Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
A |
T |
4: 144,182,464 (GRCm39) |
S335T |
probably damaging |
Het |
Abcb1b |
G |
A |
5: 8,914,238 (GRCm39) |
A1203T |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Agt |
C |
A |
8: 125,283,839 (GRCm39) |
E427* |
probably null |
Het |
Angel1 |
G |
A |
12: 86,769,681 (GRCm39) |
S193F |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,794,692 (GRCm39) |
V359A |
probably benign |
Het |
Ankrd33b |
T |
C |
15: 31,367,432 (GRCm39) |
D36G |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,931,902 (GRCm39) |
C766S |
probably benign |
Het |
Asic1 |
C |
T |
15: 99,596,700 (GRCm39) |
R499C |
probably damaging |
Het |
Atpsckmt |
T |
G |
15: 31,606,103 (GRCm39) |
S20R |
probably benign |
Het |
Bank1 |
C |
T |
3: 135,919,703 (GRCm39) |
C364Y |
probably damaging |
Het |
Bmerb1 |
T |
A |
16: 13,804,676 (GRCm39) |
S8T |
possibly damaging |
Het |
Bpifa5 |
C |
A |
2: 154,008,869 (GRCm39) |
D223E |
probably benign |
Het |
Capn5 |
C |
T |
7: 97,782,089 (GRCm39) |
R217Q |
probably damaging |
Het |
Ccm2 |
G |
A |
11: 6,540,886 (GRCm39) |
S184N |
probably damaging |
Het |
Ces5a |
T |
A |
8: 94,252,286 (GRCm39) |
D202V |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,322,528 (GRCm39) |
I284T |
probably benign |
Het |
Cog7 |
C |
A |
7: 121,540,392 (GRCm39) |
|
probably null |
Het |
Col13a1 |
A |
T |
10: 61,698,525 (GRCm39) |
M512K |
unknown |
Het |
Cps1 |
A |
C |
1: 67,254,723 (GRCm39) |
D1304A |
probably benign |
Het |
Crhbp |
C |
A |
13: 95,580,403 (GRCm39) |
|
probably null |
Het |
Ctdspl2 |
T |
A |
2: 121,837,368 (GRCm39) |
C377* |
probably null |
Het |
Ctsl |
G |
A |
13: 64,513,032 (GRCm39) |
L297F |
possibly damaging |
Het |
Ddost |
A |
G |
4: 138,038,046 (GRCm39) |
T262A |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,761,313 (GRCm39) |
|
probably null |
Het |
Ddx54 |
A |
G |
5: 120,764,927 (GRCm39) |
I769V |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,745,507 (GRCm39) |
I1463N |
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,660,872 (GRCm39) |
Y404N |
possibly damaging |
Het |
Epb42 |
T |
A |
2: 120,859,631 (GRCm39) |
K186* |
probably null |
Het |
Farp2 |
A |
G |
1: 93,504,543 (GRCm39) |
|
probably null |
Het |
Fbxl9 |
A |
T |
8: 106,039,425 (GRCm39) |
L617Q |
probably damaging |
Het |
Fev |
C |
A |
1: 74,921,692 (GRCm39) |
R86L |
possibly damaging |
Het |
Foxb2 |
G |
T |
19: 16,849,820 (GRCm39) |
C395* |
probably null |
Het |
Foxn3 |
A |
G |
12: 99,175,765 (GRCm39) |
V261A |
probably benign |
Het |
Fsd1 |
A |
G |
17: 56,298,245 (GRCm39) |
D190G |
probably benign |
Het |
Gm9930 |
A |
T |
10: 9,410,547 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma2 |
A |
T |
11: 98,545,727 (GRCm39) |
K260* |
probably null |
Het |
Hdac7 |
G |
A |
15: 97,704,380 (GRCm39) |
Q497* |
probably null |
Het |
Hic1 |
G |
A |
11: 75,057,713 (GRCm39) |
P392L |
possibly damaging |
Het |
Hk3 |
C |
T |
13: 55,162,239 (GRCm39) |
|
probably null |
Het |
Ifna6 |
G |
T |
4: 88,745,887 (GRCm39) |
V79F |
probably benign |
Het |
Il20ra |
A |
T |
10: 19,635,388 (GRCm39) |
Q543L |
probably damaging |
Het |
Itk |
T |
A |
11: 46,251,115 (GRCm39) |
D163V |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,400,916 (GRCm39) |
L688R |
probably damaging |
Het |
Kdm5b |
T |
A |
1: 134,545,771 (GRCm39) |
S977R |
possibly damaging |
Het |
Kng1 |
G |
A |
16: 22,879,232 (GRCm39) |
A45T |
possibly damaging |
Het |
Map1a |
T |
G |
2: 121,136,234 (GRCm39) |
L2350R |
probably damaging |
Het |
Mdfic |
A |
G |
6: 15,799,755 (GRCm39) |
D212G |
probably benign |
Het |
Ms4a1 |
C |
A |
19: 11,236,043 (GRCm39) |
|
probably null |
Het |
Myo9a |
T |
A |
9: 59,801,635 (GRCm39) |
F1944L |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,915,689 (GRCm39) |
W928R |
probably damaging |
Het |
Nfatc2ip |
T |
G |
7: 125,995,751 (GRCm39) |
D46A |
possibly damaging |
Het |
Ngly1 |
C |
T |
14: 16,290,774 (GRCm38) |
Q419* |
probably null |
Het |
Nsd2 |
T |
A |
5: 34,000,682 (GRCm39) |
N66K |
probably damaging |
Het |
Nsmce4a |
T |
C |
7: 130,138,732 (GRCm39) |
H304R |
probably damaging |
Het |
Odad2 |
G |
A |
18: 7,222,676 (GRCm39) |
P531L |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,965 (GRCm39) |
L310Q |
possibly damaging |
Het |
Or2y11 |
C |
T |
11: 49,443,291 (GRCm39) |
T239M |
probably damaging |
