Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Casd1 |
A |
T |
6: 4,624,142 (GRCm39) |
I312F |
probably benign |
Het |
Cdc27 |
T |
C |
11: 104,413,557 (GRCm39) |
T395A |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,405,381 (GRCm39) |
I1717T |
probably benign |
Het |
Ces1f |
A |
T |
8: 93,992,488 (GRCm39) |
V321E |
possibly damaging |
Het |
Chrnb3 |
T |
C |
8: 27,886,832 (GRCm39) |
|
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,327,099 (GRCm39) |
F1416L |
unknown |
Het |
Cplx4 |
T |
C |
18: 66,103,123 (GRCm39) |
|
probably benign |
Het |
Cubn |
A |
T |
2: 13,386,648 (GRCm39) |
I1539N |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,878,696 (GRCm39) |
T562A |
probably benign |
Het |
Dnmt1 |
C |
A |
9: 20,819,845 (GRCm39) |
V1433F |
probably damaging |
Het |
Dytn |
A |
G |
1: 63,680,251 (GRCm39) |
L436P |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,117,841 (GRCm39) |
I783V |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,942,553 (GRCm39) |
V482E |
probably damaging |
Het |
Fcrlb |
T |
A |
1: 170,734,927 (GRCm39) |
E400V |
probably benign |
Het |
Folh1 |
T |
C |
7: 86,374,626 (GRCm39) |
D656G |
probably damaging |
Het |
Frem3 |
A |
C |
8: 81,339,723 (GRCm39) |
D672A |
probably damaging |
Het |
G3bp2 |
A |
G |
5: 92,221,106 (GRCm39) |
M3T |
possibly damaging |
Het |
Gm973 |
C |
T |
1: 59,621,632 (GRCm39) |
Q26* |
probably null |
Het |
Hsp90b1 |
T |
C |
10: 86,541,222 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
G |
A |
4: 137,246,125 (GRCm39) |
|
probably null |
Het |
Lpin3 |
T |
C |
2: 160,737,753 (GRCm39) |
|
probably null |
Het |
Mtss2 |
G |
A |
8: 111,464,256 (GRCm39) |
R295Q |
probably damaging |
Het |
Muc5b |
G |
T |
7: 141,409,369 (GRCm39) |
W1151L |
unknown |
Het |
Myo3a |
A |
G |
2: 22,467,538 (GRCm39) |
Y264C |
probably benign |
Het |
Or4c123 |
A |
G |
2: 89,127,407 (GRCm39) |
V69A |
probably benign |
Het |
Or55b3 |
T |
C |
7: 102,126,742 (GRCm39) |
T112A |
possibly damaging |
Het |
Or5p60 |
T |
A |
7: 107,724,249 (GRCm39) |
I74L |
probably benign |
Het |
Pecam1 |
C |
T |
11: 106,581,807 (GRCm39) |
G380S |
probably damaging |
Het |
Phf21a |
C |
T |
2: 92,179,767 (GRCm39) |
T345I |
probably damaging |
Het |
Polg |
G |
A |
7: 79,109,485 (GRCm39) |
S444L |
probably damaging |
Het |
Prickle1 |
A |
G |
15: 93,401,027 (GRCm39) |
Y486H |
probably damaging |
Het |
Scg5 |
G |
A |
2: 113,622,382 (GRCm39) |
|
probably benign |
Het |
Septin5 |
G |
T |
16: 18,443,579 (GRCm39) |
D123E |
probably damaging |
Het |
Skint6 |
G |
A |
4: 112,944,993 (GRCm39) |
T483I |
probably benign |
Het |
Tep1 |
A |
T |
14: 51,091,581 (GRCm39) |
|
probably benign |
Het |
Tepsin |
T |
C |
11: 119,982,547 (GRCm39) |
R440G |
probably benign |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Trpm4 |
A |
T |
7: 44,959,947 (GRCm39) |
V649E |
probably damaging |
Het |
Usf3 |
C |
A |
16: 44,040,019 (GRCm39) |
Q1500K |
possibly damaging |
Het |
Vmn1r231 |
T |
C |
17: 21,110,568 (GRCm39) |
S116G |
probably damaging |
Het |
Vmn1r45 |
T |
A |
6: 89,910,035 (GRCm39) |
I312L |
probably benign |
Het |
|
Other mutations in 1810024B03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02016:1810024B03Rik
|
APN |
2 |
127,028,875 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:1810024B03Rik
|
UTSW |
2 |
127,028,933 (GRCm39) |
missense |
probably benign |
0.04 |
R0417:1810024B03Rik
|
UTSW |
2 |
127,028,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:1810024B03Rik
|
UTSW |
2 |
127,029,196 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4603:1810024B03Rik
|
UTSW |
2 |
127,029,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5396:1810024B03Rik
|
UTSW |
2 |
127,028,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5875:1810024B03Rik
|
UTSW |
2 |
127,028,737 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7729:1810024B03Rik
|
UTSW |
2 |
127,028,710 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0027:1810024B03Rik
|
UTSW |
2 |
127,028,692 (GRCm39) |
missense |
probably benign |
0.01 |
|