Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco2 |
G |
A |
15: 81,779,486 (GRCm39) |
A97T |
probably damaging |
Het |
Adat1 |
T |
C |
8: 112,705,994 (GRCm39) |
S371G |
probably benign |
Het |
Aoc3 |
T |
G |
11: 101,222,871 (GRCm39) |
I369R |
possibly damaging |
Het |
Apobr |
A |
T |
7: 126,186,694 (GRCm39) |
|
probably null |
Het |
Arhgap12 |
A |
T |
18: 6,111,774 (GRCm39) |
C69S |
probably damaging |
Het |
Astn2 |
A |
G |
4: 66,037,300 (GRCm39) |
|
probably benign |
Het |
Bcas1 |
T |
C |
2: 170,248,741 (GRCm39) |
D60G |
probably damaging |
Het |
Cacnb4 |
T |
A |
2: 52,367,783 (GRCm39) |
D62V |
probably damaging |
Het |
Cbx8 |
C |
A |
11: 118,931,618 (GRCm39) |
R20L |
probably damaging |
Het |
Ccdc92 |
G |
A |
5: 124,913,337 (GRCm39) |
T64M |
probably benign |
Het |
Cps1 |
G |
T |
1: 67,244,358 (GRCm39) |
S1135I |
probably null |
Het |
Eml2 |
G |
A |
7: 18,913,275 (GRCm39) |
R91H |
probably damaging |
Het |
Fbxl3 |
G |
A |
14: 103,320,313 (GRCm39) |
P426L |
probably damaging |
Het |
Gabrb2 |
T |
C |
11: 42,488,521 (GRCm39) |
I329T |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,898,156 (GRCm39) |
D745E |
possibly damaging |
Het |
Itprid2 |
T |
A |
2: 79,488,164 (GRCm39) |
V749E |
probably damaging |
Het |
Lacc1 |
T |
A |
14: 77,271,470 (GRCm39) |
N239I |
probably damaging |
Het |
Lamb2 |
T |
A |
9: 108,363,997 (GRCm39) |
C1008S |
probably damaging |
Het |
Man2b1 |
G |
A |
8: 85,817,565 (GRCm39) |
V349I |
probably benign |
Het |
Mib1 |
A |
G |
18: 10,811,985 (GRCm39) |
T961A |
possibly damaging |
Het |
Mmp24 |
A |
G |
2: 155,655,908 (GRCm39) |
I449V |
possibly damaging |
Het |
Myo7b |
A |
G |
18: 32,147,282 (GRCm39) |
I87T |
probably benign |
Het |
Or13c7b |
A |
G |
4: 43,821,175 (GRCm39) |
F62S |
probably damaging |
Het |
Or5p72 |
T |
A |
7: 108,022,122 (GRCm39) |
C115S |
probably benign |
Het |
Pgr |
A |
G |
9: 8,958,420 (GRCm39) |
E809G |
probably damaging |
Het |
Ppp1r3g |
T |
A |
13: 36,153,603 (GRCm39) |
V341E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,518,517 (GRCm39) |
S1091T |
probably benign |
Het |
Rab44 |
G |
A |
17: 29,358,871 (GRCm39) |
R353K |
probably benign |
Het |
Reck |
G |
A |
4: 43,891,001 (GRCm39) |
M46I |
probably benign |
Het |
Rorb |
G |
T |
19: 18,954,992 (GRCm39) |
S208Y |
possibly damaging |
Het |
Serinc2 |
G |
T |
4: 130,147,847 (GRCm39) |
T410N |
possibly damaging |
Het |
Slc23a2 |
G |
A |
2: 131,898,702 (GRCm39) |
R612* |
probably null |
Het |
Slx4 |
T |
C |
16: 3,812,773 (GRCm39) |
E145G |
probably damaging |
Het |
Spag16 |
A |
G |
1: 70,532,989 (GRCm39) |
D556G |
probably damaging |
Het |
Spopl |
C |
T |
2: 23,407,957 (GRCm39) |
V241M |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,149,293 (GRCm39) |
F485I |
probably benign |
Het |
Trmo |
C |
T |
4: 46,382,140 (GRCm39) |
V326M |
probably damaging |
Het |
Tssk5 |
T |
C |
15: 76,256,411 (GRCm39) |
D336G |
probably damaging |
Het |
Ttyh2 |
A |
T |
11: 114,601,789 (GRCm39) |
Q471L |
possibly damaging |
Het |
Wdr33 |
A |
C |
18: 32,026,132 (GRCm39) |
Q944H |
unknown |
Het |
Wdr55 |
G |
A |
18: 36,893,448 (GRCm39) |
V37M |
possibly damaging |
Het |
Zbtb18 |
A |
T |
1: 177,274,687 (GRCm39) |
S7C |
probably damaging |
Het |
Zfhx4 |
G |
A |
3: 5,464,680 (GRCm39) |
V1638M |
possibly damaging |
Het |
Zfp81 |
A |
T |
17: 33,553,677 (GRCm39) |
I379N |
possibly damaging |
Het |
|
Other mutations in Fhod3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Fhod3
|
APN |
18 |
25,127,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01139:Fhod3
|
APN |
18 |
25,199,401 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01293:Fhod3
|
APN |
18 |
25,153,709 (GRCm39) |
splice site |
probably benign |
|
IGL01313:Fhod3
|
APN |
18 |
