Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
A |
3: 121,930,651 (GRCm39) |
V1383M |
probably damaging |
Het |
Acer3 |
A |
G |
7: 97,910,832 (GRCm39) |
S77P |
probably damaging |
Het |
Adgrv1 |
G |
T |
13: 81,629,478 (GRCm39) |
T3640N |
possibly damaging |
Het |
Agmo |
T |
C |
12: 37,294,364 (GRCm39) |
L104P |
probably benign |
Het |
Alox12 |
C |
A |
11: 70,137,877 (GRCm39) |
G421V |
probably damaging |
Het |
Atad2 |
A |
G |
15: 57,989,532 (GRCm39) |
V182A |
probably damaging |
Het |
Bnc2 |
C |
T |
4: 84,194,338 (GRCm39) |
A929T |
possibly damaging |
Het |
Bola3 |
T |
C |
6: 83,335,154 (GRCm39) |
M83T |
probably damaging |
Het |
Brca2 |
T |
C |
5: 150,466,847 (GRCm39) |
F2204L |
possibly damaging |
Het |
Cachd1 |
T |
C |
4: 100,810,343 (GRCm39) |
V315A |
probably benign |
Het |
Ccdc154 |
C |
A |
17: 25,390,138 (GRCm39) |
N547K |
probably damaging |
Het |
Ccdc62 |
C |
A |
5: 124,092,470 (GRCm39) |
T485K |
probably benign |
Het |
Cdc40 |
G |
A |
10: 40,717,790 (GRCm39) |
T371I |
possibly damaging |
Het |
Cep112 |
T |
C |
11: 108,461,193 (GRCm39) |
F657L |
probably damaging |
Het |
Cirbp |
A |
G |
10: 80,005,931 (GRCm39) |
D62G |
probably damaging |
Het |
Cntf |
A |
C |
19: 12,741,664 (GRCm39) |
S65R |
probably benign |
Het |
Cxxc4 |
CGGC |
CGGCGGGGGC |
3: 133,945,912 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
G |
T |
7: 55,579,834 (GRCm39) |
G1229V |
probably benign |
Het |
Cyp4a30b |
A |
C |
4: 115,315,493 (GRCm39) |
N238T |
probably benign |
Het |
Dbx2 |
G |
A |
15: 95,552,517 (GRCm39) |
R43C |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,899,787 (GRCm39) |
I4350F |
possibly damaging |
Het |
Fbxw13 |
G |
T |
9: 109,023,833 (GRCm39) |
F70L |
possibly damaging |
Het |
Fhod3 |
A |
G |
18: 25,265,976 (GRCm39) |
T1555A |
probably damaging |
Het |
Fnbp4 |
A |
G |
2: 90,606,368 (GRCm39) |
M763V |
probably benign |
Het |
Gdf7 |
A |
G |
12: 8,348,905 (GRCm39) |
S131P |
unknown |
Het |
Gm9938 |
A |
T |
19: 23,701,941 (GRCm39) |
E93V |
unknown |
Het |
Golim4 |
A |
T |
3: 75,802,272 (GRCm39) |
M340K |
probably damaging |
Het |
Gphn |
A |
G |
12: 78,538,953 (GRCm39) |
S200G |
probably benign |
Het |
Hpse |
T |
C |
5: 100,859,248 (GRCm39) |
D99G |
probably benign |
Het |
Iqgap2 |
A |
T |
13: 95,794,392 (GRCm39) |
N1193K |
possibly damaging |
Het |
Jag2 |
A |
T |
12: 112,883,714 (GRCm39) |
C256S |
probably damaging |
Het |
Ldb3 |
T |
C |
14: 34,258,634 (GRCm39) |
Y657C |
probably damaging |
Het |
Lmtk2 |
T |
A |
5: 144,110,704 (GRCm39) |
Y475N |
probably damaging |
Het |
Mep1b |
A |
T |
18: 21,230,379 (GRCm39) |
K644* |
probably null |
Het |
Muc4 |
A |
C |
16: 32,576,889 (GRCm39) |
T60P |
possibly damaging |
Het |
Nckap5 |
G |
T |
1: 125,909,423 (GRCm39) |
Q1603K |
possibly damaging |
Het |
Npy6r |
C |
T |
18: 44,408,606 (GRCm39) |
T9I |
probably benign |
Het |
Nsd2 |
T |
C |
5: 34,039,885 (GRCm39) |
C846R |
probably damaging |
Het |
Oard1 |
A |
C |
17: 48,721,259 (GRCm39) |
K64Q |
probably benign |
Het |
Or4c103 |
T |
A |
2: 88,513,735 (GRCm39) |
I114F |
possibly damaging |
Het |
Or52e19b |
A |
T |
7: 103,032,357 (GRCm39) |
