Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
T |
C |
4: 144,250,236 (GRCm39) |
F137L |
probably benign |
Het |
Cct3 |
T |
C |
3: 88,225,835 (GRCm39) |
|
probably null |
Het |
Fermt3 |
A |
G |
19: 6,980,850 (GRCm39) |
F294L |
probably damaging |
Het |
Fndc5 |
G |
A |
4: 129,033,238 (GRCm39) |
V102M |
probably damaging |
Het |
Gle1 |
C |
T |
2: 29,839,277 (GRCm39) |
A523V |
probably damaging |
Het |
Hoxd11 |
C |
T |
2: 74,512,921 (GRCm39) |
A62V |
possibly damaging |
Het |
Il23r |
A |
G |
6: 67,455,937 (GRCm39) |
V177A |
possibly damaging |
Het |
Impdh2 |
G |
A |
9: 108,440,386 (GRCm39) |
R224Q |
probably damaging |
Het |
Larp4b |
A |
G |
13: 9,216,362 (GRCm39) |
T516A |
possibly damaging |
Het |
Mtmr2 |
T |
C |
9: 13,714,748 (GRCm39) |
Y431H |
probably benign |
Het |
N4bp1 |
T |
C |
8: 87,571,515 (GRCm39) |
T828A |
probably benign |
Het |
Nphp4 |
G |
A |
4: 152,573,186 (GRCm39) |
|
probably null |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Pabpc1l |
G |
T |
2: 163,879,091 (GRCm39) |
V313F |
possibly damaging |
Het |
Pacs1 |
G |
A |
19: 5,185,265 (GRCm39) |
P885S |
probably damaging |
Het |
Scn3a |
T |
C |
2: 65,336,491 (GRCm39) |
N705S |
probably benign |
Het |
Sema4g |
G |
T |
19: 44,986,696 (GRCm39) |
R383L |
probably benign |
Het |
Slc26a10 |
A |
G |
10: 127,009,217 (GRCm39) |
L648P |
probably damaging |
Het |
St8sia2 |
A |
T |
7: 73,621,783 (GRCm39) |
V37E |
probably benign |
Het |
Tmem209 |
C |
G |
6: 30,508,789 (GRCm39) |
V6L |
probably benign |
Het |
Tmprss11a |
T |
A |
5: 86,559,784 (GRCm39) |
|
probably null |
Het |
Ube2o |
C |
T |
11: 116,432,408 (GRCm39) |
D853N |
probably damaging |
Het |
Usp17lb |
G |
A |
7: 104,491,695 (GRCm39) |
S6F |
probably damaging |
Het |
Vmn2r74 |
G |
A |
7: 85,610,545 (GRCm39) |
T49I |
possibly damaging |
Het |
Zfp236 |
T |
A |
18: 82,646,291 (GRCm39) |
T1041S |
probably benign |
Het |
|
Other mutations in Fmn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Fmn2
|
APN |
1 |
174,330,885 (GRCm39) |
missense |
unknown |
|
IGL01085:Fmn2
|
APN |
1 |
174,523,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01784:Fmn2
|
APN |
1 |
174,329,994 (GRCm39) |
missense |
unknown |
|
IGL02095:Fmn2
|
APN |
1 |
174,330,167 (GRCm39) |
missense |
unknown |
|
IGL02330:Fmn2
|
APN |
1 |
174,437,511 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02552:Fmn2
|
APN |
1 |
174,523,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Fmn2
|
UTSW |
1 |
174,409,625 (GRCm39) |
missense |
unknown |
|
PIT4498001:Fmn2
|
UTSW |
1 |
174,440,170 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Fmn2
|
UTSW |
1 |
174,474,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Fmn2
|
UTSW |
1 |
174,618,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Fmn2
|
UTSW |
1 |
174,436,015 (GRCm39) |
unclassified |
probably benign |
|
R0062:Fmn2
|
UTSW |
1 |
174,436,015 (GRCm39) |
unclassified |
probably benign |
|
R0306:Fmn2
|
UTSW |
1 |
174,437,050 (GRCm39) |
unclassified |
probably benign |
|
R0325:Fmn2
|
UTSW |
1 |
174,437,520 (GRCm39) |
critical splice donor site |
probably null |
|
R0403:Fmn2
|
UTSW |
1 |
174,521,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Fmn2
|
UTSW |
1 |
174,409,525 (GRCm39) |
missense |
unknown |
|
R0898:Fmn2
|
UTSW |
1 |
174,331,026 (GRCm39) |
missense |
unknown |
|
R1719:Fmn2
|
UTSW |
1 |
174,436,024 (GRCm39) |
unclassified |
probably benign |
|
R1763:Fmn2
|
UTSW |
1 |
174,329,832 (GRCm39) |
missense |
unknown |
|
R1771:Fmn2
|
UTSW |
1 |
174,436,342 (GRCm39) |
unclassified |
probably benign |
|
R1777:Fmn2
|
UTSW |
1 |
174,409,488 (GRCm39) |
