| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aff3 |
A |
T |
1: 38,249,430 (GRCm39) |
V559E |
possibly damaging |
Het |
| Alpk2 |
G |
T |
18: 65,437,937 (GRCm39) |
P1619Q |
possibly damaging |
Het |
| Amz1 |
C |
A |
5: 140,737,782 (GRCm39) |
F347L |
probably benign |
Het |
| Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
| Cdc16 |
A |
G |
8: 13,809,179 (GRCm39) |
Y48C |
probably damaging |
Het |
| Cfap91 |
C |
T |
16: 38,144,498 (GRCm39) |
|
probably null |
Het |
| Cul2 |
A |
G |
18: 3,431,029 (GRCm39) |
D538G |
probably benign |
Het |
| Cyp2j13 |
T |
A |
4: 95,956,558 (GRCm39) |
I184F |
probably damaging |
Het |
| Cyp4a12b |
A |
T |
4: 115,291,005 (GRCm39) |
R344S |
possibly damaging |
Het |
| Dis3 |
A |
G |
14: 99,332,783 (GRCm39) |
|
probably benign |
Het |
| Dnah17 |
T |
C |
11: 117,985,805 (GRCm39) |
H1424R |
probably damaging |
Het |
| Eef2 |
A |
G |
10: 81,015,540 (GRCm39) |
I354V |
probably benign |
Het |
| Elmo1 |
A |
G |
13: 20,526,596 (GRCm39) |
D382G |
probably damaging |
Het |
| Epas1 |
T |
A |
17: 87,131,131 (GRCm39) |
S304T |
probably benign |
Het |
| Fry |
A |
T |
5: 150,317,696 (GRCm39) |
D892V |
probably damaging |
Het |
| Gprc5a |
G |
T |
6: 135,060,823 (GRCm39) |
D355Y |
possibly damaging |
Het |
| Hsd17b7 |
G |
A |
1: 169,787,320 (GRCm39) |
T228I |
probably damaging |
Het |
| Ift74 |
T |
C |
4: 94,510,149 (GRCm39) |
V60A |
possibly damaging |
Het |
| Insrr |
A |
T |
3: 87,716,038 (GRCm39) |
I578F |
probably damaging |
Het |
| Izumo1 |
T |
C |
7: 45,273,613 (GRCm39) |
F122S |
probably damaging |
Het |
| Lss |
G |
A |
10: 76,372,173 (GRCm39) |
R176H |
probably damaging |
Het |
| Ltb |
T |
C |
17: 35,414,044 (GRCm39) |
S61P |
probably benign |
Het |
| Mybphl |
T |
C |
3: 108,283,034 (GRCm39) |
V274A |
probably benign |
Het |
| Myo9a |
T |
G |
9: 59,776,890 (GRCm39) |
L1096W |
probably damaging |
Het |
| Nlrc5 |
T |
A |
8: 95,248,102 (GRCm39) |
L1690H |
probably damaging |
Het |
| Nrap |
A |
T |
19: 56,340,148 (GRCm39) |
S790T |
probably benign |
Het |
| Nrcam |
A |
G |
12: 44,596,689 (GRCm39) |
D308G |
probably benign |
Het |
| Or10a3 |
G |
A |
7: 108,479,982 (GRCm39) |
T277M |
probably damaging |
Het |
| Or1j17 |
A |
G |
2: 36,578,274 (GRCm39) |
T87A |
probably benign |
Het |
| Pias2 |
A |
G |
18: 77,185,354 (GRCm39) |
D138G |
probably damaging |
Het |
| Prpf4b |
T |
C |
13: 35,084,439 (GRCm39) |
|
probably benign |
Het |
| Rapgef3 |
A |
G |
15: 97,647,397 (GRCm39) |
S788P |
probably damaging |
Het |
| Slc5a6 |
T |
C |
5: 31,194,821 (GRCm39) |
Y525C |
probably damaging |
Het |
| Snx32 |
T |
C |
19: 5,546,082 (GRCm39) |
|
probably benign |
Het |
| Tnfaip3 |
T |
C |
10: 18,880,735 (GRCm39) |
E444G |
probably benign |
Het |
| Ttc27 |
T |
C |
17: 75,165,028 (GRCm39) |
Y745H |
probably benign |
Het |
|
| Other mutations in Ank1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00972:Ank1
|
APN |
8 |
23,631,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01099:Ank1
|
APN |
8 |
23,598,265 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01586:Ank1
|
APN |
8 |
23,610,928 (GRCm39) |
missense |
probably benign |
|
|
IGL01866:Ank1
|
APN |
8 |
23,583,871 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL01977:Ank1
|
APN |
8 |
23,605,449 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02109:Ank1
|
APN |
8 |
23,586,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02182:Ank1
|
APN |
8 |
23,603,868 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02261:Ank1
|
APN |
8 |
23,578,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02283:Ank1
|
APN |
8 |
23,609,450 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02335:Ank1
|
APN |
8 |
23,625,654 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL02933:Ank1
|
APN |
8 |
23,612,881 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL03056:Ank1
|
APN |
8 |
23,631,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03089:Ank1
|
APN |
8 |
23,594,848 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03257:Ank1
|
APN |
8 |
23,612,914 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Hema6
|
UTSW |
8 |
23,587,653 (GRCm39) |
intron |
