Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd4 |
T |
C |
11: 102,996,214 (GRCm39) |
S172P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,186,254 (GRCm39) |
K1223* |
probably null |
Het |
Akna |
G |
A |
4: 63,297,598 (GRCm39) |
Q819* |
probably null |
Het |
Ankrd2 |
T |
C |
19: 42,032,510 (GRCm39) |
V257A |
probably benign |
Het |
Arap1 |
T |
A |
7: 101,035,436 (GRCm39) |
D30E |
probably damaging |
Het |
Atp6v0d2 |
T |
C |
4: 19,910,578 (GRCm39) |
|
probably benign |
Het |
Blm |
T |
A |
7: 80,152,115 (GRCm39) |
I611F |
possibly damaging |
Het |
Ccng2 |
A |
G |
5: 93,421,240 (GRCm39) |
K250R |
probably benign |
Het |
Cdhr3 |
A |
G |
12: 33,142,751 (GRCm39) |
L8P |
possibly damaging |
Het |
Csf2rb |
T |
G |
15: 78,223,204 (GRCm39) |
|
probably benign |
Het |
Ctbs |
A |
G |
3: 146,163,223 (GRCm39) |
I204V |
probably benign |
Het |
Cxcl16 |
T |
A |
11: 70,349,596 (GRCm39) |
E76D |
possibly damaging |
Het |
Dhx15 |
T |
C |
5: 52,311,414 (GRCm39) |
I689V |
possibly damaging |
Het |
Dlk2 |
T |
C |
17: 46,609,868 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,311,835 (GRCm39) |
M4452K |
probably damaging |
Het |
Dok4 |
T |
A |
8: 95,591,991 (GRCm39) |
I280F |
probably benign |
Het |
Dsc3 |
T |
C |
18: 20,104,639 (GRCm39) |
T563A |
probably damaging |
Het |
Eps8l2 |
C |
T |
7: 140,942,120 (GRCm39) |
P721S |
unknown |
Het |
Evx2 |
T |
C |
2: 74,489,426 (GRCm39) |
D112G |
possibly damaging |
Het |
Fam124a |
C |
A |
14: 62,843,782 (GRCm39) |
T430K |
possibly damaging |
Het |
Fbrs |
C |
T |
7: 127,088,782 (GRCm39) |
|
probably benign |
Het |
Fbxw14 |
T |
C |
9: 109,103,647 (GRCm39) |
T22A |
probably benign |
Het |
Fmo5 |
T |
G |
3: 97,552,952 (GRCm39) |
V300G |
probably damaging |
Het |
Gadl1 |
T |
C |
9: 115,770,411 (GRCm39) |
S75P |
probably benign |
Het |
Galnt2 |
T |
G |
8: 125,065,277 (GRCm39) |
I469S |
probably benign |
Het |
Gga3 |
T |
A |
11: 115,479,805 (GRCm39) |
|
probably benign |
Het |
Gm10647 |
T |
C |
9: 66,705,771 (GRCm39) |
|
probably benign |
Het |
Gm14180 |
C |
A |
11: 99,625,043 (GRCm39) |
C25F |
unknown |
Het |
Grid2 |
A |
T |
6: 64,297,116 (GRCm39) |
D493V |
probably damaging |
Het |
Gzmc |
T |
A |
14: 56,469,754 (GRCm39) |
Y182F |
possibly damaging |
Het |
Hecw2 |
A |
C |
1: 53,869,899 (GRCm39) |
L1443R |
probably damaging |
Het |
Igkv4-62 |
A |
G |
6: 69,377,053 (GRCm39) |
I32T |
probably benign |
Het |
Ikzf1 |
T |
A |
11: 11,691,015 (GRCm39) |
|
probably null |
Het |
Il27ra |
G |
A |
8: 84,760,571 (GRCm39) |
|
probably benign |
Het |
Jmjd1c |
C |
A |
10: 67,076,587 (GRCm39) |
A2137D |
probably benign |
Het |
Kcnc2 |
T |
C |
10: 112,294,502 (GRCm39) |
C579R |
probably damaging |
Het |
Kdr |
T |
C |
5: 76,112,498 (GRCm39) |
T862A |
probably damaging |
Het |
Kif17 |
T |
C |
4: 138,005,556 (GRCm39) |
S182P |
possibly damaging |
Het |
Klf5 |
A |
T |
14: 99,539,318 (GRCm39) |
T164S |
probably benign |
Het |
Ksr2 |
T |
G |
5: 117,693,359 (GRCm39) |
V269G |
possibly damaging |
Het |
Mcm5 |
T |
A |
8: 75,847,539 (GRCm39) |
D445E |
probably damaging |
Het |
Mlkl |
T |
C |
8: 112,054,580 (GRCm39) |
I186V |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,591,978 (GRCm39) |
S3017C |
possibly damaging |
Het |
Myo15a |
T |
C |
11: 60,368,676 (GRCm39) |
F479L |
possibly damaging |
Het |
Myo6 |
A |
G |
9: 80,181,257 (GRCm39) |
|
probably benign |
Het |
Myom1 |
T |
A |
17: 71,354,782 (GRCm39) |
V393E |
probably damaging |
Het |
Nup98 |
T |
A |
7: 101,788,859 (GRCm39) |
|
probably null |
Het |
Odf2l |
A |
G |
3: 144,854,302 (GRCm39) |
N383S |
probably damaging |
Het |
