Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
A |
6: 121,631,571 (GRCm39) |
L623M |
probably benign |
Het |
Adamts13 |
A |
G |
2: 26,886,595 (GRCm39) |
E938G |
possibly damaging |
Het |
Agfg1 |
A |
T |
1: 82,871,259 (GRCm39) |
Q497L |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,986,813 (GRCm39) |
H2699R |
probably benign |
Het |
Antxrl |
G |
T |
14: 33,792,453 (GRCm39) |
|
probably null |
Het |
Apol7c |
A |
T |
15: 77,410,418 (GRCm39) |
V176E |
probably damaging |
Het |
Arid5b |
T |
C |
10: 68,113,777 (GRCm39) |
N87D |
possibly damaging |
Het |
Atp2c1 |
A |
T |
9: 105,309,897 (GRCm39) |
I560N |
probably damaging |
Het |
Atp2c2 |
T |
C |
8: 120,482,742 (GRCm39) |
F868S |
possibly damaging |
Het |
Blnk |
G |
C |
19: 40,926,122 (GRCm39) |
F326L |
probably benign |
Het |
Bltp1 |
C |
T |
3: 37,089,961 (GRCm39) |
R4130* |
probably null |
Het |
Ckap2 |
C |
T |
8: 22,665,812 (GRCm39) |
V412I |
possibly damaging |
Het |
Clmn |
A |
G |
12: 104,748,281 (GRCm39) |
V422A |
probably benign |
Het |
Ctnnal1 |
A |
G |
4: 56,813,856 (GRCm39) |
S638P |
probably benign |
Het |
Cyp2j5 |
T |
C |
4: 96,524,052 (GRCm39) |
S327G |
probably benign |
Het |
Dhx38 |
G |
A |
8: 110,280,177 (GRCm39) |
T871M |
probably damaging |
Het |
Dmxl1 |
A |
T |
18: 50,023,834 (GRCm39) |
K1706* |
probably null |
Het |
Dnah11 |
A |
G |
12: 117,979,154 (GRCm39) |
L2648P |
possibly damaging |
Het |
Elf2 |
G |
A |
3: 51,215,530 (GRCm39) |
T60I |
probably damaging |
Het |
Fam120b |
T |
A |
17: 15,622,759 (GRCm39) |
C246S |
possibly damaging |
Het |
Fcho2 |
G |
T |
13: 98,882,403 (GRCm39) |
T451K |
possibly damaging |
Het |
Fzd9 |
T |
A |
5: 135,278,602 (GRCm39) |
I428F |
probably damaging |
Het |
Galnt13 |
T |
A |
2: 54,744,667 (GRCm39) |
V122E |
probably damaging |
Het |
Gm21738 |
T |
A |
14: 19,418,908 (GRCm38) |
Y8F |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,272,029 (GRCm39) |
I940V |
possibly damaging |
Het |
Gp2 |
A |
G |
7: 119,050,721 (GRCm39) |
|
probably null |
Het |
Gpr6 |
A |
G |
10: 40,946,530 (GRCm39) |
S351P |
probably benign |
Het |
Gprin1 |
T |
C |
13: 54,887,689 (GRCm39) |
E195G |
possibly damaging |
Het |
Grm8 |
A |
T |
6: 28,125,882 (GRCm39) |
Y81* |
probably null |
Het |
Gtf3c3 |
A |
T |
1: 54,444,278 (GRCm39) |
N703K |
probably damaging |
Het |
Hhipl2 |
G |
A |
1: 183,208,921 (GRCm39) |
V495I |
probably benign |
Het |
Islr |
G |
A |
9: 58,065,502 (GRCm39) |
|
probably benign |
Het |
Lrrc36 |
T |
C |
8: 106,176,273 (GRCm39) |
Y216H |
possibly damaging |
Het |
Macroh2a1 |
T |
A |
13: 56,252,722 (GRCm39) |
N87Y |
probably damaging |
Het |
Me2 |
A |
G |
18: 73,906,205 (GRCm39) |
I528T |
probably benign |
Het |
Mecr |
A |
T |
4: 131,585,127 (GRCm39) |
I156F |
possibly damaging |
Het |
Megf6 |
A |
G |
4: 154,346,967 (GRCm39) |
|
probably benign |
Het |
Mn1 |
T |
A |
5: 111,569,435 (GRCm39) |
L1135H |
probably damaging |
Het |
Naip5 |
A |
G |
13: 100,349,177 (GRCm39) |
S1384P |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,102,213 (GRCm39) |
N337S |
probably benign |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Neb |
A |
T |
2: 52,139,293 (GRCm39) |
H3107Q |
probably benign |
Het |
Nebl |
A |
G |
2: 17,381,462 (GRCm39) |
V738A |
possibly damaging |
Het |
Nsd2 |
G |
A |
5: 34,039,464 (GRCm39) |
R825Q |
possibly damaging |
Het |
Nsun2 |
A |
G |
13: 69,775,705 (GRCm39) |
N383S |
probably damaging |
Het |
Ntrk3 |
A |
T |
7: 77,897,036 (GRCm39) |
M667K |
probably damaging |
Het |
Or10a48 |
A |
C |
7: 108,424,442 (GRCm39) |
C255G |
probably benign |
Het |
Or11h6 |
G |
A |
14: 50,880,565 (GRCm39) |
V276M |
possibly damaging |
Het |
Or1e29 |
A |
G |
11: 73,667,974 (GRCm39) |
Y60H |
possibly damaging |
Het |
Or6c2 |
A |
T |
10: 129,362,488 (GRCm39) |
M131L |
probably benign |
Het |
Pex6 |
T |
C |
17: 47,033,558 (GRCm39) |
V633A |
probably benign |
Het |
