Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c13 |
T |
A |
13: 4,247,794 (GRCm39) |
|
probably null |
Het |
Ano2 |
T |
C |
6: 125,990,240 (GRCm39) |
L787P |
probably damaging |
Het |
Arf4 |
A |
T |
14: 26,374,300 (GRCm39) |
I73F |
possibly damaging |
Het |
Atp6v1e1 |
A |
G |
6: 120,772,732 (GRCm39) |
|
probably null |
Het |
Ccdc9 |
A |
C |
7: 16,018,424 (GRCm39) |
M1R |
probably null |
Het |
Cep162 |
A |
G |
9: 87,093,864 (GRCm39) |
L838S |
probably benign |
Het |
Cfap251 |
T |
A |
5: 123,421,609 (GRCm39) |
I654N |
probably damaging |
Het |
Cfi |
T |
A |
3: 129,668,562 (GRCm39) |
|
probably benign |
Het |
Creb3l3 |
T |
C |
10: 80,927,110 (GRCm39) |
T107A |
probably benign |
Het |
Erlin2 |
T |
C |
8: 27,526,576 (GRCm39) |
L312P |
probably benign |
Het |
Etv1 |
T |
G |
12: 38,911,326 (GRCm39) |
M384R |
probably damaging |
Het |
Exph5 |
G |
T |
9: 53,285,265 (GRCm39) |
S782I |
possibly damaging |
Het |
Fsd1 |
C |
T |
17: 56,303,733 (GRCm39) |
S491F |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,823,326 (GRCm39) |
N6353S |
possibly damaging |
Het |
Gk5 |
T |
C |
9: 96,059,607 (GRCm39) |
|
probably null |
Het |
Gm11168 |
T |
G |
9: 3,005,128 (GRCm39) |
S202R |
possibly damaging |
Het |
Hdlbp |
T |
C |
1: 93,341,310 (GRCm39) |
D1016G |
possibly damaging |
Het |
Kpna4 |
A |
G |
3: 69,009,590 (GRCm39) |
|
probably benign |
Het |
Lrrn2 |
T |
C |
1: 132,866,096 (GRCm39) |
V387A |
possibly damaging |
Het |
Or4a76 |
T |
A |
2: 89,460,964 (GRCm39) |
R93* |
probably null |
Het |
Or5bw2 |
A |
G |
7: 6,573,854 (GRCm39) |
Y288C |
probably damaging |
Het |
Or6c33 |
T |
A |
10: 129,853,710 (GRCm39) |
M160K |
probably damaging |
Het |
Or8g23 |
A |
G |
9: 38,971,617 (GRCm39) |
L115S |
probably damaging |
Het |
Or8k37 |
T |
C |
2: 86,469,594 (GRCm39) |
T153A |
probably benign |
Het |
Plekhs1 |
A |
G |
19: 56,459,403 (GRCm39) |
Q51R |
probably benign |
Het |
Rab27b |
T |
A |
18: 70,118,380 (GRCm39) |
D179V |
possibly damaging |
Het |
Rprd2 |
C |
T |
3: 95,672,631 (GRCm39) |
R924H |
probably benign |
Het |
Shprh |
T |
C |
10: 11,045,998 (GRCm39) |
I905T |
probably damaging |
Het |
Trpm8 |
T |
C |
1: 88,271,009 (GRCm39) |
L433P |
probably damaging |
Het |
Urb1 |
A |
G |
16: 90,554,649 (GRCm39) |
L1861S |
possibly damaging |
Het |
Vmn2r124 |
C |
A |
17: 18,283,188 (GRCm39) |
T294K |
probably damaging |
Het |
Znrf3 |
A |
T |
11: 5,288,656 (GRCm39) |
C37* |
probably null |
Het |
|
Other mutations in Abca7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01063:Abca7
|
APN |
10 |
79,847,131 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01074:Abca7
|
APN |
10 |
79,849,726 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01313:Abca7
|
APN |
10 |
79,838,957 (GRCm39) |
splice site |
probably benign |
|
IGL01372:Abca7
|
APN |
10 |
79,842,089 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01468:Abca7
|
APN |
10 |
79,839,711 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01648:Abca7
|
APN |
10 |
79,846,914 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01796:Abca7
|
APN |
10 |
79,849,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01977:Abca7
|
APN |
10 |
79,841,986 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01982:Abca7
|
APN |
10 |
79,838,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Abca7
|
APN |
10 |
79,833,913 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02437:Abca7
|
APN |
10 |
79,844,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02721:Abca7
|
APN |
10 |
79,849,469 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02812:Abca7