Olfml3 |
A |
C |
3: 103,644,342 (GRCm39) |
|
probably null |
Het |
Or10q1 |
T |
A |
19: 13,727,352 (GRCm39) |
I294N |
probably damaging |
Het |
Or7g17 |
G |
A |
9: 18,767,925 (GRCm39) |
M1I |
probably null |
Het |
Or8g18 |
A |
G |
9: 39,149,307 (GRCm39) |
Y141H |
probably benign |
Het |
Or8j3b |
A |
T |
2: 86,205,159 (GRCm39) |
V199E |
possibly damaging |
Het |
Plxna4 |
A |
T |
6: 32,174,009 (GRCm39) |
D1195E |
probably benign |
Het |
Ppp1r1a |
T |
A |
15: 103,446,247 (GRCm39) |
H20L |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,746,085 (GRCm39) |
|
probably null |
Het |
Prom2 |
A |
G |
2: 127,380,258 (GRCm39) |
|
probably benign |
Het |
Rasal3 |
T |
C |
17: 32,622,357 (GRCm39) |
M1V |
probably null |
Het |
Rhoj |
A |
G |
12: 75,441,194 (GRCm39) |
|
probably null |
Het |
Rnf40 |
C |
T |
7: 127,196,032 (GRCm39) |
|
probably null |
Het |
Slc15a3 |
T |
C |
19: 10,820,614 (GRCm39) |
L77P |
probably damaging |
Het |
Slc26a6 |
T |
C |
9: 108,738,522 (GRCm39) |
V586A |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,370 (GRCm39) |
L37Q |
probably damaging |
Het |
Slc43a2 |
T |
A |
11: 75,454,403 (GRCm39) |
M316K |
probably benign |
Het |
Smarcal1 |
T |
C |
1: 72,672,010 (GRCm39) |
F844L |
probably benign |
Het |
Snx19 |
A |
G |
9: 30,339,912 (GRCm39) |
E350G |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,278,524 (GRCm39) |
T995S |
probably benign |
Het |
Tmc3 |
T |
G |
7: 83,261,681 (GRCm39) |
N586K |
probably damaging |
Het |
Tmem107 |
T |
A |
11: 68,963,239 (GRCm39) |
|
probably benign |
Het |
Tmem247 |
A |
G |
17: 87,225,989 (GRCm39) |
Q51R |
probably benign |
Het |
Tmpo |
G |
T |
10: 90,999,900 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
T |
A |
15: 37,996,815 (GRCm39) |
T1894S |
probably damaging |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,347,468 (GRCm39) |
H3236Q |
probably benign |
Het |
Zfand4 |
G |
A |
6: 116,291,700 (GRCm39) |
D545N |
probably benign |
Het |
Zkscan3 |
G |
T |
13: 21,578,944 (GRCm39) |
P155T |
possibly damaging |
Het |
|
Other mutations in Dsg1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Dsg1b
|
APN |
18 |
20,529,533 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00675:Dsg1b
|
APN |
18 |
20,524,975 (GRCm39) |
nonsense |
probably null |
|
IGL01071:Dsg1b
|
APN |
18 |
20,542,272 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01589:Dsg1b
|
APN |
18 |
20,542,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01729:Dsg1b
|
APN |
18 |
20,538,295 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01753:Dsg1b
|
APN |
18 |
20,530,906 (GRCm39) |
splice site |
probably benign |
|
IGL02560:Dsg1b
|
APN |
18 |
20,542,235 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02654:Dsg1b
|
APN |
18 |
20,542,319 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Dsg1b
|
APN |
18 |
20,532,542 (GRCm39) |
missense |
probably benign |
|
IGL03272:Dsg1b
|
APN |
18 |
20,530,446 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03342:Dsg1b
|
APN |
18 |
20,542,517 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02835:Dsg1b
|
UTSW |
18 |
20,525,071 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0080:Dsg1b
|
UTSW |
18 |
20,530,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0455:Dsg1b
|
UTSW |
18 |
20,529,082 (GRCm39) |
missense |
probably benign |
0.02 |
R0498:Dsg1b
|
UTSW |
18 |
20,542,390 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0518:Dsg1b
|
UTSW |
18 |
20,521,221 (GRCm39) |
missense |
probably benign |
0.00 |
R1418:Dsg1b
|
UTSW |
18 |
20,530,487 (GRCm39) |
nonsense |
probably null |
|
R1429:Dsg1b
