Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
C |
11: 9,240,834 (GRCm39) |
E899A |
possibly damaging |
Het |
Best2 |
T |
A |
8: 85,737,418 (GRCm39) |
I230F |
probably damaging |
Het |
C2cd2 |
T |
C |
16: 97,676,403 (GRCm39) |
E448G |
probably damaging |
Het |
C2cd3 |
T |
G |
7: 100,040,291 (GRCm39) |
S287A |
probably benign |
Het |
Camta2 |
G |
A |
11: 70,567,234 (GRCm39) |
P677S |
probably benign |
Het |
Cand2 |
C |
T |
6: 115,769,490 (GRCm39) |
R767C |
probably damaging |
Het |
Celsr3 |
G |
A |
9: 108,704,293 (GRCm39) |
E259K |
probably benign |
Het |
Cep250 |
C |
G |
2: 155,834,035 (GRCm39) |
Q1987E |
probably benign |
Het |
Chn1 |
T |
C |
2: 73,443,430 (GRCm39) |
D440G |
probably benign |
Het |
Cmbl |
A |
T |
15: 31,585,449 (GRCm39) |
D111V |
possibly damaging |
Het |
Col5a3 |
T |
A |
9: 20,682,453 (GRCm39) |
I1664F |
unknown |
Het |
Cp |
T |
C |
3: 20,033,158 (GRCm39) |
S662P |
possibly damaging |
Het |
Cpne5 |
G |
A |
17: 29,430,677 (GRCm39) |
R78C |
probably damaging |
Het |
Cst5 |
A |
G |
2: 149,249,261 (GRCm39) |
T104A |
probably benign |
Het |
Cyp11b2 |
A |
G |
15: 74,725,662 (GRCm39) |
F195S |
possibly damaging |
Het |
Dcaf17 |
T |
C |
2: 70,920,136 (GRCm39) |
Y475H |
probably benign |
Het |
Eeig1 |
A |
G |
2: 32,455,674 (GRCm39) |
S267G |
probably benign |
Het |
Ext2 |
A |
G |
2: 93,644,144 (GRCm39) |
W46R |
probably benign |
Het |
Gal3st3 |
T |
A |
19: 5,352,605 (GRCm39) |
S11T |
probably benign |
Het |
Garin5b |
A |
T |
7: 4,762,253 (GRCm39) |
H265Q |
|
Het |
Gfi1 |
T |
A |
5: 107,865,725 (GRCm39) |
I451F |
possibly damaging |
Het |
Gfpt2 |
T |
C |
11: 49,714,185 (GRCm39) |
L314P |
probably damaging |
Het |
Gm3250 |
A |
T |
10: 77,618,127 (GRCm39) |
C84S |
unknown |
Het |
Hmcn1 |
A |
T |
1: 150,565,320 (GRCm39) |
V2269E |
probably benign |
Het |
Ighv1-55 |
T |
C |
12: 115,172,013 (GRCm39) |
H18R |
probably benign |
Het |
Iqgap3 |
G |
A |
3: 87,998,883 (GRCm39) |
G328E |
probably benign |
Het |
Klf6 |
G |
T |
13: 5,917,233 (GRCm39) |
C303F |
probably benign |
Het |
Klhl35 |
A |
T |
7: 99,122,129 (GRCm39) |
S77C |
probably damaging |
Het |
Ktn1 |
T |
G |
14: 47,941,694 (GRCm39) |
V822G |
probably benign |
Het |
Lbhd2 |
G |
T |
12: 111,375,040 (GRCm39) |
G21W |
probably damaging |
Het |
Lrp1b |
G |
A |
2: 40,615,457 (GRCm39) |
R3649* |
probably null |
Het |
Map2 |
C |
A |
1: 66,453,312 (GRCm39) |
T734N |
probably damaging |
Het |
Mas1 |
A |
G |
17: 13,060,839 (GRCm39) |
F195L |
possibly damaging |
Het |
Med1 |
A |
T |
11: 98,080,009 (GRCm39) |
M44K |
possibly damaging |
Het |
Morc3 |
T |
C |
16: 93,667,482 (GRCm39) |
V620A |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,291,459 (GRCm39) |
D1160N |
probably benign |
Het |
Nucb2 |
T |
A |
7: 116,125,631 (GRCm39) |
I159N |
probably damaging |
Het |
Olfm5 |
A |
G |
7: 103,802,984 (GRCm39) |
L493P |
probably benign |
Het |
Or1e1 |
T |
G |
11: 73,244,797 (GRCm39) |
F73V |
probably damaging |
Het |
Or2ag15 |
A |
T |
7: 106,340,759 (GRCm39) |
C127* |
probably null |
Het |
Or56b1 |
C |
T |
7: 104,285,291 (GRCm39) |
R137C |
probably benign |
Het |
Pcdhb22 |
T |
A |
18: 37,651,813 (GRCm39) |
C94S |
probably damaging |
Het |
Pcdhga5 |
A |
G |
18: 37,829,537 (GRCm39) |
I662V |
probably benign |
Het |
Plcb2 |
G |
A |
2: 118,547,878 (GRCm39) |
T472M |
possibly damaging |
Het |
Plcb4 |
A |
G |
2: 135,849,795 (GRCm39) |
E1142G |
possibly damaging |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Polr2l |
