Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam2 |
C |
T |
14: 66,311,498 (GRCm39) |
|
probably null |
Het |
Adgrb2 |
A |
T |
4: 129,912,865 (GRCm39) |
H1373L |
probably benign |
Het |
Adgrf4 |
A |
G |
17: 42,977,547 (GRCm39) |
S599P |
probably damaging |
Het |
Atp9b |
G |
A |
18: 80,961,103 (GRCm39) |
|
probably benign |
Het |
Baiap2 |
A |
G |
11: 119,872,836 (GRCm39) |
T125A |
probably benign |
Het |
Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,404,550 (GRCm39) |
S1114P |
probably damaging |
Het |
Ccdc159 |
T |
C |
9: 21,840,765 (GRCm39) |
S111P |
possibly damaging |
Het |
Cd177 |
T |
A |
7: 24,459,176 (GRCm39) |
T78S |
possibly damaging |
Het |
Cdk5rap2 |
A |
G |
4: 70,321,709 (GRCm39) |
|
probably null |
Het |
Cdkl3 |
C |
A |
11: 51,920,683 (GRCm39) |
T462K |
probably benign |
Het |
Chid1 |
A |
C |
7: 141,102,609 (GRCm39) |
L208R |
probably damaging |
Het |
Clca3b |
A |
G |
3: 144,542,342 (GRCm39) |
S487P |
probably benign |
Het |
Col6a3 |
A |
T |
1: 90,709,748 (GRCm39) |
L1816Q |
unknown |
Het |
Dido1 |
A |
G |
2: 180,325,782 (GRCm39) |
S469P |
probably benign |
Het |
Dsg2 |
A |
G |
18: 20,734,826 (GRCm39) |
N935D |
probably benign |
Het |
Fbxw2 |
A |
G |
2: 34,702,961 (GRCm39) |
I184T |
probably benign |
Het |
Gbp9 |
T |
C |
5: 105,253,620 (GRCm39) |
I32V |
possibly damaging |
Het |
Hycc2 |
A |
T |
1: 58,579,412 (GRCm39) |
|
probably benign |
Het |
Itgb8 |
G |
A |
12: 119,153,561 (GRCm39) |
T318I |
probably damaging |
Het |
Kcnb2 |
A |
G |
1: 15,781,236 (GRCm39) |
S703G |
probably benign |
Het |
Kif26b |
A |
T |
1: 178,743,866 (GRCm39) |
S1321C |
probably damaging |
Het |
Klb |
A |
G |
5: 65,529,717 (GRCm39) |
N415S |
possibly damaging |
Het |
Mrm3 |
T |
G |
11: 76,135,319 (GRCm39) |
S177A |
probably damaging |
Het |
Nav3 |
A |
G |
10: 109,539,368 (GRCm39) |
F2011S |
probably benign |
Het |
Nipal1 |
C |
T |
5: 72,816,067 (GRCm39) |
S30L |
probably benign |
Het |
Ogdhl |
T |
C |
14: 32,068,447 (GRCm39) |
Y895H |
probably damaging |
Het |
Pif1 |
A |
G |
9: 65,500,559 (GRCm39) |
N495D |
probably damaging |
Het |
Prrc2c |
A |
T |
1: 162,548,182 (GRCm39) |
|
probably null |
Het |
Pygl |
T |
C |
12: 70,237,866 (GRCm39) |
D724G |
probably damaging |
Het |
Runx1t1 |
A |
G |
4: 13,835,663 (GRCm39) |
D40G |
probably benign |
Het |
Serhl |
A |
T |
15: 82,989,838 (GRCm39) |
D192V |
possibly damaging |
Het |
Slc12a5 |
C |
T |
2: 164,825,201 (GRCm39) |
A461V |
probably damaging |
Het |
Tomm34 |
A |
T |
2: 163,900,582 (GRCm39) |
|
probably benign |
Het |
Zfp54 |
A |
G |
17: 21,650,559 (GRCm39) |
N45D |
probably damaging |
Het |
|
Other mutations in Megf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00736:Megf10
|
APN |
18 |
57,425,782 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01631:Megf10
|
APN |
18 |
57,392,869 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02488:Megf10
|
APN |
18 |
57,425,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02747:Megf10
|
APN |
18 |
57,423,565 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03298:Megf10
|
APN |
18 |
57,416,910 (GRCm39) |
nonsense |
probably null |
|
deep
|
UTSW |
18 |
57,395,203 (GRCm39) |
missense |
probably damaging |
1.00 |
megalodon
|
UTSW |
18 |
57,421,048 (GRCm39) |
nonsense |
probably null |
|
sharkie
|
UTSW |
18 |
57,324,257 (GRCm39) |
nonsense |
probably null |
|
IGL03046:Megf10
|
UTSW |
18 |
57,421,055 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4696001:Megf10
|
UTSW |
18 |
57,410,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R0020:Megf10
|
UTSW |
18 |
57,420,965 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0020:Megf10
|
UTSW |
18 |
57,420,965 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0115:Megf10
|
UTSW |
18 |
57,392,874 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0455:Megf10
|
UTSW |
18 |
57,386,054 (GRCm39) |
missense |
probably benign |
0.34 |
R0602:Megf10
|
UTSW |
18 |
57,395,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R0630:Megf10
|
UTSW |
18 |
57,421,067 (GRCm39) |
missense |
probably benign |
0.14 |
R0652:Megf10
|
UTSW |
18 |
57,410,796 (GRCm39) |
missense |
probably benign |
0.00 |
R0658:Megf10
|
UTSW |
18 |
57,385,968 (GRCm39) |
missense |
probably benign |
0.00 |
R0761:Megf10
|
UTSW |
18 |
57,421,048 (GRCm39) |
nonsense |
probably null |
|
R1013:Megf10
|
UTSW |
18 |
57,394,291 (GRCm39) |
missense |
probably benign |
0.00 |
R1130:Megf10
|
UTSW |
18 |
57,395,078 (GRCm39) |
missense |
probably benign |
0.06 |
R1451:Megf10
|
UTSW |
18 |
57,385,931 (GRCm39) |
missense |
probably damaging |
