Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alas1 |
G |
T |
9: 106,119,000 (GRCm39) |
|
probably null |
Het |
Apba1 |
A |
T |
19: 23,921,388 (GRCm39) |
Q737L |
probably benign |
Het |
Arvcf |
T |
A |
16: 18,220,327 (GRCm39) |
D564E |
probably damaging |
Het |
Bcl11b |
G |
T |
12: 107,883,094 (GRCm39) |
P335Q |
probably damaging |
Het |
Brd9 |
G |
A |
13: 74,092,918 (GRCm39) |
V302I |
probably benign |
Het |
Brinp3 |
C |
A |
1: 146,777,430 (GRCm39) |
H626N |
possibly damaging |
Het |
C1qc |
T |
C |
4: 136,617,637 (GRCm39) |
N153S |
probably benign |
Het |
Casp3 |
G |
A |
8: 47,087,251 (GRCm39) |
G66D |
probably damaging |
Het |
Coq7 |
T |
G |
7: 118,126,701 (GRCm39) |
|
probably null |
Het |
Dach1 |
C |
T |
14: 98,138,815 (GRCm39) |
V491M |
possibly damaging |
Het |
Dda1 |
A |
G |
8: 71,926,436 (GRCm39) |
T52A |
possibly damaging |
Het |
Entpd7 |
A |
G |
19: 43,692,640 (GRCm39) |
Y65C |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,991,535 (GRCm39) |
D350G |
probably damaging |
Het |
Foxn3 |
G |
T |
12: 99,162,700 (GRCm39) |
D400E |
probably damaging |
Het |
Gbp2 |
A |
G |
3: 142,343,210 (GRCm39) |
T576A |
probably benign |
Het |
Gm15446 |
T |
A |
5: 110,088,590 (GRCm39) |
|
probably null |
Het |
Gtf2a1 |
G |
T |
12: 91,542,411 (GRCm39) |
T57K |
possibly damaging |
Het |
Hps5 |
T |
C |
7: 46,425,218 (GRCm39) |
E494G |
probably benign |
Het |
Htr2a |
G |
A |
14: 74,943,789 (GRCm39) |
M456I |
probably benign |
Het |
Hydin |
A |
G |
8: 111,268,179 (GRCm39) |
N2886S |
probably damaging |
Het |
Ighv2-6-8 |
T |
C |
12: 113,759,773 (GRCm39) |
Y112C |
probably damaging |
Het |
Kcnf1 |
A |
T |
12: 17,225,480 (GRCm39) |
L247Q |
possibly damaging |
Het |
Kndc1 |
A |
G |
7: 139,516,938 (GRCm39) |
M1606V |
possibly damaging |
Het |
Krt27 |
T |
C |
11: 99,236,619 (GRCm39) |
T431A |
probably benign |
Het |
Lama4 |
A |
T |
10: 38,973,118 (GRCm39) |
I1562F |
probably damaging |
Het |
Lrig1 |
T |
C |
6: 94,590,559 (GRCm39) |
D487G |
probably benign |
Het |
Lrp1b |
G |
A |
2: 41,339,203 (GRCm39) |
T880I |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,024,641 (GRCm39) |
V663A |
possibly damaging |
Het |
Mapt |
T |
C |
11: 104,201,362 (GRCm39) |
|
probably null |
Het |
Mpdz |
A |
T |
4: 81,302,060 (GRCm39) |
V229D |
possibly damaging |
Het |
Or10am5 |
T |
A |
7: 6,518,252 (GRCm39) |
S59C |
possibly damaging |
Het |
Or6e1 |
T |
C |
14: 54,520,188 (GRCm39) |
T55A |
probably benign |
Het |
Or8s10 |
T |
C |
15: 98,335,563 (GRCm39) |
L71P |
probably damaging |
Het |
Parm1 |
T |
C |
5: 91,742,039 (GRCm39) |
S136P |
probably benign |
Het |
Pcdhgb2 |
T |
A |
18: 37,824,003 (GRCm39) |
S331R |
probably benign |
Het |
Pdxk |
T |
C |
10: 78,300,644 (GRCm39) |
H13R |
probably damaging |
Het |
Ppp1r12c |
T |
C |
7: 4,486,366 (GRCm39) |
E601G |
probably damaging |
Het |
Rell1 |
C |
A |
5: 64,126,013 (GRCm39) |
V22L |
probably benign |
Het |
Sema6c |
T |
A |
3: 95,080,505 (GRCm39) |
L901Q |
probably benign |
Het |
Sfswap |
A |
G |
5: 129,637,805 (GRCm39) |
S821G |
possibly damaging |
Het |
Slc22a23 |
A |
G |
13: 34,489,189 (GRCm39) |
L116P |
probably damaging |
Het |
Slit1 |
A |
T |
19: 41,596,925 (GRCm39) |
|
probably benign |
Het |
Spns1 |
T |
C |
7: 125,969,958 (GRCm39) |
T481A |
probably damaging |
Het |
Tmem104 |
T |
A |
11: 115,134,749 (GRCm39) |
Y427* |
probably null |
Het |
Tmem74 |
G |
A |
15: 43,730,678 (GRCm39) |
Q122* |
probably null |
Het |
Tnpo2 |
T |
A |
8: 85,765,048 (GRCm39) |
L10Q |
probably damaging |
Het |
Trav6-2 |
G |
T |
14: 52,905,272 (GRCm39) |
A98S |
probably benign |
Het |
Ttll5 |
A |
T |
12: 86,003,376 (GRCm39) |
R214* |
probably null |
Het |
Ube2b |
A |
C |
11: 51,888,654 (GRCm39) |
V39G |
possibly damaging |
Het |
Vmn1r185 |
A |
T |
7: 26,311,208 (GRCm39) |