|
UTSW |
18 |
20,523,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Dsg1b
|
UTSW |
18 |
20,542,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Dsg1b
|
UTSW |
18 |
20,529,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Dsg1b
|
UTSW |
18 |
20,532,578 (GRCm39) |
missense |
probably benign |
|
R1934:Dsg1b
|
UTSW |
18 |
20,528,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Dsg1b
|
UTSW |
18 |
20,529,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R2191:Dsg1b
|
UTSW |
18 |
20,542,675 (GRCm39) |
makesense |
probably null |
|
R2192:Dsg1b
|
UTSW |
18 |
20,542,675 (GRCm39) |
makesense |
probably null |
|
R2927:Dsg1b
|
UTSW |
18 |
20,538,308 (GRCm39) |
missense |
probably benign |
0.23 |
R3777:Dsg1b
|
UTSW |
18 |
20,532,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Dsg1b
|
UTSW |
18 |
20,523,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Dsg1b
|
UTSW |
18 |
20,541,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4718:Dsg1b
|
UTSW |
18 |
20,530,986 (GRCm39) |
missense |
probably damaging |
0.98 |
R4853:Dsg1b
|
UTSW |
18 |
20,541,793 (GRCm39) |
missense |
probably benign |
0.01 |
R4853:Dsg1b
|
UTSW |
18 |
20,523,189 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4981:Dsg1b
|
UTSW |
18 |
20,541,925 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5125:Dsg1b
|
UTSW |
18 |
20,530,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5178:Dsg1b
|
UTSW |
18 |
20,530,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Dsg1b
|
UTSW |
18 |
20,528,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R5450:Dsg1b
|
UTSW |
18 |
20,542,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Dsg1b
|
UTSW |
18 |
20,532,596 (GRCm39) |
missense |
probably benign |
|
R5778:Dsg1b
|
UTSW |
18 |
20,542,279 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5808:Dsg1b
|
UTSW |
18 |
20,541,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R6144:Dsg1b
|
UTSW |
18 |
20,529,476 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6185:Dsg1b
|
UTSW |
18 |
20,532,543 (GRCm39) |
missense |
probably benign |
|
R6268:Dsg1b
|
UTSW |
18 |
20,521,220 (GRCm39) |
missense |
probably benign |
0.01 |
R6291:Dsg1b
|
UTSW |
18 |
20,537,848 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6342:Dsg1b
|
UTSW |
18 |
20,523,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Dsg1b
|
UTSW |
18 |
20,527,498 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6566:Dsg1b
|
UTSW |
18 |
20,530,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R6817:Dsg1b
|
UTSW |
18 |
20,527,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Dsg1b
|
UTSW |
18 |
20,532,480 (GRCm39) |
missense |
probably benign |
0.01 |
R7857:Dsg1b
|
UTSW |
18 |
20,529,520 (GRCm39) |
missense |
probably benign |
0.06 |
R8209:Dsg1b
|
UTSW |
18 |
20,541,947 (GRCm39) |
missense |
probably benign |
0.36 |
R8283:Dsg1b
|
UTSW |
18 |
20,524,963 (GRCm39) |
missense |
probably benign |
0.01 |
R8328:Dsg1b
|
UTSW |
18 |
20,510,007 (GRCm39) |
missense |
probably benign |
0.00 |
R8746:Dsg1b
|
UTSW |
18 |
20,529,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Dsg1b
|
UTSW |
18 |
20,542,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R9095:Dsg1b
|
UTSW |
18 |
20,523,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Dsg1b
|
UTSW |
18 |
20,531,004 (GRCm39) |
nonsense |
probably null |
|
R9386:Dsg1b
|
UTSW |
18 |
20,525,071 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9478:Dsg1b
|
UTSW |
18 |
20,531,008 (GRCm39) |
missense |
|
|
R9695:Dsg1b
|
UTSW |
18 |
20,532,389 (GRCm39) |
missense |
probably damaging |
0.98 |
|