Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak5 |
A |
C |
3: 152,373,444 (GRCm39) |
L18R |
probably damaging |
Het |
Atrx |
T |
C |
X: 104,923,523 (GRCm39) |
I157V |
possibly damaging |
Het |
C9 |
T |
A |
15: 6,496,939 (GRCm39) |
I212N |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,587,452 (GRCm39) |
|
probably null |
Het |
Ccnf |
A |
G |
17: 24,453,356 (GRCm39) |
V361A |
probably damaging |
Het |
Ctps1 |
T |
A |
4: 120,399,093 (GRCm39) |
H553L |
probably benign |
Het |
Dmrta1 |
C |
T |
4: 89,579,681 (GRCm39) |
Q214* |
probably null |
Het |
E230025N22Rik |
T |
C |
18: 36,824,625 (GRCm39) |
D112G |
probably damaging |
Het |
Frat1 |
T |
C |
19: 41,819,087 (GRCm39) |
C161R |
probably damaging |
Het |
H1f8 |
A |
G |
6: 115,925,757 (GRCm39) |
K185E |
probably benign |
Het |
Itpr2 |
C |
A |
6: 146,275,857 (GRCm39) |
|
probably null |
Het |
Klhl40 |
A |
G |
9: 121,609,742 (GRCm39) |
D509G |
probably benign |
Het |
Muc5ac |
T |
C |
7: 141,356,629 (GRCm39) |
V1072A |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,520,064 (GRCm39) |
Y2340H |
probably damaging |
Het |
Or10ak9 |
T |
C |
4: 118,726,179 (GRCm39) |
L66P |
probably damaging |
Het |
Or2y17 |
A |
T |
11: 49,231,820 (GRCm39) |
M154L |
probably benign |
Het |
Or51a43 |
C |
T |
7: 103,717,791 (GRCm39) |
C149Y |
probably benign |
Het |
Or5be3 |
T |
A |
2: 86,864,428 (GRCm39) |
I46F |
possibly damaging |
Het |
Or6c2 |
G |
A |
10: 129,362,100 (GRCm39) |
M1I |
probably null |
Het |
Prdm10 |
T |
C |
9: 31,258,432 (GRCm39) |
I619T |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,422,868 (GRCm39) |
T71A |
probably damaging |
Het |
Rpusd4 |
A |
G |
9: 35,183,876 (GRCm39) |
I202V |
probably benign |
Het |
Sin3a |
A |
G |
9: 57,025,421 (GRCm39) |
N1089S |
probably damaging |
Het |
St6gal2 |
A |
G |
17: 55,803,324 (GRCm39) |
D353G |
possibly damaging |
Het |
Stap2 |
A |
C |
17: 56,310,156 (GRCm39) |
F50V |
probably damaging |
Het |
Stkld1 |
T |
A |
2: 26,830,059 (GRCm39) |
|
probably null |
Het |
Tars3 |
A |
G |
7: 65,333,791 (GRCm39) |
|
probably null |
Het |
Tbl1xr1 |
G |
C |
3: 22,243,932 (GRCm39) |
D69H |
probably damaging |
Het |
Tnrc6c |
C |
T |
11: 117,614,355 (GRCm39) |
R838W |
probably damaging |
Het |
Trim61 |
A |
G |
8: 65,465,969 (GRCm39) |
F431L |
probably benign |
Het |
Trmo |
C |
T |
4: 46,382,647 (GRCm39) |
G150S |
probably damaging |
Het |
Vmn1r61 |
A |
G |
7: 5,614,176 (GRCm39) |
I46T |
probably benign |
Het |
Vmn2r19 |
T |
C |
6: 123,292,587 (GRCm39) |
Y210H |
probably benign |
Het |
|
Other mutations in Xrn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Xrn1
|
APN |
9 |
95,921,002 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00778:Xrn1
|
APN |
9 |
95,855,500 (GRCm39) |
splice site |
probably benign |
|
IGL01936:Xrn1
|
APN |
9 |
95,930,397 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01983:Xrn1
|
APN |
9 |
95,855,421 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02106:Xrn1
