Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg8 |
A |
G |
17: 84,999,916 (GRCm39) |
E189G |
possibly damaging |
Het |
Acad11 |
T |
C |
9: 103,968,931 (GRCm39) |
|
probably null |
Het |
Adcy7 |
G |
T |
8: 89,044,571 (GRCm39) |
R488L |
probably damaging |
Het |
Akt1 |
C |
T |
12: 112,625,714 (GRCm39) |
|
probably benign |
Het |
Ano9 |
C |
T |
7: 140,682,167 (GRCm39) |
|
probably benign |
Het |
Arhgap15 |
A |
G |
2: 43,953,820 (GRCm39) |
D182G |
possibly damaging |
Het |
Asxl3 |
T |
A |
18: 22,585,456 (GRCm39) |
V127D |
probably benign |
Het |
Cacna1g |
A |
G |
11: 94,319,955 (GRCm39) |
M1407T |
probably damaging |
Het |
Card9 |
A |
C |
2: 26,244,427 (GRCm39) |
|
probably benign |
Het |
Cdh5 |
A |
G |
8: 104,864,454 (GRCm39) |
N472D |
probably damaging |
Het |
Ceacam2 |
T |
A |
7: 25,227,379 (GRCm39) |
T343S |
probably benign |
Het |
Cic |
T |
A |
7: 24,990,282 (GRCm39) |
C1928S |
probably benign |
Het |
Clk3 |
C |
T |
9: 57,661,927 (GRCm39) |
W31* |
probably null |
Het |
Cntn4 |
A |
G |
6: 106,595,349 (GRCm39) |
T489A |
probably benign |
Het |
Crispld1 |
G |
A |
1: 17,826,529 (GRCm39) |
R431H |
probably damaging |
Het |
Crmp1 |
T |
A |
5: 37,436,199 (GRCm39) |
|
probably benign |
Het |
Cyld |
A |
G |
8: 89,456,218 (GRCm39) |
T423A |
possibly damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,736,198 (GRCm39) |
I84N |
probably damaging |
Het |
D2hgdh |
A |
G |
1: 93,757,507 (GRCm39) |
N141D |
probably damaging |
Het |
Dip2b |
T |
A |
15: 100,055,162 (GRCm39) |
L341Q |
probably damaging |
Het |
F3 |
C |
T |
3: 121,525,323 (GRCm39) |
T53I |
possibly damaging |
Het |
Fam227b |
T |
A |
2: 125,845,831 (GRCm39) |
Y386F |
probably benign |
Het |
Gcnt2 |
T |
A |
13: 41,040,856 (GRCm39) |
V5E |
probably benign |
Het |
Herpud1 |
G |
T |
8: 95,121,270 (GRCm39) |
E355* |
probably null |
Het |
Igf1r |
T |
C |
7: 67,843,144 (GRCm39) |
S752P |
probably benign |
Het |
Iqsec1 |
T |
C |
6: 90,649,057 (GRCm39) |
I687V |
possibly damaging |
Het |
Kdm5a |
T |
C |
6: 120,409,110 (GRCm39) |
S1598P |
probably damaging |
Het |
Klk1b9 |
A |
G |
7: 43,445,063 (GRCm39) |
E185G |
probably benign |
Het |
Myo16 |
G |
T |
8: 10,440,217 (GRCm39) |
R423L |
probably damaging |
Het |
Myo7b |
T |
C |
18: 32,100,207 (GRCm39) |
E1609G |
probably damaging |
Het |
Nom1 |
T |
A |
5: 29,644,814 (GRCm39) |
|
probably benign |
Het |
Nomo1 |
A |
G |
7: 45,727,480 (GRCm39) |
I1040V |
possibly damaging |
Het |
Or8b39 |
G |
A |
9: 37,996,741 (GRCm39) |
G203D |
probably damaging |
Het |
Paqr9 |
T |
C |
9: 95,442,748 (GRCm39) |
V246A |
probably benign |
Het |
Pfkfb4 |
A |
T |
9: 108,859,404 (GRCm39) |
D437V |
probably benign |
Het |
Phldb1 |
G |
T |
9: 44,622,223 (GRCm39) |
D797E |
probably benign |
Het |
Pkd1l3 |
A |
G |
8: 110,374,132 (GRCm39) |
E1399G |
probably damaging |
Het |
Plekhs1 |
