Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
G |
A |
14: 59,380,257 (GRCm39) |
R14C |
probably benign |
Het |
Adam29 |
A |
T |
8: 56,325,701 (GRCm39) |
L251* |
probably null |
Het |
Atpaf2 |
T |
C |
11: 60,296,650 (GRCm39) |
E161G |
probably damaging |
Het |
Brwd1 |
T |
C |
16: 95,858,666 (GRCm39) |
D381G |
probably damaging |
Het |
Cept1 |
T |
A |
3: 106,446,712 (GRCm39) |
R45* |
probably null |
Het |
Col3a1 |
A |
G |
1: 45,367,615 (GRCm39) |
E273G |
unknown |
Het |
Cuzd1 |
T |
C |
7: 130,921,832 (GRCm39) |
N57D |
probably benign |
Het |
Cyp2b13 |
A |
G |
7: 25,761,101 (GRCm39) |
K53E |
probably benign |
Het |
Fadd |
T |
C |
7: 144,134,276 (GRCm39) |
E203G |
probably benign |
Het |
Gm3159 |
G |
A |
14: 4,400,552 (GRCm38) |
|
probably null |
Het |
Gpr137c |
T |
C |
14: 45,483,890 (GRCm39) |
F206L |
possibly damaging |
Het |
Hephl1 |
G |
T |
9: 14,995,615 (GRCm39) |
T471N |
probably damaging |
Het |
Ido1 |
A |
T |
8: 25,083,345 (GRCm39) |
|
probably benign |
Het |
Krt40 |
C |
T |
11: 99,430,693 (GRCm39) |
|
probably null |
Het |
Lrp2 |
T |
A |
2: 69,285,797 (GRCm39) |
|
probably benign |
Het |
Lrrc8a |
T |
A |
2: 30,147,025 (GRCm39) |
L613H |
probably damaging |
Het |
Mettl14 |
A |
G |
3: 123,168,534 (GRCm39) |
Y169H |
probably damaging |
Het |
Nlrp4a |
A |
G |
7: 26,149,155 (GRCm39) |
Q254R |
probably benign |
Het |
Or4c15 |
A |
C |
2: 88,760,128 (GRCm39) |
M177R |
possibly damaging |
Het |
Or7c70 |
A |
T |
10: 78,683,371 (GRCm39) |
I126N |
probably damaging |
Het |
Pira12 |
T |
C |
7: 3,900,078 (GRCm39) |
T175A |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,447,670 (GRCm39) |
M2241K |
possibly damaging |
Het |
Ptprd |
G |
A |
4: 76,047,105 (GRCm39) |
S387L |
probably damaging |
Het |
Ryr1 |
A |
C |
7: 28,759,478 (GRCm39) |
L3264R |
probably damaging |
Het |
Serpina16 |
G |
A |
12: 103,641,638 (GRCm39) |
T29I |
probably benign |
Het |
Slc9a7 |
A |
G |
X: 20,052,382 (GRCm39) |
M237T |
probably benign |
Het |
Tbck |
A |
G |
3: 132,428,544 (GRCm39) |
T300A |
probably benign |
Het |
Tcaf1 |
A |
C |
6: 42,663,393 (GRCm39) |
D162E |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,717,217 (GRCm39) |
|
probably benign |
Het |
Usp17le |
A |
C |
7: 104,417,947 (GRCm39) |
H398Q |
probably benign |
Het |
Vmn2r86 |
A |
C |
10: 130,289,636 (GRCm39) |
D86E |
possibly damaging |
Het |
Zmym2 |
T |
A |
14: 57,175,870 (GRCm39) |
C822S |
probably benign |
Het |
Zp3r |
T |
C |
1: 130,511,175 (GRCm39) |
D336G |
possibly damaging |
Het |
Zpr1 |
A |
G |
9: 46,184,849 (GRCm39) |
H82R |
probably damaging |
Het |
|
Other mutations in Utp15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02951:Utp15
|
APN |
13 |
98,394,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Utp15
|
APN |
13 |
98,390,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Utp15
|
UTSW |
13 |
98,387,390 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0679:Utp15
|
UTSW |
13 |
98,395,911 (GRCm39) |
missense |
probably benign |
0.13 |
R1447:Utp15
|
UTSW |
13 |
98,389,386 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1618:Utp15
|
UTSW |
13 |
98,393,695 (GRCm39) |
missense |
probably benign |
0.16 |
R1992:Utp15
|
UTSW |
13 |
98,387,420 (GRCm39) |
missense |
probably benign |
|
R2110:Utp15
|
UTSW |
13 |
98,391,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Utp15
|
UTSW |
13 |
98,394,433 (GRCm39) |
missense |
probably benign |
0.03 |
R3888:Utp15
|
UTSW |
13 |
98,395,674 (GRCm39) |
missense |
probably benign |
0.00 |
R4355:Utp15
|
UTSW |
13 |
98,395,755 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5436:Utp15
|
UTSW |
13 |
98,397,354 (GRCm39) |
splice site |
probably null |
|
R5568:Utp15
|
UTSW |
13 |
98,394,433 (GRCm39) |
missense |
probably benign |
0.03 |
R6489:Utp15
|
UTSW |
13 |
98,387,117 (GRCm39) |
missense |
probably damaging |
0.96 |
R8116:Utp15
|
UTSW |
13 |
98,387,371 (GRCm39) |
missense |
probably benign |
|
R8360:Utp15
|
UTSW |
13 |
98,391,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R9049:Utp15
|
UTSW |
13 |
98,395,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9370:Utp15
|
UTSW |
13 |
98,387,119 (GRCm39) |
missense |
probably damaging |
0.96 |
R9654:Utp15
|
UTSW |
13 |
98,385,668 (GRCm39) |
missense |
probably benign |
|
|