Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,190,666 (GRCm39) |
N39Y |
probably benign |
Het |
Adamts10 |
C |
T |
17: 33,768,347 (GRCm39) |
Q840* |
probably null |
Het |
Aff2 |
C |
T |
X: 68,878,248 (GRCm39) |
T678I |
probably damaging |
Het |
Ahctf1 |
A |
G |
1: 179,587,836 (GRCm39) |
V1418A |
probably benign |
Het |
Ankrd11 |
G |
A |
8: 123,626,775 (GRCm39) |
R136C |
probably damaging |
Het |
Arf5 |
A |
G |
6: 28,426,075 (GRCm39) |
Y154C |
probably damaging |
Het |
AW551984 |
A |
G |
9: 39,511,912 (GRCm39) |
V33A |
probably null |
Het |
B4galt5 |
A |
G |
2: 167,151,154 (GRCm39) |
L118P |
probably damaging |
Het |
Bcl9l |
A |
G |
9: 44,417,979 (GRCm39) |
I606V |
probably benign |
Het |
Bdp1 |
A |
G |
13: 100,177,962 (GRCm39) |
I1969T |
probably benign |
Het |
Bicd1 |
A |
T |
6: 149,413,389 (GRCm39) |
D260V |
possibly damaging |
Het |
Cap1 |
A |
T |
4: 122,756,868 (GRCm39) |
H272Q |
possibly damaging |
Het |
Ccnk |
A |
G |
12: 108,165,568 (GRCm39) |
|
probably benign |
Het |
Cd209f |
A |
T |
8: 4,155,558 (GRCm39) |
|
probably null |
Het |
Cdk13 |
C |
A |
13: 17,894,079 (GRCm39) |
A1123S |
probably damaging |
Het |
Cdx1 |
C |
T |
18: 61,153,564 (GRCm39) |
R158H |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,474,663 (GRCm39) |
S123P |
probably benign |
Het |
Cwc22 |
G |
A |
2: 77,738,455 (GRCm39) |
A497V |
probably damaging |
Het |
Cwh43 |
T |
C |
5: 73,575,370 (GRCm39) |
S296P |
probably damaging |
Het |
Dhx38 |
A |
T |
8: 110,282,848 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,383,745 (GRCm39) |
M2989K |
probably benign |
Het |
F11r |
A |
T |
1: 171,288,847 (GRCm39) |
H155L |
probably benign |
Het |
Fcgbpl1 |
A |
T |
7: 27,853,174 (GRCm39) |
D1487V |
probably damaging |
Het |
Fitm2 |
A |
G |
2: 163,311,634 (GRCm39) |
V193A |
probably benign |
Het |
Foxk1 |
T |
A |
5: 142,434,578 (GRCm39) |
S281T |
probably benign |
Het |
Furin |
A |
G |
7: 80,043,297 (GRCm39) |
C305R |
probably damaging |
Het |
Fut8 |
T |
A |
12: 77,495,334 (GRCm39) |
V308D |
probably damaging |
Het |
Gjb3 |
T |
A |
4: 127,220,125 (GRCm39) |
I136F |
probably benign |
Het |
Glmn |
A |
T |
5: 107,708,800 (GRCm39) |
S385T |
probably benign |
Het |
Glp1r |
T |
A |
17: 31,150,191 (GRCm39) |
M371K |
probably benign |
Het |
Gpr179 |
T |
C |
11: 97,240,544 (GRCm39) |
H293R |
probably damaging |
Het |
H2-M11 |
A |
T |
17: 36,859,846 (GRCm39) |
R280* |
probably null |
Het |
Hadhb |
T |
A |
5: 30,373,543 (GRCm39) |
H78Q |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,433,569 (GRCm39) |
|
probably benign |
Het |
Hexa |
A |
G |
9: 59,462,693 (GRCm39) |
|
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Hyal6 |
G |
A |
6: 24,743,417 (GRCm39) |
C371Y |
probably damaging |
Het |
Il1rap |
T |
C |
16: 26,511,585 (GRCm39) |
Y210H |
probably damaging |
Het |
Ino80 |
A |
T |
2: 119,261,497 (GRCm39) |
H722Q |
probably damaging |
Het |
Kcnt1 |
A |
G |
2: 25,782,508 (GRCm39) |
N200S |
probably damaging |
Het |
Kif27 |
T |
A |
13: 58,459,078 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
C |
13: 13,852,537 (GRCm39) |
V2179A |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,377,815 (GRCm39) |
|
probably null |
Het |
Mamdc4 |
A |
G |
2: 25,461,228 (GRCm39) |
M1T |
probably null |
Het |
Mansc4 |
A |
G |
6: 146,976,725 (GRCm39) |
I297T |
possibly damaging |
Het |
Mdn1 |
G |
A |
4: 32,767,182 (GRCm39) |
|
probably benign |
Het |
Mib2 |
A |
G |
4: 155,740,519 (GRCm39) |
|
probably benign |
Het |
Mon2 |
A |
G |
10: 122,849,301 (GRCm39) |
V1333A |
possibly damaging |
Het |
Ndst2 |
T |
C |
14: 20,774,536 (GRCm39) |
D840G |
possibly damaging |
Het |
Nell2 |
A |
T |
15: 95,330,563 (GRCm39) |
|
probably null |
Het |
Or4c102 |
A |
T |
2: 88,422,999 (GRCm39) |
I284F |
probably damaging |
Het |
Or4k51 |
T |
A |
2: 111,584,930 (GRCm39) |
M112K |
