Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff1 |
A |
G |
5: 103,988,926 (GRCm39) |
D831G |
possibly damaging |
Het |
Amer2 |
A |
G |
14: 60,617,331 (GRCm39) |
K509E |
possibly damaging |
Het |
Ankrd6 |
T |
C |
4: 32,808,771 (GRCm39) |
K449E |
probably damaging |
Het |
Atp8b2 |
G |
A |
3: 89,855,828 (GRCm39) |
P459L |
probably benign |
Het |
Atr |
C |
T |
9: 95,802,875 (GRCm39) |
R1846* |
probably null |
Het |
Brd10 |
C |
T |
19: 29,694,676 (GRCm39) |
G1606R |
probably damaging |
Het |
Ccdc159 |
C |
A |
9: 21,842,992 (GRCm39) |
|
probably null |
Het |
Ccna1 |
A |
C |
3: 54,954,698 (GRCm39) |
Y338D |
probably damaging |
Het |
Cpq |
A |
T |
15: 33,213,089 (GRCm39) |
E36V |
probably damaging |
Het |
Cyp2c23 |
A |
G |
19: 44,003,371 (GRCm39) |
I268T |
probably damaging |
Het |
Dctn2 |
G |
T |
10: 127,114,057 (GRCm39) |
Q332H |
probably damaging |
Het |
Dnah17 |
T |
A |
11: 117,972,769 (GRCm39) |
I2055F |
probably damaging |
Het |
Dnmt3b |
A |
G |
2: 153,528,279 (GRCm39) |
H764R |
probably damaging |
Het |
Gphn |
T |
A |
12: 78,528,087 (GRCm39) |
I135K |
probably damaging |
Het |
Hnrnpul1 |
A |
G |
7: 25,450,409 (GRCm39) |
M1T |
probably null |
Het |
Htra4 |
T |
C |
8: 25,519,714 (GRCm39) |
D406G |
probably benign |
Het |
Klk10 |
G |
T |
7: 43,433,883 (GRCm39) |
|
probably benign |
Het |
Lilrb4a |
T |
A |
10: 51,367,616 (GRCm39) |
W53R |
probably benign |
Het |
Magel2 |
T |
C |
7: 62,028,461 (GRCm39) |
V455A |
probably benign |
Het |
Mrgprb5 |
T |
C |
7: 47,818,442 (GRCm39) |
T98A |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,951,373 (GRCm39) |
C76* |
probably null |
Het |
Myh7b |
C |
T |
2: 155,465,399 (GRCm39) |
R701C |
probably damaging |
Het |
Nbeal1 |
G |
A |
1: 60,300,745 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,215,720 (GRCm39) |
M196L |
probably benign |
Het |
Nmd3 |
A |
G |
3: 69,642,421 (GRCm39) |
K207R |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,179,129 (GRCm39) |
R962Q |
probably benign |
Het |
Pom121 |
T |
C |
5: 135,421,261 (GRCm39) |
K230E |
unknown |
Het |
Psme4 |
A |
G |
11: 30,757,788 (GRCm39) |
D307G |
possibly damaging |
Het |
Rnf41 |
T |
G |
10: 128,274,149 (GRCm39) |
M267R |
possibly damaging |
Het |
Sis |
T |
C |
3: 72,836,052 (GRCm39) |
N846D |
probably benign |
Het |
Slc22a19 |
T |
A |
19: 7,659,227 (GRCm39) |
I463L |
probably benign |
Het |
Slc25a39 |
A |
T |
11: 102,297,030 (GRCm39) |
|
probably null |
Het |
Slc35b2 |
C |
T |
17: 45,877,571 (GRCm39) |
R233C |
probably damaging |
Het |
Slc4a4 |
T |
C |
5: 89,376,695 (GRCm39) |
L983P |
probably damaging |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Tbc1d10a |
A |
G |
11: 4,159,984 (GRCm39) |
Y123C |
probably damaging |
Het |
Thbs4 |
A |
C |
13: 92,906,056 (GRCm39) |
I395S |
probably benign |
Het |
Triml2 |
A |
G |
8: 43,646,776 (GRCm39) |
T422A |
probably benign |
Het |
Ubn2 |
T |
C |
6: 38,417,382 (GRCm39) |
|
probably benign |
Het |
Vmn2r80 |
A |
G |
10: 79,005,362 (GRCm39) |
E333G |
probably damaging |
Het |
Zfp169 |
T |
C |
13: 48,644,639 (GRCm39) |
|
probably benign |
Het |
Zfp942 |
G |
A |
17: 22,148,083 (GRCm39) |
P182L |
probably benign |
Het |
|
Other mutations in Vmn1r15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01645:Vmn1r15
|
APN |
6 |
57,235,547 (GRCm39) |
nonsense |
probably null |
|
IGL02326:Vmn1r15
|
APN |
6 |
57,235,255 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02431:Vmn1r15
|
APN |
6 |
57,235,888 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02936:Vmn1r15
|
APN |
6 |
57,235,803 (GRCm39) |
nonsense |
probably null |
|
IGL02990:Vmn1r15
|
APN |
6 |
57,235,593 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03177:Vmn1r15
|
APN |
6 |
57,235,458 (GRCm39) |
missense |
probably benign |
0.27 |
R0531:Vmn1r15
|
UTSW |
6 |
57,235,236 (GRCm39) |
missense |
probably benign |
0.10 |
R1858:Vmn1r15
|
UTSW |
6 |
57,235,616 (GRCm39) |
missense |
probably benign |
0.13 |
R2010:Vmn1r15
|
UTSW |
6 |
57,235,269 (GRCm39) |
missense |
probably benign |
0.02 |
R2055:Vmn1r15
|
UTSW |
6 |
57,235,729 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2291:Vmn1r15
|
UTSW |
6 |
57,235,677 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3697:Vmn1r15
|
UTSW |
6 |
57,235,321 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5161:Vmn1r15
|
UTSW |
6 |
57,235,497 (GRCm39) |
missense |
probably benign |
0.00 |
R5884:Vmn1r15
|
UTSW |
6 |
57,235,993 (GRCm39) |
missense |
probably damaging |
0.99 |
R7287:Vmn1r15
|
UTSW |
6 |
57,235,201 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7376:Vmn1r15
|
UTSW |
6 |
57,235,342 (GRCm39) |
missense |
probably benign |
0.11 |
R7773:Vmn1r15
|
UTSW |
6 |
57,235,644 (GRCm39) |
missense |
probably benign |
0.05 |
R7980:Vmn1r15
|
UTSW |
6 |
57,235,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Vmn1r15
|
UTSW |
6 |
57,235,635 (GRCm39) |
missense |
probably benign |
0.01 |
R8753:Vmn1r15
|
UTSW |
6 |
57,235,895 (GRCm39) |
missense |
probably benign |
0.01 |
R8765:Vmn1r15
|
UTSW |
6 |
57,235,585 (GRCm39) |
missense |
probably benign |
0.01 |
R8812:Vmn1r15
|
UTSW |
6 |
57,235,123 (GRCm39) |
start gained |
probably benign |
|
|