Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox12b |
G |
T |
11: 69,054,032 (GRCm39) |
V205F |
probably benign |
Het |
Ampd3 |
T |
C |
7: 110,407,170 (GRCm39) |
|
probably benign |
Het |
Arhgef18 |
G |
A |
8: 3,494,904 (GRCm39) |
V388I |
probably benign |
Het |
Atp6v1c2 |
C |
T |
12: 17,344,741 (GRCm39) |
V169I |
probably damaging |
Het |
Ccdc88b |
G |
T |
19: 6,824,777 (GRCm39) |
L1328I |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cluh |
G |
A |
11: 74,558,591 (GRCm39) |
|
probably null |
Het |
Cpsf7 |
C |
A |
19: 10,509,159 (GRCm39) |
N23K |
probably benign |
Het |
Cyp4x1 |
A |
T |
4: 114,978,946 (GRCm39) |
F191L |
probably benign |
Het |
Dcn |
A |
G |
10: 97,345,835 (GRCm39) |
T216A |
probably benign |
Het |
Drosha |
C |
T |
15: 12,827,353 (GRCm39) |
|
probably benign |
Het |
Foxn4 |
A |
G |
5: 114,411,050 (GRCm39) |
S24P |
probably damaging |
Het |
Gm11733 |
A |
T |
11: 117,377,809 (GRCm39) |
|
probably null |
Het |
Hapln1 |
A |
C |
13: 89,749,725 (GRCm39) |
Y90S |
probably benign |
Het |
Igf2r |
C |
A |
17: 12,929,633 (GRCm39) |
|
probably benign |
Het |
Jade2 |
A |
G |
11: 51,722,074 (GRCm39) |
|
probably benign |
Het |
Kcnh7 |
A |
T |
2: 62,536,330 (GRCm39) |
L1084H |
probably benign |
Het |
Kif1a |
T |
C |
1: 92,966,985 (GRCm39) |
D1155G |
probably damaging |
Het |
Llgl2 |
A |
G |
11: 115,745,159 (GRCm39) |
M958V |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,271,740 (GRCm39) |
V4064A |
possibly damaging |
Het |
Mau2 |
A |
G |
8: 70,474,905 (GRCm39) |
|
probably benign |
Het |
Mllt10 |
T |
C |
2: 18,128,522 (GRCm39) |
|
probably benign |
Het |
Myo15a |
A |
G |
11: 60,370,266 (GRCm39) |
T1009A |
probably benign |
Het |
Myo6 |
T |
C |
9: 80,183,685 (GRCm39) |
|
probably null |
Het |
Neil2 |
G |
T |
14: 63,429,258 (GRCm39) |
H12N |
possibly damaging |
Het |
Nrde2 |
T |
C |
12: 100,108,355 (GRCm39) |
E412G |
probably damaging |
Het |
Or14j3 |
C |
T |
17: 37,900,559 (GRCm39) |
M228I |
probably benign |
Het |
Or4c115 |
T |
C |
2: 88,927,473 (GRCm39) |
Y266C |
possibly damaging |
Het |
Patl2 |
T |
G |
2: 121,954,978 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
C |
1: 20,593,187 (GRCm39) |
H1642R |
possibly damaging |
Het |
Ppp6r1 |
A |
G |
7: 4,646,022 (GRCm39) |
I199T |
possibly damaging |
Het |
Prom2 |
T |
A |
2: 127,370,734 (GRCm39) |
T817S |
probably benign |
Het |
Slc49a4 |
C |
A |
16: 35,555,861 (GRCm39) |
V200F |
possibly damaging |
Het |
Slc9b1 |
A |
G |
3: 135,100,744 (GRCm39) |
|
probably null |
Het |
Sv2c |
A |
T |
13: 96,224,886 (GRCm39) |
I141K |
probably damaging |
Het |
Tas2r139 |
A |
T |
6: 42,118,038 (GRCm39) |
I57F |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,105,703 (GRCm39) |
S106P |
possibly damaging |
Het |
Tnni3k |
T |
C |
3: 154,663,395 (GRCm39) |
D319G |
probably benign |
Het |
Tom1l2 |
C |
T |
11: 60,121,062 (GRCm39) |
D461N |
probably damaging |
Het |
Ugt1a10 |
T |
C |
1: 87,983,601 (GRCm39) |
L133S |
probably damaging |
Het |
Usf2 |
T |
G |
7: 30,654,732 (GRCm39) |
Q161P |
probably benign |
Het |
Vmn2r95 |
C |
A |
17: 18,672,298 (GRCm39) |
Y678* |
probably null |
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 |
|
IGL03177:Vmn1r15
|
APN |
6 |
57,235,458 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03382:Vmn1r15
|
APN |
6 |
57,235,555 (GRCm39) |
missense |
probably benign |
0.04 |
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 |
|
|