Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
C |
T |
9: 46,220,624 (GRCm39) |
|
probably null |
Het |
Abca13 |
T |
A |
11: 9,143,533 (GRCm39) |
|
probably null |
Het |
Akap13 |
A |
T |
7: 75,259,991 (GRCm39) |
T69S |
probably benign |
Het |
Arl1 |
T |
A |
10: 88,572,966 (GRCm39) |
C80S |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,162,916 (GRCm39) |
L926* |
probably null |
Het |
Brsk1 |
A |
G |
7: 4,712,003 (GRCm39) |
T618A |
possibly damaging |
Het |
Cep295 |
T |
C |
9: 15,235,533 (GRCm39) |
H1982R |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,226,059 (GRCm39) |
S559T |
unknown |
Het |
Clcf1 |
A |
G |
19: 4,272,213 (GRCm39) |
N90S |
possibly damaging |
Het |
Clec16a |
G |
A |
16: 10,549,543 (GRCm39) |
C872Y |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 64,933,701 (GRCm39) |
D430E |
possibly damaging |
Het |
Cyp1a2 |
T |
A |
9: 57,589,794 (GRCm39) |
I7F |
probably benign |
Het |
Cyp2b23 |
G |
A |
7: 26,380,848 (GRCm39) |
R126* |
probably null |
Het |
Daam2 |
A |
G |
17: 49,787,782 (GRCm39) |
W444R |
possibly damaging |
Het |
Dcbld2 |
T |
A |
16: 58,275,621 (GRCm39) |
C446S |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Eif2d |
T |
C |
1: 131,086,035 (GRCm39) |
*177R |
probably null |
Het |
Fkbp15 |
G |
A |
4: 62,246,114 (GRCm39) |
A438V |
probably damaging |
Het |
Gjb5 |
G |
A |
4: 127,249,652 (GRCm39) |
A164V |
probably benign |
Het |
Grin1 |
A |
T |
2: 25,188,285 (GRCm39) |
|
probably null |
Het |
Grm3 |
A |
G |
5: 9,620,233 (GRCm39) |
F337S |
probably damaging |
Het |
Hey2 |
T |
A |
10: 30,710,019 (GRCm39) |
T245S |
probably benign |
Het |
Ifi206 |
T |
C |
1: 173,308,797 (GRCm39) |
T400A |
probably benign |
Het |
Itga7 |
G |
A |
10: 128,779,902 (GRCm39) |
E480K |
probably null |
Het |
Itpr1 |
T |
C |
6: 108,470,755 (GRCm39) |
Y2227H |
possibly damaging |
Het |
Krt8 |
T |
C |
15: 101,912,337 (GRCm39) |
D113G |
probably damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lins1 |
A |
G |
7: 66,357,843 (GRCm39) |
|
probably benign |
Het |
Lmf1 |
A |
T |
17: 25,881,610 (GRCm39) |
D553V |
possibly damaging |
Het |
Lnpep |
A |
G |
17: 17,786,992 (GRCm39) |
S536P |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,620,716 (GRCm39) |
C3587* |
probably null |
Het |
Macf1 |
A |
T |
4: 123,290,917 (GRCm39) |
D3435E |
possibly damaging |
Het |
Mmp1b |
T |
C |
9: 7,384,897 (GRCm39) |
I251V |
possibly damaging |
Het |
Myg1 |
A |
T |
15: 102,245,397 (GRCm39) |
N206I |
probably damaging |
Het |
Myl12a |
T |
G |
17: 71,301,694 (GRCm39) |
R144S |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,055,179 (GRCm39) |
I454K |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,965,051 (GRCm39) |
D1545G |
probably benign |
Het |
Ogdhl |
T |
G |
14: 32,061,181 (GRCm39) |
D457E |
probably damaging |
Het |
Or5ac20 |
T |
A |
16: 59,104,704 (GRCm39) |
D52V |
probably damaging |
Het |
Or9s18 |
A |
C |
13: 65,300,588 (GRCm39) |
L183F |
probably damaging |
Het |
Paf1 |
A |
G |
7: 28,095,095 (GRCm39) |
I112V |
possibly damaging |
Het |
Pate7 |
T |
A |
9: 35,689,407 (GRCm39) |
|
probably null |
Het |
Pcdhga4 |
C |
T |
18: 37,819,798 (GRCm39) |
P449L |
probably damaging |
Het |
Pla2g6 |
A |
T |
15: 79,183,342 (GRCm39) |
I495N |
possibly damaging |
Het |
Ptprn2 |
A |
T |
12: 117,148,267 (GRCm39) |
I676F |
probably damaging |
Het |
Rev3l |
T |
C |
10: 39,700,927 (GRCm39) |
L1808P |
possibly damaging |
Het |
Sall2 |
A |
G |
14: 52,550,586 (GRCm39) |
S868P |
probably damaging |
Het |
Shoc1 |
A |
T |
4: 59,049,017 (GRCm39) |
M1116K |
probably benign |
Het |
Slc47a2 |
A |
G |
11: 61,198,412 (GRCm39) |
F428L |
probably benign |
Het |
Slco1a7 |
C |
T |
6: 141,681,826 (GRCm39) |
|
probably null |
Het |
Slco3a1 |
A |
T |
7: 73,934,363 (GRCm39) |
F603Y |
possibly damaging |
Het |
Smyd2 |
A |
T |
