Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abra |
A |
T |
15: 41,732,681 (GRCm39) |
D128E |
probably benign |
Het |
Ankrd7 |
T |
A |
6: 18,868,020 (GRCm39) |
N95K |
probably damaging |
Het |
Brd9 |
T |
C |
13: 74,095,852 (GRCm39) |
F366L |
probably benign |
Het |
Brinp2 |
A |
G |
1: 158,095,508 (GRCm39) |
F118L |
probably damaging |
Het |
Ccdc138 |
T |
C |
10: 58,343,465 (GRCm39) |
|
probably null |
Het |
Celsr3 |
T |
C |
9: 108,722,922 (GRCm39) |
F189L |
probably damaging |
Het |
Cfap45 |
A |
G |
1: 172,357,479 (GRCm39) |
T36A |
probably benign |
Het |
Clec4a1 |
G |
T |
6: 122,909,150 (GRCm39) |
V173L |
possibly damaging |
Het |
Col6a5 |
G |
A |
9: 105,739,963 (GRCm39) |
T2552I |
probably benign |
Het |
Dcaf15 |
A |
G |
8: 84,824,598 (GRCm39) |
V533A |
probably damaging |
Het |
Dhrs9 |
A |
T |
2: 69,227,997 (GRCm39) |
I204F |
probably damaging |
Het |
Dock7 |
A |
G |
4: 98,892,153 (GRCm39) |
V811A |
possibly damaging |
Het |
Eef1akmt1 |
T |
C |
14: 57,787,905 (GRCm39) |
D151G |
probably damaging |
Het |
Eif4g3 |
G |
A |
4: 137,898,556 (GRCm39) |
R1109H |
probably damaging |
Het |
Gtpbp10 |
T |
C |
5: 5,592,395 (GRCm39) |
T191A |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,424,482 (GRCm39) |
N714S |
possibly damaging |
Het |
Lima1 |
T |
C |
15: 99,678,873 (GRCm39) |
T523A |
possibly damaging |
Het |
Lipe |
A |
G |
7: 25,097,127 (GRCm39) |
L272P |
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,741,532 (GRCm39) |
E554G |
possibly damaging |
Het |
Lrrc66 |
T |
C |
5: 73,765,580 (GRCm39) |
S488G |
possibly damaging |
Het |
Man2a1 |
C |
T |
17: 65,059,494 (GRCm39) |
A1127V |
probably benign |
Het |
Naglu |
A |
T |
11: 100,962,755 (GRCm39) |
I187F |
probably damaging |
Het |
Nt5c1b |
T |
A |
12: 10,440,054 (GRCm39) |
M548K |
probably damaging |
Het |
Or10ak14 |
A |
T |
4: 118,611,090 (GRCm39) |
I217N |
probably damaging |
Het |
Or6c38 |
A |
T |
10: 128,929,027 (GRCm39) |
V272E |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,080,485 (GRCm39) |
V409A |
probably benign |
Het |
Pde6b |
A |
T |
5: 108,573,097 (GRCm39) |
|
probably null |
Het |
Pkd2 |
A |
T |
5: 104,650,210 (GRCm39) |
K857* |
probably null |
Het |
Rfx4 |
T |
A |
10: 84,680,164 (GRCm39) |
S114T |
possibly damaging |
Het |
Sacs |
G |
A |
14: 61,429,147 (GRCm39) |
G402D |
probably damaging |
Het |
Slc22a5 |
C |
T |
11: 53,782,035 (GRCm39) |
E111K |
probably damaging |
Het |
Sptbn1 |
G |
A |
11: 30,169,597 (GRCm39) |
R44C |
probably damaging |
Het |
Taf1 |
T |
C |
X: 100,637,601 (GRCm39) |
V1696A |
possibly damaging |
Het |
Tm9sf3 |
C |
A |
19: 41,244,605 (GRCm39) |
G91C |
probably damaging |
Het |
Tmie |
T |
G |
9: 110,702,865 (GRCm39) |
E32A |
probably benign |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Tsga13 |
A |
T |
6: 30,879,298 (GRCm39) |
N138K |
probably benign |
Het |
Ttc7b |
G |
A |
12: 100,466,376 (GRCm39) |
R79C |
probably damaging |
Het |
Ugt1a10 |
A |
T |
1: 87,983,463 (GRCm39) |
D87V |
possibly damaging |
Het |
Vdac3-ps1 |
A |
T |
13: 18,206,177 (GRCm39) |
|
noncoding transcript |
Het |
Vmn1r29 |
A |
C |
6: 58,285,017 (GRCm39) |
I246L |
probably damaging |
Het |
Zbtb16 |
A |
G |
9: 48,743,382 (GRCm39) |
V310A |
probably benign |
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 |
IGL02031:Akap11
|
APN |
14 |
78,751,253 (GRCm39) |
missense |
possibly damaging |
0.50 |
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 |
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 |
|
|
|