Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aipl1 |
T |
C |
11: 71,921,028 (GRCm39) |
|
probably benign |
Het |
Ankrd33b |
A |
T |
15: 31,325,329 (GRCm39) |
F129L |
probably damaging |
Het |
Apob |
A |
G |
12: 8,065,222 (GRCm39) |
K4064E |
probably benign |
Het |
Arhgef10l |
T |
C |
4: 140,302,656 (GRCm39) |
D506G |
probably damaging |
Het |
Arid4b |
A |
C |
13: 14,327,997 (GRCm39) |
|
probably benign |
Het |
Ccdc88c |
A |
T |
12: 100,899,570 (GRCm39) |
Y1263N |
probably damaging |
Het |
Ckap5 |
T |
C |
2: 91,443,117 (GRCm39) |
L1697P |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,209,253 (GRCm39) |
F230S |
probably damaging |
Het |
Cpxm1 |
C |
T |
2: 130,235,601 (GRCm39) |
V464M |
probably damaging |
Het |
Dhrs7c |
A |
G |
11: 67,706,715 (GRCm39) |
E291G |
probably benign |
Het |
Dst |
C |
A |
1: 34,228,998 (GRCm39) |
P1872H |
possibly damaging |
Het |
G6pc2 |
G |
A |
2: 69,053,335 (GRCm39) |
A130T |
probably benign |
Het |
Gm4847 |
A |
G |
1: 166,462,578 (GRCm39) |
V304A |
probably damaging |
Het |
Gm8267 |
T |
C |
14: 44,955,374 (GRCm39) |
D155G |
possibly damaging |
Het |
Kank1 |
G |
A |
19: 25,388,066 (GRCm39) |
V580I |
probably benign |
Het |
Kcnh4 |
A |
G |
11: 100,636,649 (GRCm39) |
S757P |
probably damaging |
Het |
Krt34 |
C |
A |
11: 99,929,849 (GRCm39) |
A216S |
possibly damaging |
Het |
Mfhas1 |
A |
T |
8: 36,056,526 (GRCm39) |
I334F |
probably damaging |
Het |
Mrgprb8 |
A |
G |
7: 48,039,087 (GRCm39) |
M253V |
probably benign |
Het |
Or52n4b |
A |
T |
7: 108,144,137 (GRCm39) |
H133L |
probably benign |
Het |
Pp2d1 |
T |
A |
17: 53,815,468 (GRCm39) |
T419S |
probably damaging |
Het |
Pprc1 |
T |
A |
19: 46,060,782 (GRCm39) |
|
probably benign |
Het |
Reln |
A |
G |
5: 22,184,014 (GRCm39) |
S1662P |
probably damaging |
Het |
Sema7a |
G |
A |
9: 57,862,423 (GRCm39) |
E209K |
possibly damaging |
Het |
Serinc2 |
C |
T |
4: 130,158,237 (GRCm39) |
W15* |
probably null |
Het |
Serpina3k |
A |
G |
12: 104,311,525 (GRCm39) |
T368A |
probably benign |
Het |
Setd3 |
A |
T |
12: 108,129,289 (GRCm39) |
W54R |
probably damaging |
Het |
Slc9c1 |
G |
A |
16: 45,419,833 (GRCm39) |
S1001N |
probably benign |
Het |
Snapc3 |
A |
G |
4: 83,336,213 (GRCm39) |
D75G |
probably benign |
Het |
Spata31e2 |
A |
G |
1: 26,724,104 (GRCm39) |
Y359H |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,532,820 (GRCm39) |
S333P |
probably benign |
Het |
Utrn |
T |
C |
10: 12,610,948 (GRCm39) |
D469G |
probably damaging |
Het |
|
Other mutations in Akap11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Akap11
|
APN |
14 |
78,748,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00902:Akap11
|
APN |
14 |
78,733,278 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01752:Akap11
|
APN |
14 |
78,747,318 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01972:Akap11
|
APN |
14 |
78,745,297 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02239:Akap11
|
APN |
14 |
78,751,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02528:Akap11
|
APN |
14 |
78,748,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Akap11
|
APN |
14 |
78,736,402 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03130:Akap11
|
APN |
14 |
78,747,808 (GRCm39) |
nonsense |
probably null |
|
IGL03179:Akap11
|
APN |
14 |
78,745,180 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03240:Akap11
|
APN |
14 |
78,733,345 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03331:Akap11
|
APN |
14 |
78,751,305 (GRCm39) |
missense |
probably damaging |
1.00 |
bonham
|
UTSW |
14 |
78,736,304 (GRCm39) |
nonsense |
probably null |
|
R0004:Akap11
|
UTSW |
14 |
78,752,380 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0020:Akap11
|
UTSW |
14 |
78,755,617 (GRCm39) |
missense |
probably benign |
0.37 |
R0200:Akap11
|
UTSW |
14 |
78,748,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Akap11
|
UTSW |
14 |
78,747,529 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0320:Akap11
|
UTSW |
14 |
78,750,819 (GRCm39) |
missense |
probably benign |
|
R0381:Akap11
|
UTSW |
14 |
78,750,990 (GRCm39) |
missense |
probably benign |
0.01 |
R0536:Akap11
|
UTSW |
14 |
78,751,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Akap11