|
APN |
10 |
79,841,881 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02823:Abca7
|
APN |
10 |
79,844,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02827:Abca7
|
APN |
10 |
79,845,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Abca7
|
APN |
10 |
79,837,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02952:Abca7
|
APN |
10 |
79,843,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Abca7
|
UTSW |
10 |
79,838,655 (GRCm39) |
splice site |
probably benign |
|
R0528:Abca7
|
UTSW |
10 |
79,838,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0541:Abca7
|
UTSW |
10 |
79,843,185 (GRCm39) |
missense |
probably benign |
0.01 |
R0584:Abca7
|
UTSW |
10 |
79,847,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Abca7
|
UTSW |
10 |
79,837,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Abca7
|
UTSW |
10 |
79,849,577 (GRCm39) |
nonsense |
probably null |
|
R1520:Abca7
|
UTSW |
10 |
79,844,664 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1536:Abca7
|
UTSW |
10 |
79,850,064 (GRCm39) |
missense |
probably benign |
0.39 |
R1619:Abca7
|
UTSW |
10 |
79,844,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Abca7
|
UTSW |
10 |
79,844,832 (GRCm39) |
missense |
probably benign |
|
R1752:Abca7
|
UTSW |
10 |
79,842,468 (GRCm39) |
missense |
probably benign |
0.17 |
R1762:Abca7
|
UTSW |
10 |
79,835,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Abca7
|
UTSW |
10 |
79,844,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Abca7
|
UTSW |
10 |
79,840,874 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1911:Abca7
|
UTSW |
10 |
79,842,468 (GRCm39) |
missense |
probably benign |
0.17 |
R2032:Abca7
|
UTSW |
10 |
79,844,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2188:Abca7
|
UTSW |
10 |
79,838,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Abca7
|
UTSW |
10 |
79,844,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R2974:Abca7
|
UTSW |
10 |
79,844,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R3055:Abca7
|
UTSW |
10 |
79,835,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4496:Abca7
|
UTSW |
10 |
79,838,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Abca7
|
UTSW |
10 |
79,842,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R4581:Abca7
|
UTSW |
10 |
79,842,402 (GRCm39) |
missense |
probably benign |
0.03 |
R4588:Abca7
|
UTSW |
10 |
79,833,701 (GRCm39) |
splice site |
probably null |
|
R4628:Abca7
|
UTSW |
10 |
79,851,022 (GRCm39) |
critical splice donor site |
probably null |
|
R4641:Abca7
|
UTSW |
10 |
79,841,615 (GRCm39) |
critical splice donor site |
probably null |
|
R4888:Abca7
|
UTSW |
10 |
79,838,562 (GRCm39) |
missense |
probably damaging |
0.97 |
R4911:Abca7
|
UTSW |
10 |
79,848,022 (GRCm39) |
critical splice donor site |
probably null |
|
R4979:Abca7
|
UTSW |
10 |
79,840,617 (GRCm39) |
nonsense |
probably null |
|
R4997:Abca7
|
UTSW |
10 |
79,843,154 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5147:Abca7
|
UTSW |
10 |
79,851,149 (GRCm39) |
missense |
probably benign |
0.02 |
R5176:Abca7
|
UTSW |
10 |
79,834,123 (GRCm39) |
missense |
probably benign |
0.35 |
R5190:Abca7
|
UTSW |
10 |
79,835,427 (GRCm39) |
critical splice donor site |
probably null |
|
R5358:Abca7
|
UTSW |
10 |
79,849,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R5409:Abca7
|
UTSW |
10 |
79,850,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5705:Abca7
|
UTSW |
10 |
79,851,276 (GRCm39) |
missense |
probably benign |
|
R6246:Abca7
|
UTSW |
10 |
79,850,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Abca7
|
