Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503E14Rik |
G |
A |
14: 44,401,391 (GRCm39) |
H152Y |
probably benign |
Het |
Abca1 |
T |
C |
4: 53,086,132 (GRCm39) |
D457G |
probably benign |
Het |
Atp8a1 |
T |
G |
5: 67,817,246 (GRCm39) |
K913N |
possibly damaging |
Het |
Cd180 |
G |
A |
13: 102,841,917 (GRCm39) |
S321N |
probably benign |
Het |
Cdc14b |
T |
C |
13: 64,363,470 (GRCm39) |
N264D |
probably damaging |
Het |
Cenpf |
A |
T |
1: 189,387,109 (GRCm39) |
C1724S |
probably benign |
Het |
Chil4 |
A |
G |
3: 106,109,113 (GRCm39) |
S397P |
probably benign |
Het |
Clpb |
C |
T |
7: 101,427,815 (GRCm39) |
R387* |
probably null |
Het |
Csgalnact2 |
A |
T |
6: 118,103,233 (GRCm39) |
M1K |
probably null |
Het |
Enpp3 |
C |
A |
10: 24,674,160 (GRCm39) |
C380F |
probably damaging |
Het |
Gtf3c1 |
G |
A |
7: 125,266,546 (GRCm39) |
R967W |
probably damaging |
Het |
Hnrnpr |
T |
A |
4: 136,066,856 (GRCm39) |
D472E |
unknown |
Het |
Klhl28 |
A |
T |
12: 64,996,840 (GRCm39) |
D500E |
probably damaging |
Het |
Lmo7 |
C |
T |
14: 102,148,321 (GRCm39) |
|
probably benign |
Het |
Mphosph8 |
A |
G |
14: 56,911,900 (GRCm39) |
I308V |
probably benign |
Het |
Myo6 |
T |
A |
9: 80,190,868 (GRCm39) |
|
probably null |
Het |
Nsmaf |
C |
T |
4: 6,435,056 (GRCm39) |
|
probably null |
Het |
Padi6 |
T |
A |
4: 140,454,934 (GRCm39) |
I668L |
possibly damaging |
Het |
Pigw |
A |
G |
11: 84,768,150 (GRCm39) |
I393T |
possibly damaging |
Het |
Prg3 |
G |
A |
2: 84,824,076 (GRCm39) |
C212Y |
probably damaging |
Het |
Pwp1 |
T |
C |
10: 85,715,752 (GRCm39) |
V267A |
probably benign |
Het |
Raver2 |
C |
A |
4: 100,953,468 (GRCm39) |
Q79K |
probably benign |
Het |
Sdr9c7 |
T |
C |
10: 127,745,697 (GRCm39) |
S270P |
probably damaging |
Het |
Sfmbt2 |
A |
G |
2: 10,406,818 (GRCm39) |
E39G |
probably damaging |
Het |
Strada |
A |
G |
11: 106,061,976 (GRCm39) |
|
probably benign |
Het |
Zic3 |
A |
G |
X: 57,079,779 (GRCm39) |
Y424C |
probably damaging |
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 |
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 |
R3929:Xrn1
|
UTSW |
9 |
95,870,926 (GRCm39) |
missense |
possibly damaging |
0.89 |
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 |
|