Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,882,756 (GRCm39) |
Y233H |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,885,211 (GRCm39) |
|
probably benign |
Het |
Asah2 |
T |
C |
19: 31,964,342 (GRCm39) |
Y696C |
probably damaging |
Het |
Atp8b3 |
A |
T |
10: 80,370,292 (GRCm39) |
D112E |
probably damaging |
Het |
B3gat3 |
T |
C |
19: 8,903,215 (GRCm39) |
Y191H |
probably damaging |
Het |
Capns2 |
T |
C |
8: 93,628,738 (GRCm39) |
I209T |
probably damaging |
Het |
Ccnl2 |
T |
C |
4: 155,905,479 (GRCm39) |
I303T |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,199,672 (GRCm39) |
S817R |
probably benign |
Het |
Cep57 |
A |
T |
9: 13,729,683 (GRCm39) |
L36* |
probably null |
Het |
Cers4 |
T |
A |
8: 4,566,878 (GRCm39) |
V60E |
probably damaging |
Het |
Ces2e |
T |
C |
8: 105,655,451 (GRCm39) |
Y125H |
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,742,489 (GRCm39) |
E497G |
probably benign |
Het |
Ddx24 |
A |
T |
12: 103,383,864 (GRCm39) |
M575K |
possibly damaging |
Het |
Dmxl2 |
A |
T |
9: 54,323,655 (GRCm39) |
V1243E |
probably damaging |
Het |
Elf2 |
A |
T |
3: 51,165,193 (GRCm39) |
Y270* |
probably null |
Het |
Ep400 |
A |
G |
5: 110,875,429 (GRCm39) |
L844S |
unknown |
Het |
F13a1 |
A |
T |
13: 37,172,870 (GRCm39) |
I170N |
possibly damaging |
Het |
Gm16506 |
T |
A |
14: 43,961,603 (GRCm39) |
|
probably benign |
Het |
Grm4 |
A |
G |
17: 27,653,797 (GRCm39) |
F463L |
probably damaging |
Het |
Lrrc49 |
T |
C |
9: 60,495,140 (GRCm39) |
Y691C |
probably damaging |
Het |
Mbip |
A |
C |
12: 56,384,547 (GRCm39) |
|
probably null |
Het |
Or9k2 |
T |
A |
10: 129,998,269 (GRCm39) |
K309* |
probably null |
Het |
Plod1 |
C |
T |
4: 148,007,580 (GRCm39) |
|
probably null |
Het |
Primpol |
A |
G |
8: 47,039,475 (GRCm39) |
W382R |
probably damaging |
Het |
Rufy2 |
A |
G |
10: 62,840,483 (GRCm39) |
E418G |
probably benign |
Het |
Samm50 |
T |
C |
15: 84,098,341 (GRCm39) |
V460A |
probably benign |
Het |
Senp2 |
T |
C |
16: 21,859,329 (GRCm39) |
V460A |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,698,442 (GRCm39) |
H453R |
probably benign |
Het |
Slc22a22 |
A |
G |
15: 57,112,948 (GRCm39) |
|
probably benign |
Het |
Spag1 |
A |
T |
15: 36,234,529 (GRCm39) |
D763V |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,504,167 (GRCm39) |
|
probably benign |
Het |
Tppp |
G |
T |
13: 74,169,535 (GRCm39) |
V92F |
possibly damaging |
Het |
Vmn1r32 |
G |
A |
6: 66,530,489 (GRCm39) |
L96F |
probably damaging |
Het |
Vmn2r53 |
C |
A |
7: 12,340,435 (GRCm39) |
A13S |
probably damaging |
Het |
Vmn2r75 |
G |
A |
7: 85,820,933 (GRCm39) |
|
probably benign |
Het |
Zfp750 |
C |
A |
11: 121,404,513 (GRCm39) |
G121* |
probably null |
Het |
|
Other mutations in H2-M10.2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00771:H2-M10.2
|
APN |
17 |
36,597,288 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01490:H2-M10.2
|
APN |
17 |
36,596,377 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02347:H2-M10.2
|
APN |
17 |
36,596,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:H2-M10.2
|
APN |
17 |
36,595,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:H2-M10.2
|
UTSW |
17 |
36,595,253 (GRCm39) |
missense |
probably benign |
0.04 |
R1756:H2-M10.2
|
UTSW |
17 |
36,597,015 (GRCm39) |
splice site |
probably benign |
|
R1803:H2-M10.2
|
UTSW |
17 |
36,596,763 (GRCm39) |
missense |
probably benign |
|
R2496:H2-M10.2
|
UTSW |
17 |
36,596,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3816:H2-M10.2
|
UTSW |
17 |
36,597,254 (GRCm39) |
nonsense |
probably null |
|
R4597:H2-M10.2
|
UTSW |
17 |
36,596,285 (GRCm39) |
missense |
probably benign |
0.07 |
R4832:H2-M10.2
|
UTSW |
17 |
36,595,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R5200:H2-M10.2
|
UTSW |
17 |
36,595,641 (GRCm39) |
missense |
probably benign |
0.17 |
R5325:H2-M10.2
|
UTSW |
17 |
36,596,471 (GRCm39) |
missense |
probably benign |
0.00 |
R7443:H2-M10.2
|
UTSW |
17 |
36,596,945 (GRCm39) |
missense |
probably benign |
|
R8064:H2-M10.2
|
UTSW |
17 |
36,595,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R8894:H2-M10.2
|
UTSW |
17 |
36,595,555 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9420:H2-M10.2
|
UTSW |
17 |
36,595,643 (GRCm39) |
missense |
probably benign |
0.01 |
R9489:H2-M10.2
|
UTSW |
17 |
36,596,936 (GRCm39) |
missense |
probably benign |
0.04 |
|