missense |
unknown |
|
R1831:Fmn2
|
UTSW |
1 |
174,437,511 (GRCm39) |
missense |
probably benign |
0.38 |
R2259:Fmn2
|
UTSW |
1 |
174,330,498 (GRCm39) |
missense |
unknown |
|
R2960:Fmn2
|
UTSW |
1 |
174,437,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R3545:Fmn2
|
UTSW |
1 |
174,330,192 (GRCm39) |
missense |
unknown |
|
R3840:Fmn2
|
UTSW |
1 |
174,409,599 (GRCm39) |
frame shift |
probably null |
|
R4207:Fmn2
|
UTSW |
1 |
174,409,521 (GRCm39) |
missense |
unknown |
|
R4679:Fmn2
|
UTSW |
1 |
174,330,728 (GRCm39) |
missense |
unknown |
|
R4779:Fmn2
|
UTSW |
1 |
174,437,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Fmn2
|
UTSW |
1 |
174,409,527 (GRCm39) |
missense |
unknown |
|
R4926:Fmn2
|
UTSW |
1 |
174,329,981 (GRCm39) |
missense |
unknown |
|
R5007:Fmn2
|
UTSW |
1 |
174,571,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R5247:Fmn2
|
UTSW |
1 |
174,648,794 (GRCm39) |
missense |
probably benign |
0.04 |
R5324:Fmn2
|
UTSW |
1 |
174,436,446 (GRCm39) |
unclassified |
probably benign |
|
R5353:Fmn2
|
UTSW |
1 |
174,330,572 (GRCm39) |
missense |
unknown |
|
R5420:Fmn2
|
UTSW |
1 |
174,526,344 (GRCm39) |
nonsense |
probably null |
|
R5607:Fmn2
|
UTSW |
1 |
174,437,377 (GRCm39) |
missense |
probably damaging |
0.97 |
R5668:Fmn2
|
UTSW |
1 |
174,409,603 (GRCm39) |
missense |
unknown |
|
R5982:Fmn2
|
UTSW |
1 |
174,330,019 (GRCm39) |
missense |
unknown |
|
R6148:Fmn2
|
UTSW |
1 |
174,494,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Fmn2
|
UTSW |
1 |
174,440,119 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6466:Fmn2
|
UTSW |
1 |
174,437,149 (GRCm39) |
unclassified |
probably benign |
|
R6647:Fmn2
|
UTSW |
1 |
174,420,670 (GRCm39) |
missense |
unknown |
|
R6835:Fmn2
|
UTSW |
1 |
174,527,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7231:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R7340:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R7378:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R7457:Fmn2
|
UTSW |
1 |
174,331,303 (GRCm39) |
splice site |
probably null |
|
R7474:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R7564:Fmn2
|
UTSW |
1 |
174,437,140 (GRCm39) |
missense |
unknown |
|
R7582:Fmn2
|
UTSW |
1 |
174,526,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Fmn2
|
UTSW |
1 |
174,494,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R8035:Fmn2
|
UTSW |
1 |
174,547,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R8203:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R8343:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R8371:Fmn2
|
UTSW |
1 |
174,437,173 (GRCm39) |
missense |
unknown |
|
R8377:Fmn2
|
UTSW |
1 |
174,436,011 (GRCm39) |
nonsense |
probably null |
|
R8543:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R8724:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R8726:Fmn2
|
UTSW |
1 |
174,437,404 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8891:Fmn2
|
UTSW |
1 |
174,436,769 (GRCm39) |
unclassified |
probably benign |
|
R9074:Fmn2
|
UTSW |
1 |
174,436,198 (GRCm39) |
missense |
unknown |
|
R9167:Fmn2
|
UTSW |
1 |
174,331,056 (GRCm39) |
missense |
unknown |
|
R9489:Fmn2
|
UTSW |
1 |
174,436,194 (GRCm39) |
nonsense |
probably null |
|
R9598:Fmn2
|
UTSW |
1 |
174,436,308 (GRCm39) |
missense |
unknown |
|
R9605:Fmn2
|
UTSW |
1 |
174,436,194 (GRCm39) |
nonsense |
probably null |
|
R9698:Fmn2
|
UTSW |
1 |
174,364,739 (GRCm39) |
missense |
unknown |
|
RF010:Fmn2
|
UTSW |
1 |
174,409,581 (GRCm39) |
missense |
unknown |
|
Z1176:Fmn2
|
UTSW |
1 |
174,435,960 (GRCm39) |
missense |
unknown |
|
|