probably damaging |
Het |
Or5g29 |
C |
A |
2: 85,421,448 (GRCm39) |
A188E |
possibly damaging |
Het |
Pde5a |
C |
T |
3: 122,611,726 (GRCm39) |
|
probably benign |
Het |
Phip |
A |
G |
9: 82,758,769 (GRCm39) |
|
probably benign |
Het |
Polr2b |
A |
G |
5: 77,479,929 (GRCm39) |
I561V |
possibly damaging |
Het |
Ppp4r3c2 |
T |
C |
X: 88,796,299 (GRCm39) |
S44P |
probably damaging |
Het |
Prkg2 |
A |
T |
5: 99,142,514 (GRCm39) |
|
probably null |
Het |
Prl8a6 |
T |
C |
13: 27,617,084 (GRCm39) |
D201G |
probably benign |
Het |
Ptk6 |
G |
A |
2: 180,844,320 (GRCm39) |
|
probably benign |
Het |
Ptprn2 |
T |
C |
12: 117,175,466 (GRCm39) |
|
probably benign |
Het |
Rdh1 |
G |
T |
10: 127,598,993 (GRCm39) |
R158L |
probably damaging |
Het |
Rhbdl3 |
T |
C |
11: 80,214,175 (GRCm39) |
|
probably benign |
Het |
Rims4 |
A |
T |
2: 163,706,040 (GRCm39) |
V198E |
probably damaging |
Het |
Ripk1 |
T |
C |
13: 34,193,733 (GRCm39) |
S32P |
probably damaging |
Het |
Rnf13 |
T |
A |
3: 57,686,872 (GRCm39) |
N88K |
probably damaging |
Het |
Rnf13 |
C |
A |
3: 57,714,474 (GRCm39) |
L178I |
probably damaging |
Het |
Slc17a5 |
G |
T |
9: 78,445,584 (GRCm39) |
|
probably null |
Het |
Sorcs1 |
A |
G |
19: 50,624,891 (GRCm39) |
|
probably benign |
Het |
Spata31e3 |
T |
A |
13: 50,401,000 (GRCm39) |
Q442L |
probably benign |
Het |
Srpk1 |
G |
A |
17: 28,809,218 (GRCm39) |
|
probably benign |
Het |
Stk10 |
A |
G |
11: 32,564,708 (GRCm39) |
K840E |
probably damaging |
Het |
Suco |
A |
G |
1: 161,689,882 (GRCm39) |
|
probably benign |
Het |
T2 |
G |
A |
17: 8,636,007 (GRCm39) |
|
probably null |
Het |
Tbc1d5 |
A |
G |
17: 51,226,079 (GRCm39) |
S255P |
probably damaging |
Het |
Tenm1 |
T |
C |
X: 41,625,058 (GRCm39) |
Y2254C |
probably damaging |
Het |
Tex9 |
T |
A |
9: 72,385,678 (GRCm39) |
K11* |
probably null |
Het |
Tlr4 |
A |
G |
4: 66,746,153 (GRCm39) |
I29V |
probably benign |
Het |
Tmem255a |
A |
T |
X: 37,288,523 (GRCm39) |
V278D |
probably damaging |
Het |
Trpc3 |
T |
C |
3: 36,678,566 (GRCm39) |
I840V |
probably benign |
Het |
Trpm3 |
G |
A |
19: 22,878,435 (GRCm39) |
R622Q |
possibly damaging |
Het |
Vmn1r214 |
T |
A |
13: 23,219,464 (GRCm39) |
Y319* |
probably null |
Het |
Vmn1r53 |
A |
T |
6: 90,200,700 (GRCm39) |
V208E |
probably damaging |
Het |
Vmn2r89 |
T |
C |
14: 51,693,577 (GRCm39) |
F309S |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,340,253 (GRCm39) |
F831L |
possibly damaging |
Het |
Yes1 |
G |
T |
5: 32,797,749 (GRCm39) |
E23* |
probably null |
Het |
Zfp292 |
A |
T |
4: 34,810,059 (GRCm39) |
M995K |
probably benign |
Het |
|
Other mutations in Dpy19l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Dpy19l4
|
APN |
4 |
11,290,411 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01402:Dpy19l4
|
APN |
4 |
11,273,006 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01404:Dpy19l4
|
APN |
4 |
11,273,006 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01643:Dpy19l4
|
APN |
4 |
11,290,184 (GRCm39) |
splice site |
probably benign |
|
IGL01758:Dpy19l4
|
APN |
4 |
11,265,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01896:Dpy19l4
|
APN |
4 |
11,267,752 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02222:Dpy19l4
|
APN |
4 |
11,281,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02314:Dpy19l4
|
APN |
4 |
11,267,720 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02422:Dpy19l4
|
APN |
4 |
11,265,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02565:Dpy19l4
|
APN |
4 |
11,309,440 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03121:Dpy19l4
|
APN |
4 |
11,303,334 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03357:Dpy19l4
|
APN |
4 |
11,267,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Dpy19l4
|
APN |
4 |
11,290,253 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0003:Dpy19l4
