Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
C |
5: 88,120,325 (GRCm39) |
I361L |
possibly damaging |
Het |
Aebp2 |
C |
T |
6: 140,592,594 (GRCm39) |
P446L |
probably damaging |
Het |
Arhgap32 |
C |
A |
9: 32,170,463 (GRCm39) |
A1081D |
probably damaging |
Het |
Btbd16 |
C |
T |
7: 130,417,516 (GRCm39) |
R344C |
probably damaging |
Het |
Cdc73 |
T |
A |
1: 143,545,740 (GRCm39) |
K299* |
probably null |
Het |
Cpq |
C |
T |
15: 33,250,078 (GRCm39) |
T145I |
probably benign |
Het |
Creb1 |
C |
A |
1: 64,615,413 (GRCm39) |
A215E |
probably damaging |
Het |
D630045J12Rik |
G |
T |
6: 38,173,814 (GRCm39) |
A118E |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,450,812 (GRCm39) |
F3873I |
possibly damaging |
Het |
Dock10 |
T |
C |
1: 80,583,593 (GRCm39) |
Y203C |
probably damaging |
Het |
Evi5 |
A |
G |
5: 107,990,150 (GRCm39) |
V23A |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,142,838 (GRCm39) |
D4337G |
probably damaging |
Het |
Fbxl17 |
G |
A |
17: 63,387,489 (GRCm39) |
T631I |
probably damaging |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Focad |
A |
G |
4: 88,321,583 (GRCm39) |
M1559V |
unknown |
Het |
Fras1 |
A |
T |
5: 96,900,873 (GRCm39) |
I3031L |
possibly damaging |
Het |
Gnas |
T |
C |
2: 174,139,826 (GRCm39) |
S58P |
unknown |
Het |
Hdac9 |
G |
A |
12: 34,440,327 (GRCm39) |
Q351* |
probably null |
Het |
Ibsp |
A |
T |
5: 104,457,167 (GRCm39) |
N92I |
probably damaging |
Het |
Kank1 |
C |
A |
19: 25,387,866 (GRCm39) |
T513N |
probably damaging |
Het |
Kcnh1 |
A |
G |
1: 192,101,123 (GRCm39) |
T599A |
probably benign |
Het |
Kdm5a |
T |
A |
6: 120,392,253 (GRCm39) |
L992M |
probably damaging |
Het |
Lipc |
T |
C |
9: 70,723,889 (GRCm39) |
Y245C |
probably damaging |
Het |
Mdfic2 |
T |
C |
6: 98,215,164 (GRCm39) |
H153R |
probably benign |
Het |
Morc3 |
C |
A |
16: 93,667,771 (GRCm39) |
Y716* |
probably null |
Het |
Mroh2b |
A |
T |
15: 4,963,952 (GRCm39) |
D848V |
probably damaging |
Het |
Or13c7e-ps1 |
A |
C |
4: 43,781,682 (GRCm39) |
I216S |
possibly damaging |
Het |
Or2d2b |
T |
A |
7: 106,705,336 (GRCm39) |
H244L |
probably damaging |
Het |
Or2y1b |
A |
G |
11: 49,208,459 (GRCm39) |
I29V |
probably benign |
Het |
Or5h27 |
A |
G |
16: 59,006,090 (GRCm39) |
V252A |
unknown |
Het |
Or6ae1 |
T |
A |
7: 139,741,942 (GRCm39) |
Q307L |
probably benign |
Het |
Patl1 |
A |
G |
19: 11,898,815 (GRCm39) |
E170G |
probably damaging |
Het |
Rad17 |
A |
G |
13: 100,780,074 (GRCm39) |
V112A |
probably damaging |
Het |
Rigi |
A |
G |
4: 40,229,545 (GRCm39) |
S125P |
probably benign |
Het |
Slc12a5 |
T |
C |
2: 164,832,178 (GRCm39) |
V699A |
possibly damaging |
Het |
Slc13a4 |
A |
G |
6: 35,278,742 (GRCm39) |
V49A |
probably damaging |
Het |
Slc22a6 |
A |
G |
19: 8,598,596 (GRCm39) |
T218A |
probably benign |
Het |
Slc30a9 |
A |
G |
5: 67,505,278 (GRCm39) |
