Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat2 |
C |
T |
4: 49,383,273 (GRCm38) |
M93I |
probably benign |
Het |
Adamts16 |
T |
C |
13: 70,800,954 (GRCm38) |
D196G |
probably benign |
Het |
Adhfe1 |
T |
A |
1: 9,548,153 (GRCm38) |
|
probably null |
Het |
AI661453 |
A |
G |
17: 47,467,074 (GRCm38) |
|
probably benign |
Het |
Apc |
G |
T |
18: 34,316,230 (GRCm38) |
E2026* |
probably null |
Het |
Atg2a |
GCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCC |
GCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCC |
19: 6,245,007 (GRCm38) |
|
probably benign |
Het |
BC017158 |
A |
G |
7: 128,297,470 (GRCm38) |
L134P |
probably damaging |
Het |
Cad |
T |
C |
5: 31,062,231 (GRCm38) |
S688P |
probably damaging |
Het |
Ccdc191 |
C |
T |
16: 43,931,341 (GRCm38) |
R345* |
probably null |
Het |
Dcaf13 |
T |
A |
15: 39,145,085 (GRCm38) |
|
probably benign |
Het |
Drc1 |
A |
G |
5: 30,363,136 (GRCm38) |
D607G |
probably benign |
Het |
Fam160a1 |
T |
C |
3: 85,672,376 (GRCm38) |
R841G |
probably benign |
Het |
Gli1 |
G |
T |
10: 127,331,563 (GRCm38) |
A607E |
possibly damaging |
Het |
Gls |
G |
A |
1: 52,212,375 (GRCm38) |
|
probably benign |
Het |
Gria1 |
A |
T |
11: 57,289,409 (GRCm38) |
Q728H |
probably damaging |
Het |
Hcrtr1 |
A |
G |
4: 130,135,694 (GRCm38) |
L198P |
probably damaging |
Het |
Ifngr1 |
T |
A |
10: 19,603,942 (GRCm38) |
|
probably benign |
Het |
Ipo5 |
T |
C |
14: 120,944,357 (GRCm38) |
V954A |
possibly damaging |
Het |
Kcnh5 |
G |
T |
12: 74,965,261 (GRCm38) |
A628D |
probably damaging |
Het |
Kif14 |
T |
C |
1: 136,482,472 (GRCm38) |
S646P |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 79,045,140 (GRCm38) |
S133P |
probably damaging |
Het |
Neb |
T |
C |
2: 52,137,290 (GRCm38) |
M7143V |
probably damaging |
Het |
Nelfa |
G |
A |
5: 33,901,825 (GRCm38) |
P229S |
probably damaging |
Het |
Nfatc2 |
T |
C |
2: 168,571,199 (GRCm38) |
T169A |
probably damaging |
Het |
Nr1h4 |
A |
G |
10: 89,456,567 (GRCm38) |
Y398H |
probably damaging |
Het |
Nrcam |
A |
G |
12: 44,564,032 (GRCm38) |
E511G |
probably damaging |
Het |
Ocstamp |
T |
A |
2: 165,397,751 (GRCm38) |
R172W |
probably damaging |
Het |
Olfr1130 |
A |
G |
2: 87,607,994 (GRCm38) |
E202G |
probably damaging |
Het |
Olfr26 |
T |
A |
9: 38,855,470 (GRCm38) |
M136K |
probably damaging |
Het |
Olfr27 |
T |
C |
9: 39,144,721 (GRCm38) |
V207A |
probably benign |
Het |
Phf14 |
G |
A |
6: 11,961,578 (GRCm38) |
V405I |
possibly damaging |
Het |
Plk5 |
G |
A |
10: 80,360,223 (GRCm38) |
R238H |
probably damaging |
Het |
Pole |
A |
G |
5: 110,317,926 (GRCm38) |
E1240G |
probably benign |
Het |
Prdm15 |
A |
G |
16: 97,797,761 (GRCm38) |
I899T |
possibly damaging |
Het |
Psip1 |
T |
C |
4: 83,458,144 (GRCm38) |
N486S |
probably benign |
Het |
Rlf |
A |
G |
4: 121,170,833 (GRCm38) |
|
probably benign |
Het |
Rttn |
T |
C |
18: 88,979,635 (GRCm38) |
S255P |
probably damaging |
Het |
Sema6c |
A |
G |
3: 95,172,623 (GRCm38) |
K711E |
probably damaging |
Het |