G |
A |
19: 56,460,198 (GRCm39) |
C97Y |
probably damaging |
Het |
Plscr4 |
A |
T |
9: 92,372,044 (GRCm39) |
I272L |
possibly damaging |
Het |
Prlhr |
A |
C |
19: 60,456,366 (GRCm39) |
Y67D |
probably damaging |
Het |
Rab3gap2 |
A |
G |
1: 184,984,221 (GRCm39) |
|
probably benign |
Het |
Rad23b |
T |
C |
4: 55,382,511 (GRCm39) |
V238A |
probably benign |
Het |
Sel1l2 |
T |
C |
2: 140,117,380 (GRCm39) |
T164A |
possibly damaging |
Het |
Serpinh1 |
T |
A |
7: 98,996,199 (GRCm39) |
K295M |
probably damaging |
Het |
Slc45a4 |
T |
C |
15: 73,453,687 (GRCm39) |
E770G |
probably benign |
Het |
Spag4 |
T |
C |
2: 155,911,142 (GRCm39) |
L390P |
probably damaging |
Het |
Stip1 |
A |
G |
19: 7,012,857 (GRCm39) |
|
probably benign |
Het |
Tacr1 |
A |
G |
6: 82,380,739 (GRCm39) |
N50S |
probably damaging |
Het |
Tg |
T |
C |
15: 66,613,443 (GRCm39) |
V433A |
possibly damaging |
Het |
Ubap1l |
T |
A |
9: 65,276,493 (GRCm39) |
|
probably benign |
Het |
Usp40 |
A |
T |
1: 87,909,738 (GRCm39) |
I572K |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,917,308 (GRCm39) |
E3717D |
probably damaging |
Het |
Wdr81 |
T |
C |
11: 75,335,232 (GRCm39) |
N1778S |
probably benign |
Het |
Ylpm1 |
T |
A |
12: 85,095,965 (GRCm39) |
F1162Y |
probably damaging |
Het |
Zbtb10 |
T |
A |
3: 9,330,297 (GRCm39) |
F552I |
probably damaging |
Het |
Zfp507 |
T |
C |
7: 35,475,891 (GRCm39) |
I811V |
probably damaging |
Het |
Zfp663 |
A |
T |
2: 165,195,871 (GRCm39) |
V116D |
probably benign |
Het |
|
Other mutations in Fmn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Fmn1
|
APN |
2 |
113,274,812 (GRCm39) |
intron |
probably benign |
|
IGL01520:Fmn1
|
APN |
2 |
113,274,713 (GRCm39) |
intron |
probably benign |
|
IGL02039:Fmn1
|
APN |
2 |
113,195,425 (GRCm39) |
missense |
unknown |
|
IGL02222:Fmn1
|
APN |
2 |
113,423,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02238:Fmn1
|
APN |
2 |
113,412,470 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02373:Fmn1
|
APN |
2 |
113,194,471 (GRCm39) |
missense |
unknown |
|
IGL02490:Fmn1
|
APN |
2 |
113,359,817 (GRCm39) |
splice site |
probably benign |
|
IGL02684:Fmn1
|
APN |
2 |
113,355,622 (GRCm39) |
missense |
unknown |
|
IGL03008:Fmn1
|
APN |
2 |
113,195,445 (GRCm39) |
missense |
unknown |
|
IGL03058:Fmn1
|
APN |
2 |
113,272,159 (GRCm39) |
intron |
probably benign |
|
IGL03076:Fmn1
|
APN |
2 |
113,414,437 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4304:Fmn1
|
UTSW |
2 |
113,356,128 (GRCm39) |
small insertion |
probably benign |
|
FR4304:Fmn1
|
UTSW |
2 |
113,356,119 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Fmn1
|
UTSW |
2 |
113,356,128 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Fmn1
|
UTSW |
2 |
113,356,119 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Fmn1
|
UTSW |
2 |