probably benign |
|
|
BB006:Ank1
|
UTSW |
8 |
23,606,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB016:Ank1
|
UTSW |
8 |
23,606,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0030:Ank1
|
UTSW |
8 |
23,583,909 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0077:Ank1
|
UTSW |
8 |
23,630,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0081:Ank1
|
UTSW |
8 |
23,606,258 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0147:Ank1
|
UTSW |
8 |
23,613,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0148:Ank1
|
UTSW |
8 |
23,613,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0200:Ank1
|
UTSW |
8 |
23,586,828 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0270:Ank1
|
UTSW |
8 |
23,578,941 (GRCm39) |
splice site |
probably benign |
|
|
R0309:Ank1
|
UTSW |
8 |
23,594,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0490:Ank1
|
UTSW |
8 |
23,597,890 (GRCm39) |
splice site |
probably benign |
|
|
R0675:Ank1
|
UTSW |
8 |
23,600,400 (GRCm39) |
splice site |
probably benign |
|
|
R0738:Ank1
|
UTSW |
8 |
23,604,130 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1051:Ank1
|
UTSW |
8 |
23,583,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1239:Ank1
|
UTSW |
8 |
23,586,171 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1265:Ank1
|
UTSW |
8 |
23,607,053 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R1367:Ank1
|
UTSW |
8 |
23,601,819 (GRCm39) |
splice site |
probably benign |
|
|
R1413:Ank1
|
UTSW |
8 |
23,609,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1539:Ank1
|
UTSW |
8 |
23,583,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1682:Ank1
|
UTSW |
8 |
23,599,343 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1732:Ank1
|
UTSW |
8 |
23,601,479 (GRCm39) |
splice site |
probably benign |
|
|
R1911:Ank1
|
UTSW |
8 |
23,589,666 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2087:Ank1
|
UTSW |
8 |
23,583,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2184:Ank1
|
UTSW |
8 |
23,599,270 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2302:Ank1
|
UTSW |
8 |
23,609,415 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2356:Ank1
|
UTSW |
8 |
23,575,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2495:Ank1
|
UTSW |
8 |
23,622,280 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3000:Ank1
|
UTSW |
8 |
23,609,447 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3113:Ank1
|
UTSW |
8 |
23,574,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3710:Ank1
|
UTSW |
8 |
23,577,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3768:Ank1
|
UTSW |
8 |
23,606,202 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R3771:Ank1
|
UTSW |
8 |
23,613,913 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4002:Ank1
|
UTSW |
8 |
23,629,479 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4478:Ank1
|
UTSW |
8 |
23,610,594 (GRCm39) |
missense |
probably benign |
0.30 |
|
R4755:Ank1
|
UTSW |
8 |
23,594,990 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4756:Ank1
|
UTSW |
8 |
23,612,893 (GRCm39) |
missense |
probably benign |
|
|
R4979:Ank1
|
UTSW |
8 |
23,622,212 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4989:Ank1
|
UTSW |
8 |
23,631,134 (GRCm39) |
intron |
probably benign |
|
|
R5011:Ank1
|
UTSW |
8 |
23,572,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5013:Ank1
|
UTSW |
8 |
23,572,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5031:Ank1
|
UTSW |
8 |
23,589,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5051:Ank1
|
UTSW |
8 |
23,609,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5059:Ank1
|
UTSW |
8 |
23,586,204 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5086:Ank1
|
UTSW |
8 |
23,578,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5108:Ank1
|
UTSW |
8 |
23,622,571 (GRCm39) |
missense |
probably benign |
0.11 |
|
R5235:Ank1
|
UTSW |
8 |
23,572,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5300:Ank1
|
UTSW |
8 |
23,622,517 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5408:Ank1
|
UTSW |
8 |
23,572,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5537:Ank1
|
UTSW |
8 |
