Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931422A03Rik |
G |
T |
2: 103,823,022 (GRCm39) |
T87K |
possibly damaging |
Het |
Adar |
G |
A |
3: 89,643,445 (GRCm39) |
R442Q |
probably benign |
Het |
Agtr1b |
T |
A |
3: 20,370,280 (GRCm39) |
S109C |
probably damaging |
Het |
Akr1c6 |
T |
A |
13: 4,499,373 (GRCm39) |
Y248N |
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,438,597 (GRCm39) |
V932E |
probably benign |
Het |
Apba3 |
T |
A |
10: 81,105,104 (GRCm39) |
S126T |
probably benign |
Het |
Brca2 |
T |
A |
5: 150,466,061 (GRCm39) |
S1942T |
possibly damaging |
Het |
Ccdc149 |
C |
T |
5: 52,596,552 (GRCm39) |
C20Y |
probably damaging |
Het |
Cd63 |
C |
A |
10: 128,748,071 (GRCm39) |
N156K |
probably benign |
Het |
Clvs1 |
A |
G |
4: 9,429,807 (GRCm39) |
E270G |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,216,744 (GRCm39) |
Y654C |
probably damaging |
Het |
Dgki |
A |
T |
6: 36,996,875 (GRCm39) |
D574E |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,517,056 (GRCm39) |
S63G |
probably damaging |
Het |
Exoc1 |
C |
T |
5: 76,683,412 (GRCm39) |
R46C |
probably damaging |
Het |
Fcgr4 |
C |
A |
1: 170,847,477 (GRCm39) |
A25D |
probably damaging |
Het |
Fgf4 |
T |
C |
7: 144,415,408 (GRCm39) |
V56A |
probably benign |
Het |
Gfpt2 |
A |
G |
11: 49,714,043 (GRCm39) |
I267V |
probably benign |
Het |
Gm20939 |
A |
C |
17: 95,184,648 (GRCm39) |
H432P |
probably damaging |
Het |
Gpr179 |
A |
T |
11: 97,242,739 (GRCm39) |
L35Q |
probably damaging |
Het |
Idh1 |
CA |
CAA |
1: 65,204,347 (GRCm39) |
|
probably null |
Het |
Ildr1 |
T |
C |
16: 36,528,762 (GRCm39) |
I69T |
probably damaging |
Het |
Lrfn1 |
A |
G |
7: 28,159,344 (GRCm39) |
D421G |
probably benign |
Het |
Mmp15 |
C |
T |
8: 96,096,288 (GRCm39) |
Q360* |
probably null |
Het |
Nfatc2 |
T |
C |
2: 168,378,214 (GRCm39) |
K484E |
probably damaging |
Het |
Nkpd1 |
G |
C |
7: 19,258,095 (GRCm39) |
V625L |
probably benign |
Het |
Nlrp4a |
C |
A |
7: 26,143,561 (GRCm39) |
|
probably benign |
Het |
Nme9 |
T |
A |
9: 99,350,301 (GRCm39) |
I178N |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,788,356 (GRCm39) |
T352I |
probably damaging |
Het |
Ntrk1 |
T |
C |
3: 87,686,990 (GRCm39) |
I723V |
probably damaging |
Het |
Or5p50 |
C |
T |
7: 107,422,557 (GRCm39) |
V40M |
possibly damaging |
Het |
Pias3 |
C |
A |
3: 96,612,201 (GRCm39) |
Q553K |
probably benign |
Het |
Pnp2 |
T |
G |
14: 51,200,873 (GRCm39) |
H119Q |
probably benign |
Het |
Rapgef6 |
T |
A |
11: 54,459,295 (GRCm39) |
D156E |
probably benign |
Het |
Rint1 |
T |
C |
5: 24,005,594 (GRCm39) |
V92A |
probably damaging |
Het |
Rnf148 |
A |
T |
6: 23,654,993 (GRCm39) |
M1K |
probably null |
Het |
Rnh1 |
C |
T |
7: 140,742,346 (GRCm39) |
R404H |
probably benign |
Het |
Slc4a8 |
T |
C |
15: 100,705,134 (GRCm39) |
V832A |
possibly damaging |
Het |
Spart |
A |
G |
3: 55,029,100 (GRCm39) |
D297G |
probably benign |
Het |
Spata13 |
C |
T |
14: 60,929,275 (GRCm39) |
R278C |
probably damaging |
Het |
Tmc1 |
T |
C |
19: 20,767,209 (GRCm39) |
T716A |
probably benign |
