Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,897,232 (GRCm39) |
M637K |
probably damaging |
Het |
Abca8a |
A |
G |
11: 109,922,398 (GRCm39) |
V1395A |
probably benign |
Het |
Adam20 |
A |
C |
8: 41,249,597 (GRCm39) |
D569A |
probably benign |
Het |
Axl |
A |
G |
7: 25,473,594 (GRCm39) |
L344P |
probably benign |
Het |
B3gat1 |
T |
C |
9: 26,668,283 (GRCm39) |
L291P |
probably damaging |
Het |
Cdc25c |
A |
T |
18: 34,867,910 (GRCm39) |
|
probably null |
Het |
Crat |
A |
T |
2: 30,297,736 (GRCm39) |
Y263N |
probably damaging |
Het |
Crb2 |
A |
G |
2: 37,685,523 (GRCm39) |
|
probably benign |
Het |
Dhx33 |
G |
A |
11: 70,884,687 (GRCm39) |
Q40* |
probably null |
Het |
Dnah7a |
A |
T |
1: 53,701,540 (GRCm39) |
V205D |
probably benign |
Het |
Emsy |
A |
T |
7: 98,240,077 (GRCm39) |
Y1011* |
probably null |
Het |
Fbln5 |
C |
T |
12: 101,717,146 (GRCm39) |
S414N |
probably damaging |
Het |
Fev |
T |
C |
1: 74,921,683 (GRCm39) |
E89G |
possibly damaging |
Het |
Fgg |
A |
G |
3: 82,921,535 (GRCm39) |
E406G |
possibly damaging |
Het |
Glra1 |
A |
T |
11: 55,405,715 (GRCm39) |
M425K |
possibly damaging |
Het |
Gm8214 |
C |
T |
1: 183,414,129 (GRCm39) |
|
noncoding transcript |
Het |
Kdm3b |
A |
G |
18: 34,926,067 (GRCm39) |
E69G |
probably damaging |
Het |
Kntc1 |
T |
A |
5: 123,895,877 (GRCm39) |
V89E |
probably damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,206,083 (GRCm39) |
N361I |
unknown |
Het |
Macrod2 |
A |
G |
2: 142,226,250 (GRCm39) |
N457S |
probably damaging |
Het |
Mal |
C |
A |
2: 127,482,234 (GRCm39) |
M56I |
probably damaging |
Het |
Mfsd5 |
C |
T |
15: 102,189,882 (GRCm39) |
T418M |
probably benign |
Het |
Mmaa |
C |
A |
8: 79,994,600 (GRCm39) |
R402L |
probably benign |
Het |
Myo15a |
T |
C |
11: 60,393,115 (GRCm39) |
|
probably benign |
Het |
Nme1 |
A |
G |
11: 93,850,317 (GRCm39) |
S122P |
possibly damaging |
Het |
Nxt1 |
A |
G |
2: 148,517,316 (GRCm39) |
E19G |
probably damaging |
Het |
Nynrin |
A |
T |
14: 56,107,874 (GRCm39) |
T994S |
probably benign |
Het |
Orc2 |
T |
G |
1: 58,536,551 (GRCm39) |
E56D |
probably benign |
Het |
Orc2 |
T |
C |
1: 58,536,552 (GRCm39) |
E56G |
probably benign |
Het |
Pid1 |
G |
A |
1: 84,016,026 (GRCm39) |
T113I |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 118,340,900 (GRCm39) |
|
probably benign |
Het |
Rad50 |
A |
G |
11: 53,597,848 (GRCm39) |
V12A |
probably damaging |
Het |
Serpinb9c |
C |
T |
13: 33,335,862 (GRCm39) |
V197I |
probably benign |
Het |
Sfxn2 |
A |
T |
19: 46,574,212 (GRCm39) |
N134I |
probably damaging |
Het |
Spen |
T |
C |
4: 141,244,424 (GRCm39) |
R204G |
unknown |
Het |
Strip2 |
A |
G |
6: 29,939,166 (GRCm39) |
|
probably benign |
Het |
Tas2r135 |
A |
T |
6: 42,383,078 (GRCm39) |
I206L |
probably benign |
Het |
Tmem243 |
A |
G |
5: 9,151,348 (GRCm39) |
T11A |
probably damaging |
Het |
Tmprss11c |
A |
G |
5: 86,379,666 (GRCm39) |
V401A |
probably damaging |
Het |
Trim50 |
T |
A |
5: 135,392,808 (GRCm39) |
I241N |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,781,864 (GRCm39) |
S1015A |
possibly damaging |
Het |
Wee1 |
T |
C |
7: 109,741,242 (GRCm39) |
S622P |
probably benign |
Het |
|
Other mutations in 2310022B05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02141:2310022B05Rik
|
APN |
8 |
125,364,645 (GRCm39) |
utr 3 prime |
probably benign |
|
R0245:2310022B05Rik
|
UTSW |
8 |
125,378,168 (GRCm39) |
splice site |
probably benign |
|
R2038:2310022B05Rik
|
UTSW |
8 |
125,389,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:2310022B05Rik
|
UTSW |
8 |
125,378,168 (GRCm39) |
splice site |
probably benign |
|
R4652:2310022B05Rik
|
UTSW |
8 |
125,366,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:2310022B05Rik
|
UTSW |
8 |
125,366,300 (GRCm39) |
missense |
probably benign |
0.01 |
R4867:2310022B05Rik
|
UTSW |
8 |
125,366,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6018:2310022B05Rik
|
UTSW |
8 |
125,365,853 (GRCm39) |
missense |
probably benign |
0.00 |
R6602:2310022B05Rik
|
UTSW |
8 |
125,365,993 (GRCm39) |
missense |
probably damaging |
0.98 |
R6849:2310022B05Rik
|
UTSW |
8 |
125,366,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R7924:2310022B05Rik
|
UTSW |
8 |
125,390,051 (GRCm39) |
start gained |
probably benign |
|
R8759:2310022B05Rik
|
UTSW |
8 |
125,365,916 (GRCm39) |
missense |
probably benign |
0.02 |
R9778:2310022B05Rik
|
UTSW |
8 |
125,366,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|