V284D |
probably damaging |
Het |
Or5w8 |
G |
T |
2: 87,687,545 (GRCm39) |
V9L |
probably benign |
Het |
Or6c208 |
A |
G |
10: 129,224,065 (GRCm39) |
T188A |
probably damaging |
Het |
Pkhd1l1 |
T |
G |
15: 44,368,650 (GRCm39) |
S823A |
probably benign |
Het |
Pla2r1 |
A |
G |
2: 60,259,053 (GRCm39) |
S1112P |
possibly damaging |
Het |
Plekho2 |
T |
C |
9: 65,465,963 (GRCm39) |
T142A |
probably damaging |
Het |
Prr35 |
A |
T |
17: 26,165,823 (GRCm39) |
V488E |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,102,105 (GRCm39) |
M726K |
possibly damaging |
Het |
Prrc2b |
A |
T |
2: 32,106,162 (GRCm39) |
K1514I |
possibly damaging |
Het |
Rin1 |
A |
T |
19: 5,104,947 (GRCm39) |
D669V |
probably damaging |
Het |
Setd1b |
C |
T |
5: 123,282,310 (GRCm39) |
A146V |
unknown |
Het |
Sigmar1 |
G |
A |
4: 41,741,234 (GRCm39) |
R7W |
probably damaging |
Het |
Slain1 |
C |
T |
14: 103,925,747 (GRCm39) |
T365I |
possibly damaging |
Het |
Slc38a2 |
G |
A |
15: 96,592,900 (GRCm39) |
T186I |
probably benign |
Het |
Tas2r130 |
A |
T |
6: 131,607,642 (GRCm39) |
V51E |
probably benign |
Het |
Tgfb1i1 |
A |
T |
7: 127,851,690 (GRCm39) |
H332L |
possibly damaging |
Het |
Trav7n-4 |
T |
C |
14: 53,328,846 (GRCm39) |
L15S |
probably damaging |
Het |
Ttc28 |
T |
C |
5: 111,372,041 (GRCm39) |
V861A |
probably benign |
Het |
Ttn |
A |
G |
2: 76,632,658 (GRCm39) |
I14132T |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,606,380 (GRCm39) |
E18143G |
probably damaging |
Het |
Vmn1r203 |
C |
T |
13: 22,708,720 (GRCm39) |
S167L |
possibly damaging |
Het |
Vmn2r108 |
A |
T |
17: 20,691,361 (GRCm39) |
H387Q |
probably benign |
Het |
Vps33a |
A |
T |
5: 123,709,538 (GRCm39) |
|
probably null |
Het |
Vps50 |
G |
A |
6: 3,504,926 (GRCm39) |
V31I |
probably benign |
Het |
Wdcp |
A |
G |
12: 4,901,439 (GRCm39) |
T432A |
probably benign |
Het |
Wdr36 |
T |
A |
18: 32,994,098 (GRCm39) |
Y645* |
probably null |
Het |
|
Other mutations in Abca14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00486:Abca14
|
APN |
7 |
119,846,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00800:Abca14
|
APN |
7 |
119,854,613 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00845:Abca14
|
APN |
7 |
119,823,174 (GRCm39) |
splice site |
probably benign |
|
IGL00897:Abca14
|
APN |
7 |
119,815,348 (GRCm39) |
splice site |
probably benign |
|
IGL01524:Abca14
|
APN |
7 |
119,852,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL01747:Abca14
|
APN |
7 |
119,877,310 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02214:Abca14
|
APN |
7 |
119,893,398 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02215:Abca14
|
APN |
7 |
119,852,612 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02253:Abca14
|
APN |
7 |
119,807,182 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02302:Abca14
|
APN |
7 |
119,917,968 (GRCm39) |
splice site |
probably benign |
|
IGL03391:Abca14
|
APN |
7 |
119,846,107 (GRCm39) |
missense |
probably damaging |
1.00 |
F6893:Abca14
|
UTSW |
7 |
119,924,261 (GRCm39) |
missense |
probably damaging |
0.98 |
R0109:Abca14
|
UTSW |
7 |
119,917,985 (GRCm39) |
