Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
A |
17: 24,517,958 (GRCm39) |
I784L |
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,237,598 (GRCm39) |
V473E |
probably damaging |
Het |
Agap3 |
A |
G |
5: 24,706,010 (GRCm39) |
E758G |
probably damaging |
Het |
C6 |
A |
T |
15: 4,789,343 (GRCm39) |
K263* |
probably null |
Het |
Cep78 |
T |
C |
19: 15,936,943 (GRCm39) |
T588A |
probably benign |
Het |
Cfap20dc |
T |
C |
14: 8,659,424 (GRCm38) |
N57S |
probably damaging |
Het |
Col4a3 |
C |
T |
1: 82,657,344 (GRCm39) |
Q815* |
probably null |
Het |
Dcaf10 |
A |
G |
4: 45,342,630 (GRCm39) |
M155V |
probably benign |
Het |
Fam228b |
T |
C |
12: 4,812,370 (GRCm39) |
Y136C |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,255,651 (GRCm39) |
H793Q |
probably benign |
Het |
Gm10134 |
T |
C |
2: 28,396,429 (GRCm39) |
|
probably benign |
Het |
Gm6505 |
T |
C |
3: 28,819,169 (GRCm39) |
|
noncoding transcript |
Het |
Il31ra |
A |
G |
13: 112,666,830 (GRCm39) |
F416S |
probably damaging |
Het |
Lipc |
A |
G |
9: 70,841,750 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,306,982 (GRCm39) |
K368E |
possibly damaging |
Het |
Lrriq1 |
A |
T |
10: 103,036,500 (GRCm39) |
N884K |
probably damaging |
Het |
Mrgprx1 |
T |
C |
7: 47,670,875 (GRCm39) |
R291G |
probably benign |
Het |
Myo15a |
T |
A |
11: 60,401,465 (GRCm39) |
V3057E |
possibly damaging |
Het |
Or11g1 |
T |
A |
14: 50,651,226 (GRCm39) |
I75N |
probably damaging |
Het |
Or14j8 |
T |
A |
17: 38,263,413 (GRCm39) |
R167S |
probably benign |
Het |
Postn |
A |
T |
3: 54,282,517 (GRCm39) |
I493F |
probably damaging |
Het |
Ptpn22 |
C |
A |
3: 103,810,713 (GRCm39) |
F713L |
probably benign |
Het |
Pygm |
T |
C |
19: 6,438,148 (GRCm39) |
V239A |
probably damaging |
Het |
Rangrf |
C |
A |
11: 68,863,565 (GRCm39) |
C147F |
probably benign |
Het |
Rnf112 |
C |
T |
11: 61,341,205 (GRCm39) |
R460H |
probably benign |
Het |
Sh3d19 |
A |
G |
3: 86,014,305 (GRCm39) |
E423G |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,624,736 (GRCm39) |
V1738A |
possibly damaging |
Het |
Tipin |
A |
G |
9: 64,208,467 (GRCm39) |
K204E |
probably benign |
Het |
Traf3ip1 |
A |
T |
1: 91,427,357 (GRCm39) |
Q109L |
unknown |
Het |
Ttc21b |
A |
T |
2: 66,082,229 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
A |
2: 76,804,460 (GRCm39) |
A271S |
probably benign |
Het |
Vegfb |
C |
A |
19: 6,963,386 (GRCm39) |
|
probably null |
Het |
Wipi1 |
A |
T |
11: 109,494,617 (GRCm39) |
V72D |
probably damaging |
Het |
Zmym1 |
G |
A |
4: 126,941,557 (GRCm39) |
Q944* |
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 |
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 |
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 |
|
|