Het |
Tpi1 |
A |
G |
6: 124,789,483 (GRCm39) |
V164A |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,002 (GRCm39) |
S345G |
probably benign |
Het |
Vmn1r199 |
T |
A |
13: 22,567,687 (GRCm39) |
L327Q |
probably damaging |
Het |
Washc4 |
C |
T |
10: 83,386,748 (GRCm39) |
T124I |
probably benign |
Het |
Wdr76 |
C |
T |
2: 121,357,484 (GRCm39) |
T180I |
probably benign |
Het |
Zcchc8 |
T |
C |
5: 123,845,362 (GRCm39) |
N333D |
probably benign |
Het |
Zfp516 |
T |
C |
18: 82,975,460 (GRCm39) |
S553P |
probably damaging |
Het |
|
Other mutations in Snx31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Snx31
|
APN |
15 |
36,545,761 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01627:Snx31
|
APN |
15 |
36,517,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:Snx31
|
APN |
15 |
36,525,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Snx31
|
APN |
15 |
36,525,749 (GRCm39) |
nonsense |
probably null |
|
IGL03182:Snx31
|
APN |
15 |
36,525,833 (GRCm39) |
missense |
probably benign |
0.00 |
R0755:Snx31
|
UTSW |
15 |
36,534,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R1005:Snx31
|
UTSW |
15 |
36,517,837 (GRCm39) |
splice site |
probably benign |
|
R1463:Snx31
|
UTSW |
15 |
36,539,444 (GRCm39) |
missense |
probably null |
1.00 |
R1513:Snx31
|
UTSW |
15 |
36,545,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R2030:Snx31
|
UTSW |
15 |
36,525,848 (GRCm39) |
missense |
probably benign |
0.31 |
R3404:Snx31
|
UTSW |
15 |
36,525,799 (GRCm39) |
missense |
probably benign |
0.00 |
R3720:Snx31
|
UTSW |
15 |
36,523,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4152:Snx31
|
UTSW |
15 |
36,525,785 (GRCm39) |
missense |
probably benign |
|
R4474:Snx31
|
UTSW |
15 |
36,546,256 (GRCm39) |
intron |
probably benign |
|
R4729:Snx31
|
UTSW |
15 |
36,523,698 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4998:Snx31
|
UTSW |
15 |
36,539,513 (GRCm39) |
missense |
probably damaging |
0.96 |
R5010:Snx31
|
UTSW |
15 |
36,555,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Snx31
|
UTSW |
15 |
36,525,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R5893:Snx31
|
UTSW |
15 |
36,523,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R5970:Snx31
|
UTSW |
15 |
36,523,634 (GRCm39) |
nonsense |
probably null |
|
R6211:Snx31
|
UTSW |
15 |
36,547,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R7198:Snx31
|
UTSW |
15 |
36,555,455 (GRCm39) |
missense |
probably benign |
0.04 |
R7293:Snx31
|
UTSW |
15 |
36,523,596 (GRCm39) |
missense |
probably damaging |
0.97 |
R7329:Snx31
|
UTSW |
15 |
36,555,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7741:Snx31
|
UTSW |
15 |
36,523,587 (GRCm39) |
critical splice donor site |
probably null |
|
R8057:Snx31
|
UTSW |
15 |
36,523,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R8806:Snx31
|
UTSW |
15 |
36,537,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Snx31
|
UTSW |
15 |
36,555,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Snx31
|
UTSW |
15 |
36,534,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|