113,356,118 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Fmn1
|
UTSW |
2 |
113,356,129 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Fmn1
|
UTSW |
2 |
113,356,126 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Fmn1
|
UTSW |
2 |
113,356,123 (GRCm39) |
small insertion |
probably benign |
|
R0349:Fmn1
|
UTSW |
2 |
113,196,141 (GRCm39) |
missense |
unknown |
|
R0452:Fmn1
|
UTSW |
2 |
113,467,124 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0529:Fmn1
|
UTSW |
2 |
113,538,198 (GRCm39) |
splice site |
probably benign |
|
R1215:Fmn1
|
UTSW |
2 |
113,523,375 (GRCm39) |
nonsense |
probably null |
|
R1471:Fmn1
|
UTSW |
2 |
113,523,439 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1489:Fmn1
|
UTSW |
2 |
113,195,557 (GRCm39) |
missense |
unknown |
|
R1491:Fmn1
|
UTSW |
2 |
113,426,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Fmn1
|
UTSW |
2 |
113,356,207 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1558:Fmn1
|
UTSW |
2 |
113,523,463 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1588:Fmn1
|
UTSW |
2 |
113,196,043 (GRCm39) |
missense |
unknown |
|
R1602:Fmn1
|
UTSW |
2 |
113,355,968 (GRCm39) |
missense |
unknown |
|
R1690:Fmn1
|
UTSW |
2 |
113,355,827 (GRCm39) |
missense |
unknown |
|
R1772:Fmn1
|
UTSW |
2 |
113,195,700 (GRCm39) |
missense |
unknown |
|
R1867:Fmn1
|
UTSW |
2 |
113,539,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R1923:Fmn1
|
UTSW |
2 |
113,260,066 (GRCm39) |
intron |
probably benign |
|
R1941:Fmn1
|
UTSW |
2 |
113,195,488 (GRCm39) |
missense |
unknown |
|
R2019:Fmn1
|
UTSW |
2 |
113,194,825 (GRCm39) |
missense |
unknown |
|
R2140:Fmn1
|
UTSW |
2 |
113,425,393 (GRCm39) |
missense |
probably benign |
0.45 |
R2164:Fmn1
|
UTSW |
2 |
113,195,962 (GRCm39) |
missense |
unknown |
|
R2395:Fmn1
|
UTSW |
2 |
113,195,526 (GRCm39) |
missense |
unknown |
|
R2999:Fmn1
|
UTSW |
2 |
113,195,439 (GRCm39) |
missense |
unknown |
|
R3405:Fmn1
|
UTSW |
2 |
113,194,693 (GRCm39) |
missense |
unknown |
|
R3407:Fmn1
|
UTSW |
2 |
113,195,400 (GRCm39) |
missense |
unknown |
|
R3771:Fmn1
|
UTSW |
2 |
113,412,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Fmn1
|
UTSW |
2 |
113,412,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Fmn1
|
UTSW |
2 |
113,412,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Fmn1
|
UTSW |
2 |
113,195,467 (GRCm39) |
missense |
unknown |
|
R4166:Fmn1
|
UTSW |
2 |
113,467,080 (GRCm39) |
missense |
probably benign |
0.33 |
R4477:Fmn1
|
UTSW |
2 |
113,274,744 (GRCm39) |
intron |
probably benign |
|
R4614:Fmn1
|
UTSW |
2 |
113,195,494 (GRCm39) |
missense |
unknown |
|
R4701:Fmn1
|
UTSW |
2 |
113,414,416 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4867:Fmn1
|
UTSW |
2 |
113,414,465 (GRCm39) |
critical splice donor site |
probably null |
|
R5063:Fmn1
|
UTSW |
2 |
113,195,266 (GRCm39) |
missense |
