Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
A |
G |
5: 4,093,996 (GRCm39) |
M2173V |
probably damaging |
Het |
Alas1 |
G |
T |
9: 106,119,000 (GRCm39) |
|
probably null |
Het |
Atp2c2 |
G |
A |
8: 120,476,610 (GRCm39) |
|
probably null |
Het |
Cadm2 |
A |
G |
16: 66,581,675 (GRCm39) |
V210A |
possibly damaging |
Het |
Cfap70 |
A |
T |
14: 20,459,181 (GRCm39) |
D671E |
probably damaging |
Het |
Chd2 |
C |
T |
7: 73,150,764 (GRCm39) |
E322K |
possibly damaging |
Het |
Chrnd |
C |
T |
1: 87,118,729 (GRCm39) |
Q29* |
probably null |
Het |
Cip2a |
T |
C |
16: 48,821,339 (GRCm39) |
|
probably benign |
Het |
Cym |
A |
G |
3: 107,121,582 (GRCm39) |
S237P |
probably benign |
Het |
D030068K23Rik |
A |
G |
8: 109,978,091 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma2 |
T |
A |
11: 98,541,677 (GRCm39) |
S135T |
probably benign |
Het |
Hc |
A |
T |
2: 34,873,819 (GRCm39) |
Y158* |
probably null |
Het |
Hoxb3 |
C |
A |
11: 96,236,926 (GRCm39) |
H335N |
probably damaging |
Het |
Htr2a |
G |
A |
14: 74,943,789 (GRCm39) |
M456I |
probably benign |
Het |
Ighv1-19 |
G |
A |
12: 114,672,350 (GRCm39) |
T90I |
probably damaging |
Het |
Kansl3 |
C |
A |
1: 36,384,035 (GRCm39) |
S729I |
probably damaging |
Het |
Kcnab1 |
T |
C |
3: 65,207,035 (GRCm39) |
I137T |
possibly damaging |
Het |
Kcnt1 |
A |
T |
2: 25,767,927 (GRCm39) |
E12V |
probably damaging |
Het |
Klk15 |
A |
T |
7: 43,588,204 (GRCm39) |
S171C |
possibly damaging |
Het |
Lcn2 |
A |
T |
2: 32,277,728 (GRCm39) |
M1K |
probably null |
Het |
Lrig1 |
T |
C |
6: 94,590,559 (GRCm39) |
D487G |
probably benign |
Het |
Lrp8 |
T |
A |
4: 107,700,468 (GRCm39) |
C135* |
probably null |
Het |
Lrrc31 |
C |
A |
3: 30,749,671 (GRCm39) |
S54I |
probably damaging |
Het |
Ltbp4 |
A |
G |
7: 27,024,641 (GRCm39) |
V663A |
possibly damaging |
Het |
Med27 |
G |
A |
2: 29,267,920 (GRCm39) |
|
probably benign |
Het |
Mical1 |
T |
C |
10: 41,362,933 (GRCm39) |
|
probably benign |
Het |
Myt1 |
A |
T |
2: 181,453,191 (GRCm39) |
M799L |
probably damaging |
Het |
Nlrc4 |
T |
C |
17: 74,752,953 (GRCm39) |
M477V |
probably benign |
Het |
Npy4r |
T |
C |
14: 33,869,098 (GRCm39) |
I63M |
probably benign |
Het |
Or2t43 |
A |
T |
11: 58,457,655 (GRCm39) |
I172N |
probably damaging |
Het |
Or52e15 |
C |
T |
7: 104,645,842 (GRCm39) |
G90S |
probably benign |
Het |
Or8b1b |
T |
A |
9: 38,375,379 (GRCm39) |
L14Q |
probably null |
Het |
Or8s10 |
T |
C |
15: 98,335,563 (GRCm39) |
L71P |
probably damaging |
Het |
Piezo1 |
A |
C |
8: 123,227,899 (GRCm39) |
|
probably null |
Het |
Ppp1r12c |
T |
C |
7: 4,486,366 (GRCm39) |
E601G |
probably damaging |
Het |
Proser1 |
T |
C |
3: 53,387,133 (GRCm39) |
|
probably null |
Het |
Psme2 |
A |
T |
14: 55,825,734 (GRCm39) |
N143K |
probably benign |
Het |
Pygo2 |
C |
A |
3: 89,340,571 (GRCm39) |
P323Q |
probably damaging |
Het |
Rab11b |
T |
C |
17: 33,968,763 (GRCm39) |
T77A |
possibly damaging |
Het |
Recql5 |
A |
G |
11: 115,795,714 (GRCm39) |
S190P |
probably benign |
Het |
Serpina12 |
A |
G |
12: 104,004,183 (GRCm39) |
F150L |
probably damaging |
Het |
Sfswap |
A |
G |
5: 129,637,805 (GRCm39) |
S821G |
possibly damaging |
Het |
Slc22a2 |
C |
T |
17: 12,831,281 (GRCm39) |
T357M |
probably damaging |
Het |
Spag6l |
A |
C |
16: 16,646,888 (GRCm39) |
N39K |
probably benign |
Het |
Srl |
A |
G |
16: 4,315,316 (GRCm39) |
S109P |
possibly damaging |
Het |
Tagap |
A |
T |
17: 8,148,255 (GRCm39) |
H152L |
probably damaging |
Het |
Tbx3 |
T |
A |
5: 119,818,813 (GRCm39) |
S463T |
probably benign |
Het |
Tcaf2 |
A |
G |
6: 42,619,772 (GRCm39) |
L85P |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,544,979 (GRCm39) |
S2332C |
probably damaging |
Het |
Trim60 |
A |
T |
8: 65,454,030 (GRCm39) |
M73K |
probably benign |
Het |
Trpc1 |
T |
C |
9: 95,588,918 (GRCm39) |
T769A |
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,025,958 (GRCm39) |
L601Q |
probably benign |
Het |
Unc5d |
T |
C |
8: 29,334,865 (GRCm39) |
Y154C |
possibly damaging |
Het |
Vmn1r185 |
A |
T |
7: 26,311,208 (GRCm39) |
V99E |