25,153,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01524:Fhod3
|
APN |
18 |
25,263,659 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01568:Fhod3
|
APN |
18 |
25,253,219 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01586:Fhod3
|
APN |
18 |
25,223,804 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01622:Fhod3
|
APN |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01623:Fhod3
|
APN |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01640:Fhod3
|
APN |
18 |
25,248,850 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01860:Fhod3
|
APN |
18 |
25,037,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01860:Fhod3
|
APN |
18 |
25,030,738 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Fhod3
|
APN |
18 |
25,189,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02390:Fhod3
|
APN |
18 |
25,199,332 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02550:Fhod3
|
APN |
18 |
25,156,017 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02987:Fhod3
|
APN |
18 |
25,246,610 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0328:Fhod3
|
UTSW |
18 |
25,246,657 (GRCm39) |
missense |
probably benign |
0.01 |
R0362:Fhod3
|
UTSW |
18 |
25,223,133 (GRCm39) |
nonsense |
probably null |
|
R0373:Fhod3
|
UTSW |
18 |
25,223,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0483:Fhod3
|
UTSW |
18 |
24,842,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Fhod3
|
UTSW |
18 |
25,245,640 (GRCm39) |
missense |
probably benign |
0.27 |
R0617:Fhod3
|
UTSW |
18 |
25,245,736 (GRCm39) |
splice site |
probably benign |
|
R0834:Fhod3
|
UTSW |
18 |
25,248,862 (GRCm39) |
nonsense |
probably null |
|
R0836:Fhod3
|
UTSW |
18 |
25,199,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R1157:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1160:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Fhod3
|
UTSW |
18 |
25,223,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Fhod3
|
UTSW |
18 |
25,248,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1621:Fhod3
|
UTSW |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
R1748:Fhod3
|
UTSW |
18 |
24,903,550 (GRCm39) |
nonsense |
probably null |
|
R1757:Fhod3
|
UTSW |
18 |
25,199,335 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1758:Fhod3
|
UTSW |
18 |
25,253,367 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1872:Fhod3
|
UTSW |
18 |
25,263,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Fhod3
|
UTSW |
18 |
25,245,643 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1917:Fhod3
|
UTSW |
18 |
25,218,658 (GRCm39) |
missense |
probably benign |
0.27 |
R1917:Fhod3
|
UTSW |
18 |
25,123,022 (GRCm39) |
splice site |
probably benign |
|
R1934:Fhod3
|
UTSW |
18 |
25,223,335 (GRCm39) |
missense |
probably benign |
0.35 |
R1958:Fhod3
|
UTSW |
18 |
25,223,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Fhod3
|
UTSW |
18 |
25,223,473 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3618:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R3709:Fhod3
|
UTSW |
18 |
25,223,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Fhod3
|
UTSW |
18 |
25,223,818 (GRCm39) |
missense |
probably benign |
0.44 |
R4246:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4248:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4249:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4498:Fhod3
|
UTSW |
18 |
25,243,296 (GRCm39) |
critical splice donor site |
probably null |
|
R4532:Fhod3
|
UTSW |
18 |
25,243,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Fhod3
|
UTSW |
18 |
25,248,775 (GRCm39) |
missense |
probably benign |
0.01 |
R4628:Fhod3
|
UTSW |
18 |
25,253,186 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4667:Fhod3
|
UTSW |
18 |
25,199,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4668:Fhod3