nonsense |
probably null |
|
R0109:Abca14
|
UTSW |
7 |
119,917,985 (GRCm39) |
nonsense |
probably null |
|
R0265:Abca14
|
UTSW |
7 |
119,822,850 (GRCm39) |
missense |
probably benign |
0.03 |
R0326:Abca14
|
UTSW |
7 |
119,823,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Abca14
|
UTSW |
7 |
119,877,703 (GRCm39) |
missense |
probably benign |
0.03 |
R0418:Abca14
|
UTSW |
7 |
119,806,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Abca14
|
UTSW |
7 |
119,807,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R0574:Abca14
|
UTSW |
7 |
119,823,720 (GRCm39) |
missense |
probably damaging |
0.96 |
R0611:Abca14
|
UTSW |
7 |
119,851,479 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0783:Abca14
|
UTSW |
7 |
119,893,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Abca14
|
UTSW |
7 |
119,893,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0863:Abca14
|
UTSW |
7 |
119,815,453 (GRCm39) |
missense |
probably benign |
0.03 |
R1034:Abca14
|
UTSW |
7 |
119,815,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Abca14
|
UTSW |
7 |
119,924,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1072:Abca14
|
UTSW |
7 |
119,811,992 (GRCm39) |
missense |
probably benign |
|
R1244:Abca14
|
UTSW |
7 |
119,815,561 (GRCm39) |
missense |
probably benign |
0.06 |
R1255:Abca14
|
UTSW |
7 |
119,807,016 (GRCm39) |
missense |
probably damaging |
0.97 |
R1271:Abca14
|
UTSW |
7 |
119,924,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1325:Abca14
|
UTSW |
7 |
119,846,545 (GRCm39) |
missense |
probably benign |
0.32 |
R1457:Abca14
|
UTSW |
7 |
119,888,683 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Abca14
|
UTSW |
7 |
119,815,405 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1467:Abca14
|
UTSW |
7 |
119,815,405 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1494:Abca14
|
UTSW |
7 |
119,815,524 (GRCm39) |
missense |
probably benign |
0.00 |
R1551:Abca14
|
UTSW |
7 |
119,918,101 (GRCm39) |
missense |
probably benign |
0.10 |
R1607:Abca14
|
UTSW |
7 |
119,850,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Abca14
|
UTSW |
7 |
119,877,529 (GRCm39) |
missense |
probably benign |
0.04 |
R1856:Abca14
|
UTSW |
7 |
119,877,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Abca14
|
UTSW |
7 |
119,847,190 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1892:Abca14
|
UTSW |
7 |
119,815,561 (GRCm39) |
missense |
probably benign |
0.06 |
R1898:Abca14
|
UTSW |
7 |
119,850,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Abca14
|
UTSW |
7 |
119,924,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R2018:Abca14
|
UTSW |
7 |
119,815,408 (GRCm39) |
missense |
probably benign |
0.00 |
R2039:Abca14
|
UTSW |
7 |
119,911,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Abca14
|
UTSW |
7 |
119,826,741 (GRCm39) |
nonsense |
probably null |
|
R2202:Abca14
|
UTSW |
7 |
119,888,764 (GRCm39) |
missense |
probably benign |
0.17 |
R2205:Abca14
|
UTSW |
7 |
119,846,503 (GRCm39) |
missense |
probably damaging |
0.98 |
R2360:Abca14
|
UTSW |
7 |
119,850,431 (GRCm39) |
missense |
probably benign |
0.00 |
R2401:Abca14
|
UTSW |
