Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
A |
G |
7: 82,099,308 (GRCm39) |
Q154R |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,438,234 (GRCm39) |
L1520P |
probably benign |
Het |
Brd1 |
A |
G |
15: 88,574,063 (GRCm39) |
|
probably null |
Het |
Ccdc158 |
A |
G |
5: 92,757,811 (GRCm39) |
|
probably benign |
Het |
Cep350 |
C |
A |
1: 155,754,766 (GRCm39) |
V1950F |
probably benign |
Het |
Csnk1d |
A |
G |
11: 120,863,229 (GRCm39) |
I237T |
probably damaging |
Het |
Ddah2 |
T |
C |
17: 35,280,561 (GRCm39) |
L234P |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,163,491 (GRCm39) |
|
probably null |
Het |
Ephb1 |
A |
C |
9: 101,873,973 (GRCm39) |
|
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myadml2 |
A |
T |
11: 120,538,656 (GRCm39) |
F60I |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,399,925 (GRCm39) |
V2893A |
probably damaging |
Het |
Ntn1 |
A |
G |
11: 68,276,120 (GRCm39) |
V276A |
probably benign |
Het |
Or11h6 |
T |
A |
14: 50,880,062 (GRCm39) |
I102N |
probably damaging |
Het |
Or4c111 |
A |
T |
2: 88,843,493 (GRCm39) |
I305K |
probably benign |
Het |
Or7a39 |
A |
G |
10: 78,715,765 (GRCm39) |
Y253C |
probably damaging |
Het |
Otof |
T |
C |
5: 30,527,551 (GRCm39) |
Y1962C |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,315,080 (GRCm39) |
|
probably benign |
Het |
Polr2a |
A |
G |
11: 69,626,009 (GRCm39) |
S1676P |
unknown |
Het |
Prpf40b |
A |
G |
15: 99,203,047 (GRCm39) |
|
probably benign |
Het |
Rdh16f2 |
A |
G |
10: 127,712,145 (GRCm39) |
K201E |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 82,991,691 (GRCm39) |
Y439C |
possibly damaging |
Het |
Son |
G |
T |
16: 91,444,848 (GRCm39) |
|
probably null |
Het |
Specc1 |
T |
C |
11: 62,022,713 (GRCm39) |
L710P |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,061,524 (GRCm39) |
D592G |
possibly damaging |
Het |
Tmem237 |
A |
T |
1: 59,147,863 (GRCm39) |
D209E |
probably damaging |
Het |
Vmn2r106 |
T |
C |
17: 20,488,423 (GRCm39) |
T659A |
probably benign |
Het |
Vmn2r71 |
T |
A |
7: 85,273,388 (GRCm39) |
I734N |
probably damaging |
Het |
Wdr7 |
A |
T |
18: 64,057,980 (GRCm39) |
I1270F |
possibly damaging |
Het |
|
Other mutations in Ptprh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01766:Ptprh
|
APN |
7 |
4,583,915 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02420:Ptprh
|
APN |
7 |
4,583,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02619:Ptprh
|
APN |
7 |
4,552,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02729:Ptprh
|
APN |
7 |
4,583,873 (GRCm39) |
missense |
probably damaging |
0.99 |
BB008:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
BB018:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R0018:Ptprh
|
UTSW |
7 |
4,604,845 (GRCm39) |
critical splice donor site |
probably null |
|
R0049:Ptprh
|
UTSW |
7 |
4,576,361 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0449:Ptprh
|
UTSW |
7 |
4,601,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Ptprh
|
UTSW |
7 |
4,600,997 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0626:Ptprh
|
UTSW |
7 |
4,567,271 (GRCm39) |
missense |
probably benign |
0.00 |
R0741:Ptprh
|
UTSW |
7 |
4,557,172 (GRCm39) |
critical splice donor site |
probably null |
|
R1068:Ptprh
|
UTSW |
7 |
4,552,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1226:Ptprh
|
UTSW |
7 |
4,606,091 (GRCm39) |
nonsense |
probably null |
|
R1487:Ptprh
|
UTSW |
7 |
4,555,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Ptprh
|
UTSW |
7 |
4,583,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1537:Ptprh
|
UTSW |
7 |
4,552,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Ptprh
|
UTSW |
7 |
4,555,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Ptprh
|
UTSW |
7 |
4,604,912 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Ptprh
|
UTSW |
7 |
4,552,394 (GRCm39) |
missense |
probably benign |
0.25 |
R2082:Ptprh
|
UTSW |
7 |