V99E |
probably damaging |
Het |
Wnk1 |
G |
A |
6: 119,925,087 (GRCm39) |
T1459I |
probably damaging |
Het |
Zc3h7a |
T |
C |
16: 10,963,099 (GRCm39) |
K754R |
probably damaging |
Het |
Zfp605 |
A |
G |
5: 110,275,602 (GRCm39) |
K240R |
probably damaging |
Het |
Zfp61 |
A |
G |
7: 23,990,700 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Akap6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Akap6
|
APN |
12 |
53,187,763 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00505:Akap6
|
APN |
12 |
52,933,885 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01134:Akap6
|
APN |
12 |
52,984,000 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01458:Akap6
|
APN |
12 |
52,933,601 (GRCm39) |
nonsense |
probably null |
|
IGL01589:Akap6
|
APN |
12 |
53,186,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01592:Akap6
|
APN |
12 |
53,188,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01738:Akap6
|
APN |
12 |
52,933,600 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01867:Akap6
|
APN |
12 |
52,934,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02025:Akap6
|
APN |
12 |
53,187,118 (GRCm39) |
missense |
probably benign |
|
IGL02041:Akap6
|
APN |
12 |
53,187,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Akap6
|
APN |
12 |
53,187,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Akap6
|
APN |
12 |
52,933,606 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02226:Akap6
|
APN |
12 |
53,057,250 (GRCm39) |
splice site |
probably benign |
|
IGL02323:Akap6
|
APN |
12 |
53,187,212 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02449:Akap6
|
APN |
12 |
53,186,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Akap6
|
APN |
12 |
53,186,277 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02546:Akap6
|
APN |
12 |
52,927,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02547:Akap6
|
APN |
12 |
53,187,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02588:Akap6
|
APN |
12 |
52,933,282 (GRCm39) |
nonsense |
probably null |
|
IGL02608:Akap6
|
APN |
12 |
53,057,389 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02884:Akap6
|
APN |
12 |
52,933,405 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02945:Akap6
|
APN |
12 |
52,927,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03029:Akap6
|
APN |
12 |
52,933,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03129:Akap6
|
APN |
12 |
53,187,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Akap6
|
UTSW |
12 |
53,186,254 (GRCm39) |
nonsense |
probably null |
|
R0166:Akap6
|
UTSW |
12 |
53,187,707 (GRCm39) |
missense |
probably benign |
0.04 |
R0189:Akap6
|
UTSW |
12 |
53,188,037 (GRCm39) |
missense |
probably benign |
0.41 |
R0532:Akap6
|
UTSW |
12 |
52,934,766 (GRCm39) |
missense |
probably benign |
0.00 |
R0632:Akap6
|
UTSW |
12 |
52,983,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Akap6
|
UTSW |
12 |
52,958,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Akap6
|
UTSW |
12 |
53,188,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Akap6
|
UTSW |
12 |
53,188,997 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0785:Akap6
|
UTSW |
12 |
52,933,405 (GRCm39) |
missense |
probably benign |
0.00 |
R0879:Akap6
|
UTSW |
12 |
52,927,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:Akap6
|
UTSW |
12 |
53,186,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1033:Akap6
|
UTSW |
12 |
53,116,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R1055:Akap6
|
UTSW |
12 |
52,927,455 (GRCm39) |
nonsense |
probably null |
|
R1199:Akap6
|
UTSW |
12 |
52,842,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Akap6
|
UTSW |
12 |
52,933,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Akap6
|
UTSW |
12 |
53,186,303 (GRCm39) |
missense |
probably benign |
0.15 |