|
UTSW |
18 |
25,199,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4734:Fhod3
|
UTSW |
18 |
25,161,192 (GRCm39) |
missense |
probably benign |
0.00 |
R4753:Fhod3
|
UTSW |
18 |
25,223,382 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4796:Fhod3
|
UTSW |
18 |
25,118,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Fhod3
|
UTSW |
18 |
25,223,305 (GRCm39) |
missense |
probably benign |
0.00 |
R5338:Fhod3
|
UTSW |
18 |
25,161,138 (GRCm39) |
missense |
probably damaging |
0.96 |
R5832:Fhod3
|
UTSW |
18 |
25,223,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Fhod3
|
UTSW |
18 |
25,258,810 (GRCm39) |
missense |
probably benign |
0.25 |
R6362:Fhod3
|
UTSW |
18 |
24,887,312 (GRCm39) |
missense |
probably benign |
0.00 |
R6414:Fhod3
|
UTSW |
18 |
25,223,935 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7099:Fhod3
|
UTSW |
18 |
25,223,219 (GRCm39) |
missense |
probably benign |
|
R7172:Fhod3
|
UTSW |
18 |
25,218,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Fhod3
|
UTSW |
18 |
25,223,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Fhod3
|
UTSW |
18 |
25,193,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Fhod3
|
UTSW |
18 |
25,266,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R7348:Fhod3
|
UTSW |
18 |
25,223,524 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7432:Fhod3
|
UTSW |
18 |
25,134,966 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7588:Fhod3
|
UTSW |
18 |
25,223,305 (GRCm39) |
missense |
probably benign |
0.02 |
R7629:Fhod3
|
UTSW |
18 |
24,887,374 (GRCm39) |
missense |
probably benign |
0.08 |
R7667:Fhod3
|
UTSW |
18 |
25,135,001 (GRCm39) |
missense |
probably benign |
|
R7681:Fhod3
|
UTSW |
18 |
25,123,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Fhod3
|
UTSW |
18 |
25,248,947 (GRCm39) |
critical splice donor site |
probably null |
|
R7889:Fhod3
|
UTSW |
18 |
24,903,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R8072:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R8117:Fhod3
|
UTSW |
18 |
25,248,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Fhod3
|
UTSW |
18 |
25,246,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Fhod3
|
UTSW |
18 |
25,265,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R8518:Fhod3
|
UTSW |
18 |
25,189,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R8845:Fhod3
|
UTSW |
18 |
25,265,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R8889:Fhod3
|
UTSW |
18 |
25,189,452 (GRCm39) |
critical splice donor site |
probably null |
|
R8892:Fhod3
|
UTSW |
18 |
25,189,452 (GRCm39) |
critical splice donor site |
probably null |
|
R9016:Fhod3
|
UTSW |
18 |
25,243,136 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9035:Fhod3
|
UTSW |
18 |
25,161,140 (GRCm39) |
missense |
probably benign |
0.03 |
R9063:Fhod3
|
UTSW |
18 |
25,153,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R9157:Fhod3
|
UTSW |
18 |
25,218,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R9201:Fhod3
|
UTSW |
18 |
25,127,613 (GRCm39) |
nonsense |
probably null |
|
R9244:Fhod3
|
UTSW |
18 |
25,248,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R9268:Fhod3
|
UTSW |
18 |
24,842,832 (GRCm39) |
critical splice donor site |
probably null |
|
R9272:Fhod3
|
UTSW |
18 |
25,030,681 (GRCm39) |
splice site |
probably benign |
|
R9415:Fhod3
|
UTSW |
18 |
25,102,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Fhod3
|
UTSW |
18 |
25,248,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Fhod3
|
UTSW |
18 |
25,193,392 (GRCm39) |
nonsense |
probably null |
|
R9739:Fhod3
|
UTSW |
18 |
24,903,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fhod3
|
UTSW |
18 |
25,153,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|