Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
G |
5: 114,373,578 (GRCm39) |
H1869R |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,441,748 (GRCm39) |
T950A |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,673,735 (GRCm39) |
L3110Q |
probably damaging |
Het |
Ambra1 |
A |
T |
2: 91,740,434 (GRCm39) |
|
probably benign |
Het |
Brpf3 |
A |
T |
17: 29,025,871 (GRCm39) |
N315Y |
possibly damaging |
Het |
Clxn |
A |
G |
16: 14,738,261 (GRCm39) |
D142G |
probably damaging |
Het |
Cpne7 |
C |
T |
8: 123,856,951 (GRCm39) |
P402L |
probably damaging |
Het |
Cyba |
T |
A |
8: 123,151,630 (GRCm39) |
D189V |
probably benign |
Het |
Dexi |
A |
G |
16: 10,321,385 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,420,247 (GRCm39) |
V156I |
probably benign |
Het |
Drc7 |
T |
C |
8: 95,797,077 (GRCm39) |
V420A |
probably damaging |
Het |
Eef2k |
T |
A |
7: 120,479,584 (GRCm39) |
V167E |
probably damaging |
Het |
Eid2 |
T |
C |
7: 27,968,038 (GRCm39) |
I220T |
possibly damaging |
Het |
Fggy |
A |
C |
4: 95,732,334 (GRCm39) |
T442P |
probably benign |
Het |
Foxi3 |
T |
G |
6: 70,933,683 (GRCm39) |
S57A |
probably benign |
Het |
Foxi3 |
T |
A |
6: 70,934,186 (GRCm39) |
|
probably null |
Het |
Galntl5 |
C |
T |
5: 25,415,326 (GRCm39) |
P286S |
possibly damaging |
Het |
Gm5592 |
A |
G |
7: 40,938,274 (GRCm39) |
K519E |
probably benign |
Het |
Gse1 |
T |
A |
8: 120,957,269 (GRCm39) |
S587T |
unknown |
Het |
Kcns1 |
G |
T |
2: 164,009,996 (GRCm39) |
F254L |
probably damaging |
Het |
Kif15 |
A |
G |
9: 122,840,781 (GRCm39) |
T23A |
probably benign |
Het |
Kif16b |
T |
C |
2: 142,541,577 (GRCm39) |
Q1241R |
possibly damaging |
Het |
Lck |
A |
T |
4: 129,450,098 (GRCm39) |
L205Q |
probably damaging |
Het |
Map9 |
C |
T |
3: 82,287,525 (GRCm39) |
A420V |
possibly damaging |
Het |
Mdm2 |
A |
T |
10: 117,530,960 (GRCm39) |
D170E |
|
Het |
Mllt6 |
T |
A |
11: 97,554,485 (GRCm39) |
C30S |
probably damaging |
Het |
Muc5b |
T |
G |
7: 141,411,795 (GRCm39) |
D1580E |
unknown |
Het |
Oaf |
C |
T |
9: 43,135,308 (GRCm39) |
A157T |
probably damaging |
Het |
Or13a19 |
A |
G |
7: 139,902,485 (GRCm39) |
|
probably benign |
Het |
Or2ab1 |
T |
A |
11: 58,489,126 (GRCm39) |
N295K |
possibly damaging |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Osbp2 |
T |
C |
11: 3,667,128 (GRCm39) |
I8V |
probably damaging |
Het |
Pcdh9 |
T |
C |
14: 94,124,247 (GRCm39) |
Y641C |
probably damaging |
Het |
Phf10 |
A |
T |
17: 15,166,584 (GRCm39) |
C429S |
probably damaging |
Het |
Plekha6 |
C |
G |
1: 133,201,687 (GRCm39) |
P367A |
probably benign |
Het |
Plekha6 |
C |
A |
1: 133,201,688 (GRCm39) |
P367Q |
possibly damaging |
Het |
Plod2 |
T |
A |
9: 92,489,273 (GRCm39) |
I756K |
probably damaging |
Het |
Plxnb2 |
C |
A |
15: 89,044,566 (GRCm39) |
|
probably benign |
Het |
Pop1 |
T |
A |
15: 34,530,554 (GRCm39) |
M1014K |
possibly damaging |
Het |
Prrt4 |
T |
C |
6: 29,171,540 (GRCm39) |
D304G |
probably benign |
Het |
Rcan2 |
C |
A |
17: 44,147,245 (GRCm39) |
L28I |
probably benign |
Het |
Rffl |
C |
T |
11: 82,701,020 (GRCm39) |
V269I |
probably benign |
Het |
Rhox3c |
C |
T |
X: 36,651,303 (GRCm39) |
|
probably benign |
Het |
Ric1 |
C |
T |
19: 29,577,294 (GRCm39) |
A1066V |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,752,989 (GRCm39) |
Y1777* |
probably null |
Het |
Scart2 |
G |
T |
7: 139,828,010 (GRCm39) |
G73C |
probably damaging |
Het |
Sh3tc1 |
T |
G |
5: 35,854,834 (GRCm39) |
K1288Q |
possibly damaging |
Het |
Slc10a5 |
A |
C |
3: 10,399,792 (GRCm39) |
I289M |
probably damaging |
Het |
Slc16a9 |
A |
G |
10: 70,110,797 (GRCm39) |
T128A |
probably benign |
Het |
Slc7a11 |
T |
C |
3: 50,333,632 (GRCm39) |
H373R |
probably benign |
Het |
Spesp1 |
A |
G |
9: 62,180,623 (GRCm39) |
I95T |
probably benign |
Het |
Sra1 |
C |
T |
18: 36,800,946 (GRCm39) |
V131I |
probably benign |
Het |
Stxbp5l |
