Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
T |
G |
5: 4,001,705 (GRCm39) |
S94A |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,115,856 (GRCm39) |
N3425K |
probably damaging |
Het |
Anapc7 |
T |
A |
5: 122,578,182 (GRCm39) |
I389N |
probably benign |
Het |
Aqp7 |
G |
A |
4: 41,045,321 (GRCm39) |
R20* |
probably null |
Het |
Cacna1h |
C |
T |
17: 25,602,457 (GRCm39) |
G1524R |
probably damaging |
Het |
Cacng4 |
T |
C |
11: 107,685,196 (GRCm39) |
Y32C |
probably damaging |
Het |
Cep120 |
A |
C |
18: 53,847,839 (GRCm39) |
S673R |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,135,986 (GRCm39) |
E19G |
possibly damaging |
Het |
Cpxm2 |
C |
T |
7: 131,661,540 (GRCm39) |
V416I |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,874,424 (GRCm39) |
T427A |
probably benign |
Het |
Ecm1 |
A |
T |
3: 95,641,586 (GRCm39) |
D549E |
probably benign |
Het |
Efemp1 |
T |
A |
11: 28,871,428 (GRCm39) |
N342K |
probably damaging |
Het |
Erc2 |
T |
C |
14: 27,993,526 (GRCm39) |
|
probably benign |
Het |
Fhip2b |
C |
T |
14: 70,825,130 (GRCm39) |
R402H |
probably benign |
Het |
Galnt13 |
T |
C |
2: 54,747,926 (GRCm39) |
V269A |
probably damaging |
Het |
Gm6465 |
T |
G |
5: 11,899,020 (GRCm39) |
L171R |
probably damaging |
Het |
Gpatch1 |
A |
G |
7: 34,994,703 (GRCm39) |
V521A |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,103,914 (GRCm39) |
V1087E |
possibly damaging |
Het |
Ikzf2 |
A |
T |
1: 69,578,057 (GRCm39) |
V484D |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,190,360 (GRCm39) |
V953E |
probably damaging |
Het |
Iqce |
T |
C |
5: 140,685,480 (GRCm39) |
D15G |
possibly damaging |
Het |
Kif3a |
T |
A |
11: 53,461,368 (GRCm39) |
N4K |
possibly damaging |
Het |
Lrch4 |
A |
T |
5: 137,635,271 (GRCm39) |
I254F |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,129,516 (GRCm39) |
V1623D |
probably damaging |
Het |
Mapt |
T |
A |
11: 104,180,828 (GRCm39) |
|
probably benign |
Het |
Mast1 |
A |
T |
8: 85,639,875 (GRCm39) |
|
probably null |
Het |
Mcc |
G |
T |
18: 44,892,363 (GRCm39) |
Q84K |
probably benign |
Het |
Mgat4f |
G |
A |
1: 134,318,349 (GRCm39) |
V374I |
probably benign |
Het |
Mtfr2 |
G |
A |
10: 20,224,149 (GRCm39) |
V28M |
probably benign |
Het |
Myh8 |
T |
A |
11: 67,180,520 (GRCm39) |
Y585* |
probably null |
Het |
Napsa |
T |
C |
7: 44,231,917 (GRCm39) |
V202A |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,001,080 (GRCm39) |
K199R |
probably null |
Het |
Ntpcr |
C |
T |
8: 126,462,837 (GRCm39) |
A18V |
probably benign |
Het |
Or2aj4 |
A |
T |
16: 19,385,426 (GRCm39) |
M69K |
probably damaging |
Het |
Or2g25 |
G |
T |
17: 37,970,368 (GRCm39) |
N285K |
probably damaging |
Het |
Or56b35 |
T |
A |
7: 104,963,439 (GRCm39) |
I76N |
probably damaging |
Het |
Or5g9 |
G |
T |
2: 85,552,472 (GRCm39) |
C241F |
probably damaging |
Het |
Or8b9 |
A |
G |
9: 37,766,477 (GRCm39) |
D121G |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,935,573 (GRCm39) |
V299A |
probably benign |
Het |
Pcdhb7 |
T |
C |
18: 37,476,915 (GRCm39) |
S684P |
possibly damaging |
Het |
Phf19 |
A |
C |
2: 34,787,067 (GRCm39) |
|
probably null |
Het |
Pkd1l3 |
G |
A |
8: 110,357,908 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,429,134 (GRCm39) |
I2422T |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,326,258 (GRCm39) |
V64E |
possibly damaging |
Het |
Psme4 |
T |
A |
11: 30,762,038 (GRCm39) |
C459* |
probably null |
Het |
Ptk6 |
T |
C |
2: 180,841,433 (GRCm39) |
S159G |
probably benign |
Het |
Rhd |
T |
C |
4: 134,617,650 (GRCm39) |
I329T |
possibly damaging |
Het |
Scfd1 |
A |
G |
12: 51,492,494 (GRCm39) |
Y601C |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,110,148 (GRCm39) |
