Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
G |
7: 120,023,021 (GRCm39) |
I52M |
possibly damaging |
Het |
Agbl5 |
G |
T |
5: 31,049,335 (GRCm39) |
|
probably null |
Het |
Akt2 |
T |
C |
7: 27,336,334 (GRCm39) |
|
probably benign |
Het |
Arl6ip5 |
T |
A |
6: 97,209,378 (GRCm39) |
S138T |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,952,800 (GRCm39) |
|
probably benign |
Het |
Ccdc171 |
A |
T |
4: 83,553,919 (GRCm39) |
N422Y |
probably damaging |
Het |
Ccr5 |
C |
T |
9: 123,924,951 (GRCm39) |
P185S |
possibly damaging |
Het |
Cep63 |
G |
T |
9: 102,500,759 (GRCm39) |
Q38K |
probably benign |
Het |
Cgn |
T |
C |
3: 94,682,242 (GRCm39) |
S446G |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,952,206 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
T |
A |
8: 15,968,330 (GRCm39) |
Q3099L |
probably damaging |
Het |
Dcc |
G |
A |
18: 71,708,279 (GRCm39) |
T479I |
possibly damaging |
Het |
Dclre1a |
A |
G |
19: 56,535,067 (GRCm39) |
|
probably null |
Het |
Dlg1 |
T |
A |
16: 31,502,992 (GRCm39) |
C66* |
probably null |
Het |
Dnah12 |
T |
A |
14: 26,427,272 (GRCm39) |
|
probably null |
Het |
Dnajb9 |
T |
A |
12: 44,253,987 (GRCm39) |
H140L |
probably damaging |
Het |
Dnase1 |
G |
A |
16: 3,857,413 (GRCm39) |
V237M |
probably damaging |
Het |
Dscam |
C |
A |
16: 96,456,105 (GRCm39) |
E1274D |
probably benign |
Het |
Epb41 |
T |
C |
4: 131,727,572 (GRCm39) |
H243R |
probably damaging |
Het |
Evc |
T |
A |
5: 37,473,656 (GRCm39) |
|
probably benign |
Het |
Fcgrt |
T |
A |
7: 44,752,493 (GRCm39) |
M1L |
unknown |
Het |
Flii |
T |
C |
11: 60,610,506 (GRCm39) |
|
probably null |
Het |
Gen1 |
A |
G |
12: 11,298,355 (GRCm39) |
|
probably benign |
Het |
Gm10447 |
T |
C |
11: 53,347,257 (GRCm39) |
|
probably benign |
Het |
Gm57858 |
A |
G |
3: 36,101,054 (GRCm39) |
|
probably benign |
Het |
Gm8674 |
A |
T |
13: 50,055,975 (GRCm39) |
|
noncoding transcript |
Het |
Gpr137 |
G |
C |
19: 6,916,491 (GRCm39) |
D253E |
probably damaging |
Het |
Grid2ip |
A |
T |
5: 143,343,652 (GRCm39) |
D116V |
probably benign |
Het |
Grin2c |
A |
G |
11: 115,151,554 (GRCm39) |
|
probably benign |
Het |
Havcr1 |
A |
G |
11: 46,647,051 (GRCm39) |
T162A |
possibly damaging |
Het |
Hspa1l |
A |
T |
17: 35,196,386 (GRCm39) |
T142S |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,267,409 (GRCm39) |
Y602* |
probably null |
Het |
Il18 |
T |
A |
9: 50,490,575 (GRCm39) |
|
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,309,266 (GRCm39) |
V474A |
probably damaging |
Het |
Inppl1 |
T |
C |
7: 101,476,664 (GRCm39) |
Y771C |
probably damaging |
Het |
Ints2 |
T |
C |
11: 86,125,575 (GRCm39) |
T542A |
probably benign |
Het |
Ipo7 |
T |
C |
7: 109,648,868 (GRCm39) |
Y714H |
probably benign |
Het |
Itgbl1 |
T |
A |
14: 124,077,997 (GRCm39) |
C162* |
probably null |
Het |
Kcp |
T |
C |
6: 29,496,926 (GRCm39) |
H561R |
possibly damaging |
Het |
Krt23 |
G |
T |
11: 99,376,613 (GRCm39) |
T181N |
probably benign |
Het |
Lrrc40 |
A |
T |
3: 157,746,108 (GRCm39) |
D61V |
probably damaging |
Het |
Lypd4 |
T |
A |
7: 24,564,691 (GRCm39) |
H149L |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,473,058 (GRCm39) |
F953L |
probably damaging |
Het |
Mctp1 |
C |
T |
13: 76,972,982 (GRCm39) |
P405S |
probably damaging |
Het |
Mfsd2a |
G |
A |
4: 122,845,632 (GRCm39) |
T173I |
possibly damaging |
Het |
Mtus1 |
T |
C |
8: 41,535,965 (GRCm39) |
T584A |
probably benign |
Het |
Nell2 |
A |
G |
15: 95,330,782 (GRCm39) |
V213A |
probably benign |
Het |
Nipsnap1 |
G |
A |
11: 4,839,957 (GRCm39) |
G226E |
probably damaging |
