Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
C |
3: 137,771,183 (GRCm39) |
D124A |
probably benign |
Het |
Acd |
T |
C |
8: 106,425,514 (GRCm39) |
D273G |
probably damaging |
Het |
Adam15 |
T |
C |
3: 89,254,790 (GRCm39) |
D90G |
possibly damaging |
Het |
Adam2 |
A |
T |
14: 66,287,921 (GRCm39) |
C392S |
probably damaging |
Het |
Adam23 |
T |
A |
1: 63,576,131 (GRCm39) |
N304K |
probably damaging |
Het |
Adam34l |
A |
C |
8: 44,079,304 (GRCm39) |
F307V |
probably benign |
Het |
Aldh3b3 |
T |
C |
19: 4,013,882 (GRCm39) |
F28L |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,992,993 (GRCm39) |
S920P |
probably benign |
Het |
Btc |
A |
G |
5: 91,550,515 (GRCm39) |
|
probably null |
Het |
Chchd2 |
A |
T |
5: 129,916,054 (GRCm39) |
V12E |
probably benign |
Het |
Chia1 |
A |
G |
3: 106,035,991 (GRCm39) |
|
probably benign |
Het |
Chil4 |
A |
T |
3: 106,111,382 (GRCm39) |
|
probably null |
Het |
Clock |
A |
G |
5: 76,364,671 (GRCm39) |
F815L |
unknown |
Het |
Cmtr2 |
C |
T |
8: 110,949,712 (GRCm39) |
T674M |
probably benign |
Het |
Cnbd1 |
A |
C |
4: 18,887,647 (GRCm39) |
I289R |
probably damaging |
Het |
Cog2 |
A |
T |
8: 125,253,837 (GRCm39) |
|
probably null |
Het |
Col13a1 |
T |
C |
10: 61,703,248 (GRCm39) |
I454V |
unknown |
Het |
Cyct |
T |
A |
2: 76,184,457 (GRCm39) |
Y98F |
probably benign |
Het |
Dcaf6 |
T |
C |
1: 165,227,236 (GRCm39) |
E297G |
possibly damaging |
Het |
Dgka |
T |
C |
10: 128,567,046 (GRCm39) |
H271R |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,976,300 (GRCm39) |
I1250F |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,686,155 (GRCm39) |
L130P |
probably damaging |
Het |
Dpyd |
G |
A |
3: 119,108,560 (GRCm39) |
V868I |
probably benign |
Het |
Dync1li1 |
T |
A |
9: 114,535,076 (GRCm39) |
D113E |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,932,719 (GRCm39) |
K1405E |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,342,856 (GRCm39) |
C8R |
probably benign |
Het |
Frmd4a |
A |
G |
2: 4,609,044 (GRCm39) |
M971V |
probably benign |
Het |
Glyatl3 |
C |
T |
17: 41,223,553 (GRCm39) |
|
probably null |
Het |
Grip1 |
A |
T |
10: 119,821,454 (GRCm39) |
H373L |
probably benign |
Het |
Ins1 |
T |
C |
19: 52,253,258 (GRCm39) |
L66P |
possibly damaging |
Het |
Kif21b |
A |
T |
1: 136,101,800 (GRCm39) |
I1616L |
probably benign |
Het |
Map7d1 |
A |
G |
4: 126,128,024 (GRCm39) |
M637T |
unknown |
Het |
Mc2r |
A |
T |
18: 68,540,636 (GRCm39) |
M219K |
probably benign |
Het |
Mcpt1 |
A |
G |
14: 56,256,867 (GRCm39) |
D135G |
possibly damaging |
Het |
Mturn |
T |
C |
6: 54,676,541 (GRCm39) |
|
probably null |
Het |
Mutyh |
T |
A |
4: 116,674,074 (GRCm39) |
|
probably null |
Het |
Myh3 |
A |
G |
11: 66,984,397 (GRCm39) |
D1078G |
possibly damaging |
Het |
Or4d5 |
T |
C |
9: 40,012,451 (GRCm39) |
I112V |
probably benign |
Het |
Pcdha12 |
A |
G |
18: 37,153,874 (GRCm39) |
K198E |
probably damaging |
Het |
Pcf11 |
A |
T |
7: 92,306,534 (GRCm39) |
N1211K |
possibly damaging |
Het |
Piezo1 |
G |
A |
8: 123,213,832 (GRCm39) |
P1711S |
|
Het |
Pkd1 |
T |
A |
17: 24,769,451 (GRCm39) |
L72Q |
possibly damaging |
Het |
Pramel20 |
C |
A |
4: 143,299,314 (GRCm39) |
L326I |
probably damaging |
Het |
Prss12 |
A |
G |
3: 123,299,049 (GRCm39) |
D607G |
probably benign |
Het |
R3hdml |
T |
C |
2: 163,344,372 (GRCm39) |
*254R |
probably null |
Het |
Rasal3 |
TTGGACCTGAGTGGA |
TTGGA |
17: 32,612,502 (GRCm39) |
782 |
probably null |
Het |
Relch |
A |
T |
1: 105,615,077 (GRCm39) |
Y272F |
probably benign |
Het |
Rev3l |
C |
T |
10: 39,693,149 (GRCm39) |
P410S |
probably benign |
Het |
Sec14l2 |
A |
G |
11: 4,068,665 (GRCm39) |
V5A |
probably benign |
Het |
Slc12a3 |
A |
C |
