Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano8 |
A |
G |
8: 71,936,184 (GRCm39) |
I204T |
probably damaging |
Het |
Anxa8 |
A |
G |
14: 33,815,371 (GRCm39) |
D150G |
probably damaging |
Het |
Arel1 |
T |
C |
12: 84,977,002 (GRCm39) |
T438A |
probably damaging |
Het |
Asphd1 |
T |
C |
7: 126,546,006 (GRCm39) |
|
probably benign |
Het |
Bcl2l12 |
A |
T |
7: 44,640,824 (GRCm39) |
|
probably benign |
Het |
Cand1 |
A |
G |
10: 119,055,602 (GRCm39) |
I87T |
probably damaging |
Het |
Ccdc80 |
A |
C |
16: 44,936,695 (GRCm39) |
T707P |
probably damaging |
Het |
Ccn6 |
A |
G |
10: 39,027,236 (GRCm39) |
V332A |
possibly damaging |
Het |
Cdh9 |
T |
A |
15: 16,849,162 (GRCm39) |
|
probably null |
Het |
Chrd |
T |
C |
16: 20,558,699 (GRCm39) |
|
probably benign |
Het |
Cpn1 |
T |
C |
19: 43,969,369 (GRCm39) |
Q98R |
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,172,420 (GRCm39) |
S583P |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,543,183 (GRCm39) |
I2329T |
possibly damaging |
Het |
Gfra1 |
G |
A |
19: 58,441,787 (GRCm39) |
T48I |
probably damaging |
Het |
Hapln3 |
C |
T |
7: 78,767,596 (GRCm39) |
|
probably null |
Het |
Heatr3 |
T |
C |
8: 88,871,185 (GRCm39) |
F180L |
possibly damaging |
Het |
Herc2 |
T |
A |
7: 55,813,849 (GRCm39) |
S2661T |
probably damaging |
Het |
Hook3 |
A |
T |
8: 26,551,462 (GRCm39) |
L126Q |
possibly damaging |
Het |
Hoxd8 |
T |
G |
2: 74,536,930 (GRCm39) |
L214R |
probably damaging |
Het |
Ifna1 |
T |
G |
4: 88,768,670 (GRCm39) |
L116R |
probably damaging |
Het |
Il31ra |
T |
A |
13: 112,660,886 (GRCm39) |
T487S |
probably benign |
Het |
Kifc2 |
C |
T |
15: 76,547,179 (GRCm39) |
R252W |
probably damaging |
Het |
Meox2 |
A |
G |
12: 37,228,333 (GRCm39) |
D290G |
probably damaging |
Het |
Micu2 |
A |
G |
14: 58,182,834 (GRCm39) |
|
probably benign |
Het |
Myh9 |
T |
C |
15: 77,673,130 (GRCm39) |
T406A |
possibly damaging |
Het |
Naip1 |
T |
A |
13: 100,545,626 (GRCm39) |
M1301L |
probably benign |
Het |
Pbrm1 |
T |
C |
14: 30,828,244 (GRCm39) |
L1341P |
possibly damaging |
Het |
Pcna-ps2 |
C |
A |
19: 9,261,323 (GRCm39) |
A194E |
probably benign |
Het |
Pdcd10 |
G |
A |
3: 75,434,901 (GRCm39) |
T130I |
probably damaging |
Het |
Pprc1 |
G |
A |
19: 46,051,946 (GRCm39) |
G491D |
probably damaging |
Het |
Prss57 |
A |
G |
10: 79,623,309 (GRCm39) |
V46A |
probably benign |
Het |
Ptcd3 |
A |
G |
6: 71,860,426 (GRCm39) |
|
probably null |
Het |
Riok1 |
C |
T |
13: 38,234,219 (GRCm39) |
P262S |
probably damaging |
Het |
Rnf13 |
A |
G |
3: 57,686,817 (GRCm39) |
N70S |
probably benign |
Het |
Skint7 |
T |
A |
4: 111,839,178 (GRCm39) |
D157E |
probably benign |
Het |
Sri |
T |
C |
5: 8,117,534 (GRCm39) |
F191S |
probably damaging |
Het |
Stat5b |
T |
C |
11: 100,678,200 (GRCm39) |
R638G |
probably benign |
Het |
Suds3 |
C |
T |
5: 117,232,970 (GRCm39) |
|
probably null |
Het |
Tmem19 |
A |
G |
10: 115,178,478 (GRCm39) |
L281P |
probably damaging |
Het |
Tmf1 |
A |
G |
6: 97,141,003 (GRCm39) |
|
probably benign |
Het |
Trio |
A |
G |
15: 27,768,125 (GRCm39) |
|
probably benign |
Het |
Usp28 |
T |
C |
9: 48,950,391 (GRCm39) |
I940T |
possibly damaging |
Het |
Zfp280d |
T |
A |
9: 72,219,504 (GRCm39) |
I227K |
probably benign |
Het |
Zfp335 |
A |
G |
2: 164,752,609 (GRCm39) |
V45A |
probably benign |
Het |
|
Other mutations in Egln3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03104:Egln3
|
APN |
12 |
54,249,981 (GRCm39) |
splice site |
probably benign |
|
R0036:Egln3
|
UTSW |
12 |
54,232,378 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0091:Egln3
|
UTSW |
12 |
54,228,432 (GRCm39) |
missense |
probably benign |
0.07 |
R0325:Egln3
|
UTSW |
12 |
54,250,298 (GRCm39) |
missense |
probably benign |
0.09 |
R0358:Egln3
|
UTSW |
12 |
54,250,082 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0494:Egln3
|
UTSW |
12 |
54,250,107 (GRCm39) |
missense |
probably benign |
0.01 |
R1241:Egln3
|
UTSW |
12 |
54,228,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Egln3
|
UTSW |
12 |
54,232,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R5078:Egln3
|
UTSW |
12 |
54,228,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Egln3
|
UTSW |
12 |
54,250,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R5692:Egln3
|
UTSW |
12 |
54,227,447 (GRCm39) |
splice site |
probably null |
|
R6038:Egln3
|
UTSW |
12 |
54,228,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R6038:Egln3
|
UTSW |
12 |
54,228,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R6732:Egln3
|
UTSW |
12 |
54,227,427 (GRCm39) |
missense |
probably benign |
|
R6944:Egln3
|
UTSW |
12 |
54,230,738 (GRCm39) |
missense |
probably benign |
0.00 |
R7508:Egln3
|
UTSW |
12 |
54,227,414 (GRCm39) |
missense |
probably benign |
0.28 |
R8204:Egln3
|
UTSW |
12 |
54,250,010 (GRCm39) |
missense |
probably benign |
0.00 |
|