Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,240,421 (GRCm39) |
N761K |
possibly damaging |
Het |
Adgrf3 |
T |
A |
5: 30,403,442 (GRCm39) |
L444F |
possibly damaging |
Het |
Amotl2 |
C |
T |
9: 102,607,270 (GRCm39) |
R693W |
probably damaging |
Het |
As3mt |
G |
T |
19: 46,695,968 (GRCm39) |
|
probably benign |
Het |
Atp6v1e2 |
A |
G |
17: 87,251,966 (GRCm39) |
V144A |
probably benign |
Het |
Bfar |
C |
T |
16: 13,505,331 (GRCm39) |
Q114* |
probably null |
Het |
Casd1 |
C |
T |
6: 4,621,225 (GRCm39) |
A261V |
probably damaging |
Het |
Cd177 |
A |
T |
7: 24,451,696 (GRCm39) |
I440K |
probably damaging |
Het |
Cfap54 |
G |
T |
10: 92,672,339 (GRCm39) |
Y2910* |
probably null |
Het |
Csl |
A |
G |
10: 99,593,944 (GRCm39) |
F374L |
possibly damaging |
Het |
Dctn1 |
G |
A |
6: 83,167,501 (GRCm39) |
R275H |
probably damaging |
Het |
Derl3 |
A |
G |
10: 75,729,713 (GRCm39) |
|
probably null |
Het |
Dst |
A |
G |
1: 34,007,916 (GRCm39) |
I117V |
probably benign |
Het |
Edc3 |
T |
A |
9: 57,655,680 (GRCm39) |
C477S |
possibly damaging |
Het |
Efs |
T |
C |
14: 55,154,610 (GRCm39) |
E450G |
probably damaging |
Het |
Fcrla |
T |
A |
1: 170,748,508 (GRCm39) |
I212F |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,818,786 (GRCm39) |
I4840V |
probably benign |
Het |
Gpam |
T |
A |
19: 55,066,773 (GRCm39) |
I581F |
probably benign |
Het |
Greb1l |
A |
G |
18: 10,458,358 (GRCm39) |
D45G |
probably damaging |
Het |
Heca |
A |
G |
10: 17,783,820 (GRCm39) |
Y478H |
probably damaging |
Het |
Hspa9 |
C |
T |
18: 35,072,441 (GRCm39) |
M561I |
probably damaging |
Het |
Hyal6 |
T |
A |
6: 24,734,965 (GRCm39) |
Y299* |
probably null |
Het |
Iho1 |
A |
G |
9: 108,283,877 (GRCm39) |
V189A |
probably benign |
Het |
Ik |
T |
A |
18: 36,886,310 (GRCm39) |
|
probably null |
Het |
Khsrp |
A |
G |
17: 57,330,360 (GRCm39) |
S582P |
possibly damaging |
Het |
Kif18a |
A |
G |
2: 109,122,471 (GRCm39) |
D182G |
probably damaging |
Het |
Krt1c |
T |
C |
15: 101,719,979 (GRCm39) |
T564A |
unknown |
Het |
Lig4 |
A |
G |
8: 10,021,885 (GRCm39) |
S632P |
probably benign |
Het |
Med1 |
C |
T |
11: 98,046,258 (GRCm39) |
|
probably benign |
Het |
Mgat3 |
T |
A |
15: 80,096,550 (GRCm39) |
I459N |
probably damaging |
Het |
Mkln1 |
A |
T |
6: 31,451,421 (GRCm39) |
Q454L |
probably benign |
Het |
Mn1 |
A |
G |
5: 111,567,803 (GRCm39) |
E591G |
possibly damaging |
Het |
Myo5c |
T |
A |
9: 75,199,484 (GRCm39) |
L1364Q |
probably damaging |
Het |
Oas1d |
T |
C |
5: 121,053,780 (GRCm39) |
V80A |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,929,674 (GRCm39) |
D5180E |
probably damaging |
Het |
Pax6 |
G |
A |
2: 105,522,622 (GRCm39) |
|
probably null |
Het |
Pcdh15 |
A |
C |
10: 74,160,221 (GRCm39) |
N446T |
probably damaging |
Het |
Pcnx2 |
A |
T |
8: 126,581,969 (GRCm39) |
F922L |
probably benign |
Het |
Ptpn4 |
G |
T |
1: 119,587,580 (GRCm39) |
T921K |
probably benign |
Het |
Selenov |
A |
G |
7: 27,989,746 (GRCm39) |
|
probably null |
Het |
Tmem100 |
A |
G |
11: 89,926,271 (GRCm39) |
T33A |
probably benign |
Het |
Tmem59 |
C |
T |
4: 107,044,878 (GRCm39) |
Q66* |
probably null |
Het |
Trav21-dv12 |
T |
A |
14: 54,114,070 (GRCm39) |
Y63* |
probably null |
Het |
Trim66 |
G |
T |
7: 109,056,793 (GRCm39) |
H1121Q |
probably damaging |
Het |
Trim80 |
A |
G |
11: 115,338,769 (GRCm39) |
