Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
A |
T |
5: 146,182,533 (GRCm38) |
|
probably benign |
Het |
5730409E04Rik |
A |
G |
4: 126,611,949 (GRCm38) |
E90G |
probably damaging |
Het |
Abhd6 |
T |
A |
14: 8,039,849 (GRCm38) |
I27N |
probably damaging |
Het |
Bcl2l12 |
A |
G |
7: 44,996,893 (GRCm38) |
V31A |
possibly damaging |
Het |
Cep350 |
G |
A |
1: 155,862,595 (GRCm38) |
R2501W |
probably damaging |
Het |
Cnga3 |
A |
G |
1: 37,257,991 (GRCm38) |
|
probably null |
Het |
Crcp |
T |
C |
5: 130,059,858 (GRCm38) |
|
probably benign |
Het |
Creb5 |
G |
A |
6: 53,693,924 (GRCm38) |
S304N |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,401,492 (GRCm38) |
G219V |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,219,150 (GRCm38) |
D38G |
probably benign |
Het |
Fam171a1 |
A |
G |
2: 3,223,490 (GRCm38) |
I293V |
possibly damaging |
Het |
Fbxw10 |
T |
C |
11: 62,857,735 (GRCm38) |
V396A |
possibly damaging |
Het |
Gm10340 |
G |
A |
14: 3,140,482 (GRCm38) |
|
probably benign |
Het |
Gm20390 |
A |
G |
11: 93,955,574 (GRCm38) |
V16A |
probably damaging |
Het |
Grik3 |
A |
G |
4: 125,650,517 (GRCm38) |
T344A |
probably benign |
Het |
Itga7 |
T |
C |
10: 128,934,089 (GRCm38) |
F34S |
probably damaging |
Het |
Musk |
T |
C |
4: 58,353,936 (GRCm38) |
|
probably benign |
Het |
Neb |
G |
T |
2: 52,292,819 (GRCm38) |
N1038K |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,535,667 (GRCm38) |
Y1636H |
probably damaging |
Het |
Ngef |
G |
T |
1: 87,479,150 (GRCm38) |
T632K |
possibly damaging |
Het |
Nts |
A |
G |
10: 102,490,247 (GRCm38) |
|
probably benign |
Het |
Olfml2b |
A |
G |
1: 170,682,174 (GRCm38) |
D697G |
probably damaging |
Het |
Olfr1031 |
T |
C |
2: 85,992,032 (GRCm38) |
F72L |
probably benign |
Het |
Olfr1502 |
T |
A |
19: 13,862,299 (GRCm38) |
C169S |
probably damaging |
Het |
Olfr205 |
A |
T |
16: 59,328,725 (GRCm38) |
H261Q |
probably benign |
Het |
Otof |
T |
C |
5: 30,376,682 (GRCm38) |
R1428G |
probably damaging |
Het |
Pgghg |
T |
C |
7: 140,945,720 (GRCm38) |
S479P |
|
Het |
Rnaseh2b |
T |
A |
14: 62,346,615 (GRCm38) |
F37I |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,733,801 (GRCm38) |
I1031N |
probably damaging |
Het |
Rxfp2 |
A |
G |
5: 150,063,686 (GRCm38) |
E344G |
probably benign |
Het |
Scel |
A |
G |
14: 103,537,008 (GRCm38) |
R89G |
possibly damaging |
Het |
Sirt4 |
T |
C |
5: 115,482,996 (GRCm38) |
E39G |
probably benign |
Het |
Slc6a12 |
T |
A |
6: 121,354,375 (GRCm38) |
|
probably null |
Het |
Snapc3 |
C |
A |
4: 83,450,096 (GRCm38) |
H277N |
probably benign |
Het |
Susd2 |
A |
G |
10: 75,637,499 (GRCm38) |
|
probably null |
Het |
Tagap1 |
T |
C |
17: 6,956,427 (GRCm38) |
Q290R |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,279,198 (GRCm38) |
|
probably benign |
Het |
Tmem54 |
A |
T |
4: 129,108,280 (GRCm38) |
H40L |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 85,059,377 (GRCm38) |
S683P |
probably damaging |
Het |
Tnpo2 |
A |
G |
8: 85,050,502 (GRCm38) |
D547G |