|
UTSW |
14 |
78,748,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0735:Akap11
|
UTSW |
14 |
78,747,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R1189:Akap11
|
UTSW |
14 |
78,750,787 (GRCm39) |
missense |
probably benign |
0.11 |
R1400:Akap11
|
UTSW |
14 |
78,751,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R1406:Akap11
|
UTSW |
14 |
78,750,189 (GRCm39) |
missense |
probably benign |
|
R1406:Akap11
|
UTSW |
14 |
78,750,189 (GRCm39) |
missense |
probably benign |
|
R1501:Akap11
|
UTSW |
14 |
78,750,787 (GRCm39) |
missense |
probably benign |
0.11 |
R1588:Akap11
|
UTSW |
14 |
78,747,685 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1717:Akap11
|
UTSW |
14 |
78,750,788 (GRCm39) |
missense |
probably benign |
0.02 |
R1823:Akap11
|
UTSW |
14 |
78,748,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Akap11
|
UTSW |
14 |
78,751,101 (GRCm39) |
missense |
probably benign |
0.00 |
R1874:Akap11
|
UTSW |
14 |
78,749,306 (GRCm39) |
missense |
probably benign |
0.14 |
R2031:Akap11
|
UTSW |
14 |
78,747,477 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2032:Akap11
|
UTSW |
14 |
78,747,477 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2276:Akap11
|
UTSW |
14 |
78,747,477 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2763:Akap11
|
UTSW |
14 |
78,756,332 (GRCm39) |
missense |
probably damaging |
0.98 |
R4483:Akap11
|
UTSW |
14 |
78,747,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R4582:Akap11
|
UTSW |
14 |
78,749,369 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4857:Akap11
|
UTSW |
14 |
78,736,300 (GRCm39) |
missense |
|
|
R4922:Akap11
|
UTSW |
14 |
78,750,220 (GRCm39) |
nonsense |
probably null |
|
R4993:Akap11
|
UTSW |
14 |
78,750,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Akap11
|
UTSW |
14 |
78,736,304 (GRCm39) |
nonsense |
probably null |
|
R5472:Akap11
|
UTSW |
14 |
78,750,869 (GRCm39) |
missense |
probably benign |
0.03 |
R5683:Akap11
|
UTSW |
14 |
78,750,018 (GRCm39) |
missense |
probably damaging |
0.98 |
R5774:Akap11
|
UTSW |
14 |
78,748,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Akap11
|
UTSW |
14 |
78,749,939 (GRCm39) |
missense |
probably benign |
0.00 |
R6264:Akap11
|
UTSW |
14 |
78,749,861 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6270:Akap11
|
UTSW |
14 |
78,756,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R6319:Akap11
|
UTSW |
14 |
78,750,978 (GRCm39) |
missense |
probably benign |
0.06 |
R6376:Akap11
|
UTSW |
14 |
78,752,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Akap11
|
UTSW |
14 |
78,760,029 (GRCm39) |
critical splice donor site |
probably null |
|
R6536:Akap11
|
UTSW |
14 |
78,748,754 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7048:Akap11
|
UTSW |
14 |
78,749,954 (GRCm39) |
missense |
|
|
R7147:Akap11
|
UTSW |
14 |
78,748,905 (GRCm39) |
missense |
|
|
R7473:Akap11
|
UTSW |
14 |
78,751,328 (GRCm39) |
missense |
|
|
R7503:Akap11
|
UTSW |
14 |
78,749,441 (GRCm39) |
missense |
|
|
R7542:Akap11
|
UTSW |
14 |
78,747,732 (GRCm39) |
missense |
|
|
R7618:Akap11
|
UTSW |
14 |
78,736,300 (GRCm39) |
missense |
|
|
R7679:Akap11
|
UTSW |
14 |
78,752,256 (GRCm39) |
missense |
|
|
R7973:Akap11
|
UTSW |
14 |
78,752,506 (GRCm39) |
missense |
|
|
R8094:Akap11
|
UTSW |
14 |
78,750,413 (GRCm39) |
missense |
|
|
R8098:Akap11
|
UTSW |
14 |
78,750,362 (GRCm39) |
missense |
|
|
R8226:Akap11
|
UTSW |
14 |
78,748,649 (GRCm39) |
missense |
|
|
R8269:Akap11
|
UTSW |
14 |
78,750,818 (GRCm39) |
missense |
|
|
R8304:Akap11
|
UTSW |
14 |
78,750,672 (GRCm39) |
missense |
|
|
R8343:Akap11
|
UTSW |
14 |
78,749,929 (GRCm39) |
missense |
|
|
R8389:Akap11
|
UTSW |
14 |
78,756,322 (GRCm39) |
missense |
|
|
R8824:Akap11
|
UTSW |
14 |
78,753,787 (GRCm39) |
missense |
|
|
R9034:Akap11
|
UTSW |
14 |
78,748,299 (GRCm39) |
missense |
|
|
R9189:Akap11
|
UTSW |
14 |
78,750,938 (GRCm39) |
missense |
|
|
R9259:Akap11
|
UTSW |
14 |
78,749,949 (GRCm39) |
missense |
|
|
R9275:Akap11
|
UTSW |
14 |
78,751,149 (GRCm39) |
missense |
|
|
R9434:Akap11
|
UTSW |
14 |
78,747,829 (GRCm39) |
missense |
|
|
R9500:Akap11
|
UTSW |
14 |
78,748,543 (GRCm39) |
missense |
|
|
|