Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
C |
T |
7: 45,764,477 (GRCm39) |
C1156Y |
possibly damaging |
Het |
Armh4 |
T |
C |
14: 50,011,011 (GRCm39) |
E232G |
probably damaging |
Het |
Atp8b1 |
G |
A |
18: 64,679,184 (GRCm39) |
H766Y |
probably benign |
Het |
Cacna2d1 |
C |
A |
5: 16,217,389 (GRCm39) |
|
probably null |
Het |
Card11 |
T |
A |
5: 140,863,778 (GRCm39) |
T987S |
probably benign |
Het |
Dennd2b |
T |
A |
7: 109,126,841 (GRCm39) |
K540* |
probably null |
Het |
Dmxl2 |
A |
T |
9: 54,286,017 (GRCm39) |
Y2723N |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,150,733 (GRCm39) |
I342F |
possibly damaging |
Het |
Dnajc10 |
A |
G |
2: 80,170,871 (GRCm39) |
H454R |
possibly damaging |
Het |
Dpy19l3 |
T |
C |
7: 35,394,763 (GRCm39) |
T592A |
probably benign |
Het |
Eea1 |
T |
A |
10: 95,825,451 (GRCm39) |
S49T |
probably damaging |
Het |
Esd |
T |
A |
14: 74,987,159 (GRCm39) |
N294K |
probably benign |
Het |
Fmo3 |
A |
G |
1: 162,791,575 (GRCm39) |
V234A |
possibly damaging |
Het |
Folh1 |
A |
G |
7: 86,391,435 (GRCm39) |
F420L |
probably damaging |
Het |
Gabra1 |
T |
C |
11: 42,026,389 (GRCm39) |
N301S |
probably damaging |
Het |
Gm5422 |
A |
T |
10: 31,126,069 (GRCm39) |
|
noncoding transcript |
Het |
Gorab |
A |
T |
1: 163,214,000 (GRCm39) |
L310Q |
possibly damaging |
Het |
Gsdme |
A |
G |
6: 50,228,316 (GRCm39) |
Y51H |
probably damaging |
Het |
Hrob |
T |
C |
11: 102,146,012 (GRCm39) |
L96P |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,450,560 (GRCm39) |
I1964T |
possibly damaging |
Het |
Lmbr1 |
A |
G |
5: 29,440,053 (GRCm39) |
L410P |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,395,090 (GRCm39) |
R112G |
probably benign |
Het |
Mrgpra6 |
T |
C |
7: 46,835,681 (GRCm39) |
T247A |
probably benign |
Het |
Mroh4 |
A |
G |
15: 74,483,207 (GRCm39) |
|
probably benign |
Het |
Mycbpap |
T |
C |
11: 94,394,293 (GRCm39) |
|
probably null |
Het |
Myoz2 |
T |
A |
3: 122,827,881 (GRCm39) |
K12N |
probably damaging |
Het |
Odad2 |
T |
C |
18: 7,268,491 (GRCm39) |
S343G |
probably benign |
Het |
Or1d2 |
T |
C |
11: 74,256,359 (GRCm39) |
I288T |
possibly damaging |
Het |
P3h1 |
T |
G |
4: 119,093,980 (GRCm39) |
F212V |
probably damaging |
Het |
Pcnx2 |
T |
C |
8: 126,614,656 (GRCm39) |
D265G |
probably damaging |
Het |
Pkd1l3 |
C |
T |
8: 110,361,934 (GRCm39) |
T992I |
possibly damaging |
Het |
Prss58 |
T |
C |
6: 40,874,244 (GRCm39) |
D144G |
probably damaging |
Het |
Pth2 |
T |
A |
7: 44,830,764 (GRCm39) |
L29Q |
possibly damaging |
Het |
Rab1b |
A |
C |
19: 5,154,962 (GRCm39) |
|
probably benign |
Het |
Rasa2 |
A |
T |
9: 96,464,834 (GRCm39) |
C190* |
probably null |
Het |
Scn9a |
T |
C |
2: 66,317,986 (GRCm39) |
K1501E |
possibly damaging |
Het |
Selenoi |
A |
G |
5: 30,462,821 (GRCm39) |
|
probably benign |
Het |
Slc11a2 |
T |
C |
15: 100,286,999 (GRCm39) |
N558S |
probably benign |
Het |
Sox10 |
T |
C |
15: 79,040,539 (GRCm39) |
I173V |
probably benign |
Het |
Sra1 |
A |
C |
18: 36,804,526 (GRCm39) |
F476C |
probably damaging |
Het |
Tmem119 |
T |
A |
5: 113,933,409 (GRCm39) |
K131* |
probably null |
Het |
Trim12c |
T |
A |
7: 103,994,261 (GRCm39) |
K198* |
probably null |
Het |
Ttn |
A |
G |
2: 76,681,904 (GRCm39) |
|
probably benign |
Het |
Unc119b |
C |
T |
5: 115,265,371 (GRCm39) |
V154I |
probably benign |
Het |
Usp47 |
T |
A |
7: 111,654,069 (GRCm39) |
S108R |
probably damaging |
Het |
Vmn1r191 |
T |
C |
13: 22,363,614 (GRCm39) |
I47V |
probably benign |
Het |
Wnt3 |
C |
T |
11: 103,703,204 (GRCm39) |
A229V |
probably benign |
Het |
|
Other mutations in Vmn1r15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
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 |
|
|