23,604,892 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5728:Ank1
|
UTSW |
8 |
23,612,783 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R5746:Ank1
|
UTSW |
8 |
23,606,612 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5837:Ank1
|
UTSW |
8 |
23,594,806 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5907:Ank1
|
UTSW |
8 |
23,630,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5997:Ank1
|
UTSW |
8 |
23,589,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6005:Ank1
|
UTSW |
8 |
23,622,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6046:Ank1
|
UTSW |
8 |
23,606,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6103:Ank1
|
UTSW |
8 |
23,603,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6268:Ank1
|
UTSW |
8 |
23,599,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6430:Ank1
|
UTSW |
8 |
23,622,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6457:Ank1
|
UTSW |
8 |
23,577,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6626:Ank1
|
UTSW |
8 |
23,465,207 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6935:Ank1
|
UTSW |
8 |
23,598,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7091:Ank1
|
UTSW |
8 |
23,548,679 (GRCm39) |
missense |
probably benign |
|
|
R7162:Ank1
|
UTSW |
8 |
23,622,370 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7475:Ank1
|
UTSW |
8 |
23,622,646 (GRCm39) |
missense |
probably benign |
|
|
R7546:Ank1
|
UTSW |
8 |
23,555,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7678:Ank1
|
UTSW |
8 |
23,607,074 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7768:Ank1
|
UTSW |
8 |
23,588,013 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7779:Ank1
|
UTSW |
8 |
23,586,763 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R7864:Ank1
|
UTSW |
8 |
23,577,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7929:Ank1
|
UTSW |
8 |
23,606,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7982:Ank1
|
UTSW |
8 |
23,609,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7984:Ank1
|
UTSW |
8 |
23,578,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8273:Ank1
|
UTSW |
8 |
23,575,668 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8318:Ank1
|
UTSW |
8 |
23,605,567 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8349:Ank1
|
UTSW |
8 |
23,629,302 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8449:Ank1
|
UTSW |
8 |
23,629,302 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8459:Ank1
|
UTSW |
8 |
23,605,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8506:Ank1
|
UTSW |
8 |
23,586,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8889:Ank1
|
UTSW |
8 |
23,606,990 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8893:Ank1
|
UTSW |
8 |
23,598,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8924:Ank1
|
UTSW |
8 |
23,589,011 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8993:Ank1
|
UTSW |
8 |
23,588,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9016:Ank1
|
UTSW |
8 |
23,606,264 (GRCm39) |
missense |
probably null |
0.99 |
|
R9017:Ank1
|
UTSW |
8 |
23,606,264 (GRCm39) |
missense |
probably null |
0.99 |
|
R9018:Ank1
|
UTSW |
8 |
23,606,264 (GRCm39) |
missense |
probably null |
0.99 |
|
R9086:Ank1
|
UTSW |
8 |
23,589,636 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9154:Ank1
|
UTSW |
8 |
23,605,387 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9194:Ank1
|
UTSW |
8 |
23,606,255 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9347:Ank1
|
UTSW |
8 |
23,607,076 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R9419:Ank1
|
UTSW |
8 |
23,574,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9452:Ank1
|
UTSW |
8 |
23,622,429 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9568:Ank1
|
UTSW |
8 |
23,609,381 (GRCm39) |
missense |
probably benign |
|
|
R9689:Ank1
|
UTSW |
8 |
23,631,253 (GRCm39) |
missense |
probably benign |
|
|
R9747:Ank1
|
UTSW |
8 |
23,576,993 (GRCm39) |
missense |
probably damaging |
0.97 |
|
RF024:Ank1
|
UTSW |
8 |
23,609,360 (GRCm39) |
missense |
probably benign |
0.37 |
|
X0066:Ank1
|
UTSW |
8 |
23,631,600 (GRCm39) |
splice site |
probably null |
|
|
Incidental Mutation