|
APN |
9 |
95,859,858 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02330:Xrn1
|
APN |
9 |
95,855,401 (GRCm39) |
nonsense |
probably null |
|
IGL02338:Xrn1
|
APN |
9 |
95,859,880 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02830:Xrn1
|
APN |
9 |
95,900,234 (GRCm39) |
critical splice donor site |
probably null |
|
R0063:Xrn1
|
UTSW |
9 |
95,851,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Xrn1
|
UTSW |
9 |
95,851,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0467:Xrn1
|
UTSW |
9 |
95,906,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0508:Xrn1
|
UTSW |
9 |
95,933,789 (GRCm39) |
missense |
probably benign |
0.00 |
R0605:Xrn1
|
UTSW |
9 |
95,908,930 (GRCm39) |
nonsense |
probably null |
|
R0670:Xrn1
|
UTSW |
9 |
95,873,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Xrn1
|
UTSW |
9 |
95,855,592 (GRCm39) |
missense |
probably damaging |
0.96 |
R0781:Xrn1
|
UTSW |
9 |
95,873,322 (GRCm39) |
missense |
probably benign |
0.00 |
R0947:Xrn1
|
UTSW |
9 |
95,880,316 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1034:Xrn1
|
UTSW |
9 |
95,921,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R1124:Xrn1
|
UTSW |
9 |
95,885,918 (GRCm39) |
missense |
probably benign |
0.02 |
R1171:Xrn1
|
UTSW |
9 |
95,873,064 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1199:Xrn1
|
UTSW |
9 |
95,863,814 (GRCm39) |
splice site |
probably benign |
|
R1609:Xrn1
|
UTSW |
9 |
95,856,946 (GRCm39) |
missense |
probably benign |
0.03 |
R1921:Xrn1
|
UTSW |
9 |
95,881,550 (GRCm39) |
missense |
probably benign |
0.04 |
R1953:Xrn1
|
UTSW |
9 |
95,906,274 (GRCm39) |
critical splice donor site |
probably null |
|
R2000:Xrn1
|
UTSW |
9 |
95,927,616 (GRCm39) |
nonsense |
probably null |
|
R2109:Xrn1
|
UTSW |
9 |
95,861,273 (GRCm39) |
missense |
probably benign |
0.13 |
R2111:Xrn1
|
UTSW |
9 |
95,921,885 (GRCm39) |
missense |
probably benign |
0.03 |
R2164:Xrn1
|
UTSW |
9 |
95,888,873 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2266:Xrn1
|
UTSW |
9 |
95,888,765 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3754:Xrn1
|
UTSW |
9 |
95,849,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R3783:Xrn1
|
UTSW |
9 |
95,851,338 (GRCm39) |
missense |
probably benign |
0.10 |
R3921:Xrn1
|
UTSW |
9 |
95,851,337 (GRCm39) |
missense |
probably benign |
0.01 |
R4011:Xrn1
|
UTSW |
9 |
95,867,278 (GRCm39) |
nonsense |
probably null |
|
R4082:Xrn1
|
UTSW |
9 |
95,863,973 (GRCm39) |
missense |
probably benign |
0.02 |
R4455:Xrn1
|
UTSW |
9 |
95,855,698 (GRCm39) |
intron |
probably benign |
|
R4736:Xrn1
|
UTSW |
9 |
95,915,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4756:Xrn1
|
UTSW |
9 |
95,921,862 (GRCm39) |
missense |
probably benign |
0.00 |
R4780:Xrn1
|
UTSW |
9 |
95,856,797 (GRCm39) |
intron |
probably benign |
|
R5152:Xrn1
|
UTSW |
9 |
95,846,118 (GRCm39) |
missense |
probably benign |
0.40 |
R5261:Xrn1
|
