Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,853,914 (GRCm39) |
N248Y |
possibly damaging |
Het |
Adamts13 |
G |
A |
2: 26,868,023 (GRCm39) |
V128M |
probably damaging |
Het |
Agl |
A |
T |
3: 116,566,175 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,224,621 (GRCm39) |
M1405K |
probably damaging |
Het |
Atp6v1a |
G |
T |
16: 43,920,319 (GRCm39) |
L426M |
probably damaging |
Het |
Calhm6 |
A |
G |
10: 34,002,561 (GRCm39) |
V174A |
probably damaging |
Het |
Cdc123 |
A |
G |
2: 5,808,752 (GRCm39) |
|
probably benign |
Het |
Cept1 |
A |
G |
3: 106,438,444 (GRCm39) |
|
probably benign |
Het |
Cipc |
T |
A |
12: 87,007,047 (GRCm39) |
D60E |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,581,747 (GRCm39) |
S30P |
probably benign |
Het |
Exosc3 |
A |
G |
4: 45,319,659 (GRCm39) |
I121T |
probably benign |
Het |
Fbln5 |
A |
G |
12: 101,776,128 (GRCm39) |
Y89H |
probably damaging |
Het |
Fpgt |
T |
C |
3: 154,792,483 (GRCm39) |
T515A |
probably benign |
Het |
Gas2l2 |
G |
A |
11: 83,312,906 (GRCm39) |
T802I |
probably benign |
Het |
Gm10710 |
T |
A |
3: 83,035,156 (GRCm39) |
|
probably benign |
Het |
Hdac4 |
A |
G |
1: 91,861,417 (GRCm39) |
M1051T |
probably benign |
Het |
Heatr5b |
A |
G |
17: 79,115,909 (GRCm39) |
V849A |
probably damaging |
Het |
Helb |
T |
C |
10: 119,938,738 (GRCm39) |
I579V |
probably damaging |
Het |
Hspa1l |
A |
G |
17: 35,197,787 (GRCm39) |
I609V |
probably benign |
Het |
Itgam |
C |
A |
7: 127,670,115 (GRCm39) |
Q136K |
probably benign |
Het |
Kcnc1 |
T |
C |
7: 46,077,554 (GRCm39) |
L452P |
probably damaging |
Het |
Ltbp4 |
T |
A |
7: 27,019,071 (GRCm39) |
T1083S |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,300,686 (GRCm39) |
I1449M |
probably damaging |
Het |
Nalf1 |
A |
T |
8: 9,257,831 (GRCm39) |
V439E |
probably damaging |
Het |
P2rx5 |
T |
A |
11: 73,056,385 (GRCm39) |
V103E |
probably damaging |
Het |
Pals1 |
T |
C |
12: 78,877,681 (GRCm39) |
V531A |
possibly damaging |
Het |
Pappa |
A |
G |
4: 65,123,329 (GRCm39) |
D888G |
possibly damaging |
Het |
Pcdhb21 |
G |
T |
18: 37,647,958 (GRCm39) |
M362I |
probably benign |
Het |
Pde1a |
A |
G |
2: 79,705,628 (GRCm39) |
S333P |
probably damaging |
Het |
Ppm1j |
A |
G |
3: 104,691,408 (GRCm39) |
T299A |
probably damaging |
Het |
Pramel46 |
G |
A |
5: 95,418,510 (GRCm39) |
T162I |
probably benign |
Het |
Ptdss2 |
A |
G |
7: 140,732,749 (GRCm39) |
E168G |
probably damaging |
Het |
Rspry1 |
A |
G |
8: 95,376,444 (GRCm39) |
N322S |
probably benign |
Het |
Slc7a9 |
T |
A |
7: 35,156,485 (GRCm39) |
V309E |
probably damaging |
Het |
Slco6c1 |
A |
G |
1: 97,003,548 (GRCm39) |
|
probably benign |
Het |
Tas2r120 |
T |
A |
6: 132,634,227 (GRCm39) |
M103K |
probably damaging |
Het |
Tbxas1 |
T |
A |
6: 38,925,561 (GRCm39) |
F59I |
probably damaging |
Het |
Tfpi |
A |
G |
2: 84,274,378 (GRCm39) |
S203P |
probably benign |
Het |
Tram2 |
T |
C |
1: 21,074,083 (GRCm39) |
N285S |
possibly damaging |
Het |
Trio |
T |
A |
15: 27,846,896 (GRCm39) |
D980V |
probably damaging |
Het |
Trpv5 |
T |
A |
6: 41,637,229 (GRCm39) |
H419L |
probably damaging |
Het |
Usp28 |
C |
T |
9: 48,943,543 (GRCm39) |
R361* |
probably null |
Het |
Vmn1r6 |
T |
A |
6: 56,979,674 (GRCm39) |
L112* |
probably null |
Het |
Vmn2r12 |
A |
T |
5: 109,240,025 (GRCm39) |
N179K |
probably benign |
Het |
Vmn2r82 |
G |
T |
10: 79,214,691 (GRCm39) |
A225S |
probably benign |
Het |
Zcchc4 |
A |
G |
5: 52,965,698 (GRCm39) |
Y334C |
probably damaging |
Het |
Zfp609 |
T |
C |
9: 65,610,116 (GRCm39) |
E949G |
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 |
25,030,738 (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 |
R4497:Fhod3
|
UTSW |
18 |
25,243,296 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|