Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,500,219 (GRCm39) |
F1324Y |
possibly damaging |
Het |
Abca8b |
A |
T |
11: 109,862,686 (GRCm39) |
|
probably null |
Het |
Abcc12 |
A |
G |
8: 87,244,033 (GRCm39) |
M1040T |
probably damaging |
Het |
Abtb1 |
A |
G |
6: 88,818,788 (GRCm39) |
F7L |
probably damaging |
Het |
Adcy9 |
T |
C |
16: 4,122,377 (GRCm39) |
T558A |
probably benign |
Het |
Adgrb1 |
A |
T |
15: 74,412,292 (GRCm39) |
T424S |
possibly damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ankrd31 |
C |
A |
13: 96,968,721 (GRCm39) |
P786Q |
probably benign |
Het |
Arhgap39 |
G |
T |
15: 76,621,424 (GRCm39) |
Y392* |
probably null |
Het |
Ash1l |
T |
C |
3: 88,892,326 (GRCm39) |
Y1402H |
probably damaging |
Het |
Carmil2 |
G |
T |
8: 106,419,195 (GRCm39) |
W749L |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,587,564 (GRCm39) |
Y867H |
unknown |
Het |
Cdh13 |
A |
G |
8: 119,232,437 (GRCm39) |
D47G |
probably benign |
Het |
Chst9 |
T |
A |
18: 15,585,910 (GRCm39) |
T218S |
probably benign |
Het |
Clec2i |
G |
A |
6: 128,870,587 (GRCm39) |
V67I |
probably benign |
Het |
Cox7a2 |
T |
A |
9: 79,667,028 (GRCm39) |
|
probably benign |
Het |
Cplx3 |
A |
G |
9: 57,519,030 (GRCm39) |
|
probably null |
Het |
Cpz |
A |
G |
5: 35,674,929 (GRCm39) |
C107R |
probably damaging |
Het |
Dapk1 |
T |
A |
13: 60,909,013 (GRCm39) |
C1209S |
possibly damaging |
Het |
Ddx41 |
T |
C |
13: 55,681,781 (GRCm39) |
M307V |
probably benign |
Het |
Defa24 |
A |
G |
8: 22,224,565 (GRCm39) |
I5V |
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,076,178 (GRCm39) |
N2K |
probably damaging |
Het |
Ebf2 |
A |
G |
14: 67,476,423 (GRCm39) |
D131G |
probably damaging |
Het |
Fam149b |
C |
T |
14: 20,427,985 (GRCm39) |
R424C |
probably damaging |
Het |
Fbln2 |
G |
A |
6: 91,240,335 (GRCm39) |
V714M |
probably damaging |
Het |
Fgf5 |
T |
C |
5: 98,423,385 (GRCm39) |
Y257H |
probably damaging |
Het |
Fmo3 |
A |
C |
1: 162,791,605 (GRCm39) |
V224G |
probably damaging |
Het |
Gigyf2 |
T |
C |
1: 87,338,450 (GRCm39) |
I394T |
possibly damaging |
Het |
Glmn |
T |
A |
5: 107,741,746 (GRCm39) |
|
probably null |
Het |
Greb1l |
T |
C |
18: 10,501,025 (GRCm39) |
I385T |
possibly damaging |
Het |
Grhl1 |
C |
A |
12: 24,658,449 (GRCm39) |
Q365K |
probably benign |
Het |
Gsdme |
G |
A |
6: 50,206,306 (GRCm39) |
T179M |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 89,018,962 (GRCm39) |
T349A |
probably benign |
Het |
Hax1 |
GTCATCATCATCATCATC |
GTCATCATCATCATCATCATC |
3: 89,905,247 (GRCm39) |
|
probably benign |
Het |
Il5ra |
G |
A |
6: 106,718,226 (GRCm39) |
T76I |
probably damaging |
Het |
Itga8 |
T |
C |
2: 12,196,525 (GRCm39) |
T631A |
probably benign |
Het |
Kcnh6 |
G |
A |
11: 105,909,978 (GRCm39) |
|
probably null |
Het |
Krt26 |
C |
T |
11: 99,224,415 (GRCm39) |
E368K |
probably benign |
Het |
Lhx9 |
T |
C |
1: 138,766,281 (GRCm39) |
D169G |
possibly damaging |
Het |
Lmod3 |
A |
G |
6: 97,224,234 (GRCm39) |
L529P |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,173,577 (GRCm39) |
T891A |
probably benign |
Het |
Or11g24 |
A |
G |
14: 50,661,984 (GRCm39) |
T3A |
probably benign |
Het |
Or1e1 |
T |
C |
11: 73,244,582 (GRCm39) |
M1T |
probably null |
Het |
Or1j13 |
T |
A |
2: 36,369,996 (GRCm39) |
I49F |
probably damaging |
Het |
Or1p4-ps1 |
T |
C |
11: 74,208,285 (GRCm39) |
*145R |
probably null |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Papln |
G |
C |
12: 83,821,454 (GRCm39) |
G262A |
probably damaging |
Het |
Pdcd1lg2 |
G |
A |
19: 29,423,435 (GRCm39) |
V160I |
probably benign |
Het |
Pde8b |
A |
G |
13: 95,164,105 (GRCm39) |
|
probably benign |
Het |
Ppme1 |
G |
A |
7: 100,004,002 (GRCm39) |
R68* |
probably null |
Het |
Prob1 |
T |
C |
18: 35,787,835 (GRCm39) |
S140G |
probably benign |
Het |
Ptprn2 |
A |
T |
12: 117,219,215 (GRCm39) |
N949Y |
probably damaging |
Het |
Qser1 |
C |
A |