probably benign |
Het |
Tpd52l2 |
G |
A |
2: 181,499,874 (GRCm38) |
V17M |
probably benign |
Het |
Trip11 |
T |
A |
12: 101,895,683 (GRCm38) |
T208S |
probably benign |
Het |
Ttc17 |
C |
A |
2: 94,364,376 (GRCm38) |
D551Y |
probably damaging |
Het |
Ttll12 |
A |
T |
15: 83,587,101 (GRCm38) |
W222R |
probably damaging |
Het |
Xkr8 |
A |
T |
4: 132,728,201 (GRCm38) |
I287N |
probably damaging |
Het |
Zdhhc2 |
G |
T |
8: 40,473,025 (GRCm38) |
G354C |
probably null |
Het |
Zfp13 |
C |
T |
17: 23,576,098 (GRCm38) |
A493T |
probably benign |
Het |
|
Other mutations in Akap6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Akap6
|
APN |
12 |
53,140,980 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL00505:Akap6
|
APN |
12 |
52,887,102 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL01134:Akap6
|
APN |
12 |
52,937,217 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01458:Akap6
|
APN |
12 |
52,886,818 (GRCm38) |
nonsense |
probably null |
|
IGL01589:Akap6
|
APN |
12 |
53,139,664 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01592:Akap6
|
APN |
12 |
53,142,142 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01738:Akap6
|
APN |
12 |
52,886,817 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01867:Akap6
|
APN |
12 |
52,888,008 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02025:Akap6
|
APN |
12 |
53,140,335 (GRCm38) |
missense |
probably benign |
|
IGL02041:Akap6
|
APN |
12 |
53,140,653 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02058:Akap6
|
APN |
12 |
53,140,555 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02194:Akap6
|
APN |
12 |
52,886,823 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02226:Akap6
|
APN |
12 |
53,010,467 (GRCm38) |
splice site |
probably benign |
|
IGL02323:Akap6
|
APN |
12 |
53,140,429 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02449:Akap6
|
APN |
12 |
53,140,188 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02546:Akap6
|
APN |
12 |
52,880,738 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02547:Akap6
|
APN |
12 |
53,140,696 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02588:Akap6
|
APN |
12 |
52,886,499 (GRCm38) |
nonsense |
probably null |
|
IGL02608:Akap6
|
APN |
12 |
53,010,606 (GRCm38) |
missense |
probably benign |
0.39 |
IGL02884:Akap6
|
APN |
12 |
52,886,622 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02945:Akap6
|
APN |
12 |
52,880,837 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03029:Akap6
|
APN |
12 |
52,886,412 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03129:Akap6
|
APN |
12 |
53,140,306 (GRCm38) |
missense |
probably damaging |
1.00 |
R0133:Akap6
|
UTSW |
12 |
53,139,471 (GRCm38) |
nonsense |
probably null |
|
R0166:Akap6
|
UTSW |
12 |
53,140,924 (GRCm38) |
missense |
probably benign |
0.04 |
R0189:Akap6
|
UTSW |
12 |
53,141,254 (GRCm38) |
missense |
probably benign |
0.41 |
R0532:Akap6
|
UTSW |
12 |
52,887,983 (GRCm38) |
missense |
probably benign |
0.00 |
R0632:Akap6
|
UTSW |
12 |
52,937,148 (GRCm38) |