1: 189,642,090 (GRCm39) |
C65* |
probably null |
Het |
Ssu72 |
T |
C |
4: 155,800,007 (GRCm39) |
F57L |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,813,709 (GRCm39) |
T1718A |
probably benign |
Het |
Tnks |
G |
C |
8: 35,432,720 (GRCm39) |
P34A |
unknown |
Het |
Top3a |
G |
A |
11: 60,653,348 (GRCm39) |
T42I |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,220,369 (GRCm39) |
S2369P |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubqln1 |
T |
C |
13: 58,330,997 (GRCm39) |
Q410R |
probably damaging |
Het |
Vmn2r11 |
A |
G |
5: 109,207,224 (GRCm39) |
I32T |
possibly damaging |
Het |
Xcr1 |
A |
G |
9: 123,685,375 (GRCm39) |
F129S |
probably benign |
Het |
|
Other mutations in Ptgs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00225:Ptgs1
|
APN |
2 |
36,127,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02345:Ptgs1
|
APN |
2 |
36,132,983 (GRCm39) |
missense |
probably null |
0.93 |
IGL02952:Ptgs1
|
APN |
2 |
36,141,253 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03306:Ptgs1
|
APN |
2 |
36,127,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Ptgs1
|
UTSW |
2 |
36,130,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0468:Ptgs1
|
UTSW |
2 |
36,139,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R0638:Ptgs1
|
UTSW |
2 |
36,130,868 (GRCm39) |
splice site |
probably benign |
|
R1563:Ptgs1
|
UTSW |
2 |
36,135,214 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1858:Ptgs1
|
UTSW |
2 |
36,132,782 (GRCm39) |
missense |
probably benign |
0.19 |
R2012:Ptgs1
|
UTSW |
2 |
36,127,668 (GRCm39) |
missense |
probably benign |
|
R2080:Ptgs1
|
UTSW |
2 |
36,132,859 (GRCm39) |
nonsense |
probably null |
|
R2116:Ptgs1
|
UTSW |
2 |
36,127,708 (GRCm39) |
nonsense |
probably null |
|
R4073:Ptgs1
|
UTSW |
2 |
36,127,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R4163:Ptgs1
|
UTSW |
2 |
36,141,346 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4862:Ptgs1
|
UTSW |
2 |
36,127,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Ptgs1
|
UTSW |
2 |
36,127,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Ptgs1
|
UTSW |
2 |
36,141,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Ptgs1
|
UTSW |
2 |
36,141,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Ptgs1
|
UTSW |
2 |
36,141,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Ptgs1
|
UTSW |
2 |
36,141,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5373:Ptgs1
|
UTSW |
2 |
36,141,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Ptgs1
|
UTSW |
2 |
36,141,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5428:Ptgs1
|
UTSW |
2 |
36,135,280 (GRCm39) |
missense |
probably benign |
0.00 |
R5918:Ptgs1
|
UTSW |
2 |
36,141,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6134:Ptgs1
|
UTSW |
2 |
36,141,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Ptgs1
|
UTSW |
2 |
36,141,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Ptgs1
|
UTSW |
2 |
36,127,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Ptgs1
|
UTSW |
2 |
36,141,311 (GRCm39) |
missense |
probably benign |
|
R7020:Ptgs1
|
UTSW |
2 |
36,141,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R7445:Ptgs1
|
UTSW |
2 |
36,135,222 (GRCm39) |
missense |
probably benign |
0.06 |
R7557:Ptgs1
|
UTSW |
2 |
36,135,223 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7873:Ptgs1
|
UTSW |
2 |
36,141,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R8215:Ptgs1
|
UTSW |
2 |
36,141,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R9244:Ptgs1
|
UTSW |
2 |
36,130,724 (GRCm39) |
missense |
probably damaging |
0.96 |
R9537:Ptgs1
|
UTSW |
2 |
36,120,739 (GRCm39) |
missense |
unknown |
|
R9709:Ptgs1
|
UTSW |
2 |
36,141,204 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ptgs1
|
UTSW |
2 |
36,130,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|