Slc4a10 |
A |
T |
2: 62,190,893 (GRCm38) |
|
probably benign |
Het |
Trim36 |
T |
G |
18: 46,172,576 (GRCm38) |
S435R |
probably benign |
Het |
Ucp1 |
A |
G |
8: 83,291,603 (GRCm38) |
|
probably benign |
Het |
Vmn1r17 |
T |
C |
6: 57,361,014 (GRCm38) |
Y122C |
probably benign |
Het |
Wdfy4 |
T |
A |
14: 33,041,174 (GRCm38) |
Q2166L |
probably benign |
Het |
Zc3h7b |
C |
T |
15: 81,776,998 (GRCm38) |
T346M |
possibly damaging |
Het |
Zfhx4 |
T |
A |
3: 5,402,633 (GRCm38) |
V2617D |
probably damaging |
Het |
|
Other mutations in Vmn1r23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01563:Vmn1r23
|
APN |
6 |
57,926,076 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01980:Vmn1r23
|
APN |
6 |
57,926,490 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02934:Vmn1r23
|
APN |
6 |
57,925,929 (GRCm38) |
missense |
probably benign |
0.26 |
IGL03153:Vmn1r23
|
APN |
6 |
57,925,932 (GRCm38) |
missense |
probably damaging |
0.98 |
R0410:Vmn1r23
|
UTSW |
6 |
57,926,190 (GRCm38) |
missense |
probably benign |
0.11 |
R0452:Vmn1r23
|
UTSW |
6 |
57,926,484 (GRCm38) |
missense |
possibly damaging |
0.90 |
R0647:Vmn1r23
|
UTSW |
6 |
57,926,184 (GRCm38) |
missense |
probably benign |
|
R0692:Vmn1r23
|
UTSW |
6 |
57,926,125 (GRCm38) |
nonsense |
probably null |
|
R1674:Vmn1r23
|
UTSW |
6 |
57,926,061 (GRCm38) |
missense |
possibly damaging |
0.75 |
R1744:Vmn1r23
|
UTSW |
6 |
57,925,925 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1774:Vmn1r23
|
UTSW |
6 |
57,926,690 (GRCm38) |
missense |
probably damaging |
0.97 |
R2101:Vmn1r23
|
UTSW |
6 |
57,926,452 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2202:Vmn1r23
|
UTSW |
6 |
57,926,619 (GRCm38) |
missense |
probably benign |
0.01 |
R2204:Vmn1r23
|
UTSW |
6 |
57,926,619 (GRCm38) |
missense |
probably benign |
0.01 |
R2205:Vmn1r23
|
UTSW |
6 |
57,926,619 (GRCm38) |
missense |
probably benign |
0.01 |
R4282:Vmn1r23
|
UTSW |
6 |
57,926,467 (GRCm38) |
missense |
probably benign |
0.27 |
R4408:Vmn1r23
|
UTSW |
6 |
57,926,368 (GRCm38) |
missense |
probably benign |
0.01 |
R4532:Vmn1r23
|
UTSW |
6 |
57,925,929 (GRCm38) |
missense |
probably benign |
0.21 |
R4690:Vmn1r23
|
UTSW |
6 |
57,926,025 (GRCm38) |
missense |
probably benign |
|
R4700:Vmn1r23
|
UTSW |
6 |
57,926,205 (GRCm38) |
missense |
probably benign |
0.17 |
R4894:Vmn1r23
|
UTSW |
6 |
57,926,325 (GRCm38) |
missense |
probably benign |
0.00 |
R6164:Vmn1r23
|
UTSW |
6 |
57,926,055 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6930:Vmn1r23
|
UTSW |
6 |
57,926,145 (GRCm38) |
missense |
probably benign |
|
R7129:Vmn1r23
|
UTSW |
6 |
57,926,076 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7731:Vmn1r23
|
UTSW |
6 |
57,926,334 (GRCm38) |
missense |
probably benign |
0.03 |
R7877:Vmn1r23
|
UTSW |
6 |
57,926,556 (GRCm38) |
missense |
probably benign |
|
R8751:Vmn1r23
|
UTSW |
6 |
57,926,467 (GRCm38) |
missense |
probably benign |
0.27 |
R8809:Vmn1r23
|
UTSW |
6 |
57,926,367 (GRCm38) |
missense |
probably damaging |
0.97 |
|