Het |
Nudt15 |
T |
C |
14: 73,760,824 (GRCm39) |
Y89C |
probably damaging |
Het |
Or10g7 |
T |
A |
9: 39,905,459 (GRCm39) |
S118T |
possibly damaging |
Het |
Or10h28 |
T |
A |
17: 33,488,109 (GRCm39) |
M137K |
probably damaging |
Het |
Or13p3 |
T |
A |
4: 118,566,808 (GRCm39) |
M68K |
probably benign |
Het |
Or7a37 |
T |
G |
10: 78,806,267 (GRCm39) |
S261R |
probably damaging |
Het |
Phf24 |
A |
C |
4: 42,933,891 (GRCm39) |
E91A |
probably damaging |
Het |
Plbd1 |
T |
A |
6: 136,618,165 (GRCm39) |
N17I |
possibly damaging |
Het |
Por |
C |
T |
5: 135,761,438 (GRCm39) |
S308L |
probably benign |
Het |
Prmt8 |
T |
A |
6: 127,688,837 (GRCm39) |
K178* |
probably null |
Het |
Rev3l |
A |
G |
10: 39,693,282 (GRCm39) |
N454S |
probably damaging |
Het |
Rps6ka2 |
T |
C |
17: 7,539,009 (GRCm39) |
V309A |
probably benign |
Het |
Slc15a5 |
A |
G |
6: 137,995,112 (GRCm39) |
|
probably benign |
Het |
Slc30a6 |
G |
A |
17: 74,730,198 (GRCm39) |
V363I |
probably benign |
Het |
Snf8 |
G |
A |
11: 95,930,125 (GRCm39) |
M42I |
probably benign |
Het |
Tacr3 |
C |
T |
3: 134,637,989 (GRCm39) |
T382I |
probably benign |
Het |
Tenm3 |
A |
G |
8: 48,682,010 (GRCm39) |
V2540A |
probably damaging |
Het |
Trabd |
A |
G |
15: 88,969,816 (GRCm39) |
T314A |
possibly damaging |
Het |
Tyk2 |
T |
C |
9: 21,025,486 (GRCm39) |
|
probably null |
Het |
Ube4a |
T |
C |
9: 44,856,099 (GRCm39) |
|
probably benign |
Het |
Unc80 |
A |
G |
1: 66,589,015 (GRCm39) |
H1060R |
possibly damaging |
Het |
Virma |
A |
T |
4: 11,528,626 (GRCm39) |
K1288* |
probably null |
Het |
Vmn2r100 |
A |
C |
17: 19,751,582 (GRCm39) |
I542L |
probably benign |
Het |
Vwde |
T |
C |
6: 13,187,806 (GRCm39) |
|
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,245,018 (GRCm39) |
I797T |
possibly damaging |
Het |
Zfp74 |
C |
T |
7: 29,653,466 (GRCm39) |
|
probably benign |
Het |
Zkscan7 |
T |
A |
9: 122,717,872 (GRCm39) |
L89Q |
probably damaging |
Het |
|
Other mutations in Stom |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01318:Stom
|
APN |
2 |
35,226,889 (GRCm39) |
missense |
probably benign |
|
IGL02103:Stom
|
APN |
2 |
35,210,401 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02825:Stom
|
APN |
2 |
35,211,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03078:Stom
|
APN |
2 |
35,205,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Stom
|
UTSW |
2 |
35,211,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R0417:Stom
|
UTSW |
2 |
35,211,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Stom
|
UTSW |
2 |
35,205,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Stom
|
UTSW |
2 |
35,206,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Stom
|
UTSW |
2 |
35,211,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2509:Stom
|
UTSW |
2 |
35,210,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Stom
|
UTSW |
2 |
35,205,977 (GRCm39) |
nonsense |
probably null |
|
R4469:Stom
|
UTSW |
2 |
35,211,545 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4592:Stom
|
UTSW |
2 |
35,213,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5240:Stom
|
UTSW |
2 |
35,226,889 (GRCm39) |
missense |
probably benign |
|
R7338:Stom
|
UTSW |
2 |
35,213,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7532:Stom
|
UTSW |
2 |
35,211,589 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7652:Stom
|
UTSW |
2 |
35,206,041 (GRCm39) |
missense |
probably benign |
0.03 |
R8928:Stom
|
UTSW |
2 |
35,205,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Stom
|
UTSW |
2 |
35,211,697 (GRCm39) |
missense |
possibly damaging |
0.55 |
|