S1753P |
probably damaging |
Het |
Slc8a1 |
A |
C |
17: 81,749,630 (GRCm39) |
|
probably null |
Het |
Spg7 |
T |
A |
8: 123,803,669 (GRCm39) |
L233Q |
probably damaging |
Het |
Strip1 |
C |
A |
3: 107,529,198 (GRCm39) |
R353L |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,764,823 (GRCm39) |
N544D |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,204,469 (GRCm39) |
T4794A |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,266,095 (GRCm39) |
|
probably benign |
Het |
Vmn1r193 |
A |
T |
13: 22,403,984 (GRCm39) |
C3S |
probably benign |
Het |
Yju2b |
G |
T |
8: 84,987,163 (GRCm39) |
|
probably benign |
Het |
Zdhhc5 |
C |
T |
2: 84,520,836 (GRCm39) |
R447H |
probably benign |
Het |
Zfp202 |
A |
G |
9: 40,123,124 (GRCm39) |
I629V |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,023,441 (GRCm39) |
C990S |
probably damaging |
Het |
|
Other mutations in Abca8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00862:Abca8b
|
APN |
11 |
109,844,374 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00952:Abca8b
|
APN |
11 |
109,859,886 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01141:Abca8b
|
APN |
11 |
109,828,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Abca8b
|
APN |
11 |
109,867,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Abca8b
|
APN |
11 |
109,827,580 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01963:Abca8b
|
APN |
11 |
109,862,589 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02169:Abca8b
|
APN |
11 |
109,843,408 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02536:Abca8b
|
APN |
11 |
109,872,574 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02658:Abca8b
|
APN |
11 |
109,843,386 (GRCm39) |
missense |
probably benign |
|
IGL02828:Abca8b
|
APN |
11 |
109,871,720 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03118:Abca8b
|
APN |
11 |
109,838,007 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03302:Abca8b
|
APN |
11 |
109,858,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03325:Abca8b
|
APN |
11 |
109,844,422 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0057:Abca8b
|
UTSW |
11 |
109,832,385 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0131:Abca8b
|
UTSW |
11 |
109,833,115 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0226:Abca8b
|
UTSW |
11 |
109,847,844 (GRCm39) |
splice site |
probably null |
|
R0426:Abca8b
|
UTSW |
11 |
109,845,853 (GRCm39) |
splice site |
probably benign |
|
R0432:Abca8b
|
UTSW |
11 |
109,870,841 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0512:Abca8b
|
UTSW |
11 |
109,841,476 (GRCm39) |
missense |
probably benign |
0.32 |
R0589:Abca8b
|
UTSW |
11 |
109,833,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R0690:Abca8b
|
UTSW |
11 |
109,860,634 (GRCm39) |
splice site |
probably benign |
|
R1263:Abca8b
|
UTSW |
11 |
109,832,433 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1371:Abca8b
|
UTSW |
11 |
109,844,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R1497:Abca8b
|
UTSW |
11 |
109,864,647 (GRCm39) |
splice site |
probably benign |
|
R1502:Abca8b
|
UTSW |
11 |
109,865,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1517:Abca8b
|
UTSW |
11 |
109,862,640 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1543:Abca8b
|
UTSW |
11 |
109,865,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R1618:Abca8b
|
UTSW |
11 |
109,840,714 (GRCm39) |
splice site |
probably benign |
|
R1625:Abca8b
|
UTSW |
11 |
109,857,947 (GRCm39) |
missense |
probably benign |
0.11 |
R1753:Abca8b
|
UTSW |
11 |
109,864,542 (GRCm39) |
missense |
probably benign |
0.00 |
R1819:Abca8b
|
UTSW |
11 |
109,871,882 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1822:Abca8b
