Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre4 |
A |
G |
17: 56,092,121 (GRCm39) |
Y127C |
probably damaging |
Het |
Aif1l |
A |
T |
2: 31,852,251 (GRCm39) |
S40C |
probably damaging |
Het |
Alkal1 |
A |
G |
1: 6,458,839 (GRCm39) |
K76R |
probably damaging |
Het |
Atm |
T |
C |
9: 53,391,969 (GRCm39) |
S1807G |
probably benign |
Het |
Bhmt-ps1 |
T |
A |
4: 26,369,352 (GRCm39) |
|
noncoding transcript |
Het |
Brd10 |
A |
T |
19: 29,696,149 (GRCm39) |
S1115T |
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,797,276 (GRCm39) |
Y368N |
probably damaging |
Het |
Gar1 |
A |
T |
3: 129,624,455 (GRCm39) |
|
probably benign |
Het |
Gm5265 |
A |
T |
1: 169,281,370 (GRCm39) |
|
noncoding transcript |
Het |
Gm7964 |
T |
G |
7: 83,406,030 (GRCm39) |
N281K |
probably damaging |
Het |
Grin1 |
T |
C |
2: 25,187,332 (GRCm39) |
|
probably benign |
Het |
H1f5 |
A |
T |
13: 21,964,147 (GRCm39) |
|
probably benign |
Het |
Hapln4 |
T |
A |
8: 70,539,610 (GRCm39) |
W214R |
probably damaging |
Het |
Ift56 |
A |
G |
6: 38,372,010 (GRCm39) |
Y200C |
probably damaging |
Het |
Irgq |
C |
A |
7: 24,233,050 (GRCm39) |
A297D |
possibly damaging |
Het |
Kri1 |
T |
C |
9: 21,192,359 (GRCm39) |
E145G |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,583,460 (GRCm39) |
C683R |
probably damaging |
Het |
Mrpl22 |
T |
A |
11: 58,062,693 (GRCm39) |
|
probably benign |
Het |
Myo7a |
T |
A |
7: 97,722,436 (GRCm39) |
Q1163L |
possibly damaging |
Het |
Nipsnap3a |
T |
A |
4: 52,997,251 (GRCm39) |
D172E |
probably benign |
Het |
Nrxn3 |
G |
T |
12: 89,499,762 (GRCm39) |
G718* |
probably null |
Het |
Olfm3 |
C |
T |
3: 114,883,820 (GRCm39) |
Q41* |
probably null |
Het |
Or52z12 |
A |
G |
7: 103,233,966 (GRCm39) |
T246A |
probably damaging |
Het |
Or8u8 |
G |
T |
2: 86,012,341 (GRCm39) |
T38K |
probably damaging |
Het |
Parm1 |
G |
A |
5: 91,741,726 (GRCm39) |
M31I |
probably benign |
Het |
Phc3 |
A |
T |
3: 30,990,968 (GRCm39) |
S383R |
probably damaging |
Het |
Pkn2 |
A |
T |
3: 142,499,627 (GRCm39) |
L950* |
probably null |
Het |
Plec |
C |
T |
15: 76,061,519 (GRCm39) |
R2671H |
probably damaging |
Het |
Ptbp1 |
T |
C |
10: 79,695,047 (GRCm39) |
I125T |
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,682,143 (GRCm39) |
R537H |
probably damaging |
Het |
Ptk7 |
A |
T |
17: 46,885,389 (GRCm39) |
M679K |
probably benign |
Het |
Ptx3 |
C |
T |
3: 66,132,127 (GRCm39) |
T216I |
probably damaging |
Het |
Rrp8 |
T |
C |
7: 105,383,229 (GRCm39) |
I346V |
possibly damaging |
Het |
Rsrc1 |
A |
G |
3: 66,901,900 (GRCm39) |
K17E |
unknown |
Het |
Ryr2 |
T |
A |
13: 11,752,759 (GRCm39) |
E1854V |
possibly damaging |
Het |
Semp2l2a |
T |
C |
8: 13,888,061 (GRCm39) |
E10G |
probably benign |
Het |
Slc25a45 |
A |
T |
19: 5,930,146 (GRCm39) |
I39F |
probably damaging |
Het |
Spag5 |
G |
A |
11: 78,195,337 (GRCm39) |
V215I |
probably damaging |
Het |
Ston1 |
A |
G |
17: 88,944,199 (GRCm39) |
Y535C |
