Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
G |
T |
13: 31,742,978 (GRCm39) |
R92S |
unknown |
Het |
Adamts14 |
T |
C |
10: 61,041,176 (GRCm39) |
S842G |
possibly damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Ccdc7a |
A |
G |
8: 129,562,654 (GRCm39) |
I1108T |
possibly damaging |
Het |
Col12a1 |
T |
A |
9: 79,548,863 (GRCm39) |
M2161L |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,364,832 (GRCm39) |
I1647T |
probably benign |
Het |
Defb26 |
A |
T |
2: 152,350,156 (GRCm39) |
C41* |
probably null |
Het |
Dennd3 |
T |
G |
15: 73,439,964 (GRCm39) |
|
probably benign |
Het |
Edem1 |
C |
T |
6: 108,831,338 (GRCm39) |
R600W |
possibly damaging |
Het |
F13a1 |
C |
A |
13: 37,172,913 (GRCm39) |
G156W |
probably damaging |
Het |
Foxk2 |
A |
G |
11: 121,190,553 (GRCm39) |
T565A |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,808,168 (GRCm39) |
I1496F |
possibly damaging |
Het |
Fyb1 |
T |
C |
15: 6,690,197 (GRCm39) |
|
probably null |
Het |
Gapdhs |
T |
C |
7: 30,436,146 (GRCm39) |
Y148C |
probably damaging |
Het |
H1f3 |
T |
C |
13: 23,739,505 (GRCm39) |
I81T |
probably damaging |
Het |
Hddc2 |
A |
T |
10: 31,192,289 (GRCm39) |
R64S |
probably damaging |
Het |
Hddc2 |
T |
A |
10: 31,196,338 (GRCm39) |
|
probably null |
Het |
Klk10 |
T |
A |
7: 43,432,942 (GRCm39) |
S113T |
probably benign |
Het |
Lin7a |
T |
C |
10: 107,159,843 (GRCm39) |
S52P |
possibly damaging |
Het |
Nbeal1 |
A |
T |
1: 60,331,029 (GRCm39) |
I2213L |
probably damaging |
Het |
Nbeal2 |
T |
C |
9: 110,466,615 (GRCm39) |
T763A |
probably benign |
Het |
Nlrp4a |
T |
A |
7: 26,149,482 (GRCm39) |
I363N |
possibly damaging |
Het |
Oat |
C |
T |
7: 132,161,393 (GRCm39) |
V381I |
probably benign |
Het |
Or52n2c |
A |
G |
7: 104,574,557 (GRCm39) |
L138P |
probably damaging |
Het |
Plpp2 |
A |
T |
10: 79,363,378 (GRCm39) |
I207N |
possibly damaging |
Het |
Rps6ka4 |
T |
C |
19: 6,808,679 (GRCm39) |
E522G |
possibly damaging |
Het |
Sars2 |
T |
C |
7: 28,441,628 (GRCm39) |
V63A |
probably benign |
Het |
Sgf29 |
C |
T |
7: 126,271,350 (GRCm39) |
R209C |
probably damaging |
Het |
Sptbn1 |
G |
A |
11: 30,086,048 (GRCm39) |
A1220V |
probably damaging |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tnrc18 |
T |
C |
5: 142,757,902 (GRCm39) |
E1055G |
|
Het |
Vmn2r120 |
T |
G |
17: 57,816,244 (GRCm39) |
I704L |
possibly damaging |
Het |
Vwa8 |
A |
G |
14: 79,329,731 (GRCm39) |
S1188G |
probably benign |
Het |
Zfp12 |
A |
G |
5: 143,231,535 (GRCm39) |
K653E |
probably damaging |
Het |
Zfp933 |
T |
A |
4: 147,911,058 (GRCm39) |
R179S |
probably damaging |
Het |
Zfp937 |
A |
T |
2: 150,080,681 (GRCm39) |
H237L |
probably damaging |
Het |
Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably damaging |
Het |
|
Other mutations in Vmn1r158 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01147:Vmn1r158
|
APN |
7 |
22,490,204 (GRCm39) |
missense |
probably benign |
0.01 |
R1173:Vmn1r158
|
UTSW |
7 |
22,489,870 (GRCm39) |
missense |
probably benign |
0.19 |
R1574:Vmn1r158
|
UTSW |
7 |
22,489,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Vmn1r158
|
UTSW |
7 |
22,489,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Vmn1r158
|
UTSW |
7 |
22,490,072 (GRCm39) |
missense |
probably benign |
0.08 |
R1777:Vmn1r158
|
UTSW |
7 |
22,489,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Vmn1r158
|
UTSW |
7 |
22,490,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Vmn1r158
|
UTSW |
7 |
22,490,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Vmn1r158
|
UTSW |
7 |
22,489,815 (GRCm39) |
missense |
probably benign |
0.03 |
R3749:Vmn1r158
|
UTSW |
7 |
22,489,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Vmn1r158
|
UTSW |
7 |
22,490,179 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5238:Vmn1r158
|
UTSW |
7 |
22,489,799 (GRCm39) |
missense |
probably benign |
|
R6500:Vmn1r158
|
UTSW |
7 |
22,490,078 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6511:Vmn1r158
|
UTSW |
7 |
22,490,116 (GRCm39) |
missense |
probably benign |
0.00 |
R6581:Vmn1r158
|
UTSW |
7 |
22,489,465 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6751:Vmn1r158
|
UTSW |
7 |
22,489,306 (GRCm39) |
missense |
probably damaging |
0.96 |
R7168:Vmn1r158
|
UTSW |
7 |
22,490,101 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7337:Vmn1r158
|
UTSW |
7 |
22,489,649 (GRCm39) |
missense |
probably benign |
0.00 |
R7747:Vmn1r158
|
UTSW |
7 |
22,489,725 (GRCm39) |
missense |
probably benign |
0.15 |
R8328:Vmn1r158
|
UTSW |
7 |
22,489,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Vmn1r158
|
UTSW |
7 |
22,489,305 (GRCm39) |
nonsense |
probably null |
|
R8809:Vmn1r158
|
UTSW |
7 |
22,489,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R9227:Vmn1r158
|
UTSW |
7 |
22,489,469 (GRCm39) |
missense |
probably benign |
0.02 |
R9468:Vmn1r158
|
UTSW |
7 |
22,489,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R9702:Vmn1r158
|
UTSW |
7 |
22,490,065 (GRCm39) |
missense |
probably benign |
0.00 |
R9719:Vmn1r158
|
UTSW |
7 |
22,489,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Vmn1r158
|
UTSW |
7 |
22,489,883 (GRCm39) |
missense |
possibly damaging |
0.46 |
|