Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930009A15Rik |
A |
T |
10: 115,415,717 (GRCm39) |
|
probably benign |
Het |
Acaa2 |
T |
C |
18: 74,937,223 (GRCm39) |
L369S |
probably damaging |
Het |
Akna |
A |
G |
4: 63,313,140 (GRCm39) |
S328P |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,719,546 (GRCm39) |
Y214C |
probably damaging |
Het |
Apc |
A |
G |
18: 34,354,140 (GRCm39) |
|
probably benign |
Het |
Brca2 |
C |
T |
5: 150,466,716 (GRCm39) |
T2160I |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,204,330 (GRCm39) |
S1251P |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,395,573 (GRCm39) |
E488G |
probably damaging |
Het |
Ccdc158 |
T |
A |
5: 92,797,908 (GRCm39) |
I411F |
probably damaging |
Het |
Cd163 |
C |
T |
6: 124,297,595 (GRCm39) |
Q914* |
probably null |
Het |
Cd22 |
T |
C |
7: 30,566,083 (GRCm39) |
D827G |
probably damaging |
Het |
Ces1e |
A |
G |
8: 93,946,001 (GRCm39) |
|
probably null |
Het |
Col14a1 |
T |
C |
15: 55,315,779 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,713,135 (GRCm39) |
D1509V |
probably damaging |
Het |
Ddx51 |
A |
G |
5: 110,804,717 (GRCm39) |
D543G |
probably damaging |
Het |
Diaph3 |
T |
A |
14: 87,222,261 (GRCm39) |
I408F |
probably damaging |
Het |
Dld |
G |
A |
12: 31,390,325 (GRCm39) |
P213L |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,037,262 (GRCm39) |
T3327A |
probably benign |
Het |
Dnttip2 |
T |
A |
3: 122,078,817 (GRCm39) |
|
probably benign |
Het |
Dock10 |
T |
C |
1: 80,546,225 (GRCm39) |
E791G |
possibly damaging |
Het |
Ehd3 |
G |
T |
17: 74,134,356 (GRCm39) |
W238C |
probably damaging |
Het |
Ehd3 |
T |
G |
17: 74,134,361 (GRCm39) |
L240R |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,824,766 (GRCm39) |
V2357A |
unknown |
Het |
Fam20c |
T |
C |
5: 138,741,932 (GRCm39) |
V181A |
probably damaging |
Het |
Gm4781 |
T |
C |
10: 100,232,814 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch8 |
A |
T |
11: 102,371,058 (GRCm39) |
S827T |
unknown |
Het |
Grm3 |
A |
T |
5: 9,561,930 (GRCm39) |
I640N |
probably damaging |
Het |
Gstm7 |
A |
G |
3: 107,838,747 (GRCm39) |
|
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,700,372 (GRCm39) |
H572Q |
probably damaging |
Het |
Ift140 |
C |
T |
17: 25,313,735 (GRCm39) |
Q1389* |
probably null |
Het |
Igfn1 |
A |
G |
1: 135,893,152 (GRCm39) |
V2099A |
probably damaging |
Het |
Ik |
A |
G |
18: 36,888,531 (GRCm39) |
N443S |
possibly damaging |
Het |
Impact |
A |
G |
18: 13,123,601 (GRCm39) |
K315E |
probably benign |
Het |
Insr |
C |
A |
8: 3,308,697 (GRCm39) |
R113L |
probably benign |
Het |
Jak2 |
T |
A |
19: 29,260,954 (GRCm39) |
Y317N |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,122,411 (GRCm39) |
V162E |
probably damaging |
Het |
L3mbtl3 |
A |
G |
10: 26,207,762 (GRCm39) |
V319A |
unknown |
Het |
Lepr |
T |
C |
4: 101,649,324 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
C |
T |
14: 102,137,938 (GRCm39) |
T647I |
possibly damaging |
Het |
Mindy3 |
C |
T |
2: 12,405,854 (GRCm39) |
R147Q |
probably benign |
Het |
Mtr |
T |
C |
13: 12,230,453 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
T |
16: 32,576,652 (GRCm39) |
|
probably benign |
Het |
Nrip1 |
G |
A |
16: 76,090,471 (GRCm39) |
T362M |
possibly damaging |
Het |
Or1j17 |
G |
T |
2: 36,578,074 (GRCm39) |
R20L |
probably null |
Het |
Or1q1 |
T |
C |
2: 36,886,957 (GRCm39) |
I45T |
possibly damaging |
Het |
Or5d45 |
A |
G |
2: 88,153,222 (GRCm39) |
S276P |
probably benign |
Het |
Ovol1 |
G |
A |
19: 5,601,630 (GRCm39) |
R131C |
probably damaging |
Het |
Pcdhb14 |
A |
T |
18: 37,581,295 (GRCm39) |
M134L |
probably benign |
Het |
Pecam1 |
G |
A |
11: 106,581,887 (GRCm39) |
T252M |
probably benign |
Het |
Rnd3 |
T |
A |
2: 51,022,536 (GRCm39) |
I169F |
probably damaging |
Het |
Rnmt |
T |
A |
18: 68,444,689 (GRCm39) |
D219E |
probably benign |
Het |
Rufy1 |
A |
T |
11: 50,292,315 (GRCm39) |
F491L |
probably benign |
Het |
Ryr2 |
G |
T |
13: 11,677,124 (GRCm39) |
C3242* |
probably null |
Het |
Smurf2 |
G |
T |
11: 106,766,727 (GRCm39) |
R31S |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,074,873 (GRCm39) |
I1333T |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,527,580 (GRCm39) |
C1279Y |
probably damaging |
Het |
Sugp2 |
T |
C |
8: 70,704,753 (GRCm39) |
|
probably null |
Het |
Sulf1 |
A |
T |
1: 12,929,636 (GRCm39) |
D301V |
probably benign |
Het |
Tbcd |
G |
T |
11: 121,492,737 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
T |
C |
14: 50,599,712 (GRCm39) |
