Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610528J11Rik |
A |
T |
4: 118,386,490 (GRCm39) |
M1L |
probably benign |
Het |
5730596B20Rik |
T |
A |
6: 52,156,182 (GRCm39) |
|
probably benign |
Het |
Acrbp |
T |
C |
6: 125,030,917 (GRCm39) |
|
probably null |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Acss3 |
A |
G |
10: 106,920,732 (GRCm39) |
I126T |
possibly damaging |
Het |
Aff3 |
T |
C |
1: 38,574,650 (GRCm39) |
E110G |
probably damaging |
Het |
Aldh1a3 |
T |
C |
7: 66,059,000 (GRCm39) |
I113V |
probably benign |
Het |
Aplp2 |
T |
C |
9: 31,069,086 (GRCm39) |
E525G |
probably damaging |
Het |
Atp2b4 |
A |
G |
1: 133,657,440 (GRCm39) |
|
probably benign |
Het |
Atp8a1 |
C |
T |
5: 67,970,435 (GRCm39) |
|
probably null |
Het |
Bhmt |
A |
G |
13: 93,761,972 (GRCm39) |
C104R |
probably damaging |
Het |
Cct5 |
T |
G |
15: 31,591,177 (GRCm39) |
E508A |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,787,065 (GRCm39) |
E2761D |
probably benign |
Het |
Clstn1 |
T |
C |
4: 149,728,131 (GRCm39) |
S600P |
probably damaging |
Het |
Cnppd1 |
A |
G |
1: 75,113,573 (GRCm39) |
S232P |
probably damaging |
Het |
Crybb3 |
T |
C |
5: 113,227,619 (GRCm39) |
|
probably null |
Het |
Csmd1 |
A |
G |
8: 16,273,249 (GRCm39) |
I861T |
probably damaging |
Het |
Cyp2d10 |
A |
C |
15: 82,289,540 (GRCm39) |
S191A |
possibly damaging |
Het |
Ddx10 |
T |
C |
9: 53,146,604 (GRCm39) |
D206G |
probably damaging |
Het |
Dnah1 |
G |
T |
14: 31,024,332 (GRCm39) |
H916N |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,802,615 (GRCm39) |
|
probably null |
Het |
Epb42 |
G |
A |
2: 120,859,525 (GRCm39) |
|
probably benign |
Het |
Etnppl |
A |
G |
3: 130,423,062 (GRCm39) |
R248G |
probably damaging |
Het |
Eya3 |
T |
C |
4: 132,446,558 (GRCm39) |
F369L |
probably damaging |
Het |
Fam170b |
T |
C |
14: 32,556,025 (GRCm39) |
|
probably benign |
Het |
Fli1 |
A |
T |
9: 32,372,723 (GRCm39) |
V105D |
probably damaging |
Het |
Fndc3b |
C |
A |
3: 27,511,155 (GRCm39) |
C785F |
probably benign |
Het |
Foxe3 |
T |
C |
4: 114,782,765 (GRCm39) |
D149G |
probably damaging |
Het |
Gk5 |
T |
C |
9: 96,056,857 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
A |
G |
2: 154,867,372 (GRCm39) |
D443G |
possibly damaging |
Het |
Gm9796 |
C |
T |
11: 95,588,821 (GRCm39) |
|
noncoding transcript |
Het |
Golga4 |
A |
T |
9: 118,398,061 (GRCm39) |
R52S |
probably benign |
Het |
Hey2 |
C |
A |
10: 30,710,006 (GRCm39) |
C249F |
probably damaging |
Het |
Ipo9 |
A |
T |
1: 135,348,101 (GRCm39) |
|
probably benign |
Het |
Ireb2 |
C |
A |
9: 54,793,877 (GRCm39) |
T269K |
probably benign |
Het |
Kansl3 |
A |
G |
1: 36,391,050 (GRCm39) |
V274A |
probably damaging |
Het |
Kcnk2 |
C |
T |
1: 188,942,169 (GRCm39) |
A352T |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,006,442 (GRCm39) |
E903G |
probably benign |
Het |
Lepr |
A |
G |
4: 101,607,541 (GRCm39) |
K253R |
probably benign |
Het |
Lmntd2 |
T |
C |
7: 140,793,536 (GRCm39) |
|
probably benign |
Het |
Lrrc39 |
A |
T |
3: 116,371,952 (GRCm39) |
T240S |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,635,085 (GRCm39) |
|
probably null |
Het |
Maf |
T |
C |
8: 116,432,495 (GRCm39) |
M370V |
possibly damaging |
Het |
Mib2 |
G |
A |
4: 155,745,673 (GRCm39) |
S46L |
possibly damaging |
Het |
Mms22l |
C |
T |
4: 24,497,867 (GRCm39) |
T63I |
probably damaging |
Het |
Morc2a |
T |
A |
