Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
T |
C |
3: 59,659,513 (GRCm39) |
V322A |
probably benign |
Het |
Adam4 |
T |
C |
12: 81,466,348 (GRCm39) |
T758A |
probably benign |
Het |
B3galnt2 |
T |
C |
13: 14,169,814 (GRCm39) |
I424T |
probably damaging |
Het |
Cacna1g |
T |
C |
11: 94,321,312 (GRCm39) |
Y1316C |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,517,517 (GRCm39) |
S388P |
probably damaging |
Het |
Ccdc157 |
A |
G |
11: 4,098,765 (GRCm39) |
L247S |
probably damaging |
Het |
Cdh8 |
A |
G |
8: 99,757,498 (GRCm39) |
I700T |
possibly damaging |
Het |
Cdhr3 |
G |
T |
12: 33,098,985 (GRCm39) |
Y535* |
probably null |
Het |
Clasp2 |
T |
C |
9: 113,641,836 (GRCm39) |
|
probably null |
Het |
Col16a1 |
T |
A |
4: 129,947,151 (GRCm39) |
D165E |
probably damaging |
Het |
Col9a1 |
A |
T |
1: 24,234,436 (GRCm39) |
|
probably benign |
Het |
Cpa3 |
A |
T |
3: 20,296,307 (GRCm39) |
I10N |
possibly damaging |
Het |
Cstf3 |
T |
A |
2: 104,439,347 (GRCm39) |
|
probably benign |
Het |
Dnah3 |
C |
A |
7: 119,570,689 (GRCm39) |
|
probably null |
Het |
E2f6 |
T |
C |
12: 16,874,706 (GRCm39) |
C263R |
probably benign |
Het |
Eps8l2 |
C |
A |
7: 140,936,534 (GRCm39) |
Q288K |
possibly damaging |
Het |
Fam193a |
T |
A |
5: 34,578,199 (GRCm39) |
V231D |
probably damaging |
Het |
Gjd3 |
C |
T |
11: 102,691,029 (GRCm39) |
G325S |
probably benign |
Het |
Gpatch8 |
T |
A |
11: 102,429,111 (GRCm39) |
E39D |
unknown |
Het |
Gpr107 |
C |
T |
2: 31,042,375 (GRCm39) |
A2V |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,385,045 (GRCm39) |
H629N |
possibly damaging |
Het |
Kcna10 |
C |
A |
3: 107,101,545 (GRCm39) |
H59N |
probably benign |
Het |
Kitl |
A |
T |
10: 99,915,886 (GRCm39) |
E138D |
possibly damaging |
Het |
Kpna2 |
T |
C |
11: 106,881,571 (GRCm39) |
K353R |
probably damaging |
Het |
M1ap |
T |
A |
6: 82,958,798 (GRCm39) |
I143N |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,420,538 (GRCm39) |
S239P |
possibly damaging |
Het |
Med13l |
T |
A |
5: 118,880,105 (GRCm39) |
S1066T |
probably damaging |
Het |
Mettl23 |
G |
T |
11: 116,739,865 (GRCm39) |
E47* |
probably null |
Het |
Or52i2 |
T |
C |
7: 102,319,433 (GRCm39) |
F102S |
probably damaging |
Het |
Or5af1 |
C |
T |
11: 58,722,039 (GRCm39) |
Q20* |
probably null |
Het |
Proca1 |
T |
A |
11: 78,092,699 (GRCm39) |
D48E |
possibly damaging |
Het |
Rab34 |
T |
G |
11: 78,082,458 (GRCm39) |
V227G |
probably damaging |
Het |
Rab7 |
A |
T |
6: 87,990,632 (GRCm39) |
L14Q |
probably damaging |
Het |
Rasgef1c |
C |
T |
11: 49,847,934 (GRCm39) |
S23F |
probably benign |
Het |
Rit1 |
A |
G |
3: 88,633,457 (GRCm39) |
|
probably benign |
Het |
Scin |
T |
C |
12: 40,174,568 (GRCm39) |
T172A |
probably benign |
Het |
Scmh1 |
C |
A |
4: 120,325,575 (GRCm39) |
N97K |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,846,162 (GRCm39) |
E655G |
possibly damaging |
Het |
Slc22a15 |
A |
G |
3: 101,771,905 (GRCm39) |
V243A |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,789,042 (GRCm39) |
|
probably benign |
Het |
Smim7 |
C |
T |
8: 73,324,867 (GRCm39) |
G3R |
probably damaging |
Het |
Snurf |
C |
T |
7: 59,645,282 (GRCm39) |
R44H |
possibly damaging |
Het |
Snx13 |
G |
A |
12: 35,174,471 (GRCm39) |
A667T |
possibly damaging |
Het |
Sowaha |
T |
G |
11: 53,369,590 (GRCm39) |
H382P |
probably damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tmem259 |
G |
T |
10: 79,814,442 (GRCm39) |
|
probably null |
Het |
Topbp1 |
A |
G |
9: 103,211,277 (GRCm39) |
T945A |
probably damaging |
Het |
Tor1aip2 |
T |
C |
1: 155,939,307 (GRCm39) |
|
probably benign |
Het |
Ube3b |
T |
C |
5: 114,527,136 (GRCm39) |
V118A |
probably damaging |
Het |
Usp38 |
T |
C |
8: 81,711,717 (GRCm39) |
K773E |
probably damaging |
Het |
Wnk1 |
G |
A |
6: 119,925,852 (GRCm39) |
|
probably benign |
Het |
Zfp871 |
A |
G |
17: 32,994,842 (GRCm39) |
V111A |
possibly 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 |
IGL01862:Abca8b
|
APN |
11 |
109,837,997 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|