2: 104,617,468 (GRCm39) |
D1115Y |
probably damaging |
Het |
Rad54l |
G |
T |
4: 115,954,666 (GRCm39) |
D674E |
probably damaging |
Het |
Ripk4 |
T |
A |
16: 97,545,387 (GRCm39) |
D420V |
probably damaging |
Het |
Ros1 |
G |
T |
10: 51,954,067 (GRCm39) |
S1857R |
probably benign |
Het |
Rsf1 |
A |
G |
7: 97,311,316 (GRCm39) |
E682G |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Homo |
Samd4 |
G |
A |
14: 47,325,329 (GRCm39) |
R515H |
probably damaging |
Het |
Selp |
T |
A |
1: 163,969,079 (GRCm39) |
W560R |
probably benign |
Het |
Shc3 |
A |
T |
13: 51,615,468 (GRCm39) |
L163Q |
probably damaging |
Het |
Shh |
G |
A |
5: 28,666,397 (GRCm39) |
A163V |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,427,937 (GRCm39) |
R113G |
possibly damaging |
Het |
Slc5a6 |
C |
A |
5: 31,206,168 (GRCm39) |
|
probably benign |
Het |
Smarcd2 |
A |
G |
11: 106,157,715 (GRCm39) |
|
probably null |
Het |
Sytl3 |
A |
G |
17: 6,995,664 (GRCm39) |
D148G |
probably damaging |
Het |
Tnks |
G |
T |
8: 35,385,615 (GRCm39) |
H297Q |
possibly damaging |
Het |
Trbv21 |
A |
T |
6: 41,179,568 (GRCm39) |
|
probably benign |
Het |
Ube3c |
T |
C |
5: 29,806,161 (GRCm39) |
F268L |
probably benign |
Het |
Ugt2b5 |
T |
C |
5: 87,287,541 (GRCm39) |
I209V |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,818,082 (GRCm39) |
N140S |
probably damaging |
Het |
Vcam1 |
T |
C |
3: 115,919,606 (GRCm39) |
Y226C |
probably damaging |
Het |
Vmn1r129 |
T |
A |
7: 21,094,534 (GRCm39) |
Q228L |
probably damaging |
Het |
Vmn1r209 |
T |
A |
13: 22,990,202 (GRCm39) |
N163Y |
probably benign |
Het |
Vmn1r85 |
A |
G |
7: 12,818,854 (GRCm39) |
S97P |
probably damaging |
Het |
Vmn2r30 |
C |
T |
7: 7,337,350 (GRCm39) |
M95I |
probably benign |
Het |
Vmn2r74 |
G |
A |
7: 85,601,098 (GRCm39) |
R847C |
probably damaging |
Het |
Wdr70 |
G |
A |
15: 7,916,830 (GRCm39) |
T529I |
possibly damaging |
Het |
Zfp532 |
T |
G |
18: 65,757,005 (GRCm39) |
S313A |
possibly damaging |
Het |
Zhx3 |
A |
T |
2: 160,621,463 (GRCm39) |
N901K |
probably benign |
Het |
|
Other mutations in A2m |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00494:A2m
|
APN |
6 |
121,621,108 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL00798:A2m
|
APN |
6 |
121,647,969 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:A2m
|
APN |
6 |
121,650,501 (GRCm39) |
nonsense |
probably null |
|
IGL01313:A2m
|
APN |
6 |
121,621,969 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01337:A2m
|
APN |
6 |
121,645,529 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01505:A2m
|
APN |
6 |
121,653,906 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01508:A2m
|
APN |
6 |
121,636,326 (GRCm39) |
nonsense |
probably null |
|
IGL01672:A2m
|
APN |
6 |
121,618,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:A2m
|
APN |
6 |
121,644,149 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02012:A2m
|
APN |
6 |
121,651,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:A2m
|
APN |
6 |
121,626,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:A2m
|
APN |
6 |
121,645,179 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02397:A2m
|
APN |
6 |
121,623,834 (GRCm39) |
missense |
probably benign |
|
IGL02407:A2m
|
APN |
6 |
121,645,575 (GRCm39) |
nonsense |
probably null |
|
IGL02408:A2m
|
APN |
6 |
121,621,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02469:A2m
|
APN |
6 |
121,645,074 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02527:A2m
|
APN |
6 |
121,638,392 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02612:A2m
|
APN |
6 |
121,654,971 (GRCm39) |
missense |
probably benign |
|
IGL02746:A2m
|
APN |
6 |
121,646,462 (GRCm39) |
splice site |
probably benign |
|
IGL02952:A2m
|
APN |
6 |
121,654,984 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03056:A2m
|
APN |
6 |
121,647,862 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03121:A2m
|
APN |
6 |