Phactr1 |
C |
T |
13: 43,110,147 (GRCm39) |
T95M |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,564,408 (GRCm39) |
D1334G |
probably damaging |
Het |
Pkhd1l1 |
A |
C |
15: 44,460,513 (GRCm39) |
I4241L |
probably benign |
Het |
Ppwd1 |
T |
C |
13: 104,356,771 (GRCm39) |
E248G |
probably damaging |
Het |
Prepl |
A |
C |
17: 85,379,509 (GRCm39) |
M393R |
probably benign |
Het |
Ptpn6 |
T |
C |
6: 124,698,148 (GRCm39) |
S532G |
probably benign |
Het |
Rnase11 |
G |
T |
14: 51,287,058 (GRCm39) |
H165Q |
possibly damaging |
Het |
Sf1 |
A |
G |
19: 6,422,090 (GRCm39) |
N172S |
possibly damaging |
Het |
Shprh |
T |
A |
10: 11,032,822 (GRCm39) |
D269E |
probably benign |
Het |
Slc16a1 |
T |
C |
3: 104,556,798 (GRCm39) |
I61T |
possibly damaging |
Het |
Slc38a2 |
A |
C |
15: 96,590,417 (GRCm39) |
I309S |
probably damaging |
Het |
Sry |
C |
G |
Y: 2,663,149 (GRCm39) |
Q170H |
unknown |
Het |
Stk3 |
A |
C |
15: 35,008,454 (GRCm39) |
|
probably null |
Het |
Tg |
C |
A |
15: 66,568,015 (GRCm39) |
C1306* |
probably null |
Het |
Tnik |
A |
G |
3: 28,719,889 (GRCm39) |
M1254V |
probably damaging |
Het |
U2surp |
T |
C |
9: 95,366,280 (GRCm39) |
E474G |
possibly damaging |
Het |
Vmn1r224 |
T |
A |
17: 20,639,587 (GRCm39) |
F55I |
probably benign |
Het |
Zc2hc1a |
A |
G |
3: 7,581,543 (GRCm39) |
D15G |
probably benign |
Het |
Zfp827 |
C |
A |
8: 79,802,975 (GRCm39) |
P516T |
possibly damaging |
Het |
Zfyve9 |
A |
T |
4: 108,542,104 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn1r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01449:Vmn1r32
|
APN |
6 |
66,529,916 (GRCm39) |
missense |
probably benign |
|
IGL02399:Vmn1r32
|
APN |
6 |
66,529,913 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02964:Vmn1r32
|
APN |
6 |
66,529,922 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03161:Vmn1r32
|
APN |
6 |
66,530,204 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03244:Vmn1r32
|
APN |
6 |
66,530,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Vmn1r32
|
APN |
6 |
66,529,897 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0668:Vmn1r32
|
UTSW |
6 |
66,530,644 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0732:Vmn1r32
|
UTSW |
6 |
66,530,690 (GRCm39) |
missense |
probably benign |
0.01 |
R1205:Vmn1r32
|
UTSW |
6 |
66,530,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1732:Vmn1r32
|
UTSW |
6 |
66,530,285 (GRCm39) |
missense |
probably benign |
0.19 |
R2049:Vmn1r32
|
UTSW |
6 |
66,530,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Vmn1r32
|
UTSW |
6 |
66,530,533 (GRCm39) |
missense |
probably benign |
0.09 |
R3773:Vmn1r32
|
UTSW |
6 |
66,530,351 (GRCm39) |
missense |
probably benign |
0.01 |
R3834:Vmn1r32
|
UTSW |
6 |
66,530,647 (GRCm39) |
missense |
probably benign |
0.02 |
R3980:Vmn1r32
|
UTSW |
6 |
66,530,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R4737:Vmn1r32
|
UTSW |
6 |
66,530,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Vmn1r32
|
UTSW |
6 |
66,530,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R6382:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
probably benign |
0.07 |
R6894:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7394:Vmn1r32
|
UTSW |
6 |
66,530,173 (GRCm39) |
missense |
probably benign |
0.06 |
R7980:Vmn1r32
|
UTSW |
6 |
66,530,305 (GRCm39) |
nonsense |
probably null |
|
R8833:Vmn1r32
|
UTSW |
6 |
66,530,623 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8867:Vmn1r32
|
UTSW |
6 |
66,530,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R8975:Vmn1r32
|
UTSW |
6 |
66,530,189 (GRCm39) |
missense |
probably benign |
0.03 |
R9131:Vmn1r32
|
UTSW |
6 |
66,530,020 (GRCm39) |
missense |
probably benign |
0.30 |
R9135:Vmn1r32
|
UTSW |
6 |
66,530,120 (GRCm39) |
nonsense |
probably null |
|
R9429:Vmn1r32
|
UTSW |
6 |
66,530,237 (GRCm39) |
missense |
probably benign |
0.03 |
|