Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110070M22Rik |
A |
T |
13: 119,624,721 (GRCm39) |
D8E |
unknown |
Het |
Abca5 |
T |
A |
11: 110,192,371 (GRCm39) |
I714L |
probably benign |
Het |
Abce1 |
T |
A |
8: 80,426,043 (GRCm39) |
S245C |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,325,105 (GRCm39) |
D310E |
probably benign |
Het |
Adhfe1 |
T |
A |
1: 9,637,030 (GRCm39) |
I394N |
probably benign |
Het |
Apob |
A |
T |
12: 8,059,591 (GRCm39) |
D2691V |
probably benign |
Het |
Arhgap18 |
A |
G |
10: 26,748,734 (GRCm39) |
T340A |
possibly damaging |
Het |
Arsb |
A |
T |
13: 94,077,124 (GRCm39) |
Q497L |
probably benign |
Het |
Asic5 |
T |
C |
3: 81,919,318 (GRCm39) |
I354T |
probably benign |
Het |
Atp6v0a1 |
T |
C |
11: 100,924,868 (GRCm39) |
C318R |
probably damaging |
Het |
Cftr |
T |
C |
6: 18,226,137 (GRCm39) |
Y362H |
probably benign |
Het |
Crip3 |
T |
C |
17: 46,741,716 (GRCm39) |
Y113H |
probably benign |
Het |
Dcaf4 |
AT |
A |
12: 83,584,571 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
A |
1: 80,481,573 (GRCm39) |
I475F |
|
Het |
Dqx1 |
T |
A |
6: 83,043,436 (GRCm39) |
Y674N |
probably damaging |
Het |
Dync2h1 |
G |
T |
9: 7,113,214 (GRCm39) |
Q2437K |
possibly damaging |
Het |
Ednra |
A |
T |
8: 78,391,734 (GRCm39) |
C385* |
probably null |
Het |
Fam216a |
G |
A |
5: 122,507,623 (GRCm39) |
T68I |
probably benign |
Het |
Fbxw22 |
A |
G |
9: 109,233,291 (GRCm39) |
L14P |
probably damaging |
Het |
Fem1al |
G |
T |
11: 29,775,009 (GRCm39) |
H149Q |
probably damaging |
Het |
Fkbp10 |
A |
G |
11: 100,312,129 (GRCm39) |
I230V |
possibly damaging |
Het |
Ggn |
C |
A |
7: 28,872,423 (GRCm39) |
A637E |
probably damaging |
Het |
Hcrtr2 |
T |
C |
9: 76,137,942 (GRCm39) |
D391G |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,117,992 (GRCm39) |
V817D |
possibly damaging |
Het |
Il1f10 |
G |
A |
2: 24,183,682 (GRCm39) |
W120* |
probably null |
Het |
Irf5 |
C |
A |
6: 29,535,876 (GRCm39) |
R297S |
probably damaging |
Het |
Jak2 |
A |
G |
19: 29,263,798 (GRCm39) |
T438A |
possibly damaging |
Het |
Jsrp1 |
T |
C |
10: 80,644,410 (GRCm39) |
D332G |
possibly damaging |
Het |
Kank4 |
A |
T |
4: 98,659,582 (GRCm39) |
V832D |
probably damaging |
Het |
Kcnip3 |
C |
T |
2: 127,352,856 (GRCm39) |
S25N |
probably benign |
Het |
Klk1b16 |
C |
T |
7: 43,788,910 (GRCm39) |
H48Y |
probably benign |
Het |
Klrh1 |
C |
A |
6: 129,743,673 (GRCm39) |
A204S |
possibly damaging |
Het |
Krtap5-4 |
G |
A |
7: 141,857,609 (GRCm39) |
C93Y |
unknown |
Het |
Lacc1 |
T |
A |
14: 77,267,096 (GRCm39) |
Q389L |
probably benign |
Het |
Lin9 |
C |
A |
1: 180,515,661 (GRCm39) |
T477K |
probably benign |
Het |
Lpar2 |
A |
T |
8: 70,276,256 (GRCm39) |
N15I |
probably damaging |
Het |
Ltbp2 |
C |
A |
12: 84,915,459 (GRCm39) |
C200F |
probably damaging |
Het |
Mall |
G |
T |
2: 127,550,793 (GRCm39) |
H122Q |
probably benign |