UTSW |
9 |
95,927,596 (GRCm39) |
missense |
probably benign |
0.00 |
R5741:Xrn1
|
UTSW |
9 |
95,927,604 (GRCm39) |
missense |
probably benign |
0.24 |
R6108:Xrn1
|
UTSW |
9 |
95,856,480 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6127:Xrn1
|
UTSW |
9 |
95,851,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R6268:Xrn1
|
UTSW |
9 |
95,846,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6418:Xrn1
|
UTSW |
9 |
95,915,763 (GRCm39) |
splice site |
probably null |
|
R7002:Xrn1
|
UTSW |
9 |
95,929,843 (GRCm39) |
missense |
probably benign |
0.00 |
R7067:Xrn1
|
UTSW |
9 |
95,851,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R7155:Xrn1
|
UTSW |
9 |
95,861,198 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7439:Xrn1
|
UTSW |
9 |
95,933,682 (GRCm39) |
missense |
probably benign |
|
R7447:Xrn1
|
UTSW |
9 |
95,927,547 (GRCm39) |
missense |
probably benign |
|
R7454:Xrn1
|
UTSW |
9 |
95,930,411 (GRCm39) |
missense |
probably benign |
0.03 |
R7473:Xrn1
|
UTSW |
9 |
95,861,194 (GRCm39) |
missense |
probably benign |
0.07 |
R7561:Xrn1
|
UTSW |
9 |
95,881,511 (GRCm39) |
missense |
probably benign |
0.18 |
R7580:Xrn1
|
UTSW |
9 |
95,893,732 (GRCm39) |
missense |
not run |
|
R7642:Xrn1
|
UTSW |
9 |
95,903,906 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7763:Xrn1
|
UTSW |
9 |
95,880,401 (GRCm39) |
critical splice donor site |
probably null |
|
R8225:Xrn1
|
UTSW |
9 |
95,917,720 (GRCm39) |
missense |
probably benign |
|
R8372:Xrn1
|
UTSW |
9 |
95,906,166 (GRCm39) |
missense |
probably benign |
0.42 |
R8516:Xrn1
|
UTSW |
9 |
95,930,444 (GRCm39) |
nonsense |
probably null |
|
R8710:Xrn1
|
UTSW |
9 |
95,884,285 (GRCm39) |
missense |
|
|
R8850:Xrn1
|
UTSW |
9 |
95,920,732 (GRCm39) |
missense |
probably benign |
|
R8865:Xrn1
|
UTSW |
9 |
95,873,246 (GRCm39) |
missense |
probably benign |
0.00 |
R8951:Xrn1
|
UTSW |
9 |
95,870,999 (GRCm39) |
missense |
probably benign |
0.00 |
R9013:Xrn1
|
UTSW |
9 |
95,920,981 (GRCm39) |
missense |
probably benign |
0.00 |
R9162:Xrn1
|
UTSW |
9 |
95,915,660 (GRCm39) |
missense |
probably benign |
0.01 |
R9163:Xrn1
|
UTSW |
9 |
95,880,274 (GRCm39) |
missense |
probably benign |
0.00 |
R9415:Xrn1
|
UTSW |
9 |
95,851,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R9438:Xrn1
|
UTSW |
9 |
95,893,287 (GRCm39) |
missense |
probably benign |
0.30 |
R9544:Xrn1
|
UTSW |
9 |
95,920,756 (GRCm39) |
missense |
probably benign |
|
R9588:Xrn1
|
UTSW |
9 |
95,920,756 (GRCm39) |
missense |
probably benign |
|
R9674:Xrn1
|
UTSW |
9 |
95,855,647 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9674:Xrn1
|
UTSW |
9 |
95,855,645 (GRCm39) |
missense |
probably damaging |
0.99 |
R9716:Xrn1
|
UTSW |
9 |
95,927,632 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1176:Xrn1
|
UTSW |
9 |
95,846,243 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Xrn1
|
UTSW |
9 |
95,873,058 (GRCm39) |
missense |
probably benign |
0.00 |
|