Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
T |
C |
5: 81,836,516 (GRCm39) |
V758A |
possibly damaging |
Het |
Arf4 |
T |
C |
14: 26,359,609 (GRCm39) |
L12P |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 36,996,441 (GRCm39) |
N1051S |
probably benign |
Het |
C4bp |
A |
T |
1: 130,575,801 (GRCm39) |
V230E |
possibly damaging |
Het |
Carm1 |
T |
A |
9: 21,480,878 (GRCm39) |
|
probably null |
Het |
Cd4 |
G |
A |
6: 124,856,341 (GRCm39) |
T50I |
probably benign |
Het |
Ceacam16 |
T |
C |
7: 19,595,054 (GRCm39) |
Y8C |
probably benign |
Het |
Ckap2l |
A |
T |
2: 129,111,136 (GRCm39) |
V687E |
probably damaging |
Het |
Dcaf4 |
A |
G |
12: 83,588,148 (GRCm39) |
D449G |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 110,278,746 (GRCm39) |
Y1113C |
probably benign |
Het |
Fry |
A |
G |
5: 150,362,253 (GRCm39) |
I161V |
probably benign |
Het |
Gm17093 |
A |
C |
14: 44,758,984 (GRCm39) |
M169L |
unknown |
Het |
Gm20721 |
A |
G |
2: 174,187,295 (GRCm39) |
D999G |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,713,361 (GRCm39) |
H840R |
probably damaging |
Het |
Hoxc12 |
C |
A |
15: 102,845,755 (GRCm39) |
H156Q |
probably benign |
Het |
Htr3b |
T |
C |
9: 48,858,934 (GRCm39) |
D68G |
probably damaging |
Het |
Inpp5b |
T |
C |
4: 124,639,880 (GRCm39) |
V99A |
probably damaging |
Het |
Klhl42 |
C |
T |
6: 147,009,241 (GRCm39) |
T360M |
probably benign |
Het |
Lmo7 |
C |
T |
14: 102,031,713 (GRCm39) |
R36* |
probably null |
Het |
Lmod3 |
T |
G |
6: 97,229,513 (GRCm39) |
N7T |
probably damaging |
Het |
Malrd1 |
G |
A |
2: 16,106,768 (GRCm39) |
|
probably null |
Het |
Mthfd2l |
T |
A |
5: 91,148,425 (GRCm39) |
I284K |
possibly damaging |
Het |
Myo1e |
T |
A |
9: 70,234,448 (GRCm39) |
I267N |
probably damaging |
Het |
Or13c7d |
T |
C |
4: 43,770,112 (GRCm39) |
R300G |
probably damaging |
Het |
Or2y1g |
T |
A |
11: 49,171,314 (GRCm39) |
V113E |
possibly damaging |
Het |
Prkce |
T |
C |
17: 86,476,268 (GRCm39) |
V83A |
probably damaging |
Het |
Resf1 |
A |
G |
6: 149,228,394 (GRCm39) |
E480G |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,606,238 (GRCm39) |
E4448V |
possibly damaging |
Het |
Scn1a |
A |
T |
2: 66,119,455 (GRCm39) |
N1349K |
probably damaging |
Het |
Smarcc1 |
T |
C |
9: 109,979,033 (GRCm39) |
I172T |
possibly damaging |
Het |
Syt16 |
T |
C |
12: 74,269,437 (GRCm39) |
V92A |
possibly damaging |
Het |
Tenm4 |
A |
G |
7: 96,523,474 (GRCm39) |
Y1672C |
probably damaging |
Het |
Tmem131 |
A |
G |
1: 36,838,468 (GRCm39) |
Y1486H |
probably damaging |
Het |
Tmem132a |
A |
G |
19: 10,838,888 (GRCm39) |
|
probably benign |
Het |
Usp40 |
A |
T |
1: 87,921,920 (GRCm39) |
D314E |
probably damaging |
Het |
Vmn2r79 |
G |
A |
7: 86,686,481 (GRCm39) |
V621I |
probably benign |
Het |
Wnk4 |
A |
G |
11: 101,167,509 (GRCm39) |
|
probably benign |
Het |
Wwc1 |
C |
A |
11: 35,789,445 (GRCm39) |
|
probably null |
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 |
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 |
|
R3116:Pxdn
|
UTSW |
12 |
30,052,306 (GRCm39) |
missense |
possibly damaging |
0.89 |
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 |
|