Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh18a1 |
T |
C |
19: 40,562,800 (GRCm39) |
N191S |
probably benign |
Het |
Cacnb2 |
T |
A |
2: 14,879,630 (GRCm39) |
L84* |
probably null |
Het |
Cdhr2 |
C |
T |
13: 54,866,052 (GRCm39) |
T284M |
possibly damaging |
Het |
Defb45 |
T |
C |
2: 152,438,394 (GRCm39) |
|
probably benign |
Het |
Dkk3 |
C |
T |
7: 111,718,679 (GRCm39) |
V236M |
probably benign |
Het |
Dscc1 |
A |
T |
15: 54,945,711 (GRCm39) |
V328D |
probably benign |
Het |
Epha3 |
T |
C |
16: 63,372,889 (GRCm39) |
Y938C |
probably damaging |
Het |
Erc1 |
A |
T |
6: 119,756,452 (GRCm39) |
F435I |
possibly damaging |
Het |
Fbxl5 |
T |
C |
5: 43,908,323 (GRCm39) |
Y626C |
possibly damaging |
Het |
Gabrr1 |
C |
T |
4: 33,160,225 (GRCm39) |
S303F |
probably damaging |
Het |
Ggt1 |
T |
C |
10: 75,414,689 (GRCm39) |
V169A |
possibly damaging |
Het |
Gm10800 |
CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA |
CAAGAAAACTGAAAATCA |
2: 98,497,361 (GRCm39) |
|
probably null |
Het |
Gm3182 |
T |
A |
14: 4,481,832 (GRCm38) |
C9S |
probably damaging |
Het |
Gpr88 |
A |
C |
3: 116,046,264 (GRCm39) |
S16A |
unknown |
Het |
Kalrn |
A |
T |
16: 33,851,952 (GRCm39) |
M2076K |
possibly damaging |
Het |
Katnip |
A |
G |
7: 125,412,768 (GRCm39) |
T371A |
probably benign |
Het |
Kcnd3 |
T |
C |
3: 105,566,025 (GRCm39) |
I402T |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,489,714 (GRCm39) |
D57G |
probably benign |
Het |
Ncl |
T |
C |
1: 86,279,162 (GRCm39) |
T584A |
possibly damaging |
Het |
Nfx1 |
A |
T |
4: 40,977,244 (GRCm39) |
Q306L |
probably benign |
Het |
Ogdh |
A |
T |
11: 6,290,504 (GRCm39) |
D374V |
probably benign |
Het |
Or5d39 |
T |
A |
2: 87,980,259 (GRCm39) |
T35S |
probably benign |
Het |
Pak5 |
T |
A |
2: 135,925,211 (GRCm39) |
H697L |
probably damaging |
Het |
Pappa |
T |
C |
4: 65,234,469 (GRCm39) |
C1425R |
probably damaging |
Het |
Pramel26 |
T |
C |
4: 143,539,406 (GRCm39) |
E29G |
possibly damaging |
Het |
Rab3gap2 |
T |
A |
1: 185,013,882 (GRCm39) |
I1196N |
probably damaging |
Het |
Ralyl |
A |
T |
3: 14,172,299 (GRCm39) |
D56V |
probably damaging |
Het |
Scin |
C |
T |
12: 40,119,446 (GRCm39) |
|
probably null |
Het |
Slc25a19 |
T |
C |
11: 115,514,781 (GRCm39) |
I69V |
possibly damaging |
Het |
Slc8a1 |
G |
T |
17: 81,956,269 (GRCm39) |
Y256* |
probably null |
Het |
Smyd1 |
T |
C |
6: 71,196,272 (GRCm39) |
H372R |
probably benign |
Het |
St8sia1 |
T |
C |
6: 142,859,848 (GRCm39) |
T94A |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,527,916 (GRCm39) |
M1391K |
possibly damaging |
Het |
Tlr9 |
G |
A |
9: 106,100,721 (GRCm39) |
R4H |
probably benign |
Het |
Trim50 |
A |
G |
5: 135,382,331 (GRCm39) |
D61G |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,597,295 (GRCm39) |
P19873S |
probably damaging |
Het |
Vmn1r228 |
G |
T |
17: 20,996,772 (GRCm39) |
H249N |
probably benign |
Het |
Vmn2r108 |
C |
T |
17: 20,683,279 (GRCm39) |
G642S |
probably damaging |
Het |
Wdr27 |
A |
G |
17: 15,154,831 (GRCm39) |
S29P |
probably benign |
Het |
Zan |
A |
G |
5: 137,415,298 (GRCm39) |
|
probably null |
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 |
|
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 |
|
R1202:Fmn2
|
UTSW |
1 |
174,440,101 (GRCm39) |
nonsense |
probably null |
|
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 |
|
|