8: 95,061,625 (GRCm39) |
I291L |
probably benign |
Het |
Slc4a10 |
T |
C |
2: 62,083,662 (GRCm39) |
F372L |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,035,978 (GRCm39) |
W1095R |
probably damaging |
Het |
Synj1 |
T |
C |
16: 90,785,095 (GRCm39) |
T254A |
probably damaging |
Het |
Taar2 |
T |
C |
10: 23,817,237 (GRCm39) |
F259S |
probably damaging |
Het |
Tns2 |
C |
A |
15: 102,018,996 (GRCm39) |
L396I |
probably damaging |
Het |
Tom1l1 |
TTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTG |
11: 90,540,648 (GRCm39) |
|
probably benign |
Het |
Traf5 |
T |
C |
1: 191,747,033 (GRCm39) |
D96G |
probably damaging |
Het |
Trgv3 |
A |
G |
13: 19,427,441 (GRCm39) |
E108G |
probably damaging |
Het |
Trpv6 |
A |
G |
6: 41,602,378 (GRCm39) |
V336A |
probably benign |
Het |
Usp45 |
A |
T |
4: 21,824,998 (GRCm39) |
L583F |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,554,475 (GRCm39) |
D1538G |
probably benign |
Het |
Vmn1r209 |
T |
A |
13: 22,990,072 (GRCm39) |
H206L |
probably damaging |
Het |
Zfp51 |
T |
A |
17: 21,684,733 (GRCm39) |
H449Q |
probably benign |
Het |
Zfp653 |
G |
A |
9: 21,969,321 (GRCm39) |
S315F |
possibly damaging |
Het |
|
Other mutations in Acte1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02202:Acte1
|
APN |
7 |
143,447,910 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0128:Acte1
|
UTSW |
7 |
143,445,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0217:Acte1
|
UTSW |
7 |
143,447,956 (GRCm39) |
splice site |
probably benign |
|
R0726:Acte1
|
UTSW |
7 |
143,425,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R1025:Acte1
|
UTSW |
7 |
143,450,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R2879:Acte1
|
UTSW |
7 |
143,447,800 (GRCm39) |
nonsense |
probably null |
|
R2925:Acte1
|
UTSW |
7 |
143,437,736 (GRCm39) |
nonsense |
probably null |
|
R3625:Acte1
|
UTSW |
7 |
143,425,591 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4003:Acte1
|
UTSW |
7 |
143,451,040 (GRCm39) |
missense |
probably benign |
0.16 |
R4184:Acte1
|
UTSW |
7 |
143,447,858 (GRCm39) |
nonsense |
probably null |
|
R4205:Acte1
|
UTSW |
7 |
143,422,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R6179:Acte1
|
UTSW |
7 |
143,425,524 (GRCm39) |
missense |
probably benign |
0.12 |
R7170:Acte1
|
UTSW |
7 |
143,450,102 (GRCm39) |
missense |
probably damaging |
0.97 |
R8023:Acte1
|
UTSW |
7 |
143,445,528 (GRCm39) |
missense |
probably damaging |
0.97 |
R8109:Acte1
|
UTSW |
7 |
143,451,203 (GRCm39) |
splice site |
probably null |
|
R8120:Acte1
|
UTSW |
7 |
143,425,524 (GRCm39) |
missense |
probably benign |
0.12 |
R8309:Acte1
|
UTSW |
7 |
143,437,680 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8516:Acte1
|
UTSW |
7 |
143,451,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R8748:Acte1
|
UTSW |
7 |
143,445,556 (GRCm39) |
missense |
probably benign |
|
R8944:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8964:Acte1
|
UTSW |
7 |
143,423,030 (GRCm39) |
missense |
probably benign |
|
R9220:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9221:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9222:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9303:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9304:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9306:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9308:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9428:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9429:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9457:Acte1
|
UTSW |
7 |
143,437,713 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9596:Acte1
|
UTSW |
7 |
143,434,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
|