UTSW |
10 |
79,838,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Abca7
|
UTSW |
10 |
79,844,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Abca7
|
UTSW |
10 |
79,833,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Abca7
|
UTSW |
10 |
79,841,992 (GRCm39) |
missense |
probably benign |
0.04 |
R6284:Abca7
|
UTSW |
10 |
79,840,244 (GRCm39) |
missense |
probably benign |
|
R6307:Abca7
|
UTSW |
10 |
79,843,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Abca7
|
UTSW |
10 |
79,842,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Abca7
|
UTSW |
10 |
79,850,984 (GRCm39) |
missense |
probably null |
0.69 |
R6460:Abca7
|
UTSW |
10 |
79,844,862 (GRCm39) |
missense |
probably benign |
0.04 |
R6560:Abca7
|
UTSW |
10 |
79,843,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R6565:Abca7
|
UTSW |
10 |
79,847,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Abca7
|
UTSW |
10 |
79,844,598 (GRCm39) |
missense |
probably damaging |
0.98 |
R6814:Abca7
|
UTSW |
10 |
79,838,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Abca7
|
UTSW |
10 |
79,845,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Abca7
|
UTSW |
10 |
79,850,822 (GRCm39) |
missense |
probably benign |
0.17 |
R7493:Abca7
|
UTSW |
10 |
79,837,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R7535:Abca7
|
UTSW |
10 |
79,837,463 (GRCm39) |
missense |
probably benign |
0.04 |
R7602:Abca7
|
UTSW |
10 |
79,833,846 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7607:Abca7
|
UTSW |
10 |
79,847,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Abca7
|
UTSW |
10 |
79,836,656 (GRCm39) |
missense |
probably benign |
0.00 |
R7821:Abca7
|
UTSW |
10 |
79,838,424 (GRCm39) |
small deletion |
probably benign |
|
R7863:Abca7
|
UTSW |
10 |
79,844,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Abca7
|
UTSW |
10 |
79,840,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Abca7
|
UTSW |
10 |
79,840,867 (GRCm39) |
missense |
probably benign |
0.00 |
R8114:Abca7
|
UTSW |
10 |
79,844,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Abca7
|
UTSW |
10 |
79,842,360 (GRCm39) |
missense |
probably benign |
0.05 |
R8439:Abca7
|
UTSW |
10 |
79,841,995 (GRCm39) |
missense |
probably benign |
0.03 |
R8456:Abca7
|
UTSW |
10 |
79,842,360 (GRCm39) |
missense |
probably benign |
0.05 |
R8830:Abca7
|
UTSW |
10 |
79,844,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Abca7
|
UTSW |
10 |
79,841,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9066:Abca7
|
UTSW |
10 |
79,849,188 (GRCm39) |
missense |
probably damaging |
0.98 |
R9116:Abca7
|
UTSW |
10 |
79,838,973 (GRCm39) |
missense |
|
|
R9128:Abca7
|
UTSW |
10 |
79,838,352 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9141:Abca7
|
UTSW |
10 |
79,851,264 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9184:Abca7
|
UTSW |
10 |
79,838,690 (GRCm39) |
missense |
probably damaging |
0.97 |
R9246:Abca7
|
UTSW |
10 |
79,838,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9320:Abca7
|
UTSW |
10 |
79,833,471 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9426:Abca7
|
UTSW |
10 |
79,851,264 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9490:Abca7
|
UTSW |
10 |
79,834,601 (GRCm39) |
missense |
probably benign |
|
R9561:Abca7
|
UTSW |
10 |
79,837,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9672:Abca7
|
UTSW |
10 |
79,838,563 (GRCm39) |
missense |
probably null |
1.00 |
Z1176:Abca7
|
UTSW |
10 |
79,842,393 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Abca7
|
UTSW |
10 |
79,835,266 (GRCm39) |
nonsense |
probably null |
|
|