Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,381,772 (GRCm39) |
I1398V |
probably benign |
Het |
Abca5 |
G |
A |
11: 110,188,995 (GRCm39) |
Q821* |
probably null |
Het |
Bcl9 |
A |
T |
3: 97,116,009 (GRCm39) |
L895Q |
probably damaging |
Het |
Daxx |
A |
G |
17: 34,131,351 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
A |
G |
15: 95,522,628 (GRCm39) |
Y360H |
probably damaging |
Het |
Dpy19l2 |
T |
C |
9: 24,607,321 (GRCm39) |
T47A |
probably benign |
Het |
Ephb3 |
T |
C |
16: 21,040,174 (GRCm39) |
V512A |
probably benign |
Het |
Exoc2 |
T |
C |
13: 31,090,842 (GRCm39) |
D254G |
probably benign |
Het |
Gtpbp1 |
G |
T |
15: 79,575,127 (GRCm39) |
R7L |
probably benign |
Het |
Gucy2c |
A |
T |
6: 136,706,201 (GRCm39) |
I500N |
probably benign |
Het |
H2ac6 |
A |
T |
13: 23,867,783 (GRCm39) |
Y40N |
probably damaging |
Het |
H2ac6 |
G |
T |
13: 23,867,784 (GRCm39) |
N39K |
possibly damaging |
Het |
Hormad2 |
T |
C |
11: 4,358,580 (GRCm39) |
|
probably benign |
Het |
Impg2 |
A |
G |
16: 56,089,445 (GRCm39) |
Q1130R |
probably damaging |
Het |
Itga4 |
T |
A |
2: 79,150,903 (GRCm39) |
D836E |
probably benign |
Het |
Loxhd1 |
A |
T |
18: 77,427,797 (GRCm39) |
T456S |
possibly damaging |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Map1b |
T |
C |
13: 99,568,036 (GRCm39) |
T1562A |
unknown |
Het |
Mre11a |
C |
T |
9: 14,726,572 (GRCm39) |
|
probably benign |
Het |
Myh1 |
A |
C |
11: 67,102,313 (GRCm39) |
E868A |
possibly damaging |
Het |
Nlrp4e |
T |
G |
7: 23,020,300 (GRCm39) |
S262R |
probably damaging |
Het |
Nlrp9a |
C |
T |
7: 26,257,318 (GRCm39) |
T223I |
probably benign |
Het |
Nosip |
A |
G |
7: 44,723,466 (GRCm39) |
D44G |
probably benign |
Het |
Nr6a1 |
C |
T |
2: 38,630,565 (GRCm39) |
M217I |
probably benign |
Het |
Numa1 |
A |
G |
7: 101,649,601 (GRCm39) |
T1111A |
probably benign |
Het |
Or6c6c |
T |
A |
10: 129,541,608 (GRCm39) |
I287N |
probably damaging |
Het |
Pms1 |
A |
G |
1: 53,246,519 (GRCm39) |
L340P |
probably damaging |
Het |
Prmt7 |
T |
C |
8: 106,963,937 (GRCm39) |
V277A |
probably benign |
Het |
Pxmp4 |
T |
C |
2: 154,429,870 (GRCm39) |
Y173C |
probably damaging |
Het |
Rbm11 |
G |
T |
16: 75,389,896 (GRCm39) |
V21L |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,416,712 (GRCm39) |
S1123P |
probably damaging |
Het |
Rnf220 |
C |
T |
4: 117,156,734 (GRCm39) |
|
probably benign |
Het |
Rnf41 |
T |
G |
10: 128,273,196 (GRCm39) |
*123G |
probably null |
Het |
Samhd1 |
C |
T |
2: 156,952,475 (GRCm39) |
D426N |
possibly damaging |
Het |
Scn10a |
A |
G |
9: 119,501,218 (GRCm39) |
W189R |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,055,150 (GRCm39) |
F265L |
probably damaging |
Het |
Spag16 |
A |
G |
1: 69,897,661 (GRCm39) |
D137G |
probably benign |
Het |
Srsf12 |
G |
A |
4: 33,209,103 (GRCm39) |
|
probably benign |
Het |
Suclg2 |
A |
G |
6: 95,572,722 (GRCm39) |
I81T |
possibly damaging |
Het |
Tmc1 |
C |
T |
19: 20,776,556 (GRCm39) |
R601H |
probably damaging |
Het |
Trim33 |
T |
C |
3: 103,254,086 (GRCm39) |
|
probably null |
Het |
Vit |
A |
G |
17: 78,932,480 (GRCm39) |
D529G |
probably damaging |
Het |
Wbp1l |
C |
T |
19: 46,643,057 (GRCm39) |
H353Y |
possibly damaging |
Het |
Wdr70 |
A |
T |
15: 8,075,965 (GRCm39) |
V170D |
possibly damaging |
Het |
Ythdc2 |
T |
A |
18: 44,995,751 (GRCm39) |
I947N |
possibly damaging |
Het |
Zfp280b |
T |
C |
10: 75,875,197 (GRCm39) |
S359P |
probably benign |
Het |
Zfp936 |
T |
C |
7: 42,836,722 (GRCm39) |
|
probably null |
Het |
Zscan4d |
T |
A |
7: 10,896,716 (GRCm39) |
Y218F |
probably benign |
Het |
|
Other mutations in Cpne7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01919:Cpne7
|
APN |
8 |
123,852,382 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02111:Cpne7
|
APN |
8 |
123,852,392 (GRCm39) |
intron |
probably benign |
|
IGL03000:Cpne7
|
APN |
8 |
123,853,435 (GRCm39) |
missense |
probably benign |
0.07 |
R0501:Cpne7
|
UTSW |
8 |
123,852,994 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0727:Cpne7
|
UTSW |
8 |
123,853,025 (GRCm39) |
missense |
probably damaging |
0.98 |
R1750:Cpne7
|
UTSW |
8 |
123,861,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Cpne7
|
UTSW |
8 |
123,854,176 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2103:Cpne7
|
UTSW |
8 |
123,854,176 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2219:Cpne7
|
UTSW |
8 |
123,851,177 (GRCm39) |
missense |
probably benign |
0.12 |
R2350:Cpne7
|
UTSW |
8 |
123,851,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Cpne7
|
UTSW |
8 |
123,844,406 (GRCm39) |
splice site |
probably null |
|
R4657:Cpne7
|
UTSW |
8 |
123,861,314 (GRCm39) |
makesense |
probably null |
|
R4961:Cpne7
|
UTSW |
8 |
123,860,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R6148:Cpne7
|
UTSW |
8 |
123,854,171 (GRCm39) |
missense |
probably benign |
0.00 |
R7566:Cpne7
|
UTSW |
8 |
123,860,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Cpne7
|
UTSW |
8 |
123,850,920 (GRCm39) |
missense |
probably damaging |
0.98 |
R7984:Cpne7
|
UTSW |
8 |
123,846,461 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8185:Cpne7
|
UTSW |
8 |
123,854,168 (GRCm39) |
missense |
probably benign |
0.04 |
R8978:Cpne7
|
UTSW |
8 |
123,861,177 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9031:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9044:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9079:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9080:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9084:Cpne7
|
UTSW |
8 |
123,856,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9443:Cpne7
|
UTSW |
8 |
123,853,411 (GRCm39) |
missense |
probably damaging |
0.99 |
|