D422G |
probably damaging |
Het |
Slc37a3 |
T |
C |
6: 39,324,363 (GRCm39) |
Y295C |
possibly damaging |
Het |
Slc39a8 |
T |
C |
3: 135,563,923 (GRCm39) |
V256A |
probably benign |
Het |
Slc45a2 |
G |
A |
15: 11,026,005 (GRCm39) |
E452K |
possibly damaging |
Het |
Slc4a11 |
C |
T |
2: 130,533,664 (GRCm39) |
A100T |
probably damaging |
Het |
Slc7a12 |
G |
A |
3: 14,546,035 (GRCm39) |
C60Y |
probably damaging |
Het |
St8sia3 |
T |
A |
18: 64,398,640 (GRCm39) |
L33Q |
probably damaging |
Het |
Tiam1 |
A |
G |
16: 89,594,918 (GRCm39) |
|
probably null |
Het |
Trim37 |
T |
A |
11: 87,077,257 (GRCm39) |
V529E |
probably benign |
Het |
Trpv3 |
A |
T |
11: 73,178,225 (GRCm39) |
T431S |
probably benign |
Het |
Tsc22d1 |
TCAGCAGCAGCAGCAGCAGCAGCAGCA |
TCAGCAGCAGCAGCAGCAGCAGCA |
14: 76,654,707 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,544,679 (GRCm39) |
V32808M |
probably damaging |
Het |
Vmn2r27 |
T |
C |
6: 124,168,856 (GRCm39) |
Y758C |
probably damaging |
Het |
Vwa5b2 |
C |
T |
16: 20,423,046 (GRCm39) |
P1015S |
probably benign |
Het |
Whamm |
A |
G |
7: 81,236,035 (GRCm39) |
R413G |
probably damaging |
Het |
Zbtb41 |
C |
T |
1: 139,350,781 (GRCm39) |
|
probably benign |
Het |
Zfp119b |
A |
G |
17: 56,246,536 (GRCm39) |
S217P |
possibly damaging |
Het |
|
Other mutations in Sertad2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03008:Sertad2
|
APN |
11 |
20,597,798 (GRCm39) |
splice site |
probably benign |
|
wisteria
|
UTSW |
11 |
20,598,664 (GRCm39) |
frame shift |
probably null |
|
PIT4366001:Sertad2
|
UTSW |
11 |
20,598,116 (GRCm39) |
missense |
probably benign |
0.03 |
R1171:Sertad2
|
UTSW |
11 |
20,598,091 (GRCm39) |
missense |
probably benign |
0.01 |
R1306:Sertad2
|
UTSW |
11 |
20,598,388 (GRCm39) |
missense |
probably benign |
|
R3834:Sertad2
|
UTSW |
11 |
20,598,482 (GRCm39) |
missense |
probably benign |
0.15 |
R4087:Sertad2
|
UTSW |
11 |
20,598,664 (GRCm39) |
frame shift |
probably null |
|
R4940:Sertad2
|
UTSW |
11 |
20,597,899 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5232:Sertad2
|
UTSW |
11 |
20,598,344 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5621:Sertad2
|
UTSW |
11 |
20,598,061 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5891:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R5956:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6006:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6007:Sertad2
|
UTSW |
11 |
20,597,884 (GRCm39) |
missense |
probably benign |
0.30 |
R6048:Sertad2
|
UTSW |
11 |
20,598,436 (GRCm39) |
missense |
probably benign |
|
R9135:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9136:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9137:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
R9138:Sertad2
|
UTSW |
11 |
20,598,425 (GRCm39) |
missense |
probably benign |
0.00 |
|