probably damaging |
Het |
Tbc1d14 |
A |
T |
5: 36,650,452 (GRCm39) |
S395T |
probably benign |
Het |
Tlr11 |
C |
T |
14: 50,599,306 (GRCm39) |
P431S |
probably damaging |
Het |
Trerf1 |
G |
T |
17: 47,625,727 (GRCm39) |
|
noncoding transcript |
Het |
Trim43b |
T |
A |
9: 88,972,692 (GRCm39) |
Q154L |
probably benign |
Het |
Vmn1r-ps103 |
C |
A |
13: 22,626,198 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r14 |
A |
G |
5: 109,364,149 (GRCm39) |
M589T |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,765,952 (GRCm39) |
T20S |
probably benign |
Het |
Zbtb5 |
A |
G |
4: 44,993,855 (GRCm39) |
|
probably null |
Het |
Zfp35 |
T |
G |
18: 24,136,246 (GRCm39) |
F197V |
possibly damaging |
Het |
|
Other mutations in Vmn1r49 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01293:Vmn1r49
|
APN |
6 |
90,049,394 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03230:Vmn1r49
|
APN |
6 |
90,049,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Vmn1r49
|
APN |
6 |
90,049,341 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0517:Vmn1r49
|
UTSW |
6 |
90,049,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R0638:Vmn1r49
|
UTSW |
6 |
90,049,648 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1498:Vmn1r49
|
UTSW |
6 |
90,049,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Vmn1r49
|
UTSW |
6 |
90,049,623 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1668:Vmn1r49
|
UTSW |
6 |
90,049,764 (GRCm39) |
missense |
probably benign |
0.07 |
R1816:Vmn1r49
|
UTSW |
6 |
90,049,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2071:Vmn1r49
|
UTSW |
6 |
90,049,184 (GRCm39) |
missense |
probably benign |
0.00 |
R2155:Vmn1r49
|
UTSW |
6 |
90,049,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R2274:Vmn1r49
|
UTSW |
6 |
90,049,126 (GRCm39) |
missense |
probably benign |
0.23 |
R4614:Vmn1r49
|
UTSW |
6 |
90,049,534 (GRCm39) |
missense |
probably benign |
0.00 |
R4797:Vmn1r49
|
UTSW |
6 |
90,049,612 (GRCm39) |
missense |
probably benign |
0.13 |
R4978:Vmn1r49
|
UTSW |
6 |
90,049,872 (GRCm39) |
missense |
probably benign |
0.30 |
R5227:Vmn1r49
|
UTSW |
6 |
90,049,753 (GRCm39) |
missense |
probably benign |
0.00 |
R5959:Vmn1r49
|
UTSW |
6 |
90,049,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Vmn1r49
|
UTSW |
6 |
90,049,195 (GRCm39) |
missense |
probably benign |
0.19 |
R6744:Vmn1r49
|
UTSW |
6 |
90,049,184 (GRCm39) |
missense |
probably benign |
0.00 |
R7173:Vmn1r49
|
UTSW |
6 |
90,049,250 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7457:Vmn1r49
|
UTSW |
6 |
90,049,534 (GRCm39) |
missense |
probably benign |
0.00 |
R7573:Vmn1r49
|
UTSW |
6 |
90,049,843 (GRCm39) |
missense |
probably benign |
0.06 |
R8360:Vmn1r49
|
UTSW |
6 |
90,049,991 (GRCm39) |
missense |
probably benign |
0.06 |
R8399:Vmn1r49
|
UTSW |
6 |
90,049,689 (GRCm39) |
nonsense |
probably null |
|
R9560:Vmn1r49
|
UTSW |
6 |
90,049,382 (GRCm39) |
missense |
probably benign |
0.03 |
|