Het |
Mast3 |
T |
C |
8: 71,232,117 (GRCm39) |
I1287V |
probably benign |
Het |
Mindy4 |
T |
C |
6: 55,255,220 (GRCm39) |
I566T |
probably benign |
Het |
Mme |
T |
C |
3: 63,235,638 (GRCm39) |
Y195H |
probably damaging |
Het |
Mpzl1 |
T |
C |
1: 165,432,267 (GRCm39) |
T173A |
probably benign |
Het |
Mri1 |
G |
T |
8: 84,977,708 (GRCm39) |
T209N |
|
Het |
Myo1e |
A |
G |
9: 70,245,083 (GRCm39) |
I394V |
probably damaging |
Het |
Nat14 |
T |
C |
7: 4,927,329 (GRCm39) |
V167A |
possibly damaging |
Het |
Nfasc |
A |
G |
1: 132,498,247 (GRCm39) |
Y1212H |
unknown |
Het |
Nsun7 |
T |
A |
5: 66,452,764 (GRCm39) |
L493Q |
probably damaging |
Het |
Obsl1 |
A |
T |
1: 75,464,394 (GRCm39) |
S1637R |
probably benign |
Het |
Ocstamp |
A |
T |
2: 165,239,957 (GRCm39) |
Y76* |
probably null |
Het |
Or5b95 |
A |
C |
19: 12,658,198 (GRCm39) |
H242P |
probably damaging |
Het |
Or6c2b |
T |
A |
10: 128,947,416 (GRCm39) |
K293* |
probably null |
Het |
Or8b52 |
G |
A |
9: 38,576,565 (GRCm39) |
R192C |
probably benign |
Het |
Otog |
T |
A |
7: 45,947,990 (GRCm39) |
C145* |
probably null |
Het |
Padi6 |
T |
A |
4: 140,468,869 (GRCm39) |
K5* |
probably null |
Het |
Pcdha5 |
T |
A |
18: 37,094,615 (GRCm39) |
S375T |
probably benign |
Het |
Pde10a |
C |
T |
17: 9,159,994 (GRCm39) |
P140S |
probably benign |
Het |
Pgbd1 |
C |
G |
13: 21,607,300 (GRCm39) |
C298S |
possibly damaging |
Het |
Plch2 |
C |
T |
4: 155,071,448 (GRCm39) |
G977D |
probably benign |
Het |
Pou2f3 |
T |
C |
9: 43,040,188 (GRCm39) |
T367A |
probably damaging |
Het |
Ppm1j |
T |
A |
3: 104,692,276 (GRCm39) |
Y352N |
probably damaging |
Het |
Prkag2 |
T |
C |
5: 25,226,967 (GRCm39) |
T97A |
probably benign |
Het |
Rpl36a-ps1 |
T |
A |
14: 99,231,660 (GRCm39) |
Y26F |
probably benign |
Het |
Sctr |
A |
T |
1: 119,991,001 (GRCm39) |
N445Y |
possibly damaging |
Het |
Serping1 |
C |
T |
2: 84,603,835 (GRCm39) |
V69I |
probably benign |
Het |
Slc8a2 |
T |
A |
7: 15,878,963 (GRCm39) |
L483Q |
probably benign |
Het |
Spag17 |
T |
C |
3: 99,846,586 (GRCm39) |
F37L |
probably benign |
Het |
Tcp11 |
T |
C |
17: 28,285,995 (GRCm39) |
Q540R |
probably benign |
Het |
Thnsl1 |
G |
T |
2: 21,217,141 (GRCm39) |
R298S |
possibly damaging |
Het |
Tigd5 |
T |
A |
15: 75,782,230 (GRCm39) |
Y197* |
probably null |
Het |
Tmprss11g |
A |
T |
5: 86,640,059 (GRCm39) |
L203Q |
probably damaging |
Het |
Trim35 |
T |
A |
14: 66,546,271 (GRCm39) |
V346E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,598,708 (GRCm39) |
I19402V |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,749,689 (GRCm39) |
E3787K |
probably benign |
Het |
Tut1 |
G |
A |
19: 8,942,778 (GRCm39) |
V622I |
probably benign |
Het |
Vmn1r2 |
A |
G |
4: 3,172,134 (GRCm39) |
I18V |
probably benign |
Het |
Zbbx |
T |
C |
3: 75,046,853 (GRCm39) |
N22S |
possibly damaging |
Het |
Zfp169 |
A |
C |
13: 48,652,339 (GRCm39) |
M26R |