missense |
probably damaging |
1.00 |
R0666:Akap6
|
UTSW |
12 |
52,911,808 (GRCm38) |
missense |
probably damaging |
1.00 |
R0723:Akap6
|
UTSW |
12 |
53,141,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R0763:Akap6
|
UTSW |
12 |
53,142,214 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0785:Akap6
|
UTSW |
12 |
52,886,622 (GRCm38) |
missense |
probably benign |
0.00 |
R0879:Akap6
|
UTSW |
12 |
52,880,799 (GRCm38) |
missense |
probably damaging |
1.00 |
R0880:Akap6
|
UTSW |
12 |
53,139,508 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1033:Akap6
|
UTSW |
12 |
53,069,222 (GRCm38) |
missense |
probably damaging |
0.97 |
R1055:Akap6
|
UTSW |
12 |
52,880,672 (GRCm38) |
nonsense |
probably null |
|
R1199:Akap6
|
UTSW |
12 |
52,796,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R1295:Akap6
|
UTSW |
12 |
52,887,029 (GRCm38) |
missense |
probably damaging |
1.00 |
R1389:Akap6
|
UTSW |
12 |
53,139,520 (GRCm38) |
missense |
probably benign |
0.15 |
R1471:Akap6
|
UTSW |
12 |
53,141,496 (GRCm38) |
missense |
probably benign |
0.05 |
R1483:Akap6
|
UTSW |
12 |
52,796,087 (GRCm38) |
missense |
probably damaging |
1.00 |
R1512:Akap6
|
UTSW |
12 |
52,937,154 (GRCm38) |
missense |
probably damaging |
1.00 |
R1648:Akap6
|
UTSW |
12 |
53,142,006 (GRCm38) |
nonsense |
probably null |
|
R1791:Akap6
|
UTSW |
12 |
53,069,125 (GRCm38) |
missense |
probably damaging |
1.00 |
R1888:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1888:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1891:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1899:Akap6
|
UTSW |
12 |
53,141,852 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1917:Akap6
|
UTSW |
12 |
53,104,612 (GRCm38) |
missense |
probably benign |
0.13 |
R1970:Akap6
|
UTSW |
12 |
52,938,475 (GRCm38) |
missense |
probably damaging |
0.96 |
R1987:Akap6
|
UTSW |
12 |
53,140,795 (GRCm38) |
missense |
possibly damaging |
0.78 |
R1988:Akap6
|
UTSW |
12 |
53,140,795 (GRCm38) |
missense |
possibly damaging |
0.78 |
R2153:Akap6
|
UTSW |
12 |
53,141,404 (GRCm38) |
missense |
probably benign |
0.03 |
R2567:Akap6
|
UTSW |
12 |
52,938,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R2568:Akap6
|
UTSW |
12 |
52,887,278 (GRCm38) |
missense |
possibly damaging |
0.77 |
R3025:Akap6
|
UTSW |
12 |
53,140,143 (GRCm38) |
missense |
probably benign |
|
R3051:Akap6
|
UTSW |
12 |
52,887,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R3195:Akap6
|
UTSW |
12 |
53,072,457 (GRCm38) |
nonsense |
probably null |
|
R3196:Akap6
|
UTSW |
12 |
53,072,457 (GRCm38) |
nonsense |
probably null |
|
R3426:Akap6
|
UTSW |
12 |
52,888,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R3783:Akap6
|
UTSW |
12 |
52,880,769 (GRCm38) |
missense |
probably damaging |
1.00 |
R3934:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3936:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3967:Akap6
|
UTSW |
12 |
53,141,453 (GRCm38) |
missense |
probably damaging |
1.00 |
R3970:Akap6
|
UTSW |
12 |