I566T |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,374,921 (GRCm39) |
|
probably benign |
Het |
Tnfaip8l1 |
T |
C |
17: 56,478,799 (GRCm39) |
F30L |
probably benign |
Het |
Trav15-2-dv6-2 |
T |
A |
14: 53,887,433 (GRCm39) |
C118S |
probably damaging |
Het |
Ttc13 |
A |
G |
8: 125,408,959 (GRCm39) |
|
probably benign |
Het |
Ubqln3 |
A |
T |
7: 103,790,906 (GRCm39) |
S395T |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,754,827 (GRCm39) |
D178G |
probably benign |
Het |
Usf3 |
A |
G |
16: 44,041,222 (GRCm39) |
I1901V |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,402,112 (GRCm39) |
I116F |
probably benign |
Het |
Vmn1r69 |
T |
A |
7: 10,314,717 (GRCm39) |
T5S |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Wfikkn2 |
C |
T |
11: 94,129,688 (GRCm39) |
R151H |
probably damaging |
Het |
|
Other mutations in Pcca |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Pcca
|
APN |
14 |
122,820,041 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00906:Pcca
|
APN |
14 |
122,927,545 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00975:Pcca
|
APN |
14 |
123,114,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01329:Pcca
|
APN |
14 |
122,927,545 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01353:Pcca
|
APN |
14 |
122,820,029 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01672:Pcca
|
APN |
14 |
122,927,557 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02621:Pcca
|
APN |
14 |
122,922,391 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02695:Pcca
|
APN |
14 |
122,820,150 (GRCm39) |
splice site |
probably benign |
|
IGL02749:Pcca
|
APN |
14 |
122,771,800 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02971:Pcca
|
APN |
14 |
123,126,945 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03290:Pcca
|
APN |
14 |
122,822,518 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL03052:Pcca
|
UTSW |
14 |
123,124,513 (GRCm39) |
missense |
probably benign |
|
PIT4812001:Pcca
|
UTSW |
14 |
123,027,794 (GRCm39) |
missense |
probably benign |
0.00 |
R0549:Pcca
|
UTSW |
14 |
122,875,789 (GRCm39) |
splice site |
probably benign |
|
R0866:Pcca
|
UTSW |
14 |
123,126,957 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1498:Pcca
|
UTSW |
14 |
122,854,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Pcca
|
UTSW |
14 |
122,938,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R2002:Pcca
|
UTSW |
14 |
123,124,477 (GRCm39) |
missense |
probably benign |
0.00 |
R2020:Pcca
|
UTSW |
14 |
123,050,634 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2086:Pcca
|
UTSW |
14 |
122,923,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R3780:Pcca
|
UTSW |
14 |
122,922,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Pcca
|
UTSW |
14 |
123,027,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Pcca
|
UTSW |
14 |
123,124,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Pcca
|
UTSW |
14 |
123,124,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Pcca
|
UTSW |
14 |
122,896,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R6295:Pcca
|
UTSW |
14 |
122,896,187 (GRCm39) |
missense |
probably benign |
0.10 |
R6317:Pcca
|
UTSW |
14 |
122,820,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6319:Pcca
|
UTSW |
14 |
122,820,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Pcca
|
UTSW |
14 |
122,875,794 (GRCm39) |
missense |
probably benign |
0.07 |
R6989:Pcca
|
UTSW |
14 |
122,887,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7243:Pcca
|
UTSW |
14 |
123,114,186 (GRCm39) |
missense |
probably benign |
|
R7841:Pcca
|
UTSW |
14 |
122,800,384 (GRCm39) |
missense |
probably benign |
0.03 |
R8026:Pcca
|
UTSW |
14 |
122,875,794 (GRCm39) |
missense |
probably benign |
0.07 |
R8463:Pcca
|
UTSW |
14 |
122,922,526 (GRCm39) |
splice site |
probably null |
|
R8769:Pcca
|
UTSW |
14 |
122,854,260 (GRCm39) |
missense |
probably benign |
0.01 |
R8889:Pcca
|
UTSW |
14 |
122,795,123 (GRCm39) |
splice site |
probably benign |
|
R8956:Pcca
|
UTSW |
14 |
122,975,324 (GRCm39) |
missense |
probably benign |
|
R9287:Pcca
|
UTSW |
14 |
122,854,178 (GRCm39) |
missense |
probably benign |
0.00 |
R9336:Pcca
|
UTSW |
14 |
122,887,738 (GRCm39) |
missense |
probably benign |
0.04 |
R9447:Pcca
|
UTSW |
14 |
122,854,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R9606:Pcca
|
UTSW |
14 |
122,901,717 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Pcca
|
UTSW |
14 |
122,922,310 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Pcca
|
UTSW |
14 |
122,854,203 (GRCm39) |
missense |
possibly damaging |
0.51 |
|