7 |
119,882,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R2426:Abca14
|
UTSW |
7 |
119,882,446 (GRCm39) |
missense |
probably benign |
0.04 |
R3433:Abca14
|
UTSW |
7 |
119,893,455 (GRCm39) |
missense |
probably damaging |
0.97 |
R4598:Abca14
|
UTSW |
7 |
119,854,626 (GRCm39) |
missense |
probably benign |
0.11 |
R4599:Abca14
|
UTSW |
7 |
119,854,626 (GRCm39) |
missense |
probably benign |
0.11 |
R4700:Abca14
|
UTSW |
7 |
119,911,928 (GRCm39) |
critical splice donor site |
probably null |
|
R4751:Abca14
|
UTSW |
7 |
119,911,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4826:Abca14
|
UTSW |
7 |
119,815,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Abca14
|
UTSW |
7 |
119,815,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Abca14
|
UTSW |
7 |
119,846,203 (GRCm39) |
missense |
probably benign |
|
R4881:Abca14
|
UTSW |
7 |
119,877,472 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4895:Abca14
|
UTSW |
7 |
119,846,572 (GRCm39) |
critical splice donor site |
probably null |
|
R4928:Abca14
|
UTSW |
7 |
119,923,803 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4990:Abca14
|
UTSW |
7 |
119,911,388 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Abca14
|
UTSW |
7 |
119,911,505 (GRCm39) |
missense |
probably benign |
0.05 |
R5091:Abca14
|
UTSW |
7 |
119,851,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Abca14
|
UTSW |
7 |
119,852,652 (GRCm39) |
missense |
probably benign |
|
R5209:Abca14
|
UTSW |
7 |
119,832,130 (GRCm39) |
missense |
probably benign |
0.01 |
R5333:Abca14
|
UTSW |
7 |
119,888,769 (GRCm39) |
nonsense |
probably null |
|
R5424:Abca14
|
UTSW |
7 |
119,810,777 (GRCm39) |
missense |
probably benign |
0.01 |
R5488:Abca14
|
UTSW |
7 |
119,851,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R5489:Abca14
|
UTSW |
7 |
119,851,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R5716:Abca14
|
UTSW |
7 |
119,846,217 (GRCm39) |
critical splice donor site |
probably null |
|
R6450:Abca14
|
UTSW |
7 |
119,815,449 (GRCm39) |
missense |
probably benign |
0.17 |
R6477:Abca14
|
UTSW |
7 |
119,924,325 (GRCm39) |
missense |
probably benign |
0.44 |
R6652:Abca14
|
UTSW |
7 |
119,846,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R6782:Abca14
|
UTSW |
7 |
119,847,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6874:Abca14
|
UTSW |
7 |
119,851,428 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6965:Abca14
|
UTSW |
7 |
119,882,452 (GRCm39) |
nonsense |
probably null |
|
R7142:Abca14
|
UTSW |
7 |
119,850,406 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7146:Abca14
|
UTSW |
7 |
119,854,520 (GRCm39) |
missense |
probably benign |
0.15 |
R7202:Abca14
|
UTSW |
7 |
119,917,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7220:Abca14
|
UTSW |
7 |
119,826,667 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7241:Abca14
|
UTSW |
7 |
119,846,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7291:Abca14
|
UTSW |
7 |
119,888,832 (GRCm39) |
nonsense |
probably null |
|
R7296:Abca14
|
UTSW |
7 |
119,877,534 (GRCm39) |
missense |
probably benign |
|
R7298:Abca14
|
UTSW |
7 |