Y533C |
probably damaging |
Het |
Ttc17 |
G |
A |
2: 94,194,955 (GRCm39) |
P520L |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,622,093 (GRCm39) |
V15483E |
probably damaging |
Het |
Vinac1 |
G |
T |
2: 128,882,721 (GRCm39) |
N98K |
probably damaging |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
C |
A |
3: 5,468,974 (GRCm39) |
T3069K |
probably benign |
Het |
Zfp281 |
A |
G |
1: 136,553,448 (GRCm39) |
H142R |
probably benign |
Het |
Zfp462 |
G |
T |
4: 55,060,044 (GRCm39) |
R1190L |
probably damaging |
Het |
Zfp935 |
T |
A |
13: 62,602,231 (GRCm39) |
H323L |
probably damaging |
Het |
|
Other mutations in Akap8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Akap8
|
APN |
17 |
32,536,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01450:Akap8
|
APN |
17 |
32,534,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Akap8
|
APN |
17 |
32,528,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02223:Akap8
|
APN |
17 |
32,535,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02315:Akap8
|
APN |
17 |
32,524,475 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03404:Akap8
|
APN |
17 |
32,531,250 (GRCm39) |
splice site |
probably benign |
|
BB006:Akap8
|
UTSW |
17 |
32,528,419 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Akap8
|
UTSW |
17 |
32,528,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Akap8
|
UTSW |
17 |
32,535,234 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0526:Akap8
|
UTSW |
17 |
32,536,266 (GRCm39) |
missense |
probably benign |
0.28 |
R1795:Akap8
|
UTSW |
17 |
32,534,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Akap8
|
UTSW |
17 |
32,535,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R2571:Akap8
|
UTSW |
17 |
32,534,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R2918:Akap8
|
UTSW |
17 |
32,524,622 (GRCm39) |
missense |
probably benign |
0.01 |
R3423:Akap8
|
UTSW |
17 |
32,535,429 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3870:Akap8
|
UTSW |
17 |
32,536,813 (GRCm39) |
unclassified |
probably benign |
|
R4077:Akap8
|
UTSW |
17 |
32,531,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4078:Akap8
|
UTSW |
17 |
32,531,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Akap8
|
UTSW |
17 |
32,525,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R4756:Akap8
|
UTSW |
17 |
32,535,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R5091:Akap8
|
UTSW |
17 |
32,535,208 (GRCm39) |
missense |
probably benign |
0.05 |
R5761:Akap8
|
UTSW |
17 |
32,536,159 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6896:Akap8
|
UTSW |
17 |
32,536,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7138:Akap8
|
UTSW |
17 |
32,535,515 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7350:Akap8
|
UTSW |
17 |
32,535,549 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7929:Akap8
|
UTSW |
17 |
32,528,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Akap8
|
UTSW |
17 |
32,529,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Akap8
|
UTSW |
17 |
32,525,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Akap8
|
UTSW |
17 |
32,530,036 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0020:Akap8
|
UTSW |
17 |
32,534,724 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Akap8
|
UTSW |
17 |
32,525,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|