Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,946,610 (GRCm39) |
I37F |
possibly damaging |
Het |
Aoc1l3 |
A |
G |
6: 48,964,331 (GRCm39) |
Y113C |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,521,953 (GRCm39) |
N357S |
probably benign |
Het |
Csmd3 |
A |
G |
15: 47,520,995 (GRCm39) |
F2783S |
probably damaging |
Het |
Desi2 |
T |
A |
1: 178,072,008 (GRCm39) |
M104K |
probably damaging |
Het |
Disp1 |
C |
T |
1: 182,870,486 (GRCm39) |
V645I |
probably benign |
Het |
Dock8 |
A |
T |
19: 25,165,858 (GRCm39) |
H1914L |
probably benign |
Het |
Fdft1 |
T |
C |
14: 63,415,147 (GRCm39) |
I28M |
probably benign |
Het |
Ffar3 |
T |
C |
7: 30,555,231 (GRCm39) |
M30V |
probably benign |
Het |
Grm3 |
A |
T |
5: 9,620,752 (GRCm39) |
F164Y |
probably damaging |
Het |
Ints5 |
T |
C |
19: 8,872,136 (GRCm39) |
S32P |
possibly damaging |
Het |
Itgam |
T |
A |
7: 127,715,201 (GRCm39) |
S908R |
probably damaging |
Het |
Kif20b |
C |
T |
19: 34,947,480 (GRCm39) |
P1565L |
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,940,121 (GRCm39) |
E1610G |
probably damaging |
Het |
Krt24 |
T |
A |
11: 99,173,262 (GRCm39) |
T298S |
possibly damaging |
Het |
Magoh |
T |
C |
4: 107,744,409 (GRCm39) |
V126A |
possibly damaging |
Het |
Marchf6 |
G |
A |
15: 31,486,265 (GRCm39) |
S362F |
probably benign |
Het |
Meak7 |
G |
A |
8: 120,495,056 (GRCm39) |
A234V |
probably benign |
Het |
Mier3 |
T |
A |
13: 111,843,182 (GRCm39) |
I178N |
probably damaging |
Het |
Moxd1 |
G |
T |
10: 24,177,429 (GRCm39) |
E582* |
probably null |
Het |
Ncor2 |
A |
T |
5: 125,101,230 (GRCm39) |
L2195Q |
probably damaging |
Het |
Neil1 |
A |
T |
9: 57,053,947 (GRCm39) |
D124E |
probably benign |
Het |
Nhsl1 |
A |
T |
10: 18,400,916 (GRCm39) |
Q714L |
probably damaging |
Het |
Nipbl |
T |
A |
15: 8,373,076 (GRCm39) |
M1057L |
probably benign |
Het |
Npas3 |
G |
A |
12: 54,114,508 (GRCm39) |
|
probably null |
Het |
Oas1h |
C |
T |
5: 120,999,679 (GRCm39) |
Q55* |
probably null |
Het |
Or2a5 |
T |
C |
6: 42,873,784 (GRCm39) |
V133A |
probably benign |
Het |
Or2ag2b |
T |
A |
7: 106,417,571 (GRCm39) |
F94I |
probably damaging |
Het |
Or52h9 |
C |
A |
7: 104,202,295 (GRCm39) |
H56Q |
probably benign |
Het |
Or5p61 |
T |
C |
7: 107,759,029 (GRCm39) |
E17G |
probably benign |
Het |
Or7d9 |
A |
T |
9: 20,197,523 (GRCm39) |
H176L |
probably benign |
Het |
Phactr2 |
C |
A |
10: 13,137,645 (GRCm39) |
E166* |
probably null |
Het |
Prkdc |
C |
T |
16: 15,482,222 (GRCm39) |
L422F |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,499,971 (GRCm39) |
V1051A |
probably damaging |
Het |
Rad21 |
T |
A |
15: 51,828,397 (GRCm39) |
E557V |
probably null |
Het |
Rtn3 |
T |
G |
19: 7,409,355 (GRCm39) |
N888H |
probably damaging |
Het |
Slc12a5 |
T |
A |
2: 164,838,101 (GRCm39) |
|
probably null |
Het |
Slc7a11 |
T |
A |
3: 50,338,588 (GRCm39) |
M274L |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,360,979 (GRCm39) |
N825S |
probably damaging |
Het |
Tln2 |
T |
A |
9: 67,262,421 (GRCm39) |
D610V |
probably benign |
Het |
Tmed11 |
C |
T |
5: 108,927,705 (GRCm39) |
V110M |
probably damaging |
Het |
Tmem92 |
T |
C |
11: 94,673,254 (GRCm39) |
D3G |
possibly damaging |
Het |
Trp53rkb |
C |
T |
2: 166,636,009 (GRCm39) |
|
probably benign |
Het |
Wdr91 |
A |
G |
6: 34,882,522 (GRCm39) |
L209P |
probably damaging |
Het |
Zfp511 |
T |
A |
7: 139,616,504 (GRCm39) |
D46E |
probably benign |
Het |
Zfp804a |
C |
A |
2: 82,089,761 (GRCm39) |
Q1197K |
probably damaging |
Het |
|