0.97 |
R1699:Megf10
|
UTSW |
18 |
57,410,802 (GRCm39) |
splice site |
probably null |
|
R1729:Megf10
|
UTSW |
18 |
57,373,864 (GRCm39) |
critical splice donor site |
probably null |
|
R1784:Megf10
|
UTSW |
18 |
57,373,864 (GRCm39) |
critical splice donor site |
probably null |
|
R1870:Megf10
|
UTSW |
18 |
57,324,257 (GRCm39) |
nonsense |
probably null |
|
R1961:Megf10
|
UTSW |
18 |
57,345,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R2094:Megf10
|
UTSW |
18 |
57,414,785 (GRCm39) |
nonsense |
probably null |
|
R2213:Megf10
|
UTSW |
18 |
57,421,081 (GRCm39) |
nonsense |
probably null |
|
R2853:Megf10
|
UTSW |
18 |
57,427,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Megf10
|
UTSW |
18 |
57,416,934 (GRCm39) |
missense |
probably benign |
0.39 |
R3774:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3775:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3776:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Megf10
|
UTSW |
18 |
57,408,907 (GRCm39) |
splice site |
probably benign |
|
R3911:Megf10
|
UTSW |
18 |
57,422,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R3966:Megf10
|
UTSW |
18 |
57,313,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Megf10
|
UTSW |
18 |
57,392,870 (GRCm39) |
missense |
probably damaging |
0.98 |
R4131:Megf10
|
UTSW |
18 |
57,313,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Megf10
|
UTSW |
18 |
57,322,675 (GRCm39) |
critical splice donor site |
probably null |
|
R4598:Megf10
|
UTSW |
18 |
57,420,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Megf10
|
UTSW |
18 |
57,420,864 (GRCm39) |
missense |
probably benign |
0.32 |
R4765:Megf10
|
UTSW |
18 |
57,420,866 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4874:Megf10
|
UTSW |
18 |
57,426,930 (GRCm39) |
missense |
probably benign |
0.00 |
R4928:Megf10
|
UTSW |
18 |
57,373,745 (GRCm39) |
missense |
probably benign |
|
R5412:Megf10
|
UTSW |
18 |
57,324,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Megf10
|
UTSW |
18 |
57,410,180 (GRCm39) |
missense |
probably benign |
0.11 |
R6015:Megf10
|
UTSW |
18 |
57,386,100 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:Megf10
|
UTSW |
18 |
57,375,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Megf10
|
UTSW |
18 |
57,375,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Megf10
|
UTSW |
18 |
57,313,621 (GRCm39) |
missense |
probably benign |
|
R6369:Megf10
|
UTSW |
18 |
57,394,259 (GRCm39) |
missense |
probably benign |
0.06 |
R6479:Megf10
|
UTSW |
18 |
57,379,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6489:Megf10
|
UTSW |
18 |
57,424,879 (GRCm39) |
missense |
probably benign |
0.01 |
R7228:Megf10
|
UTSW |
18 |
57,322,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Megf10
|
UTSW |
18 |
57,408,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Megf10
|
UTSW |
18 |
57,395,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Megf10
|
UTSW |
18 |
57,385,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R7488:Megf10
|
UTSW |
18 |
57,324,187 (GRCm39) |
missense |
probably damaging |
0.99 |
R7492:Megf10
|
UTSW |
18 |
57,424,866 (GRCm39) |
missense |
probably benign |
0.00 |
R7542:Megf10
|
UTSW |
18 |
57,322,642 (GRCm39) |
missense |
probably benign |
0.07 |
R7636:Megf10
|
UTSW |
18 |
57,410,061 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7646:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7650:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7713:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7714:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7716:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7796:Megf10
|
UTSW |
18 |
57,410,731 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7915:Megf10
|
UTSW |
18 |
57,373,807 (GRCm39) |
missense |
probably benign |
0.05 |
R8221:Megf10
|
UTSW |
18 |
57,416,893 (GRCm39) |
missense |
probably benign |
0.00 |
R8527:Megf10
|
UTSW |
18 |
57,425,790 (GRCm39) |
missense |
probably benign |
0.00 |
R8559:Megf10
|
UTSW |
18 |
57,373,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Megf10
|
UTSW |
18 |
57,392,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Megf10
|
UTSW |
18 |
57,394,252 (GRCm39) |
nonsense |
probably null |
|
R9481:Megf10
|
UTSW |
18 |
57,395,090 (GRCm39) |
missense |
probably benign |
0.38 |
R9644:Megf10
|
UTSW |
18 |
57,375,773 (GRCm39) |
missense |
probably benign |
|
RF003:Megf10
|
UTSW |
18 |
57,427,099 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Megf10
|
UTSW |
18 |
57,410,766 (GRCm39) |
missense |
probably damaging |
0.96 |
|