Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahr |
T |
G |
12: 35,554,448 (GRCm39) |
D557A |
possibly damaging |
Het |
Alpi |
T |
A |
1: 87,027,431 (GRCm39) |
T312S |
probably damaging |
Het |
Cacna1b |
C |
A |
2: 24,525,107 (GRCm39) |
|
probably null |
Het |
Car5a |
C |
T |
8: 122,653,821 (GRCm39) |
|
probably null |
Het |
Cubn |
T |
C |
2: 13,450,883 (GRCm39) |
T841A |
possibly damaging |
Het |
Eml6 |
A |
T |
11: 29,788,451 (GRCm39) |
F545I |
possibly damaging |
Het |
Fam114a2 |
G |
A |
11: 57,400,220 (GRCm39) |
T156I |
probably damaging |
Het |
Fbxl21 |
C |
T |
13: 56,684,672 (GRCm39) |
R259* |
probably null |
Het |
Fhip1b |
T |
C |
7: 105,039,352 (GRCm39) |
N5S |
probably damaging |
Het |
Gm5117 |
C |
T |
8: 32,227,787 (GRCm39) |
|
noncoding transcript |
Het |
Hc |
T |
C |
2: 34,873,784 (GRCm39) |
Y1650C |
probably damaging |
Het |
Med12l |
C |
A |
3: 59,169,314 (GRCm39) |
T1568K |
probably damaging |
Het |
Mtrex |
T |
C |
13: 113,017,595 (GRCm39) |
K853E |
probably damaging |
Het |
Or2ag2b |
A |
G |
7: 106,417,739 (GRCm39) |
I150V |
probably benign |
Het |
Or5g27 |
T |
C |
2: 85,410,117 (GRCm39) |
F178S |
probably damaging |
Het |
Or6n1 |
G |
T |
1: 173,916,987 (GRCm39) |
C127F |
probably damaging |
Het |
Orm3 |
A |
G |
4: 63,277,563 (GRCm39) |
S184G |
probably benign |
Het |
Padi1 |
A |
G |
4: 140,546,170 (GRCm39) |
|
probably benign |
Het |
Rnf133 |
T |
C |
6: 23,648,988 (GRCm39) |
T357A |
probably benign |
Het |
Tmem17 |
A |
G |
11: 22,467,265 (GRCm39) |
S60G |
probably benign |
Het |
Ubqlnl |
G |
T |
7: 103,798,904 (GRCm39) |
Q198K |
probably benign |
Het |
Vmn1r69 |
A |
T |
7: 10,314,586 (GRCm39) |
Y48* |
probably null |
Het |
Zfp658 |
G |
A |
7: 43,222,134 (GRCm39) |
W136* |
probably null |
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 |
|
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 |
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 |
|
|
|