign |
Het |
Scyl1 |
A |
G |
19: 5,810,853 (GRCm39) |
V488A |
probably damaging |
Het |
Slc1a6 |
G |
C |
10: 78,648,706 (GRCm39) |
V476L |
possibly damaging |
Het |
Slc22a4 |
A |
C |
11: 53,888,269 (GRCm39) |
I253S |
possibly damaging |
Het |
Speer2 |
T |
C |
16: 69,657,412 (GRCm39) |
H77R |
possibly damaging |
Het |
Speg |
T |
C |
1: 75,398,894 (GRCm39) |
S2114P |
probably damaging |
Het |
Synpo2 |
T |
A |
3: 122,911,041 (GRCm39) |
R201S |
possibly damaging |
Het |
Ttpa |
C |
A |
4: 20,028,419 (GRCm39) |
H225Q |
probably damaging |
Het |
Vmn1r45 |
A |
T |
6: 89,910,261 (GRCm39) |
H236Q |
possibly damaging |
Het |
Vmn2r7 |
A |
T |
3: 64,623,507 (GRCm39) |
V271D |
probably benign |
Het |
Zfp53 |
A |
T |
17: 21,729,274 (GRCm39) |
T436S |
probably benign |
Het |
|
Other mutations in Slc22a17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01701:Slc22a17
|
APN |
14 |
55,144,718 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02216:Slc22a17
|
APN |
14 |
55,145,433 (GRCm39) |
makesense |
probably null |
|
IGL02588:Slc22a17
|
APN |
14 |
55,145,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1576:Slc22a17
|
UTSW |
14 |
55,145,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Slc22a17
|
UTSW |
14 |
55,145,957 (GRCm39) |
critical splice donor site |
probably null |
|
R2027:Slc22a17
|
UTSW |
14 |
55,145,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Slc22a17
|
UTSW |
14 |
55,146,282 (GRCm39) |
nonsense |
probably null |
|
R3547:Slc22a17
|
UTSW |
14 |
55,144,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5175:Slc22a17
|
UTSW |
14 |
55,144,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5609:Slc22a17
|
UTSW |
14 |
55,146,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Slc22a17
|
UTSW |
14 |
55,149,716 (GRCm39) |
missense |
probably benign |
0.05 |
R7538:Slc22a17
|
UTSW |
14 |
55,149,575 (GRCm39) |
missense |
probably benign |
0.00 |
R8351:Slc22a17
|
UTSW |
14 |
55,146,051 (GRCm39) |
missense |
probably benign |
0.00 |
R8852:Slc22a17
|
UTSW |
14 |
55,146,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Slc22a17
|
UTSW |
14 |
55,147,139 (GRCm39) |
missense |
possibly damaging |
0.83 |
|