53,141,453 (GRCm38) |
missense |
probably damaging |
1.00 |
R4042:Akap6
|
UTSW |
12 |
53,139,379 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4095:Akap6
|
UTSW |
12 |
53,139,462 (GRCm38) |
missense |
probably damaging |
1.00 |
R4152:Akap6
|
UTSW |
12 |
53,140,407 (GRCm38) |
missense |
probably benign |
0.45 |
R4231:Akap6
|
UTSW |
12 |
53,141,038 (GRCm38) |
missense |
probably damaging |
1.00 |
R4232:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4233:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4234:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4235:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4236:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4475:Akap6
|
UTSW |
12 |
53,141,643 (GRCm38) |
missense |
probably benign |
0.00 |
R4513:Akap6
|
UTSW |
12 |
52,796,004 (GRCm38) |
missense |
probably benign |
0.03 |
R4686:Akap6
|
UTSW |
12 |
52,887,623 (GRCm38) |
frame shift |
probably null |
|
R4724:Akap6
|
UTSW |
12 |
52,795,885 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4782:Akap6
|
UTSW |
12 |
52,887,623 (GRCm38) |
frame shift |
probably null |
|
R4852:Akap6
|
UTSW |
12 |
53,104,675 (GRCm38) |
missense |
probably damaging |
1.00 |
R5024:Akap6
|
UTSW |
12 |
53,142,562 (GRCm38) |
missense |
probably benign |
0.01 |
R5116:Akap6
|
UTSW |
12 |
53,141,515 (GRCm38) |
missense |
probably benign |
0.01 |
R5164:Akap6
|
UTSW |
12 |
53,142,466 (GRCm38) |
missense |
probably benign |
|
R5225:Akap6
|
UTSW |
12 |
52,886,546 (GRCm38) |
missense |
probably damaging |
1.00 |
R5269:Akap6
|
UTSW |
12 |
53,139,843 (GRCm38) |
missense |
probably damaging |
0.99 |
R5352:Akap6
|
UTSW |
12 |
52,796,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R5496:Akap6
|
UTSW |
12 |
53,140,653 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5551:Akap6
|
UTSW |
12 |
52,795,964 (GRCm38) |
missense |
probably damaging |
1.00 |
R5997:Akap6
|
UTSW |
12 |
52,937,233 (GRCm38) |
critical splice donor site |
probably null |
|
R6137:Akap6
|
UTSW |
12 |
53,140,354 (GRCm38) |
missense |
probably damaging |
1.00 |
R6151:Akap6
|
UTSW |
12 |
53,025,792 (GRCm38) |
missense |
probably damaging |
1.00 |
R6169:Akap6
|
UTSW |
12 |
53,142,358 (GRCm38) |
missense |
probably benign |
|
R6307:Akap6
|
UTSW |
12 |
53,141,568 (GRCm38) |
missense |
possibly damaging |
0.85 |
R6351:Akap6
|
UTSW |
12 |
53,142,025 (GRCm38) |
missense |
probably damaging |
0.98 |
R6479:Akap6
|
UTSW |
12 |
53,141,169 (GRCm38) |
missense |
probably damaging |
1.00 |
R6502:Akap6
|
UTSW |
12 |
53,140,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R6760:Akap6
|
UTSW |
12 |
53,139,778 (GRCm38) |
missense |
probably damaging |
1.00 |
R6778:Akap6
|
UTSW |
12 |
53,025,816 (GRCm38) |
missense |
probably damaging |
1.00 |
R6837:Akap6
|
UTSW |
12 |
53,141,262 (GRCm38) |
missense |
probably damaging |
1.00 |
R6896:Akap6
|
UTSW |
12 |
52,887,494 (GRCm38) |
missense |
probably benign |
0.06 |
R6917:Akap6
|
UTSW |
12 |
53,069,168 (GRCm38) |
missense |
probably null |
0.97 |