121,618,265 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03303:A2m
|
APN |
6 |
121,644,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:A2m
|
APN |
6 |
121,653,862 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03046:A2m
|
UTSW |
6 |
121,636,282 (GRCm39) |
missense |
probably benign |
0.04 |
R0040:A2m
|
UTSW |
6 |
121,622,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0049:A2m
|
UTSW |
6 |
121,615,267 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0049:A2m
|
UTSW |
6 |
121,615,267 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0109:A2m
|
UTSW |
6 |
121,636,262 (GRCm39) |
missense |
probably benign |
0.00 |
R0147:A2m
|
UTSW |
6 |
121,639,405 (GRCm39) |
critical splice donor site |
probably null |
|
R0148:A2m
|
UTSW |
6 |
121,639,405 (GRCm39) |
critical splice donor site |
probably null |
|
R0345:A2m
|
UTSW |
6 |
121,615,231 (GRCm39) |
splice site |
probably benign |
|
R0445:A2m
|
UTSW |
6 |
121,634,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:A2m
|
UTSW |
6 |
121,653,849 (GRCm39) |
splice site |
probably benign |
|
R1186:A2m
|
UTSW |
6 |
121,638,493 (GRCm39) |
missense |
probably benign |
0.00 |
R1436:A2m
|
UTSW |
6 |
121,621,172 (GRCm39) |
missense |
probably benign |
0.09 |
R1452:A2m
|
UTSW |
6 |
121,655,015 (GRCm39) |
missense |
probably benign |
0.01 |
R1636:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1637:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1638:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1698:A2m
|
UTSW |
6 |
121,622,117 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1776:A2m
|
UTSW |
6 |
121,618,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1918:A2m
|
UTSW |
6 |
121,621,895 (GRCm39) |
missense |
probably benign |
0.16 |
R1921:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1927:A2m
|
UTSW |
6 |
121,613,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R1934:A2m
|
UTSW |
6 |
121,626,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R1943:A2m
|
UTSW |
6 |
121,645,506 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1996:A2m
|
UTSW |
6 |
121,646,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R2039:A2m
|
UTSW |
6 |
121,636,908 (GRCm39) |
missense |
probably benign |
0.32 |
R2085:A2m
|
UTSW |
6 |
121,653,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:A2m
|
UTSW |
6 |
121,651,896 (GRCm39) |
nonsense |
probably null |
|
R2105:A2m
|
UTSW |
6 |
121,650,459 (GRCm39) |
missense |
probably benign |
0.04 |
R2107:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R2235:A2m
|
UTSW |
6 |
121,619,023 (GRCm39) |
missense |
probably benign |
0.21 |
R2292:A2m
|
UTSW |
6 |
121,650,518 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2350:A2m
|
UTSW |
6 |
121,655,047 (GRCm39) |
splice site |
probably benign |
|
R3001:A2m
|
UTSW |
6 |
121,638,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3002:A2m
|
UTSW |
6 |
121,638,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3023:A2m
|
UTSW |
6 |
121,646,531 (GRCm39) |
missense |
probably benign |
0.08 |
R3429:A2m
|
UTSW |
6 |
121,613,249 (GRCm39) |
start codon destroyed |
probably null |
|
R3437:A2m
|
UTSW |
6 |
121,616,253 (GRCm39) |
missense |
probably null |
0.03 |
R3909:A2m
|
UTSW |
6 |
121,625,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:A2m
|
UTSW |
6 |
121,650,434 (GRCm39) |
missense |
probably benign |
0.00 |
R4332:A2m
|
UTSW |
6 |
121,634,406 (GRCm39) |
missense |
probably benign |
0.01 |
R4584:A2m
|
UTSW |
6 |
121,634,365 (GRCm39) |
missense |
probably benign |
0.07 |
R4697:A2m
|
UTSW |
6 |
121,615,243 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R4710:A2m
|
UTSW |
6 |
121,618,262 (GRCm39) |
missense |
probably benign |
0.03 |
R4841:A2m
|
UTSW |
6 |
121,623,803 (GRCm39) |
missense |
probably benign |
0.06 |
R5206:A2m
|
UTSW |
6 |
121,651,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:A2m
|
UTSW |
6 |