unknown |
|
R5224:Fmn1
|
UTSW |
2 |
113,195,470 (GRCm39) |
missense |
unknown |
|
R5510:Fmn1
|
UTSW |
2 |
113,426,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R6083:Fmn1
|
UTSW |
2 |
113,194,648 (GRCm39) |
missense |
unknown |
|
R6234:Fmn1
|
UTSW |
2 |
113,196,000 (GRCm39) |
missense |
unknown |
|
R6266:Fmn1
|
UTSW |
2 |
113,426,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6764:Fmn1
|
UTSW |
2 |
113,355,560 (GRCm39) |
missense |
unknown |
|
R7054:Fmn1
|
UTSW |
2 |
113,195,353 (GRCm39) |
missense |
unknown |
|
R7311:Fmn1
|
UTSW |
2 |
113,356,025 (GRCm39) |
missense |
unknown |
|
R7439:Fmn1
|
UTSW |
2 |
113,271,956 (GRCm39) |
missense |
unknown |
|
R7440:Fmn1
|
UTSW |
2 |
113,271,956 (GRCm39) |
missense |
unknown |
|
R7441:Fmn1
|
UTSW |
2 |
113,271,956 (GRCm39) |
missense |
unknown |
|
R7444:Fmn1
|
UTSW |
2 |
113,271,956 (GRCm39) |
missense |
unknown |
|
R7461:Fmn1
|
UTSW |
2 |
113,194,416 (GRCm39) |
missense |
unknown |
|
R7526:Fmn1
|
UTSW |
2 |
113,518,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R7540:Fmn1
|
UTSW |
2 |
113,359,655 (GRCm39) |
splice site |
probably null |
|
R7576:Fmn1
|
UTSW |
2 |
113,195,353 (GRCm39) |
missense |
unknown |
|
R7657:Fmn1
|
UTSW |
2 |
113,355,538 (GRCm39) |
missense |
unknown |
|
R7669:Fmn1
|
UTSW |
2 |
113,195,822 (GRCm39) |
missense |
unknown |
|
R7713:Fmn1
|
UTSW |
2 |
113,356,159 (GRCm39) |
missense |
unknown |
|
R7841:Fmn1
|
UTSW |
2 |
113,359,810 (GRCm39) |
critical splice donor site |
probably null |
|
R7953:Fmn1
|
UTSW |
2 |
113,426,689 (GRCm39) |
missense |
probably benign |
0.03 |
R7959:Fmn1
|
UTSW |
2 |
113,195,967 (GRCm39) |
missense |
unknown |
|
R8041:Fmn1
|
UTSW |
2 |
113,194,939 (GRCm39) |
missense |
unknown |
|
R8152:Fmn1
|
UTSW |
2 |
113,196,037 (GRCm39) |
missense |
unknown |
|
R8203:Fmn1
|
UTSW |
2 |
113,355,620 (GRCm39) |
missense |
unknown |
|
R8318:Fmn1
|
UTSW |
2 |
113,195,502 (GRCm39) |
missense |
unknown |
|
R8356:Fmn1
|
UTSW |
2 |
113,195,385 (GRCm39) |
missense |
unknown |
|
R8456:Fmn1
|
UTSW |
2 |
113,195,385 (GRCm39) |
missense |
unknown |
|
R8698:Fmn1
|
UTSW |
2 |
113,260,152 (GRCm39) |
missense |
unknown |
|
R8861:Fmn1
|
UTSW |
2 |
113,195,149 (GRCm39) |
missense |
unknown |
|
R8907:Fmn1
|
UTSW |
2 |
113,355,914 (GRCm39) |
missense |
unknown |
|
R9147:Fmn1
|
UTSW |
2 |
113,271,973 (GRCm39) |
missense |
unknown |
|
R9148:Fmn1
|
UTSW |
2 |
113,271,973 (GRCm39) |
missense |
unknown |
|
R9536:Fmn1
|
UTSW |
2 |
113,309,262 (GRCm39) |
missense |
unknown |
|
R9574:Fmn1
|
UTSW |
2 |
113,425,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R9577:Fmn1
|
UTSW |
2 |
113,194,470 (GRCm39) |
missense |
unknown |
|
RF003:Fmn1
|
UTSW |
2 |
113,356,131 (GRCm39) |
small insertion |
probably benign |
|
Z1088:Fmn1
|
UTSW |
2 |
113,272,270 (GRCm39) |
intron |
probably benign |
|
|