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 |
Dpy19l4 |
A |
C |
4: 11,272,993 (GRCm39) |
|
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 |
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 Polr2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02026:Polr2b
|
APN |
5 |
77,480,099 (GRCm39) |
missense |
probably benign |
|
IGL02069:Polr2b
|
APN |
5 |
77,491,044 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03218:Polr2b
|
APN |
5 |
77,463,764 (GRCm39) |
missense |
probably benign |
0.03 |
R0007:Polr2b
|
UTSW |
5 |
77,488,284 (GRCm39) |
missense |
probably benign |
0.02 |
R0056:Polr2b
|
UTSW |
5 |
77,482,382 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0076:Polr2b
|
UTSW |
5 |
77,474,408 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0099:Polr2b
|
UTSW |
5 |
77,468,797 (GRCm39) |
splice site |
probably benign |
|
R0114:Polr2b
|
UTSW |
5 |
77,491,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Polr2b
|
UTSW |
5 |
77,467,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Polr2b
|
UTSW |
5 |
77,461,006 (GRCm39) |
unclassified |
probably benign |
|
R1233:Polr2b
|
UTSW |
5 |
77,482,412 (GRCm39) |
missense |
probably benign |
|
R1597:Polr2b
|
UTSW |
5 |
77,473,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Polr2b
|
UTSW |
5 |
77,474,470 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1696:Polr2b
|
UTSW |
5 |
77,490,495 (GRCm39) |
missense |
probably benign |
0.12 |
R1704:Polr2b
|
UTSW |
5 |
77,490,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1871:Polr2b
|
UTSW |
5 |
77,474,374 (GRCm39) |
splice site |
probably benign |
|
R2114:Polr2b
|
UTSW |
5 |
77,468,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Polr2b
|
UTSW |
5 |
77,468,193 (GRCm39) |
missense |
probably benign |
0.18 |
R2305:Polr2b
|
UTSW |
5 |
77,468,284 (GRCm39) |
splice site |
probably benign |
|
R3921:Polr2b
|
UTSW |
5 |
77,474,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Polr2b
|
UTSW |
5 |
77,496,252 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4031:Polr2b
|
UTSW |
5 |
77,496,252 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4526:Polr2b
|
UTSW |
5 |
77,474,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Polr2b
|
UTSW |
5 |
77,479,886 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4827:Polr2b
|
UTSW |
5 |
77,490,398 (GRCm39) |
missense |
probably benign |
|
R5244:Polr2b
|
UTSW |
5 |
77,490,847 (GRCm39) |
intron |
probably benign |
|
R5360:Polr2b
|
UTSW |
5 |
77,496,993 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5628:Polr2b
|
UTSW |
5 |
77,461,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R5928:Polr2b
|
UTSW |
5 |
77,493,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Polr2b
|
UTSW |
5 |
77,468,099 (GRCm39) |
missense |
probably benign |
|
R6179:Polr2b
|
UTSW |
5 |
77,468,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Polr2b
|
UTSW |
5 |
77,496,141 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Polr2b
|
UTSW |
5 |
77,491,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Polr2b
|
UTSW |
5 |
77,468,868 (GRCm39) |
missense |
probably benign |
0.04 |
R7328:Polr2b
|
UTSW |
5 |
77,463,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Polr2b
|
UTSW |
5 |
77,496,966 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7471:Polr2b
|
UTSW |
5 |
77,468,913 (GRCm39) |
nonsense |
probably null |
|
R7581:Polr2b
|
UTSW |
5 |
77,474,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Polr2b
|
UTSW |
5 |
77,468,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Polr2b
|
UTSW |
5 |
77,488,268 (GRCm39) |
missense |
probably benign |
0.00 |
R7700:Polr2b
|
UTSW |
5 |
77,488,268 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Polr2b
|
UTSW |
5 |
77,468,092 (GRCm39) |
missense |
probably benign |
0.35 |
R7995:Polr2b
|
UTSW |
5 |
77,473,614 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8015:Polr2b
|
UTSW |
5 |
77,484,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Polr2b
|
UTSW |
5 |
77,468,062 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8318:Polr2b
|
UTSW |
5 |
77,483,576 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Polr2b
|
UTSW |
5 |
77,483,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8850:Polr2b
|
UTSW |
5 |
77,463,761 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Polr2b
|
UTSW |
5 |
77,493,224 (GRCm39) |
missense |
probably benign |
0.16 |
R9275:Polr2b
|
UTSW |
5 |
77,471,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Polr2b
|
UTSW |
5 |
77,471,485 (GRCm39) |
missense |
probably damaging |
1.00 |
X0054:Polr2b
|
UTSW |
5 |
77,496,152 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1088:Polr2b
|
UTSW |
5 |
77,493,248 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Polr2b
|
UTSW |
5 |
77,490,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Polr2b
|
UTSW |
5 |
77,479,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|