probably benign |
Het |
Zfp180 |
T |
A |
7: 23,804,686 (GRCm39) |
H368Q |
probably damaging |
Het |
Zfp638 |
T |
A |
6: 83,930,108 (GRCm39) |
S770T |
possibly damaging |
Het |
Znrf1 |
T |
C |
8: 112,263,774 (GRCm39) |
M1T |
probably null |
Het |
|
Other mutations in Srrm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Srrm2
|
APN |
17 |
24,031,452 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00484:Srrm2
|
APN |
17 |
24,037,492 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01413:Srrm2
|
APN |
17 |
24,034,999 (GRCm39) |
unclassified |
probably benign |
|
IGL02272:Srrm2
|
APN |
17 |
24,034,756 (GRCm39) |
unclassified |
probably benign |
|
IGL02279:Srrm2
|
APN |
17 |
24,034,306 (GRCm39) |
unclassified |
probably benign |
|
IGL02325:Srrm2
|
APN |
17 |
24,029,453 (GRCm39) |
unclassified |
probably benign |
|
IGL02947:Srrm2
|
APN |
17 |
24,029,720 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03002:Srrm2
|
APN |
17 |
24,034,708 (GRCm39) |
unclassified |
probably benign |
|
BB009:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
BB019:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R0173:Srrm2
|
UTSW |
17 |
24,034,103 (GRCm39) |
unclassified |
probably benign |
|
R1018:Srrm2
|
UTSW |
17 |
24,041,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R1109:Srrm2
|
UTSW |
17 |
24,038,591 (GRCm39) |
unclassified |
probably benign |
|
R1199:Srrm2
|
UTSW |
17 |
24,036,725 (GRCm39) |
unclassified |
probably benign |
|
R1471:Srrm2
|
UTSW |
17 |
24,039,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Srrm2
|
UTSW |
17 |
24,034,876 (GRCm39) |
missense |
probably benign |
0.23 |
R1618:Srrm2
|
UTSW |
17 |
24,037,906 (GRCm39) |
unclassified |
probably benign |
|
R1678:Srrm2
|
UTSW |
17 |
24,037,960 (GRCm39) |
missense |
probably benign |
0.23 |
R1853:Srrm2
|
UTSW |
17 |
24,039,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Srrm2
|
UTSW |
17 |
24,040,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Srrm2
|
UTSW |
17 |
24,031,403 (GRCm39) |
unclassified |
probably benign |
|
R2102:Srrm2
|
UTSW |
17 |
24,036,722 (GRCm39) |
unclassified |
probably benign |
|
R2156:Srrm2
|
UTSW |
17 |
24,037,237 (GRCm39) |
missense |
probably benign |
0.23 |
R2214:Srrm2
|
UTSW |
17 |
24,035,719 (GRCm39) |
unclassified |
probably benign |
|
R2913:Srrm2
|
UTSW |
17 |
24,034,658 (GRCm39) |
unclassified |
probably benign |
|
R3721:Srrm2
|
UTSW |
17 |
24,041,549 (GRCm39) |
small deletion |
probably benign |
|
R4411:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4412:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4413:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4583:Srrm2
|
UTSW |
17 |
24,038,593 (GRCm39) |
unclassified |
probably benign |
|
R4682:Srrm2
|
UTSW |
17 |
24,034,666 (GRCm39) |
missense |
probably benign |
0.23 |
R4910:Srrm2
|
UTSW |
17 |
24,034,362 (GRCm39) |
unclassified |
probably benign |