|
UTSW |
11 |
109,847,901 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1829:Abca8b
|
UTSW |
11 |
109,833,167 (GRCm39) |
missense |
probably damaging |
0.97 |
R1873:Abca8b
|
UTSW |
11 |
109,870,781 (GRCm39) |
missense |
probably benign |
0.01 |
R1899:Abca8b
|
UTSW |
11 |
109,828,744 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1908:Abca8b
|
UTSW |
11 |
109,847,924 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1962:Abca8b
|
UTSW |
11 |
109,870,724 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Abca8b
|
UTSW |
11 |
109,868,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Abca8b
|
UTSW |
11 |
109,847,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2092:Abca8b
|
UTSW |
11 |
109,857,534 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2100:Abca8b
|
UTSW |
11 |
109,828,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Abca8b
|
UTSW |
11 |
109,845,974 (GRCm39) |
missense |
probably benign |
0.03 |
R2871:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2871:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2872:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2872:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2873:Abca8b
|
UTSW |
11 |
109,846,002 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3711:Abca8b
|
UTSW |
11 |
109,837,081 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3937:Abca8b
|
UTSW |
11 |
109,865,393 (GRCm39) |
missense |
probably benign |
0.01 |
R4052:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4060:Abca8b
|
UTSW |
11 |
109,848,027 (GRCm39) |
missense |
probably benign |
0.04 |
R4207:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4208:Abca8b
|
UTSW |
11 |
109,872,551 (GRCm39) |
nonsense |
probably null |
|
R4354:Abca8b
|
UTSW |
11 |
109,862,518 (GRCm39) |
missense |
probably benign |
0.27 |
R4399:Abca8b
|
UTSW |
11 |
109,827,211 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4456:Abca8b
|
UTSW |
11 |
109,833,071 (GRCm39) |
missense |
probably benign |
0.27 |
R4509:Abca8b
|
UTSW |
11 |
109,857,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Abca8b
|
UTSW |
11 |
109,827,274 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4868:Abca8b
|
UTSW |
11 |
109,865,338 (GRCm39) |
missense |
probably benign |
0.05 |
R5002:Abca8b
|
UTSW |
11 |
109,852,623 (GRCm39) |
missense |
probably damaging |
0.96 |
R5007:Abca8b
|
UTSW |
11 |
109,827,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Abca8b
|
UTSW |
11 |
109,840,957 (GRCm39) |
missense |
probably damaging |
0.98 |
R5023:Abca8b
|
UTSW |
11 |
109,865,814 (GRCm39) |
critical splice donor site |
probably null |
|
R5091:Abca8b
|
UTSW |
11 |
109,827,210 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5098:Abca8b
|
UTSW |
11 |
109,847,944 (GRCm39) |
missense |
probably benign |
0.05 |
R5117:Abca8b
|
UTSW |
11 |
109,857,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Abca8b
|
UTSW |
11 |
109,867,420 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5302:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5487:Abca8b
|
UTSW |
11 |
109,844,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R5512:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5564:Abca8b
|
UTSW |
11 |
109,825,407 (GRCm39) |
missense |
probably benign |
0.08 |
R5610:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Abca8b
|
UTSW |
11 |
109,831,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Abca8b
|
UTSW |
11 |
109,844,445 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5827:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5848:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5854:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Abca8b