4,553,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptprh
|
UTSW |
7 |
4,604,867 (GRCm39) |
missense |
probably benign |
0.26 |
R2214:Ptprh
|
UTSW |
7 |
4,555,921 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2271:Ptprh
|
UTSW |
7 |
4,606,132 (GRCm39) |
start gained |
probably benign |
|
R3693:Ptprh
|
UTSW |
7 |
4,557,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R3713:Ptprh
|
UTSW |
7 |
4,574,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4081:Ptprh
|
UTSW |
7 |
4,583,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Ptprh
|
UTSW |
7 |
4,600,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R4689:Ptprh
|
UTSW |
7 |
4,600,996 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4782:Ptprh
|
UTSW |
7 |
4,572,576 (GRCm39) |
missense |
probably benign |
0.08 |
R4838:Ptprh
|
UTSW |
7 |
4,576,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4974:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R5218:Ptprh
|
UTSW |
7 |
4,600,919 (GRCm39) |
missense |
probably benign |
0.05 |
R5430:Ptprh
|
UTSW |
7 |
4,554,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Ptprh
|
UTSW |
7 |
4,552,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5544:Ptprh
|
UTSW |
7 |
4,583,909 (GRCm39) |
nonsense |
probably null |
|
R5547:Ptprh
|
UTSW |
7 |
4,557,221 (GRCm39) |
nonsense |
probably null |
|
R5869:Ptprh
|
UTSW |
7 |
4,604,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Ptprh
|
UTSW |
7 |
4,576,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Ptprh
|
UTSW |
7 |
4,576,361 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6112:Ptprh
|
UTSW |
7 |
4,600,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6493:Ptprh
|
UTSW |
7 |
4,583,989 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6733:Ptprh
|
UTSW |
7 |
4,606,043 (GRCm39) |
splice site |
probably null |
|
R6836:Ptprh
|
UTSW |
7 |
4,554,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Ptprh
|
UTSW |
7 |
4,552,370 (GRCm39) |
nonsense |
probably null |
|
R6868:Ptprh
|
UTSW |
7 |
4,604,864 (GRCm39) |
missense |
probably benign |
|
R7015:Ptprh
|
UTSW |
7 |
4,555,626 (GRCm39) |
critical splice donor site |
probably null |
|
R7092:Ptprh
|
UTSW |
7 |
4,583,860 (GRCm39) |
critical splice donor site |
probably null |
|
R7147:Ptprh
|
UTSW |
7 |
4,553,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Ptprh
|
UTSW |
7 |
4,572,480 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7358:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R7436:Ptprh
|
UTSW |
7 |
4,555,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Ptprh
|
UTSW |
7 |
4,574,780 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7863:Ptprh
|
UTSW |
7 |
4,606,097 (GRCm39) |
start codon destroyed |
probably benign |
0.31 |
R7931:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R7973:Ptprh
|
UTSW |
7 |
4,583,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8239:Ptprh
|
UTSW |
7 |
4,584,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8331:Ptprh
|
UTSW |
7 |
4,552,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Ptprh
|
UTSW |
7 |
4,554,022 (GRCm39) |
missense |
probably benign |
0.03 |
R8700:Ptprh
|
UTSW |
7 |
4,567,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Ptprh
|
UTSW |
7 |
4,567,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Ptprh
|
UTSW |
7 |
4,583,944 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9119:Ptprh
|
UTSW |
7 |
4,555,712 (GRCm39) |
missense |
probably benign |
0.25 |
R9203:Ptprh
|
UTSW |
7 |
4,574,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Ptprh
|
UTSW |
7 |
4,583,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R9250:Ptprh
|
UTSW |
7 |
4,576,289 (GRCm39) |
missense |
probably benign |
0.03 |
RF022:Ptprh
|
UTSW |
7 |
4,552,367 (GRCm39) |
missense |
probably benign |
|
Z1177:Ptprh
|
UTSW |
7 |
4,601,117 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ptprh
|
UTSW |
7 |
4,600,970 (GRCm39) |
missense |
probably damaging |
0.99 |
|