Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
T |
C |
15: 57,895,444 (GRCm39) |
D18G |
probably null |
Het |
A530064D06Rik |
A |
G |
17: 48,473,653 (GRCm39) |
V88A |
probably damaging |
Het |
Abhd6 |
T |
C |
14: 8,055,589 (GRCm38) |
L272P |
probably damaging |
Het |
Adam25 |
C |
T |
8: 41,207,627 (GRCm39) |
R298C |
possibly damaging |
Het |
Adam34l |
T |
C |
8: 44,078,988 (GRCm39) |
N412S |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,916,818 (GRCm39) |
N219D |
possibly damaging |
Het |
Brd3 |
A |
G |
2: 27,353,938 (GRCm39) |
F58S |
probably damaging |
Het |
Ceacam3 |
G |
A |
7: 16,892,253 (GRCm39) |
R332H |
possibly damaging |
Het |
Cfap57 |
C |
A |
4: 118,446,172 (GRCm39) |
|
probably null |
Het |
Chd2 |
A |
G |
7: 73,130,154 (GRCm39) |
F834L |
probably damaging |
Het |
Crocc2 |
A |
G |
1: 93,111,126 (GRCm39) |
K140E |
possibly damaging |
Het |
Fam117b |
A |
G |
1: 60,020,731 (GRCm39) |
T534A |
probably benign |
Het |
Fchsd1 |
C |
T |
18: 38,102,487 (GRCm39) |
V14I |
probably damaging |
Het |
Grid2ip |
A |
T |
5: 143,359,257 (GRCm39) |
E291V |
probably damaging |
Het |
Hbp1 |
A |
G |
12: 31,987,720 (GRCm39) |
L146S |
probably damaging |
Het |
Hr |
A |
G |
14: 70,799,276 (GRCm39) |
D616G |
possibly damaging |
Het |
Igfbp5 |
A |
C |
1: 72,902,300 (GRCm39) |
|
probably null |
Het |
Jak2 |
C |
T |
19: 29,287,022 (GRCm39) |
|
probably null |
Het |
Mpl |
T |
C |
4: 118,305,750 (GRCm39) |
D425G |
probably damaging |
Het |
Ms4a4c |
T |
C |
19: 11,398,676 (GRCm39) |
S165P |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,392,911 (GRCm39) |
S3217P |
probably benign |
Het |
Nfatc3 |
T |
A |
8: 106,810,502 (GRCm39) |
L426* |
probably null |
Het |
Or4f47 |
T |
C |
2: 111,972,509 (GRCm39) |
V73A |
probably benign |
Het |
Or5ak24 |
T |
C |
2: 85,261,068 (GRCm39) |
Y35C |
probably damaging |
Het |
Or7a42 |
T |
A |
10: 78,791,818 (GRCm39) |
Y260N |
probably damaging |
Het |
Phf1 |
G |
T |
17: 27,155,586 (GRCm39) |
V384L |
probably benign |
Het |
Rangap1 |
T |
C |
15: 81,596,336 (GRCm39) |
T259A |
probably benign |
Het |
Rec8 |
A |
G |
14: 55,856,076 (GRCm39) |
N6S |
possibly damaging |
Het |
Rmdn2 |
G |
A |
17: 79,934,971 (GRCm39) |
|
probably benign |
Het |
Scin |
T |
C |
12: 40,118,945 (GRCm39) |
Y617C |
probably damaging |
Het |
Ttc13 |
T |
C |
8: 125,400,221 (GRCm39) |
S744G |
probably benign |
Het |
Ttc14 |
T |
C |
3: 33,862,968 (GRCm39) |
|
probably benign |
Het |
Uggt1 |
T |
C |
1: 36,214,032 (GRCm39) |
E219G |
possibly damaging |
Het |
Vmn1r72 |
A |
T |
7: 11,413,064 (GRCm39) |
|
probably null |
Het |
Zfp326 |
T |
G |
5: 106,036,584 (GRCm39) |
M76R |
probably null |
Het |
|
Other mutations in Vmn1r183 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Vmn1r183
|
APN |
7 |
23,754,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Vmn1r183
|
APN |
7 |
23,754,985 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03377:Vmn1r183
|
APN |
7 |
23,754,817 (GRCm39) |
missense |
possibly damaging |
0.70 |
PIT4791001:Vmn1r183
|
UTSW |
7 |
23,754,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R0463:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Vmn1r183
|
UTSW |
7 |
23,754,250 (GRCm39) |
missense |
probably benign |
0.03 |
R0666:Vmn1r183
|
UTSW |
7 |
23,754,601 (GRCm39) |
missense |
probably benign |
|
R3928:Vmn1r183
|
UTSW |
7 |
23,754,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R4425:Vmn1r183
|
UTSW |
7 |
23,754,973 (GRCm39) |
missense |
probably benign |
0.00 |
R4767:Vmn1r183
|
UTSW |
7 |
23,754,531 (GRCm39) |
frame shift |
probably null |
|
R4835:Vmn1r183
|
UTSW |
7 |
23,754,564 (GRCm39) |
missense |
probably benign |
0.07 |
R5267:Vmn1r183
|
UTSW |
7 |
23,754,971 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5693:Vmn1r183
|
UTSW |
7 |
23,754,227 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Vmn1r183
|
UTSW |
7 |
23,754,982 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7073:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Vmn1r183
|
UTSW |
7 |
23,754,890 (GRCm39) |
missense |
possibly damaging |
0.89 |
|