R1471:Akap6
|
UTSW |
12 |
53,188,279 (GRCm39) |
missense |
probably benign |
0.05 |
R1483:Akap6
|
UTSW |
12 |
52,842,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Akap6
|
UTSW |
12 |
52,983,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Akap6
|
UTSW |
12 |
53,188,789 (GRCm39) |
nonsense |
probably null |
|
R1791:Akap6
|
UTSW |
12 |
53,115,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1888:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1891:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1899:Akap6
|
UTSW |
12 |
53,188,635 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1917:Akap6
|
UTSW |
12 |
53,151,395 (GRCm39) |
missense |
probably benign |
0.13 |
R1970:Akap6
|
UTSW |
12 |
52,985,258 (GRCm39) |
missense |
probably damaging |
0.96 |
R1987:Akap6
|
UTSW |
12 |
53,187,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1988:Akap6
|
UTSW |
12 |
53,187,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2153:Akap6
|
UTSW |
12 |
53,188,187 (GRCm39) |
missense |
probably benign |
0.03 |
R2567:Akap6
|
UTSW |
12 |
52,985,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Akap6
|
UTSW |
12 |
52,934,061 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3025:Akap6
|
UTSW |
12 |
53,186,926 (GRCm39) |
missense |
probably benign |
|
R3051:Akap6
|
UTSW |
12 |
52,933,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Akap6
|
UTSW |
12 |
53,119,240 (GRCm39) |
nonsense |
probably null |
|
R3196:Akap6
|
UTSW |
12 |
53,119,240 (GRCm39) |
nonsense |
probably null |
|
R3426:Akap6
|
UTSW |
12 |
52,934,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R3783:Akap6
|
UTSW |
12 |
52,927,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R3934:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3936:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3967:Akap6
|
UTSW |
12 |
53,188,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Akap6
|
UTSW |
12 |
53,188,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Akap6
|
UTSW |
12 |
53,186,162 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4152:Akap6
|
UTSW |
12 |
53,187,190 (GRCm39) |
missense |
probably benign |
0.45 |
R4231:Akap6
|
UTSW |
12 |
53,187,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4236:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4475:Akap6
|
UTSW |
12 |
53,188,426 (GRCm39) |
missense |
probably benign |
0.00 |
R4513:Akap6
|
UTSW |
12 |
52,842,787 (GRCm39) |
missense |
probably benign |
0.03 |
R4686:Akap6
|
UTSW |
12 |
52,934,406 (GRCm39) |
frame shift |
probably null |
|
R4724:Akap6
|
UTSW |
12 |
52,842,668 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4782:Akap6
|
UTSW |
12 |
52,934,406 (GRCm39) |
frame shift |
probably null |
|
R4852:Akap6
|
UTSW |
12 |
53,151,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Akap6
|
UTSW |
12 |
53,189,345 (GRCm39) |
missense |
probably benign |
0.01 |
R5116:Akap6
|
UTSW |
12 |
53,188,298 (GRCm39) |
missense |
probably benign |
0.01 |
R5164:Akap6
|
UTSW |
12 |
53,189,249 (GRCm39) |
missense |
probably benign |
|
R5225:Akap6
|
UTSW |
12 |
52,933,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Akap6
|
UTSW |
12 |
53,186,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R5352:Akap6
|
UTSW |
12 |
52,842,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Akap6
|
UTSW |
12 |
53,187,436 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5551:Akap6
|
UTSW |
12 |
52,842,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:Akap6
|
UTSW |
12 |
52,984,016 (GRCm39) |
critical splice donor site |
probably null |
|
R6137:Akap6
|
UTSW |
12 |
53,187,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Akap6
|
UTSW |
12 |
53,072,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Akap6
|
UTSW |
12 |
53,189,141 (GRCm39) |