R6983:Akap6
|
UTSW |
12 |
52,887,653 (GRCm38) |
missense |
probably damaging |
1.00 |
R7142:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7143:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7216:Akap6
|
UTSW |
12 |
53,140,457 (GRCm38) |
missense |
probably benign |
0.02 |
R7297:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7356:Akap6
|
UTSW |
12 |
52,911,864 (GRCm38) |
missense |
probably damaging |
1.00 |
R7378:Akap6
|
UTSW |
12 |
53,142,574 (GRCm38) |
missense |
probably benign |
0.00 |
R7382:Akap6
|
UTSW |
12 |
53,142,171 (GRCm38) |
missense |
probably benign |
0.00 |
R7498:Akap6
|
UTSW |
12 |
53,142,705 (GRCm38) |
nonsense |
probably null |
|
R7542:Akap6
|
UTSW |
12 |
53,069,234 (GRCm38) |
missense |
probably damaging |
1.00 |
R7589:Akap6
|
UTSW |
12 |
53,142,063 (GRCm38) |
nonsense |
probably null |
|
R7676:Akap6
|
UTSW |
12 |
52,886,850 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7814:Akap6
|
UTSW |
12 |
53,140,961 (GRCm38) |
missense |
probably benign |
0.28 |
R7971:Akap6
|
UTSW |
12 |
53,139,795 (GRCm38) |
missense |
probably damaging |
1.00 |
R8039:Akap6
|
UTSW |
12 |
53,141,676 (GRCm38) |
missense |
probably benign |
0.00 |
R8425:Akap6
|
UTSW |
12 |
52,886,621 (GRCm38) |
missense |
probably benign |
0.00 |
R8747:Akap6
|
UTSW |
12 |
53,142,216 (GRCm38) |
missense |
probably benign |
0.01 |
R8885:Akap6
|
UTSW |
12 |
53,141,536 (GRCm38) |
missense |
probably benign |
|
R8956:Akap6
|
UTSW |
12 |
53,140,344 (GRCm38) |
missense |
probably benign |
0.00 |
R8989:Akap6
|
UTSW |
12 |
52,880,871 (GRCm38) |
missense |
probably damaging |
1.00 |
R9014:Akap6
|
UTSW |
12 |
53,139,620 (GRCm38) |
missense |
possibly damaging |
0.60 |
R9031:Akap6
|
UTSW |
12 |
53,142,048 (GRCm38) |
missense |
probably benign |
0.36 |
R9216:Akap6
|
UTSW |
12 |
52,880,885 (GRCm38) |
missense |
probably benign |
0.05 |
R9220:Akap6
|
UTSW |
12 |
53,140,449 (GRCm38) |
missense |
possibly damaging |
0.49 |
R9243:Akap6
|
UTSW |
12 |
53,141,252 (GRCm38) |
missense |
probably benign |
0.08 |
R9286:Akap6
|
UTSW |
12 |
53,072,471 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9347:Akap6
|
UTSW |
12 |
53,069,111 (GRCm38) |
missense |
probably damaging |
1.00 |
R9475:Akap6
|
UTSW |
12 |
53,010,552 (GRCm38) |
missense |
probably damaging |
1.00 |
R9509:Akap6
|
UTSW |
12 |
53,142,238 (GRCm38) |
missense |
probably damaging |
0.99 |
R9523:Akap6
|
UTSW |
12 |
52,795,889 (GRCm38) |
missense |
probably benign |
0.02 |
R9600:Akap6
|
UTSW |
12 |
52,886,558 (GRCm38) |
missense |
probably benign |
0.04 |
R9612:Akap6
|
UTSW |
12 |
52,911,907 (GRCm38) |
missense |
probably damaging |
1.00 |
R9627:Akap6
|
UTSW |
12 |
53,104,630 (GRCm38) |
missense |
|
|
R9666:Akap6
|
UTSW |
12 |
53,141,535 (GRCm38) |
missense |
probably benign |
|
R9784:Akap6
|
UTSW |
12 |
53,141,070 (GRCm38) |
missense |
probably damaging |
1.00 |
X0062:Akap6
|
UTSW |
12 |
53,142,361 (GRCm38) |
missense |
probably benign |
0.43 |
Z1176:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
|