Other mutations in Pxdn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Pxdn
|
APN |
12 |
30,037,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01152:Pxdn
|
APN |
12 |
30,051,936 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01286:Pxdn
|
APN |
12 |
30,032,753 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01323:Pxdn
|
APN |
12 |
30,037,136 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01338:Pxdn
|
APN |
12 |
30,052,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01341:Pxdn
|
APN |
12 |
30,052,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Pxdn
|
APN |
12 |
30,051,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01580:Pxdn
|
APN |
12 |
30,034,492 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01650:Pxdn
|
APN |
12 |
30,052,400 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01679:Pxdn
|
APN |
12 |
30,049,901 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01866:Pxdn
|
APN |
12 |
30,034,570 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02354:Pxdn
|
APN |
12 |
30,049,188 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Pxdn
|
APN |
12 |
30,049,188 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Pxdn
|
APN |
12 |
30,034,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Pxdn
|
APN |
12 |
30,053,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03079:Pxdn
|
APN |
12 |
30,052,997 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03111:Pxdn
|
APN |
12 |
30,032,755 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02988:Pxdn
|
UTSW |
12 |
30,053,113 (GRCm39) |
nonsense |
probably null |
|
PIT4280001:Pxdn
|
UTSW |
12 |
30,045,327 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4469001:Pxdn
|
UTSW |
12 |
30,055,828 (GRCm39) |
missense |
probably benign |
0.00 |
R0070:Pxdn
|
UTSW |
12 |
30,032,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R0070:Pxdn
|
UTSW |
12 |
30,032,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R0086:Pxdn
|
UTSW |
12 |
30,052,418 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0140:Pxdn
|
UTSW |
12 |
30,032,753 (GRCm39) |
missense |
probably benign |
0.04 |
R0201:Pxdn
|
UTSW |
12 |
30,052,430 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0282:Pxdn
|
UTSW |
12 |
30,034,439 (GRCm39) |
nonsense |
probably null |
|
R0310:Pxdn
|
UTSW |
12 |
30,065,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Pxdn
|
UTSW |
12 |
30,037,065 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0468:Pxdn
|
UTSW |
12 |
30,044,485 (GRCm39) |
missense |
probably damaging |
0.99 |
R0825:Pxdn
|
UTSW |
12 |
30,034,995 (GRCm39) |
splice site |
probably benign |
|
R0885:Pxdn
|
UTSW |
12 |
30,053,401 (GRCm39) |
missense |
probably benign |
0.30 |
R1420:Pxdn
|
UTSW |
12 |
30,052,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Pxdn
|
UTSW |
12 |
30,052,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Pxdn
|
UTSW |
12 |
30,055,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R2280:Pxdn
|
UTSW |
12 |
30,034,905 (GRCm39) |
missense |
probably damaging |
0.98 |
R2504:Pxdn
|
UTSW |
12 |
30,053,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Pxdn
|
UTSW |
12 |
30,025,568 (GRCm39) |
splice site |
probably benign |
|
R3607:Pxdn
|
UTSW |
12 |
30,040,917 (GRCm39) |
missense |
probably benign |
0.04 |
R4033:Pxdn
|
UTSW |
12 |
30,053,224 (GRCm39) |
missense |
probably benign |
0.19 |
R4576:Pxdn
|
UTSW |
12 |
30,061,922 (GRCm39) |
missense |
probably benign |
|
R4659:Pxdn
|
UTSW |
12 |
30,044,552 (GRCm39) |
missense |
probably benign |
0.01 |
R4681:Pxdn