missense |
probably benign |
|
R6307:Akap6
|
UTSW |
12 |
53,188,351 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6351:Akap6
|
UTSW |
12 |
53,188,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R6479:Akap6
|
UTSW |
12 |
53,187,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Akap6
|
UTSW |
12 |
53,186,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Akap6
|
UTSW |
12 |
53,186,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6778:Akap6
|
UTSW |
12 |
53,072,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Akap6
|
UTSW |
12 |
53,188,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Akap6
|
UTSW |
12 |
52,934,277 (GRCm39) |
missense |
probably benign |
0.06 |
R6917:Akap6
|
UTSW |
12 |
53,115,951 (GRCm39) |
missense |
probably null |
0.97 |
R6983:Akap6
|
UTSW |
12 |
52,934,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R7142:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7143:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7216:Akap6
|
UTSW |
12 |
53,187,240 (GRCm39) |
missense |
probably benign |
0.02 |
R7297:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7356:Akap6
|
UTSW |
12 |
52,958,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Akap6
|
UTSW |
12 |
53,189,357 (GRCm39) |
missense |
probably benign |
0.00 |
R7382:Akap6
|
UTSW |
12 |
53,188,954 (GRCm39) |
missense |
probably benign |
0.00 |
R7498:Akap6
|
UTSW |
12 |
53,189,488 (GRCm39) |
nonsense |
probably null |
|
R7542:Akap6
|
UTSW |
12 |
53,116,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7589:Akap6
|
UTSW |
12 |
53,188,846 (GRCm39) |
nonsense |
probably null |
|
R7676:Akap6
|
UTSW |
12 |
52,933,633 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7814:Akap6
|
UTSW |
12 |
53,187,744 (GRCm39) |
missense |
probably benign |
0.28 |
R7971:Akap6
|
UTSW |
12 |
53,186,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Akap6
|
UTSW |
12 |
53,188,459 (GRCm39) |
missense |
probably benign |
0.00 |
R8425:Akap6
|
UTSW |
12 |
52,933,404 (GRCm39) |
missense |
probably benign |
0.00 |
R8747:Akap6
|
UTSW |
12 |
53,188,999 (GRCm39) |
missense |
probably benign |
0.01 |
R8885:Akap6
|
UTSW |
12 |
53,188,319 (GRCm39) |
missense |
probably benign |
|
R8956:Akap6
|
UTSW |
12 |
53,187,127 (GRCm39) |
missense |
probably benign |
0.00 |
R8989:Akap6
|
UTSW |
12 |
52,927,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Akap6
|
UTSW |
12 |
53,186,403 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9031:Akap6
|
UTSW |
12 |
53,188,831 (GRCm39) |
missense |
probably benign |
0.36 |
R9216:Akap6
|
UTSW |
12 |
52,927,668 (GRCm39) |
missense |
probably benign |
0.05 |
R9220:Akap6
|
UTSW |
12 |
53,187,232 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9243:Akap6
|
UTSW |
12 |
53,188,035 (GRCm39) |
missense |
probably benign |
0.08 |
R9286:Akap6
|
UTSW |
12 |
53,119,254 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9347:Akap6
|
UTSW |
12 |
53,115,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Akap6
|
UTSW |
12 |
53,057,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Akap6
|
UTSW |
12 |
53,189,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R9523:Akap6
|
UTSW |
12 |
52,842,672 (GRCm39) |
missense |
probably benign |
0.02 |
R9600:Akap6
|
UTSW |
12 |
52,933,341 (GRCm39) |
missense |
probably benign |
0.04 |
R9612:Akap6
|
UTSW |
12 |
52,958,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Akap6
|
UTSW |
12 |
53,151,413 (GRCm39) |
missense |
|
|
R9666:Akap6
|
UTSW |
12 |
53,188,318 (GRCm39) |
missense |
probably benign |
|
R9784:Akap6
|
UTSW |
12 |
53,187,853 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Akap6
|
UTSW |
12 |
53,189,144 (GRCm39) |
missense |
probably benign |
0.43 |
Z1176:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
|