11: 3,633,989 (GRCm39) |
S700R |
probably benign |
Het |
Mpz |
A |
G |
1: 170,987,498 (GRCm39) |
|
probably benign |
Het |
Ncam2 |
T |
C |
16: 81,420,225 (GRCm39) |
|
probably benign |
Het |
Niban1 |
T |
C |
1: 151,584,957 (GRCm39) |
|
probably null |
Het |
Nudt14 |
C |
T |
12: 112,902,037 (GRCm39) |
A123T |
probably damaging |
Het |
Odad3 |
A |
G |
9: 21,901,543 (GRCm39) |
|
probably benign |
Het |
Or10h1 |
C |
T |
17: 33,418,298 (GRCm39) |
T92I |
probably benign |
Het |
Or2a7 |
G |
A |
6: 43,151,692 (GRCm39) |
M257I |
probably benign |
Het |
Or9g20 |
A |
T |
2: 85,629,879 (GRCm39) |
I245N |
possibly damaging |
Het |
Otoa |
T |
C |
7: 120,710,302 (GRCm39) |
|
probably benign |
Het |
Pik3cg |
G |
A |
12: 32,254,790 (GRCm39) |
T399I |
probably damaging |
Het |
Pkn3 |
C |
T |
2: 29,973,309 (GRCm39) |
A377V |
probably benign |
Het |
Ppan |
A |
G |
9: 20,802,825 (GRCm39) |
N327S |
probably benign |
Het |
Prkca |
T |
C |
11: 107,944,937 (GRCm39) |
|
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,543,033 (GRCm39) |
V320E |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,444,278 (GRCm39) |
V1442A |
probably damaging |
Het |
Rapgef1 |
C |
T |
2: 29,616,239 (GRCm39) |
R834C |
probably damaging |
Het |
Rbms1 |
G |
T |
2: 60,672,754 (GRCm39) |
N44K |
probably damaging |
Het |
Rfwd3 |
A |
C |
8: 112,009,365 (GRCm39) |
F404V |
probably benign |
Het |
Rimbp3 |
G |
T |
16: 17,027,317 (GRCm39) |
R247L |
probably benign |
Het |
Serpinb1b |
T |
C |
13: 33,277,696 (GRCm39) |
S310P |
possibly damaging |
Het |
Smtn |
C |
A |
11: 3,480,235 (GRCm39) |
V329L |
probably damaging |
Het |
Snapc2 |
T |
C |
8: 4,304,979 (GRCm39) |
|
probably benign |
Het |
Spam1 |
A |
T |
6: 24,800,418 (GRCm39) |
M386L |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,142,387 (GRCm39) |
E6208G |
probably damaging |
Het |
Teddm1a |
T |
C |
1: 153,768,369 (GRCm39) |
Y278H |
probably damaging |
Het |
Tnfaip6 |
A |
T |
2: 51,945,928 (GRCm39) |
N258I |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 44,971,472 (GRCm39) |
R188Q |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,579,441 (GRCm39) |
H491Q |
probably benign |
Het |
Urgcp |
C |
T |
11: 5,666,989 (GRCm39) |
E450K |
probably benign |
Het |
Vmn1r228 |
T |
C |
17: 20,996,637 (GRCm39) |
N294D |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,015,958 (GRCm39) |
C2606S |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,021,377 (GRCm39) |
H642Q |
unknown |
Het |
Zbtb46 |
A |
G |
2: 181,053,567 (GRCm39) |
S382P |
possibly damaging |
Het |
Zfp217 |
A |
G |
2: 169,961,700 (GRCm39) |
I209T |
probably benign |
Het |
Zranb3 |
T |
A |
1: 127,891,510 (GRCm39) |
N822I |
probably benign |
Het |
|
Other mutations in Fmo1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Fmo1
|
APN |
1 |
162,663,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00479:Fmo1
|
APN |
1 |
162,657,632 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01612:Fmo1
|
APN |
1 |
162,661,168 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01650:Fmo1
|
APN |
1 |
162,661,153 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02052:Fmo1
|
APN |
1 |
162,677,629 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02340:Fmo1
|
APN |
1 |
162,660,559 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03348:Fmo1
|
APN |
1 |
162,677,720 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03388:Fmo1
|
APN |
1 |
162,663,716 (GRCm39) |
