Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI661453 |
C |
A |
17: 47,779,442 (GRCm39) |
|
probably benign |
Het |
Arhgap29 |
G |
A |
3: 121,807,977 (GRCm39) |
V1052I |
probably benign |
Het |
Arhgef17 |
A |
G |
7: 100,577,862 (GRCm39) |
S1029P |
probably benign |
Het |
Arpc5l |
T |
C |
2: 38,898,226 (GRCm39) |
S7P |
probably damaging |
Het |
Asf1b |
A |
G |
8: 84,682,533 (GRCm39) |
I26V |
probably benign |
Het |
Cep95 |
T |
C |
11: 106,697,197 (GRCm39) |
L240P |
probably damaging |
Het |
Cnmd |
A |
G |
14: 79,879,508 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
T |
A |
6: 102,180,846 (GRCm39) |
N783I |
probably damaging |
Het |
Col6a2 |
C |
A |
10: 76,440,676 (GRCm39) |
|
probably benign |
Het |
Col9a2 |
T |
C |
4: 120,907,607 (GRCm39) |
|
probably null |
Het |
Cry2 |
T |
C |
2: 92,254,977 (GRCm39) |
E126G |
probably benign |
Het |
Cxcl15 |
T |
C |
5: 90,942,467 (GRCm39) |
V13A |
possibly damaging |
Het |
Dbr1 |
A |
G |
9: 99,465,952 (GRCm39) |
D510G |
probably benign |
Het |
Dct |
A |
G |
14: 118,271,655 (GRCm39) |
F392L |
probably damaging |
Het |
Dgkz |
A |
G |
2: 91,764,395 (GRCm39) |
|
probably benign |
Het |
Dhrs7b |
A |
G |
11: 60,721,541 (GRCm39) |
I2V |
probably benign |
Het |
Efnb3 |
A |
T |
11: 69,447,730 (GRCm39) |
|
probably null |
Het |
Fbf1 |
T |
A |
11: 116,041,846 (GRCm39) |
R565S |
probably null |
Het |
Gimap5 |
T |
C |
6: 48,729,727 (GRCm39) |
I99T |
probably damaging |
Het |
Gm9912 |
A |
G |
3: 148,891,085 (GRCm39) |
L16P |
unknown |
Het |
Gpr17 |
A |
G |
18: 32,080,187 (GRCm39) |
L292P |
probably damaging |
Het |
Hdac10 |
C |
T |
15: 89,011,801 (GRCm39) |
V129M |
probably damaging |
Het |
Mfap3l |
A |
G |
8: 61,124,498 (GRCm39) |
I247V |
possibly damaging |
Het |
Mtus1 |
A |
T |
8: 41,537,457 (GRCm39) |
S86R |
probably damaging |
Het |
Mylk3 |
A |
G |
8: 86,085,890 (GRCm39) |
S55P |
possibly damaging |
Het |
Nol6 |
A |
T |
4: 41,118,567 (GRCm39) |
C745S |
probably damaging |
Het |
Nudt13 |
A |
T |
14: 20,356,385 (GRCm39) |
E103D |
probably damaging |
Het |
Or10ag59 |
A |
G |
2: 87,405,806 (GRCm39) |
Y126C |
probably damaging |
Het |
Or1e35 |
A |
G |
11: 73,798,261 (GRCm39) |
I19T |
possibly damaging |
Het |
Pdzk1 |
G |
T |
3: 96,764,687 (GRCm39) |
A324S |
probably benign |
Het |
Pofut2 |
T |
C |
10: 77,096,515 (GRCm39) |
V80A |
possibly damaging |
Het |
Rasip1 |
A |
G |
7: 45,286,240 (GRCm39) |
D821G |
probably damaging |
Het |
Rnf10 |
T |
A |
5: 115,389,161 (GRCm39) |
K273* |
probably null |
Het |
Slc4a9 |
A |
G |
18: 36,672,828 (GRCm39) |
M811V |
possibly damaging |
Het |
Smchd1 |
T |
C |
17: 71,751,015 (GRCm39) |
D301G |
probably damaging |
Het |
Tm9sf2 |
A |
T |
14: 122,380,883 (GRCm39) |
T159S |
probably benign |
Het |
Tom1l1 |
G |
A |
11: 90,540,687 (GRCm39) |
P327S |
probably damaging |
Het |
Trim3 |
A |
G |
7: 105,267,689 (GRCm39) |
|
probably benign |
Het |
Trpm6 |
A |
C |
19: 18,807,691 (GRCm39) |
|
probably benign |
Het |
Ttc13 |
A |
C |
8: 125,415,621 (GRCm39) |
L245R |
probably damaging |
Het |
Txnrd1 |
T |
A |
10: 82,713,118 (GRCm39) |
V60E |
probably damaging |
Het |
Ung |
T |
A |
5: 114,274,447 (GRCm39) |
D173E |
probably benign |
Het |
Zbtb5 |
A |
G |
4: 44,995,294 (GRCm39) |
V30A |
probably damaging |
Het |
|
Other mutations in 4930503E14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00778:4930503E14Rik
|
APN |
14 |
44,401,391 (GRCm39) |
missense |
probably benign |
0.10 |
R2925:4930503E14Rik
|
UTSW |
14 |
44,407,755 (GRCm39) |
missense |
probably damaging |
0.98 |
R4067:4930503E14Rik
|
UTSW |
14 |
44,406,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R4347:4930503E14Rik
|
UTSW |
14 |
44,408,635 (GRCm39) |
missense |
probably damaging |
0.96 |
R4414:4930503E14Rik
|
UTSW |
14 |
44,406,690 (GRCm39) |
missense |
probably benign |
0.00 |
R4504:4930503E14Rik
|
UTSW |
14 |
44,407,899 (GRCm39) |
missense |
probably damaging |
0.98 |
R5047:4930503E14Rik
|
UTSW |
14 |
44,406,698 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7489:4930503E14Rik
|
UTSW |
14 |
44,407,756 (GRCm39) |
missense |
probably damaging |
0.99 |
R9665:4930503E14Rik
|
UTSW |
14 |
44,407,796 (GRCm39) |
missense |
probably damaging |
0.99 |
|