Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018B08Rik |
T |
A |
8: 122,266,712 (GRCm39) |
Y58F |
probably benign |
Het |
Asap2 |
T |
C |
12: 21,218,251 (GRCm39) |
V58A |
probably damaging |
Het |
Bccip |
A |
G |
7: 133,322,520 (GRCm39) |
M289V |
probably benign |
Het |
Bhmt2 |
A |
T |
13: 93,798,819 (GRCm39) |
I334N |
probably benign |
Het |
Copa |
T |
A |
1: 171,938,253 (GRCm39) |
I513N |
possibly damaging |
Het |
Cspg4b |
T |
C |
13: 113,505,800 (GRCm39) |
S2310P |
probably benign |
Het |
Ctif |
G |
A |
18: 75,568,431 (GRCm39) |
T569M |
probably benign |
Het |
Dennd1a |
A |
T |
2: 37,691,225 (GRCm39) |
M231K |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,653,824 (GRCm39) |
|
probably null |
Het |
Fat3 |
T |
C |
9: 16,288,252 (GRCm39) |
I424V |
probably damaging |
Het |
Foxred2 |
G |
T |
15: 77,836,530 (GRCm39) |
C328* |
probably null |
Het |
Gemin5 |
A |
T |
11: 58,038,738 (GRCm39) |
H590Q |
probably damaging |
Het |
Gm5475 |
T |
C |
15: 100,325,007 (GRCm39) |
|
probably benign |
Het |
Gmip |
A |
G |
8: 70,273,576 (GRCm39) |
T956A |
probably benign |
Het |
Hmbox1 |
A |
T |
14: 65,134,281 (GRCm39) |
D106E |
probably benign |
Het |
Irs2 |
A |
T |
8: 11,054,697 (GRCm39) |
I1245N |
probably damaging |
Het |
Kcnk1 |
A |
G |
8: 126,752,129 (GRCm39) |
Y245C |
probably damaging |
Het |
Krtap4-9 |
A |
T |
11: 99,676,708 (GRCm39) |
R210* |
probably null |
Het |
Lama1 |
A |
G |
17: 68,081,538 (GRCm39) |
D1325G |
probably benign |
Het |
Lyz3 |
C |
T |
10: 117,074,413 (GRCm39) |
D25N |
probably benign |
Het |
Mep1a |
A |
T |
17: 43,793,121 (GRCm39) |
V361E |
probably damaging |
Het |
Mrgprx2 |
A |
G |
7: 48,131,813 (GRCm39) |
I92T |
possibly damaging |
Het |
Nup214 |
A |
T |
2: 31,872,683 (GRCm39) |
R242* |
probably null |
Het |
Nynrin |
T |
G |
14: 56,101,335 (GRCm39) |
S335A |
probably benign |
Het |
Or13a24 |
T |
G |
7: 140,154,564 (GRCm39) |
L166R |
probably damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,026 (GRCm39) |
V148A |
probably benign |
Het |
Or8b1c |
T |
G |
9: 38,384,472 (GRCm39) |
I143S |
probably benign |
Het |
Orc2 |
T |
C |
1: 58,539,523 (GRCm39) |
K39E |
probably benign |
Het |
Ppl |
C |
T |
16: 4,912,373 (GRCm39) |
G736D |
probably benign |
Het |
Ppp2r1a |
A |
G |
17: 21,181,895 (GRCm39) |
E471G |
possibly damaging |
Het |
Prrc2c |
G |
A |
1: 162,548,074 (GRCm39) |
P161S |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,310,893 (GRCm39) |
I804V |
probably benign |
Het |
Saal1 |
A |
G |
7: 46,352,088 (GRCm39) |
C144R |
probably benign |
Het |
Slc29a4 |
G |
A |
5: 142,698,713 (GRCm39) |
V125I |
probably benign |
Het |
Smarcc2 |
A |
G |
10: 128,305,541 (GRCm39) |
T322A |
probably benign |
Het |
Srgap2 |
A |
T |
1: 131,244,969 (GRCm39) |
M591K |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,528,176 (GRCm39) |
I1478V |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,188,998 (GRCm39) |
|
probably null |
Het |
Tmem150c |
C |
T |
5: 100,243,465 (GRCm39) |
|
probably null |
Het |
Tmem39b |
T |
A |
4: 129,572,366 (GRCm39) |
H412L |
possibly damaging |
Het |
Tox |
A |
C |
4: 6,697,635 (GRCm39) |
H389Q |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,202,158 (GRCm39) |
I1595T |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,653,558 (GRCm39) |
H1941R |
probably damaging |
Het |
|
Other mutations in Vmn2r-ps117 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6903:Vmn2r-ps117
|
UTSW |
17 |
19,058,552 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6912:Vmn2r-ps117
|
UTSW |
17 |
19,047,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6953:Vmn2r-ps117
|
UTSW |
17 |
19,045,095 (GRCm39) |
missense |
probably benign |
|
R6974:Vmn2r-ps117
|
UTSW |
17 |
19,058,495 (GRCm39) |
missense |
probably benign |
0.15 |
R7373:Vmn2r-ps117
|
UTSW |
17 |
19,044,948 (GRCm39) |
missense |
probably benign |
|
R7630:Vmn2r-ps117
|
UTSW |
17 |
19,044,909 (GRCm39) |
missense |
probably benign |
0.01 |
R7776:Vmn2r-ps117
|
UTSW |
17 |
19,043,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R8060:Vmn2r-ps117
|
UTSW |
17 |
19,058,124 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8126:Vmn2r-ps117
|
UTSW |
17 |
19,042,814 (GRCm39) |
missense |
probably benign |
0.00 |
R8751:Vmn2r-ps117
|
UTSW |
17 |
19,044,021 (GRCm39) |
missense |
probably benign |
|
R8986:Vmn2r-ps117
|
UTSW |
17 |
19,044,943 (GRCm39) |
nonsense |
probably null |
|
R9324:Vmn2r-ps117
|
UTSW |
17 |
19,042,911 (GRCm39) |
missense |
probably benign |
0.20 |
R9417:Vmn2r-ps117
|
UTSW |
17 |
19,044,037 (GRCm39) |
nonsense |
probably null |
|
R9607:Vmn2r-ps117
|
UTSW |
17 |
19,043,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Vmn2r-ps117
|
UTSW |
17 |
19,058,338 (GRCm39) |
missense |
probably benign |
0.01 |
|