missense |
probably benign |
0.17 |
PIT1430001:Fmo1
|
UTSW |
1 |
162,657,622 (GRCm39) |
missense |
probably benign |
0.00 |
R0314:Fmo1
|
UTSW |
1 |
162,687,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R0348:Fmo1
|
UTSW |
1 |
162,663,704 (GRCm39) |
missense |
probably benign |
0.00 |
R0385:Fmo1
|
UTSW |
1 |
162,663,773 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0699:Fmo1
|
UTSW |
1 |
162,661,341 (GRCm39) |
missense |
probably benign |
0.00 |
R1413:Fmo1
|
UTSW |
1 |
162,661,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R1424:Fmo1
|
UTSW |
1 |
162,657,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Fmo1
|
UTSW |
1 |
162,667,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Fmo1
|
UTSW |
1 |
162,657,554 (GRCm39) |
nonsense |
probably null |
|
R1929:Fmo1
|
UTSW |
1 |
162,661,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Fmo1
|
UTSW |
1 |
162,667,325 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2272:Fmo1
|
UTSW |
1 |
162,661,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Fmo1
|
UTSW |
1 |
162,663,828 (GRCm39) |
missense |
probably benign |
0.00 |
R3787:Fmo1
|
UTSW |
1 |
162,657,583 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3825:Fmo1
|
UTSW |
1 |
162,678,916 (GRCm39) |
splice site |
probably benign |
|
R3904:Fmo1
|
UTSW |
1 |
162,661,337 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4320:Fmo1
|
UTSW |
1 |
162,661,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Fmo1
|
UTSW |
1 |
162,661,217 (GRCm39) |
nonsense |
probably null |
|
R4431:Fmo1
|
UTSW |
1 |
162,661,281 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4473:Fmo1
|
UTSW |
1 |
162,677,732 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5340:Fmo1
|
UTSW |
1 |
162,657,551 (GRCm39) |
missense |
probably benign |
0.39 |
R5354:Fmo1
|
UTSW |
1 |
162,657,714 (GRCm39) |
missense |
probably benign |
0.01 |
R5479:Fmo1
|
UTSW |
1 |
162,677,793 (GRCm39) |
missense |
probably damaging |
0.99 |
R5930:Fmo1
|
UTSW |
1 |
162,667,185 (GRCm39) |
critical splice donor site |
probably null |
|
R6148:Fmo1
|
UTSW |
1 |
162,679,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R6160:Fmo1
|
UTSW |
1 |
162,663,867 (GRCm39) |
missense |
probably benign |
0.00 |
R6164:Fmo1
|
UTSW |
1 |
162,678,979 (GRCm39) |
missense |
probably benign |
0.24 |
R6263:Fmo1
|
UTSW |
1 |
162,677,629 (GRCm39) |
critical splice donor site |
probably null |
|
R7046:Fmo1
|
UTSW |
1 |
162,667,263 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7590:Fmo1
|
UTSW |
1 |
162,687,251 (GRCm39) |
intron |
probably benign |
|
R7663:Fmo1
|
UTSW |
1 |
162,663,866 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7692:Fmo1
|
UTSW |
1 |
162,661,402 (GRCm39) |
missense |
probably benign |
0.16 |
R7712:Fmo1
|
UTSW |
1 |
162,663,704 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Fmo1
|
UTSW |
1 |
162,677,676 (GRCm39) |
missense |
probably benign |
0.28 |
R8895:Fmo1
|
UTSW |
1 |
162,657,827 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Fmo1
|
UTSW |
1 |
162,663,773 (GRCm39) |
missense |
probably benign |
0.03 |
R9583:Fmo1
|
UTSW |
1 |
162,686,996 (GRCm39) |
missense |
|
|
R9620:Fmo1
|
UTSW |
1 |
162,661,390 (GRCm39) |
missense |
probably benign |
|
X0022:Fmo1
|
UTSW |
1 |
162,657,569 (GRCm39) |
missense |
possibly damaging |
0.57 |
X0066:Fmo1
|
UTSW |
1 |
162,667,273 (GRCm39) |
missense |
probably benign |
0.00 |
|