probably damaging |
Het |
Vmn1r57 |
G |
T |
7: 5,223,856 (GRCm39) |
S127I |
possibly damaging |
Het |
Vmn1r62 |
T |
A |
7: 5,678,943 (GRCm39) |
M208K |
probably damaging |
Het |
Vmn2r110 |
T |
C |
17: 20,803,642 (GRCm39) |
D311G |
possibly damaging |
Het |
Vmn2r48 |
C |
A |
7: 9,676,185 (GRCm39) |
S432I |
probably benign |
Het |
Vmn2r48 |
T |
A |
7: 9,676,186 (GRCm39) |
S432C |
probably damaging |
Het |
Vmn2r71 |
T |
C |
7: 85,270,442 (GRCm39) |
V536A |
probably benign |
Het |
Vstm2a |
A |
G |
11: 16,209,884 (GRCm39) |
T37A |
probably damaging |
Het |
Wfs1 |
T |
C |
5: 37,124,809 (GRCm39) |
H694R |
probably damaging |
Het |
Zdbf2 |
T |
C |
1: 63,348,940 (GRCm39) |
S2440P |
possibly damaging |
Het |
Zfp61 |
A |
G |
7: 23,990,700 (GRCm39) |
|
probably null |
Het |
Zfp64 |
T |
C |
2: 168,767,855 (GRCm39) |
T586A |
probably benign |
Het |
Zfp943 |
T |
A |
17: 22,211,963 (GRCm39) |
C350S |
probably damaging |
Het |
|
Other mutations in Angpt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Angpt1
|
APN |
15 |
42,339,863 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02671:Angpt1
|
APN |
15 |
42,539,790 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02876:Angpt1
|
APN |
15 |
42,290,373 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03077:Angpt1
|
APN |
15 |
42,339,818 (GRCm39) |
nonsense |
probably null |
|
IGL03334:Angpt1
|
APN |
15 |
42,359,808 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0226:Angpt1
|
UTSW |
15 |
42,331,631 (GRCm39) |
missense |
probably benign |
0.01 |
R1774:Angpt1
|
UTSW |
15 |
42,387,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R1800:Angpt1
|
UTSW |
15 |
42,375,800 (GRCm39) |
missense |
probably damaging |
0.96 |
R1967:Angpt1
|
UTSW |
15 |
42,301,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4477:Angpt1
|
UTSW |
15 |
42,331,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Angpt1
|
UTSW |
15 |
42,301,796 (GRCm39) |
missense |
probably benign |
0.01 |
R4647:Angpt1
|
UTSW |
15 |
42,539,580 (GRCm39) |
missense |
probably benign |
0.02 |
R4648:Angpt1
|
UTSW |
15 |
42,539,580 (GRCm39) |
missense |
probably benign |
0.02 |
R4750:Angpt1
|
UTSW |
15 |
42,539,797 (GRCm39) |
missense |
probably benign |
0.00 |
R5222:Angpt1
|
UTSW |
15 |
42,539,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Angpt1
|
UTSW |
15 |
42,301,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Angpt1
|
UTSW |
15 |
42,386,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Angpt1
|
UTSW |
15 |
42,375,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Angpt1
|
UTSW |
15 |
42,387,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R6904:Angpt1
|
UTSW |
15 |
42,323,136 (GRCm39) |
missense |
probably benign |
0.00 |
R7009:Angpt1
|
UTSW |
15 |
42,386,991 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7101:Angpt1
|
UTSW |
15 |
42,386,965 (GRCm39) |
missense |
probably benign |
0.18 |
R7139:Angpt1
|
UTSW |
15 |
42,539,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Angpt1
|
UTSW |
15 |
42,323,121 (GRCm39) |
missense |
probably benign |
0.25 |
R7830:Angpt1
|
UTSW |
15 |
42,539,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Angpt1
|
UTSW |
15 |
42,359,752 (GRCm39) |
missense |
probably benign |
0.00 |
R8073:Angpt1
|
UTSW |
15 |
42,301,699 (GRCm39) |
missense |
probably benign |
0.00 |
R8093:Angpt1
|
UTSW |
15 |
42,339,873 (GRCm39) |
missense |
probably benign |
0.01 |
R8331:Angpt1
|
UTSW |
15 |
42,539,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8391:Angpt1
|
UTSW |
15 |
42,375,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Angpt1
|
UTSW |
15 |
42,290,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8508:Angpt1
|
UTSW |
15 |
42,375,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Angpt1
|
UTSW |
15 |
42,375,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Angpt1
|
UTSW |
15 |
42,301,751 (GRCm39) |
missense |
probably benign |
|
R9318:Angpt1
|
UTSW |
15 |
42,301,751 (GRCm39) |
missense |
probably benign |
|
R9746:Angpt1
|
UTSW |
15 |
42,539,837 (GRCm39) |
missense |
probably benign |
|
|