121,653,909 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5230:A2m
|
UTSW |
6 |
121,651,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:A2m
|
UTSW |
6 |
121,615,375 (GRCm39) |
missense |
probably benign |
0.11 |
R5331:A2m
|
UTSW |
6 |
121,615,375 (GRCm39) |
missense |
probably benign |
0.11 |
R5377:A2m
|
UTSW |
6 |
121,622,212 (GRCm39) |
missense |
probably benign |
|
R5590:A2m
|
UTSW |
6 |
121,653,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:A2m
|
UTSW |
6 |
121,616,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:A2m
|
UTSW |
6 |
121,645,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:A2m
|
UTSW |
6 |
121,644,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:A2m
|
UTSW |
6 |
121,655,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:A2m
|
UTSW |
6 |
121,647,862 (GRCm39) |
missense |
probably benign |
0.38 |
R5996:A2m
|
UTSW |
6 |
121,636,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:A2m
|
UTSW |
6 |
121,615,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R6090:A2m
|
UTSW |
6 |
121,624,972 (GRCm39) |
missense |
probably benign |
0.45 |
R6241:A2m
|
UTSW |
6 |
121,623,788 (GRCm39) |
missense |
probably benign |
0.09 |
R6294:A2m
|
UTSW |
6 |
121,631,440 (GRCm39) |
missense |
probably benign |
|
R6492:A2m
|
UTSW |
6 |
121,631,464 (GRCm39) |
missense |
probably benign |
0.35 |
R6554:A2m
|
UTSW |
6 |
121,618,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:A2m
|
UTSW |
6 |
121,625,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R6742:A2m
|
UTSW |
6 |
121,654,995 (GRCm39) |
missense |
probably benign |
0.01 |
R6795:A2m
|
UTSW |
6 |
121,625,281 (GRCm39) |
splice site |
probably null |
|
R6843:A2m
|
UTSW |
6 |
121,615,360 (GRCm39) |
missense |
probably benign |
0.01 |
R7013:A2m
|
UTSW |
6 |
121,618,345 (GRCm39) |
missense |
probably null |
0.00 |
R7137:A2m
|
UTSW |
6 |
121,654,944 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7167:A2m
|
UTSW |
6 |
121,624,930 (GRCm39) |
missense |
probably benign |
|
R7294:A2m
|
UTSW |
6 |
121,650,541 (GRCm39) |
nonsense |
probably null |
|
R7452:A2m
|
UTSW |
6 |
121,618,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:A2m
|
UTSW |
6 |
121,652,177 (GRCm39) |
missense |
probably benign |
0.01 |
R7602:A2m
|
UTSW |
6 |
121,647,895 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7602:A2m
|
UTSW |
6 |
121,618,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:A2m
|
UTSW |
6 |
121,637,063 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7766:A2m
|
UTSW |
6 |
121,615,300 (GRCm39) |
missense |
probably benign |
0.08 |
R7921:A2m
|
UTSW |
6 |
121,654,954 (GRCm39) |
missense |
probably benign |
0.00 |
R8007:A2m
|
UTSW |
6 |
121,647,845 (GRCm39) |
intron |
probably benign |
|
R8291:A2m
|
UTSW |
6 |
121,655,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:A2m
|
UTSW |
6 |
121,634,369 (GRCm39) |
missense |
probably benign |
0.03 |
R8856:A2m
|
UTSW |
6 |
121,618,349 (GRCm39) |
missense |
probably benign |
0.00 |
R9023:A2m
|
UTSW |
6 |
121,636,917 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9154:A2m
|
UTSW |
6 |
121,645,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:A2m
|
UTSW |
6 |
121,647,957 (GRCm39) |
missense |
probably damaging |
0.98 |
R9255:A2m
|
UTSW |
6 |
121,626,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:A2m
|
UTSW |
6 |
121,637,865 (GRCm39) |
missense |
probably benign |
0.38 |
R9325:A2m
|
UTSW |
6 |
121,646,578 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9393:A2m
|
UTSW |
6 |
121,616,270 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9563:A2m
|
UTSW |
6 |
121,645,009 (GRCm39) |
missense |
probably damaging |
0.99 |
X0057:A2m
|
UTSW |
6 |
121,645,135 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:A2m
|
UTSW |
6 |
121,653,039 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:A2m
|
UTSW |
6 |
121,623,835 (GRCm39) |
missense |
probably benign |
|
|