|
UTSW |
11 |
109,844,423 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5994:Abca8b
|
UTSW |
11 |
109,840,592 (GRCm39) |
splice site |
probably null |
|
R6035:Abca8b
|
UTSW |
11 |
109,862,686 (GRCm39) |
splice site |
probably null |
|
R6035:Abca8b
|
UTSW |
11 |
109,862,686 (GRCm39) |
splice site |
probably null |
|
R6050:Abca8b
|
UTSW |
11 |
109,868,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Abca8b
|
UTSW |
11 |
109,864,634 (GRCm39) |
missense |
probably benign |
0.03 |
R6223:Abca8b
|
UTSW |
11 |
109,868,672 (GRCm39) |
missense |
probably benign |
0.00 |
R6349:Abca8b
|
UTSW |
11 |
109,825,544 (GRCm39) |
splice site |
probably null |
|
R7002:Abca8b
|
UTSW |
11 |
109,832,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Abca8b
|
UTSW |
11 |
109,864,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7107:Abca8b
|
UTSW |
11 |
109,867,299 (GRCm39) |
missense |
probably damaging |
0.98 |
R7158:Abca8b
|
UTSW |
11 |
109,825,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Abca8b
|
UTSW |
11 |
109,836,654 (GRCm39) |
missense |
probably benign |
0.09 |
R7197:Abca8b
|
UTSW |
11 |
109,836,648 (GRCm39) |
nonsense |
probably null |
|
R7220:Abca8b
|
UTSW |
11 |
109,872,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Abca8b
|
UTSW |
11 |
109,829,275 (GRCm39) |
missense |
probably benign |
0.01 |
R7590:Abca8b
|
UTSW |
11 |
109,829,341 (GRCm39) |
missense |
probably damaging |
0.97 |
R7658:Abca8b
|
UTSW |
11 |
109,826,543 (GRCm39) |
missense |
probably benign |
0.00 |
R7739:Abca8b
|
UTSW |
11 |
109,865,417 (GRCm39) |
missense |
probably benign |
0.05 |
R7797:Abca8b
|
UTSW |
11 |
109,862,509 (GRCm39) |
critical splice donor site |
probably null |
|
R7934:Abca8b
|
UTSW |
11 |
109,865,865 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8074:Abca8b
|
UTSW |
11 |
109,829,320 (GRCm39) |
missense |
probably benign |
|
R8302:Abca8b
|
UTSW |
11 |
109,853,406 (GRCm39) |
critical splice donor site |
probably null |
|
R8341:Abca8b
|
UTSW |
11 |
109,845,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8486:Abca8b
|
UTSW |
11 |
109,857,937 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8748:Abca8b
|
UTSW |
11 |
109,836,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Abca8b
|
UTSW |
11 |
109,838,003 (GRCm39) |
missense |
probably benign |
0.00 |
R9002:Abca8b
|
UTSW |
11 |
109,843,456 (GRCm39) |
missense |
probably benign |
0.02 |
R9032:Abca8b
|
UTSW |
11 |
109,848,073 (GRCm39) |
missense |
probably benign |
0.04 |
R9099:Abca8b
|
UTSW |
11 |
109,871,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9124:Abca8b
|
UTSW |
11 |
109,828,593 (GRCm39) |
missense |
probably damaging |
0.97 |
R9178:Abca8b
|
UTSW |
11 |
109,840,937 (GRCm39) |
missense |
probably benign |
0.00 |
R9188:Abca8b
|
UTSW |
11 |
109,872,561 (GRCm39) |
nonsense |
probably null |
|
R9277:Abca8b
|
UTSW |
11 |
109,867,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R9340:Abca8b
|
UTSW |
11 |
109,840,939 (GRCm39) |
missense |
probably benign |
0.43 |
R9371:Abca8b
|
UTSW |
11 |
109,858,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Abca8b
|
UTSW |
11 |
109,870,711 (GRCm39) |
missense |
probably benign |
|
R9450:Abca8b
|
UTSW |
11 |
109,859,930 (GRCm39) |
missense |
probably damaging |
0.98 |
R9462:Abca8b
|
UTSW |
11 |
109,844,433 (GRCm39) |
missense |
|
|
R9712:Abca8b
|
UTSW |
11 |
109,833,163 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Abca8b
|
UTSW |
11 |
109,867,308 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Abca8b
|
UTSW |
11 |
109,865,470 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Abca8b
|
UTSW |
11 |
109,852,734 (GRCm39) |
missense |
possibly damaging |
0.52 |
|