|
UTSW |
12 |
30,062,325 (GRCm39) |
missense |
probably benign |
0.45 |
R4968:Pxdn
|
UTSW |
12 |
30,050,011 (GRCm39) |
missense |
probably benign |
0.25 |
R5032:Pxdn
|
UTSW |
12 |
30,053,140 (GRCm39) |
missense |
probably benign |
0.08 |
R5232:Pxdn
|
UTSW |
12 |
30,040,987 (GRCm39) |
missense |
probably benign |
0.08 |
R5366:Pxdn
|
UTSW |
12 |
30,052,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5504:Pxdn
|
UTSW |
12 |
30,052,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Pxdn
|
UTSW |
12 |
30,053,141 (GRCm39) |
missense |
probably damaging |
0.99 |
R5739:Pxdn
|
UTSW |
12 |
30,032,333 (GRCm39) |
missense |
probably benign |
0.03 |
R5877:Pxdn
|
UTSW |
12 |
30,053,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6167:Pxdn
|
UTSW |
12 |
30,024,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Pxdn
|
UTSW |
12 |
30,032,716 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6200:Pxdn
|
UTSW |
12 |
30,053,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6609:Pxdn
|
UTSW |
12 |
30,052,940 (GRCm39) |
missense |
probably benign |
0.00 |
R6628:Pxdn
|
UTSW |
12 |
30,049,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Pxdn
|
UTSW |
12 |
30,064,582 (GRCm39) |
splice site |
probably null |
|
R6921:Pxdn
|
UTSW |
12 |
30,065,504 (GRCm39) |
missense |
probably damaging |
0.96 |
R6995:Pxdn
|
UTSW |
12 |
30,045,370 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7211:Pxdn
|
UTSW |
12 |
30,034,903 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7220:Pxdn
|
UTSW |
12 |
30,044,479 (GRCm39) |
missense |
probably benign |
0.02 |
R7347:Pxdn
|
UTSW |
12 |
30,062,260 (GRCm39) |
missense |
probably benign |
0.01 |
R7402:Pxdn
|
UTSW |
12 |
30,052,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R7408:Pxdn
|
UTSW |
12 |
30,040,944 (GRCm39) |
missense |
probably benign |
0.29 |
R7413:Pxdn
|
UTSW |
12 |
30,052,927 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Pxdn
|
UTSW |
12 |
30,034,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R7572:Pxdn
|
UTSW |
12 |
30,056,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R7708:Pxdn
|
UTSW |
12 |
30,056,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R7815:Pxdn
|
UTSW |
12 |
30,055,824 (GRCm39) |
missense |
probably damaging |
0.96 |
R7972:Pxdn
|
UTSW |
12 |
30,056,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R8097:Pxdn
|
UTSW |
12 |
30,056,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R8098:Pxdn
|
UTSW |
12 |
30,056,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R8205:Pxdn
|
UTSW |
12 |
30,056,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8262:Pxdn
|
UTSW |
12 |
30,049,195 (GRCm39) |
nonsense |
probably null |
|
R8335:Pxdn
|
UTSW |
12 |
30,052,096 (GRCm39) |
missense |
probably damaging |
0.99 |
R8356:Pxdn
|
UTSW |
12 |
30,061,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R8437:Pxdn
|
UTSW |
12 |
30,052,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R8456:Pxdn
|
UTSW |
12 |
30,061,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R8709:Pxdn
|
UTSW |
12 |
30,056,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R8772:Pxdn
|
UTSW |
12 |
30,065,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Pxdn
|
UTSW |
12 |
30,040,992 (GRCm39) |
missense |
probably benign |
|
R9310:Pxdn
|
UTSW |
12 |
30,052,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:Pxdn
|
UTSW |
12 |
30,044,552 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Pxdn
|
UTSW |
12 |
30,040,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|