|
UTSW |
4 |
11,267,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Dpy19l4
|
UTSW |
4 |
11,289,715 (GRCm39) |
missense |
probably benign |
0.07 |
R1114:Dpy19l4
|
UTSW |
4 |
11,287,643 (GRCm39) |
splice site |
probably benign |
|
R1332:Dpy19l4
|
UTSW |
4 |
11,276,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1336:Dpy19l4
|
UTSW |
4 |
11,276,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Dpy19l4
|
UTSW |
4 |
11,303,371 (GRCm39) |
nonsense |
probably null |
|
R1421:Dpy19l4
|
UTSW |
4 |
11,304,011 (GRCm39) |
missense |
probably benign |
0.09 |
R1422:Dpy19l4
|
UTSW |
4 |
11,317,168 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1465:Dpy19l4
|
UTSW |
4 |
11,296,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Dpy19l4
|
UTSW |
4 |
11,296,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1766:Dpy19l4
|
UTSW |
4 |
11,303,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Dpy19l4
|
UTSW |
4 |
11,281,020 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2090:Dpy19l4
|
UTSW |
4 |
11,304,344 (GRCm39) |
missense |
probably benign |
0.34 |
R2324:Dpy19l4
|
UTSW |
4 |
11,276,857 (GRCm39) |
unclassified |
probably benign |
|
R2446:Dpy19l4
|
UTSW |
4 |
11,304,143 (GRCm39) |
splice site |
probably null |
|
R3769:Dpy19l4
|
UTSW |
4 |
11,276,868 (GRCm39) |
splice site |
probably null |
|
R4151:Dpy19l4
|
UTSW |
4 |
11,309,485 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4472:Dpy19l4
|
UTSW |
4 |
11,304,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4609:Dpy19l4
|
UTSW |
4 |
11,295,999 (GRCm39) |
nonsense |
probably null |
|
R4708:Dpy19l4
|
UTSW |
4 |
11,277,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4722:Dpy19l4
|
UTSW |
4 |
11,290,521 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4997:Dpy19l4
|
UTSW |
4 |
11,287,493 (GRCm39) |
missense |
probably benign |
0.01 |
R5085:Dpy19l4
|
UTSW |
4 |
11,265,943 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5088:Dpy19l4
|
UTSW |
4 |
11,303,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Dpy19l4
|
UTSW |
4 |
11,304,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Dpy19l4
|
UTSW |
4 |
11,289,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R5413:Dpy19l4
|
UTSW |
4 |
11,289,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5758:Dpy19l4
|
UTSW |
4 |
11,276,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R6024:Dpy19l4
|
UTSW |
4 |
11,276,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Dpy19l4
|
UTSW |
4 |
11,289,671 (GRCm39) |
nonsense |
probably null |
|
R6339:Dpy19l4
|
UTSW |
4 |
11,285,111 (GRCm39) |
missense |
probably damaging |
0.98 |
R7055:Dpy19l4
|
UTSW |
4 |
11,290,291 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7359:Dpy19l4
|
UTSW |
4 |
11,273,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Dpy19l4
|
UTSW |
4 |
11,317,160 (GRCm39) |
nonsense |
probably null |
|
R7579:Dpy19l4
|
UTSW |
4 |
11,265,909 (GRCm39) |
missense |
probably benign |
0.39 |
R7913:Dpy19l4
|
UTSW |
4 |
11,265,859 (GRCm39) |
nonsense |
probably null |
|
R8047:Dpy19l4
|
UTSW |
4 |
11,317,139 (GRCm39) |
missense |
probably benign |
0.00 |
R8049:Dpy19l4
|
UTSW |
4 |
11,303,982 (GRCm39) |
missense |
probably benign |
0.44 |
R8495:Dpy19l4
|
UTSW |
4 |
11,267,659 (GRCm39) |
missense |
probably benign |
|
R8911:Dpy19l4
|
UTSW |
4 |
11,317,078 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8928:Dpy19l4
|
UTSW |
4 |
11,304,674 (GRCm39) |
intron |
probably benign |
|
R8955:Dpy19l4
|
UTSW |
4 |
11,290,195 (GRCm39) |
missense |
probably benign |
0.00 |
R9332:Dpy19l4
|
UTSW |
4 |
11,304,298 (GRCm39) |
critical splice donor site |
probably null |
|
R9372:Dpy19l4
|
UTSW |
4 |
11,303,343 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9401:Dpy19l4
|
UTSW |
4 |
11,265,806 (GRCm39) |
missense |
probably benign |
0.29 |
|