|
R4943:Srrm2
|
UTSW |
17 |
24,041,389 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5023:Srrm2
|
UTSW |
17 |
24,038,291 (GRCm39) |
unclassified |
probably benign |
|
R5033:Srrm2
|
UTSW |
17 |
24,039,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Srrm2
|
UTSW |
17 |
24,038,524 (GRCm39) |
unclassified |
probably benign |
|
R5186:Srrm2
|
UTSW |
17 |
24,035,561 (GRCm39) |
missense |
probably benign |
0.23 |
R5197:Srrm2
|
UTSW |
17 |
24,036,358 (GRCm39) |
missense |
probably benign |
0.23 |
R5366:Srrm2
|
UTSW |
17 |
24,037,678 (GRCm39) |
missense |
probably benign |
0.23 |
R5483:Srrm2
|
UTSW |
17 |
24,040,246 (GRCm39) |
missense |
probably damaging |
0.96 |
R5551:Srrm2
|
UTSW |
17 |
24,037,450 (GRCm39) |
unclassified |
probably benign |
|
R5602:Srrm2
|
UTSW |
17 |
24,038,311 (GRCm39) |
unclassified |
probably benign |
|
R5733:Srrm2
|
UTSW |
17 |
24,040,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R5774:Srrm2
|
UTSW |
17 |
24,037,249 (GRCm39) |
unclassified |
probably benign |
|
R5909:Srrm2
|
UTSW |
17 |
24,040,291 (GRCm39) |
missense |
probably benign |
0.27 |
R5961:Srrm2
|
UTSW |
17 |
24,039,083 (GRCm39) |
unclassified |
probably benign |
|
R6122:Srrm2
|
UTSW |
17 |
24,039,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6906:Srrm2
|
UTSW |
17 |
24,039,337 (GRCm39) |
missense |
probably damaging |
0.97 |
R7177:Srrm2
|
UTSW |
17 |
24,035,747 (GRCm39) |
missense |
unknown |
|
R7197:Srrm2
|
UTSW |
17 |
24,037,198 (GRCm39) |
missense |
unknown |
|
R7442:Srrm2
|
UTSW |
17 |
24,039,091 (GRCm39) |
missense |
unknown |
|
R7644:Srrm2
|
UTSW |
17 |
24,038,294 (GRCm39) |
missense |
unknown |
|
R7664:Srrm2
|
UTSW |
17 |
24,039,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R7874:Srrm2
|
UTSW |
17 |
24,034,652 (GRCm39) |
missense |
unknown |
|
R7932:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R7950:Srrm2
|
UTSW |
17 |
24,027,084 (GRCm39) |
missense |
unknown |
|
R7958:Srrm2
|
UTSW |
17 |
24,040,286 (GRCm39) |
missense |
probably benign |
0.25 |
R8081:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Srrm2
|
UTSW |
17 |
24,027,057 (GRCm39) |
missense |
unknown |
|
R8174:Srrm2
|
UTSW |
17 |
24,034,297 (GRCm39) |
missense |
unknown |
|
R8191:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Srrm2
|
UTSW |
17 |
24,027,330 (GRCm39) |
missense |
unknown |
|
R8523:Srrm2
|
UTSW |
17 |
24,027,489 (GRCm39) |
unclassified |
probably benign |
|
R8728:Srrm2
|
UTSW |
17 |
24,038,831 (GRCm39) |
missense |
unknown |
|
R8912:Srrm2
|
UTSW |
17 |
24,038,575 (GRCm39) |
missense |
probably benign |
0.23 |
R9209:Srrm2
|
UTSW |
17 |
24,039,880 (GRCm39) |
missense |
probably benign |
0.05 |
RF006:Srrm2
|
UTSW |
17 |
24,031,562 (GRCm39) |
missense |
unknown |
|
Z1176:Srrm2
|
UTSW |
17 |
24,036,157 (GRCm39) |
missense |
unknown |
|
Z1177:Srrm2
|
UTSW |
17 |
24,036,484 (GRCm39) |
missense |
unknown |
|
|