T |
C |
7: 141,053,285 (GRCm39) |
Y43C |
probably damaging |
Het |
Prkcb |
T |
A |
7: 122,127,771 (GRCm39) |
N298K |
probably benign |
Het |
Ptar1 |
T |
A |
19: 23,695,414 (GRCm39) |
C294S |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,401,736 (GRCm39) |
I1919V |
|
Het |
Slc25a18 |
C |
T |
6: 120,769,022 (GRCm39) |
R180C |
probably benign |
Het |
Slc27a3 |
A |
C |
3: 90,295,768 (GRCm39) |
S285R |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,783,032 (GRCm39) |
V1092I |
unknown |
Het |
Spata19 |
T |
G |
9: 27,309,024 (GRCm39) |
I54R |
possibly damaging |
Het |
St6galnac5 |
T |
C |
3: 152,551,956 (GRCm39) |
T204A |
probably benign |
Het |
Tdpoz8 |
T |
A |
3: 92,981,341 (GRCm39) |
C46S |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,694,831 (GRCm39) |
I708V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,775,183 (GRCm39) |
E1999G |
unknown |
Het |
Ube3b |
C |
T |
5: 114,542,607 (GRCm39) |
T488M |
probably damaging |
Het |
Vmn1r235 |
A |
T |
17: 21,482,271 (GRCm39) |
I199F |
probably benign |
Het |
Vsig8 |
A |
T |
1: 172,388,340 (GRCm39) |
N215Y |
possibly damaging |
Het |
Wapl |
A |
G |
14: 34,399,417 (GRCm39) |
K162R |
possibly damaging |
Het |
Wdpcp |
A |
G |
11: 21,614,014 (GRCm39) |
T60A |
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,010,351 (GRCm39) |
I566N |
probably damaging |
Het |
Wdr46 |
C |
T |
17: 34,163,555 (GRCm39) |
T371M |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,344,923 (GRCm39) |
S1101P |
possibly damaging |
Het |
|
Other mutations in Edem2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01141:Edem2
|
APN |
2 |
155,550,948 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01417:Edem2
|
APN |
2 |
155,570,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02043:Edem2
|
APN |
2 |
155,547,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02403:Edem2
|
APN |
2 |
155,550,983 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0488:Edem2
|
UTSW |
2 |
155,558,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Edem2
|
UTSW |
2 |
155,544,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R1547:Edem2
|
UTSW |
2 |
155,564,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:Edem2
|
UTSW |
2 |
155,550,969 (GRCm39) |
missense |
probably benign |
0.03 |
R2114:Edem2
|
UTSW |
2 |
155,544,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R2250:Edem2
|
UTSW |
2 |
155,552,893 (GRCm39) |
splice site |
probably null |
|
R2268:Edem2
|
UTSW |
2 |
155,544,137 (GRCm39) |
missense |
probably benign |
|
R2287:Edem2
|
UTSW |
2 |
155,555,279 (GRCm39) |
missense |
probably benign |
|
R2919:Edem2
|
UTSW |
2 |
155,550,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Edem2
|
UTSW |
2 |
155,547,618 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4806:Edem2
|
UTSW |
2 |
155,570,913 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5574:Edem2
|
UTSW |
2 |
155,558,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6714:Edem2
|
UTSW |
2 |
155,570,809 (GRCm39) |
critical splice donor site |
probably null |
|
R6913:Edem2
|
UTSW |
2 |
155,568,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R7016:Edem2
|
UTSW |
2 |
155,557,992 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7234:Edem2
|
UTSW |
2 |
155,552,886 (GRCm39) |
missense |
probably benign |
0.19 |
R8063:Edem2
|
UTSW |
2 |
155,544,376 (GRCm39) |
missense |
probably benign |
0.00 |
|