Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
A |
6: 142,539,870 (GRCm39) |
|
probably null |
Het |
Adam4 |
A |
T |
12: 81,466,657 (GRCm39) |
C655S |
probably damaging |
Het |
Adamts13 |
A |
C |
2: 26,880,568 (GRCm39) |
D717A |
probably damaging |
Het |
Atf7ip2 |
A |
G |
16: 10,019,262 (GRCm39) |
N30S |
possibly damaging |
Het |
Bmp8b |
T |
C |
4: 123,008,532 (GRCm39) |
V166A |
probably benign |
Het |
Bpifb9a |
G |
A |
2: 154,104,646 (GRCm39) |
G261R |
probably benign |
Het |
Cdipt |
G |
T |
7: 126,578,732 (GRCm39) |
M174I |
probably benign |
Het |
Cep128 |
T |
C |
12: 90,966,419 (GRCm39) |
T1063A |
probably benign |
Het |
Ciao1 |
A |
G |
2: 127,088,404 (GRCm39) |
Y140H |
probably damaging |
Het |
Cngb1 |
A |
G |
8: 96,024,408 (GRCm39) |
S217P |
unknown |
Het |
Cnot2 |
T |
A |
10: 116,346,294 (GRCm39) |
I103F |
probably benign |
Het |
Col27a1 |
T |
G |
4: 63,144,040 (GRCm39) |
V576G |
probably damaging |
Het |
Dapk1 |
T |
A |
13: 60,878,710 (GRCm39) |
H566Q |
probably benign |
Het |
Dhrs2 |
T |
A |
14: 55,478,637 (GRCm39) |
C261S |
possibly damaging |
Het |
Ercc4 |
G |
C |
16: 12,948,001 (GRCm39) |
R406P |
probably benign |
Het |
Fer1l4 |
A |
G |
2: 155,886,934 (GRCm39) |
|
probably null |
Het |
Fsip1 |
T |
A |
2: 118,075,359 (GRCm39) |
K218M |
unknown |
Het |
Fsip2 |
G |
T |
2: 82,811,346 (GRCm39) |
S2555I |
possibly damaging |
Het |
Gfpt2 |
A |
G |
11: 49,714,785 (GRCm39) |
K358E |
probably benign |
Het |
Gm9637 |
A |
T |
14: 19,402,598 (GRCm38) |
V1D |
noncoding transcript |
Het |
H2-M10.6 |
T |
C |
17: 37,124,155 (GRCm39) |
|
probably null |
Het |
Hand2 |
A |
G |
8: 57,774,994 (GRCm39) |
Y18C |
probably damaging |
Het |
Helz2 |
A |
T |
2: 180,879,895 (GRCm39) |
V607E |
probably damaging |
Het |
Hps5 |
G |
A |
7: 46,418,485 (GRCm39) |
R862* |
probably null |
Het |
Ildr1 |
A |
G |
16: 36,529,883 (GRCm39) |
D90G |
probably damaging |
Het |
Ints12 |
A |
G |
3: 132,814,633 (GRCm39) |
N280S |
probably benign |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Itpr2 |
T |
A |
6: 146,274,604 (GRCm39) |
K859N |
probably damaging |
Het |
Lhx9 |
G |
T |
1: 138,766,179 (GRCm39) |
A212D |
probably benign |
Het |
Myo6 |
C |
T |
9: 80,162,229 (GRCm39) |
T322I |
unknown |
Het |
Ndufaf4 |
A |
G |
4: 24,898,648 (GRCm39) |
D71G |
probably benign |
Het |
Nrp1 |
T |
A |
8: 129,214,434 (GRCm39) |
S641T |
probably benign |
Het |
Nudt7 |
A |
T |
8: 114,863,080 (GRCm39) |
N37I |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,913,066 (GRCm39) |
I271F |
|
Het |
Or2ag16 |
T |
C |
7: 106,352,374 (GRCm39) |
T74A |
probably benign |
Het |
Or4d2b |
G |
A |
11: 87,780,443 (GRCm39) |
S93F |
probably damaging |
Het |
Or6c5b |
T |
C |
10: 129,245,975 (GRCm39) |
S247P |
probably damaging |
Het |
Or7g18 |
T |
C |
9: 18,787,126 (GRCm39) |
Y168H |
probably benign |
Het |
Or9g4b |
A |
G |
2: 85,616,119 (GRCm39) |
E88G |
probably benign |
Het |
Oxa1l |
T |
C |
14: 54,605,274 (GRCm39) |
S317P |
probably damaging |
Het |
Poglut2 |
A |
T |
1: 44,156,226 (GRCm39) |
H120Q |
probably benign |
Het |
Polr2a |
C |
T |
11: 69,630,779 (GRCm39) |
R1213H |
probably damaging |
Het |
Postn |
A |
T |
3: 54,283,468 (GRCm39) |
S516C |
probably null |
Het |
Rabep2 |
A |
G |
7: 126,039,580 (GRCm39) |
T336A |
possibly damaging |
Het |
Ralgapb |
G |
A |
2: 158,285,256 (GRCm39) |
C585Y |
probably damaging |
Het |
Rexo4 |
A |
G |
2: 26,850,350 (GRCm39) |
S276P |
probably damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCTGCGGCGGC |
7: 97,229,122 (GRCm39) |
|
probably benign |
Het |
Sall3 |
G |
A |
18: 81,016,969 (GRCm39) |
P320S |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,099,789 (GRCm39) |
L160P |
probably damaging |
Het |
Sphkap |
A |
G |
1: 83,256,492 (GRCm39) |
F419S |
probably benign |
Het |
Stag1 |
C |
A |
9: 100,811,946 (GRCm39) |
T808K |
probably benign |
Het |
Stam2 |
G |
T |
2: 52,604,931 (GRCm39) |
N201K |
possibly damaging |
Het |
Stat1 |
G |
A |
1: 52,194,178 (GRCm39) |
R704Q |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,331,303 (GRCm39) |
D2236G |
probably damaging |
Het |
Thsd7a |
T |
A |
6: 12,379,592 (GRCm39) |
Y944F |
|
Het |
Tmem225 |
G |
T |
9: 40,061,955 (GRCm39) |
V190F |
probably damaging |
Het |
Tonsl |
A |
T |
15: 76,521,022 (GRCm39) |
V400D |
probably benign |
Het |
Tpp2 |
G |
A |
1: 44,022,712 (GRCm39) |
G971D |
probably damaging |
Het |
Trh |
C |
T |
6: 92,220,050 (GRCm39) |
V89I |
probably benign |
Het |
Txlnb |
A |
G |
10: 17,717,205 (GRCm39) |
D404G |
probably damaging |
Het |
Uggt1 |
A |
G |
1: 36,204,645 (GRCm39) |
V990A |
probably damaging |
Het |
Vmn1r179 |
T |
A |
7: 23,628,396 (GRCm39) |
Y196N |
possibly damaging |
Het |
Vmn2r8 |
T |
C |
5: 108,945,936 (GRCm39) |
D557G |
probably damaging |
Het |
Zfp516 |
G |
T |
18: 82,974,458 (GRCm39) |
G219C |
probably 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 |
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 |
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 |
|