119,807,106 (GRCm39) |
missense |
probably benign |
0.00 |
R7315:Abca14
|
UTSW |
7 |
119,893,341 (GRCm39) |
missense |
probably benign |
0.00 |
R7776:Abca14
|
UTSW |
7 |
119,832,214 (GRCm39) |
critical splice donor site |
probably null |
|
R7820:Abca14
|
UTSW |
7 |
119,811,944 (GRCm39) |
missense |
probably benign |
0.42 |
R7873:Abca14
|
UTSW |
7 |
119,888,792 (GRCm39) |
missense |
probably benign |
0.17 |
R8215:Abca14
|
UTSW |
7 |
119,893,425 (GRCm39) |
missense |
probably benign |
|
R8332:Abca14
|
UTSW |
7 |
119,815,436 (GRCm39) |
missense |
probably benign |
|
R8419:Abca14
|
UTSW |
7 |
119,815,489 (GRCm39) |
missense |
probably benign |
0.08 |
R8444:Abca14
|
UTSW |
7 |
119,918,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R8818:Abca14
|
UTSW |
7 |
119,815,524 (GRCm39) |
missense |
probably benign |
0.00 |
R8834:Abca14
|
UTSW |
7 |
119,877,372 (GRCm39) |
missense |
probably benign |
0.02 |
R8889:Abca14
|
UTSW |
7 |
119,815,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Abca14
|
UTSW |
7 |
119,815,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8894:Abca14
|
UTSW |
7 |
119,847,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Abca14
|
UTSW |
7 |
119,815,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R8950:Abca14
|
UTSW |
7 |
119,823,595 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8950:Abca14
|
UTSW |
7 |
119,823,644 (GRCm39) |
nonsense |
probably null |
|
R9018:Abca14
|
UTSW |
7 |
119,918,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R9018:Abca14
|
UTSW |
7 |
119,888,763 (GRCm39) |
missense |
probably benign |
0.01 |
R9110:Abca14
|
UTSW |
7 |
119,831,615 (GRCm39) |
intron |
probably benign |
|
R9254:Abca14
|
UTSW |
7 |
119,807,202 (GRCm39) |
nonsense |
probably null |
|
R9376:Abca14
|
UTSW |
7 |
119,893,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R9378:Abca14
|
UTSW |
7 |
119,807,191 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9379:Abca14
|
UTSW |
7 |
119,807,202 (GRCm39) |
nonsense |
probably null |
|
R9388:Abca14
|
UTSW |
7 |
119,882,261 (GRCm39) |
missense |
probably benign |
0.01 |
R9445:Abca14
|
UTSW |
7 |
119,877,691 (GRCm39) |
missense |
probably benign |
0.05 |
R9522:Abca14
|
UTSW |
7 |
119,847,368 (GRCm39) |
missense |
probably null |
0.98 |
R9577:Abca14
|
UTSW |
7 |
119,810,768 (GRCm39) |
missense |
probably benign |
0.27 |
R9627:Abca14
|
UTSW |
7 |
119,854,530 (GRCm39) |
missense |
probably benign |
0.00 |
R9639:Abca14
|
UTSW |
7 |
119,893,345 (GRCm39) |
missense |
probably benign |
0.01 |
R9660:Abca14
|
UTSW |
7 |
119,851,478 (GRCm39) |
missense |
probably benign |
0.00 |
R9696:Abca14
|
UTSW |
7 |
119,888,734 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9709:Abca14
|
UTSW |
7 |
119,888,739 (GRCm39) |
nonsense |
probably null |
|
R9780:Abca14
|
UTSW |
7 |
119,911,447 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Abca14
|
UTSW |
7 |
119,815,358 (GRCm39) |
missense |
probably benign |
0.14 |
Z1176:Abca14
|
UTSW |
7 |
119,846,146 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abca14
|
UTSW |
7 |
119,917,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|