Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
A |
G |
4: 62,450,896 (GRCm39) |
R120G |
probably null |
Het |
Abcb9 |
T |
C |
5: 124,211,665 (GRCm39) |
Y628C |
probably damaging |
Het |
Adrm1b |
A |
T |
3: 92,336,637 (GRCm39) |
Y22N |
probably benign |
Het |
Alpk2 |
C |
T |
18: 65,482,901 (GRCm39) |
C369Y |
probably damaging |
Het |
Caskin1 |
T |
G |
17: 24,723,195 (GRCm39) |
L661R |
probably damaging |
Het |
Cep83 |
A |
C |
10: 94,573,804 (GRCm39) |
N231T |
probably damaging |
Het |
Cfap44 |
G |
A |
16: 44,234,054 (GRCm39) |
G338D |
probably benign |
Het |
Chrna7 |
T |
G |
7: 62,753,541 (GRCm39) |
K326T |
possibly damaging |
Het |
Col4a4 |
A |
G |
1: 82,431,689 (GRCm39) |
S1532P |
unknown |
Het |
Cplx4 |
A |
T |
18: 66,090,190 (GRCm39) |
|
probably null |
Het |
Csf1r |
G |
C |
18: 61,257,947 (GRCm39) |
G639R |
probably damaging |
Het |
Dnajc27 |
T |
C |
12: 4,147,270 (GRCm39) |
L151P |
possibly damaging |
Het |
Epha5 |
A |
G |
5: 84,381,513 (GRCm39) |
V446A |
probably benign |
Het |
Esam |
T |
C |
9: 37,448,317 (GRCm39) |
V252A |
probably damaging |
Het |
Flnc |
C |
A |
6: 29,447,828 (GRCm39) |
D1210E |
probably damaging |
Het |
Fstl4 |
T |
C |
11: 52,891,050 (GRCm39) |
S63P |
probably benign |
Het |
Gas2l2 |
A |
G |
11: 83,314,070 (GRCm39) |
V414A |
possibly damaging |
Het |
Glra1 |
G |
A |
11: 55,424,688 (GRCm39) |
P174L |
probably damaging |
Het |
Gm16485 |
A |
T |
9: 8,972,196 (GRCm39) |
N21Y |
unknown |
Het |
Golga7 |
A |
T |
8: 23,746,731 (GRCm39) |
C24S |
possibly damaging |
Het |
Ints8 |
T |
C |
4: 11,227,128 (GRCm39) |
T582A |
probably benign |
Het |
Irx2 |
A |
T |
13: 72,777,343 (GRCm39) |
T55S |
probably benign |
Het |
Lce1j |
A |
T |
3: 92,696,390 (GRCm39) |
C129* |
probably null |
Het |
Mettl25b |
T |
C |
3: 87,834,955 (GRCm39) |
N115S |
possibly damaging |
Het |
Mocs1 |
G |
A |
17: 49,761,799 (GRCm39) |
G631E |
possibly damaging |
Het |
Mpi |
A |
T |
9: 57,457,881 (GRCm39) |
L107Q |
probably damaging |
Het |
Msrb2 |
A |
G |
2: 19,399,166 (GRCm39) |
*176W |
probably null |
Het |
Myh13 |
T |
A |
11: 67,231,206 (GRCm39) |
L401Q |
probably damaging |
Het |
Npffr2 |
G |
A |
5: 89,730,513 (GRCm39) |
V148I |
probably benign |
Het |
Oas1a |
T |
C |
5: 121,035,080 (GRCm39) |
E360G |
probably benign |
Het |
Or4k15c |
A |
T |
14: 50,321,367 (GRCm39) |
I257N |
possibly damaging |
Het |
Or5b96 |
A |
C |
19: 12,867,095 (GRCm39) |
V282G |
probably damaging |
Het |
Or9g20 |
A |
T |
2: 85,630,239 (GRCm39) |
I125N |
probably damaging |
Het |
Pcdha2 |
A |
G |
18: 37,072,579 (GRCm39) |
D70G |
probably benign |
Het |
Phf11b |
T |
C |
14: 59,568,722 (GRCm39) |
S64G |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Plpp2 |
A |
C |
10: 79,366,374 (GRCm39) |
L146R |
possibly damaging |
Het |
Poc5 |
T |
A |
13: 96,539,408 (GRCm39) |
N316K |
probably benign |
Het |
Rad51ap2 |
A |
T |
12: 11,512,593 (GRCm39) |
R947* |
probably null |
Het |
Ralgapb |
A |
G |
2: 158,307,803 (GRCm39) |
H1037R |
probably benign |
Het |
Rpl21 |
T |
C |
5: 146,772,702 (GRCm39) |
V141A |
probably benign |
Het |
Rufy3 |
C |
A |
5: 88,790,851 (GRCm39) |
D517E |
probably benign |
Het |
Scn7a |
A |
G |
2: 66,587,670 (GRCm39) |
V11A |
possibly damaging |
Het |
Sipa1l1 |
A |
C |
12: 82,496,700 (GRCm39) |
Q1744P |
probably damaging |
Het |
Smc2 |
T |
C |
4: 52,470,911 (GRCm39) |
|
probably null |
Het |
Sorcs3 |
T |
A |
19: 48,752,734 (GRCm39) |
L843Q |
possibly damaging |
Het |
Strc |
A |
T |
2: 121,207,844 (GRCm39) |
F509Y |
probably damaging |
Het |
Tas2r117 |
A |
C |
6: 132,780,281 (GRCm39) |
T140P |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,928,509 (GRCm39) |
I2641N |
possibly damaging |
Het |
Tnxb |
C |
A |
17: 34,929,077 (GRCm39) |
P2707T |
probably benign |
Het |
Vmn1r4 |
T |
A |
6: 56,933,515 (GRCm39) |
N6K |
probably benign |
Het |
Vmn1r91 |
T |
A |
7: 19,835,218 (GRCm39) |
S46T |
possibly damaging |
Het |
Zfp750 |
T |
C |
11: 121,402,706 (GRCm39) |
T681A |
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 |
|
IGL02506:Fmn1
|
APN |
2 |
113,355,640 (GRCm39) |
missense |
unknown |
|
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 |
|
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 |
|
|