Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,166,371 (GRCm39) |
M1K |
probably null |
Het |
Adra1b |
A |
T |
11: 43,726,263 (GRCm39) |
V218D |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,606,255 (GRCm39) |
S1216G |
possibly damaging |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cfap44 |
G |
T |
16: 44,288,824 (GRCm39) |
D1525Y |
probably damaging |
Het |
Chd8 |
A |
T |
14: 52,439,650 (GRCm39) |
M2341K |
probably benign |
Het |
Chst11 |
A |
G |
10: 83,027,319 (GRCm39) |
T249A |
probably damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,434,850 (GRCm39) |
V336A |
probably benign |
Het |
Dennd3 |
T |
C |
15: 73,419,153 (GRCm39) |
L648P |
probably benign |
Het |
Dhx16 |
T |
C |
17: 36,200,173 (GRCm39) |
V864A |
probably benign |
Het |
Enpp3 |
G |
A |
10: 24,675,092 (GRCm39) |
H362Y |
possibly damaging |
Het |
Ess2 |
A |
T |
16: 17,728,028 (GRCm39) |
D79E |
probably damaging |
Het |
Fam83c |
T |
A |
2: 155,671,299 (GRCm39) |
Y712F |
probably damaging |
Het |
Helz |
C |
T |
11: 107,561,113 (GRCm39) |
Q1392* |
probably null |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Iqch |
T |
C |
9: 63,479,961 (GRCm39) |
H143R |
probably benign |
Het |
Itgb5 |
A |
G |
16: 33,720,881 (GRCm39) |
D315G |
probably damaging |
Het |
Kcnmb2 |
A |
G |
3: 32,236,174 (GRCm39) |
K141R |
probably benign |
Het |
Lrrc37a |
G |
A |
11: 103,391,676 (GRCm39) |
P1250S |
probably benign |
Het |
Mcm5 |
T |
G |
8: 75,836,962 (GRCm39) |
V110G |
probably damaging |
Het |
Med27 |
G |
A |
2: 29,361,312 (GRCm39) |
D163N |
probably damaging |
Het |
Mms22l |
C |
A |
4: 24,600,185 (GRCm39) |
Y1129* |
probably null |
Het |
Mov10l1 |
G |
A |
15: 88,931,023 (GRCm39) |
R1081H |
probably damaging |
Het |
Mtpap |
C |
G |
18: 4,380,833 (GRCm39) |
N170K |
probably benign |
Het |
Mtpap |
C |
T |
18: 4,380,834 (GRCm39) |
Q171* |
probably null |
Het |
Myo6 |
T |
A |
9: 80,153,836 (GRCm39) |
F271I |
unknown |
Het |
Ndst4 |
C |
T |
3: 125,518,385 (GRCm39) |
S354L |
probably benign |
Het |
Nfatc1 |
C |
T |
18: 80,751,258 (GRCm39) |
A26T |
probably benign |
Het |
Or7d11 |
C |
A |
9: 19,966,543 (GRCm39) |
C72F |
probably damaging |
Het |
Piezo2 |
G |
C |
18: 63,250,815 (GRCm39) |
T428S |
probably benign |
Het |
Prkch |
A |
G |
12: 73,768,616 (GRCm39) |
E462G |
probably damaging |
Het |
Rbm20 |
A |
G |
19: 53,823,131 (GRCm39) |
Y576C |
probably damaging |
Het |
Riok3 |
TTTCATT |
TTT |
18: 12,282,642 (GRCm39) |
|
probably null |
Het |
Rpp40 |
C |
T |
13: 36,080,898 (GRCm39) |
D302N |
probably benign |
Het |
Sash1 |
A |
G |
10: 8,615,969 (GRCm39) |
V631A |
probably damaging |
Het |
Sstr2 |
A |
G |
11: 113,515,203 (GRCm39) |
T41A |
probably benign |
Het |
Thsd7b |
T |
A |
1: 129,843,371 (GRCm39) |
V861E |
possibly damaging |
Het |
Tomm70a |
A |
G |
16: 56,973,070 (GRCm39) |
K603E |
possibly damaging |
Het |
Tpd52l2 |
T |
A |
2: 181,141,683 (GRCm39) |
M22K |
possibly damaging |
Het |
Tpst1 |
T |
A |
5: 130,130,860 (GRCm39) |
L110Q |
possibly damaging |
Het |
Tram1l1 |
A |
G |
3: 124,115,137 (GRCm39) |
Y99C |
possibly damaging |
Het |
Ttc39b |
A |
G |
4: 83,181,977 (GRCm39) |
F81L |
possibly damaging |
Het |
Ubr1 |
A |
G |
2: 120,778,325 (GRCm39) |
Y238H |
probably damaging |
Het |
Vmn1r202 |
G |
T |
13: 22,686,316 (GRCm39) |
H34N |
possibly damaging |
Het |
Xpnpep1 |
A |
T |
19: 53,000,289 (GRCm39) |
V187E |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,349 (GRCm39) |
I438V |
probably benign |
Het |
|
Other mutations in Vmn1r36 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01384:Vmn1r36
|
APN |
6 |
66,693,446 (GRCm39) |
missense |
probably damaging |
0.98 |
R0610:Vmn1r36
|
UTSW |
6 |
66,693,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R0864:Vmn1r36
|
UTSW |
6 |
66,693,840 (GRCm39) |
missense |
probably null |
|
R1754:Vmn1r36
|
UTSW |
6 |
66,693,517 (GRCm39) |
frame shift |
probably null |
|
R1813:Vmn1r36
|
UTSW |
6 |
66,693,756 (GRCm39) |
missense |
probably benign |
|
R1844:Vmn1r36
|
UTSW |
6 |
66,693,747 (GRCm39) |
missense |
probably benign |
0.00 |
R1896:Vmn1r36
|
UTSW |
6 |
66,693,756 (GRCm39) |
missense |
probably benign |
|
R2987:Vmn1r36
|
UTSW |
6 |
66,693,700 (GRCm39) |
missense |
probably benign |
0.05 |
R4852:Vmn1r36
|
UTSW |
6 |
66,693,872 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4899:Vmn1r36
|
UTSW |
6 |
66,693,549 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5985:Vmn1r36
|
UTSW |
6 |
66,693,855 (GRCm39) |
missense |
probably benign |
0.02 |
R6235:Vmn1r36
|
UTSW |
6 |
66,693,230 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Vmn1r36
|
UTSW |
6 |
66,693,107 (GRCm39) |
missense |
probably benign |
|
R7511:Vmn1r36
|
UTSW |
6 |
66,693,914 (GRCm39) |
start gained |
probably benign |
|
R8046:Vmn1r36
|
UTSW |
6 |
66,692,964 (GRCm39) |
nonsense |
probably null |
|
R8143:Vmn1r36
|
UTSW |
6 |
66,693,036 (GRCm39) |
nonsense |
probably null |
|
R8870:Vmn1r36
|
UTSW |
6 |
66,693,720 (GRCm39) |
missense |
probably benign |
0.00 |
R8871:Vmn1r36
|
UTSW |
6 |
66,693,442 (GRCm39) |
nonsense |
probably null |
|
R9335:Vmn1r36
|
UTSW |
6 |
66,693,430 (GRCm39) |
nonsense |
probably null |
|
|