A |
G |
16: 37,024,930 (GRCm39) |
V556A |
possibly damaging |
Het |
Sycp2 |
T |
C |
2: 177,989,617 (GRCm39) |
E1414G |
probably damaging |
Het |
Trac |
A |
T |
14: 54,458,148 (GRCm39) |
K57* |
probably null |
Het |
Trps1 |
T |
C |
15: 50,686,003 (GRCm39) |
E724G |
probably benign |
Het |
Tubgcp6 |
T |
G |
15: 88,987,397 (GRCm39) |
D1192A |
possibly damaging |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Vps18 |
T |
G |
2: 119,128,034 (GRCm39) |
I952M |
probably damaging |
Het |
Wdr36 |
T |
C |
18: 32,970,499 (GRCm39) |
F20S |
probably damaging |
Het |
Wdr62 |
C |
A |
7: 29,962,062 (GRCm39) |
R450L |
probably benign |
Het |
Xab2 |
T |
C |
8: 3,668,641 (GRCm39) |
K76E |
probably benign |
Het |
Zpr1 |
A |
G |
9: 46,190,995 (GRCm39) |
D300G |
probably damaging |
Het |
|
Other mutations in 2610008E11Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01551:2610008E11Rik
|
APN |
10 |
78,924,147 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01905:2610008E11Rik
|
APN |
10 |
78,903,582 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02522:2610008E11Rik
|
APN |
10 |
78,903,633 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02999:2610008E11Rik
|
APN |
10 |
78,903,424 (GRCm39) |
missense |
possibly damaging |
0.74 |
K7371:2610008E11Rik
|
UTSW |
10 |
78,903,767 (GRCm39) |
missense |
probably benign |
0.01 |
R0557:2610008E11Rik
|
UTSW |
10 |
78,903,519 (GRCm39) |
missense |
probably damaging |
0.99 |
R0761:2610008E11Rik
|
UTSW |
10 |
78,903,833 (GRCm39) |
missense |
probably benign |
0.00 |
R1528:2610008E11Rik
|
UTSW |
10 |
78,903,530 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1801:2610008E11Rik
|
UTSW |
10 |
78,903,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R1923:2610008E11Rik
|
UTSW |
10 |
78,903,743 (GRCm39) |
missense |
probably damaging |
0.98 |
R2444:2610008E11Rik
|
UTSW |
10 |
78,904,561 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4223:2610008E11Rik
|
UTSW |
10 |
78,930,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R4653:2610008E11Rik
|
UTSW |
10 |
78,903,264 (GRCm39) |
missense |
probably benign |
0.42 |
R5127:2610008E11Rik
|
UTSW |
10 |
78,902,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R5784:2610008E11Rik
|
UTSW |
10 |
78,903,441 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6175:2610008E11Rik
|
UTSW |
10 |
78,902,448 (GRCm39) |
missense |
probably damaging |
0.98 |
R6990:2610008E11Rik
|
UTSW |
10 |
78,902,925 (GRCm39) |
missense |
probably damaging |
0.99 |
R7055:2610008E11Rik
|
UTSW |
10 |
78,903,681 (GRCm39) |
missense |
probably damaging |
0.98 |
R7133:2610008E11Rik
|
UTSW |
10 |
78,902,474 (GRCm39) |
missense |
probably benign |
0.33 |
R7133:2610008E11Rik
|
UTSW |
10 |
78,902,473 (GRCm39) |
missense |
probably benign |
0.02 |
R7142:2610008E11Rik
|
UTSW |
10 |
78,903,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:2610008E11Rik
|
UTSW |
10 |
78,903,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:2610008E11Rik
|
UTSW |
10 |
78,902,325 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8103:2610008E11Rik
|
UTSW |
10 |
78,903,668 (GRCm39) |
missense |
probably benign |
|
R8117:2610008E11Rik
|
UTSW |
10 |
78,930,289 (GRCm39) |
missense |
probably benign |
0.07 |
R8296:2610008E11Rik
|
UTSW |
10 |
78,903,568 (GRCm39) |
missense |
probably benign |
0.09 |
R8316:2610008E11Rik
|
UTSW |
10 |
78,903,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8477:2610008E11Rik
|
UTSW |
10 |
78,924,174 (GRCm39) |
missense |
probably benign |
0.00 |
R8790:2610008E11Rik
|
UTSW |
10 |
78,928,285 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9147:2610008E11Rik
|
UTSW |
10 |
78,903,406 (GRCm39) |
nonsense |
probably null |
|
R9148:2610008E11Rik
|
UTSW |
10 |
78,903,406 (GRCm39) |
nonsense |
probably null |
|
R9474:2610008E11Rik
|
UTSW |
10 |
78,903,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|