Het |
Or4a2 |
T |
C |
2: 89,248,544 (GRCm39) |
Y71C |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,319,696 (GRCm39) |
I181F |
possibly damaging |
Het |
Or7e168 |
G |
A |
9: 19,720,156 (GRCm39) |
V181I |
probably benign |
Het |
Or8c20 |
A |
C |
9: 38,260,499 (GRCm39) |
N40T |
probably damaging |
Het |
Or8h9 |
C |
T |
2: 86,789,190 (GRCm39) |
G204D |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,714,427 (GRCm39) |
E265G |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,814,193 (GRCm39) |
S4188G |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,559 (GRCm39) |
N37K |
probably damaging |
Het |
R3hdm1 |
G |
A |
1: 128,121,440 (GRCm39) |
V315I |
probably benign |
Het |
Rab24 |
A |
T |
13: 55,468,738 (GRCm39) |
|
probably null |
Het |
Rap1gap2 |
A |
T |
11: 74,332,592 (GRCm39) |
M71K |
probably damaging |
Het |
Rergl |
T |
G |
6: 139,473,524 (GRCm39) |
K42T |
probably damaging |
Het |
Septin5 |
T |
C |
16: 18,443,647 (GRCm39) |
T92A |
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,246,140 (GRCm39) |
V595A |
probably benign |
Het |
Slc17a8 |
A |
G |
10: 89,412,192 (GRCm39) |
S414P |
probably benign |
Het |
Tie1 |
A |
C |
4: 118,333,343 (GRCm39) |
I841R |
probably damaging |
Het |
Tll1 |
T |
G |
8: 64,551,505 (GRCm39) |
D292A |
probably damaging |
Het |
Tnfaip8l1 |
A |
T |
17: 56,478,727 (GRCm39) |
T6S |
probably damaging |
Het |
Trim17 |
T |
A |
11: 58,859,320 (GRCm39) |
V178E |
probably damaging |
Het |
Ttc27 |
A |
T |
17: 75,163,544 (GRCm39) |
R717S |
possibly damaging |
Het |
Upk2 |
G |
T |
9: 44,365,418 (GRCm39) |
P50Q |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,307,880 (GRCm39) |
C2319S |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,742,178 (GRCm39) |
D184V |
probably damaging |
Het |
Vmn2r9 |
C |
A |
5: 108,996,154 (GRCm39) |
G165* |
probably null |
Het |
Xkr6 |
A |
T |
14: 64,056,871 (GRCm39) |
I261F |
probably benign |
Het |
Xpnpep3 |
T |
G |
15: 81,311,693 (GRCm39) |
I133S |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,193,387 (GRCm39) |
Y91C |
probably benign |
Het |
Zfp442 |
T |
C |
2: 150,253,169 (GRCm39) |
D31G |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,939 (GRCm39) |
Q387L |
probably damaging |
Het |
Zfp804a |
C |
T |
2: 82,089,761 (GRCm39) |
Q1197* |
probably null |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Thnsl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Thnsl2
|
APN |
6 |
71,108,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00814:Thnsl2
|
APN |
6 |
71,116,867 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01139:Thnsl2
|
APN |
6 |
71,115,718 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01380:Thnsl2
|
APN |
6 |
71,115,740 (GRCm39) |
missense |
probably benign |
|
IGL01511:Thnsl2
|
APN |
6 |
71,116,777 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02000:Thnsl2
|
APN |
6 |
71,111,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Thnsl2
|
APN |
6 |
71,108,930 (GRCm39) |
missense |
probably benign |
0.00 |
R0372:Thnsl2
|
UTSW |
6 |
71,116,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Thnsl2
|
UTSW |
6 |
71,118,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Thnsl2
|
UTSW |
6 |
71,111,208 (GRCm39) |
nonsense |
probably null |
|
R0863:Thnsl2
|
UTSW |
6 |
71,111,208 (GRCm39) |
nonsense |
probably null |
|
R1300:Thnsl2
|
UTSW |
6 |
71,111,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Thnsl2
|
UTSW |
6 |
71,108,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Thnsl2
|
UTSW |
6 |
71,108,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R4767:Thnsl2
|
UTSW |
6 |
71,111,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Thnsl2
|
UTSW |
6 |
71,115,749 (GRCm39) |
missense |
probably benign |
0.40 |
R5818:Thnsl2
|
UTSW |
6 |
71,111,127 (GRCm39) |
missense |
probably benign |
0.01 |
R6627:Thnsl2
|
UTSW |
6 |
71,111,199 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6800:Thnsl2
|
UTSW |
6 |
71,118,264 (GRCm39) |
missense |
probably benign |
0.29 |
R7192:Thnsl2
|
UTSW |
6 |
71,116,739 (GRCm39) |
missense |
probably benign |
0.02 |
R7391:Thnsl2
|
UTSW |
6 |
71,108,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Thnsl2
|
UTSW |
6 |
71,108,990 (GRCm39) |
nonsense |
probably null |
|
R7565:Thnsl2
|
UTSW |
6 |
71,118,311 (GRCm39) |
missense |
probably benign |
0.00 |
R7980:Thnsl2
|
UTSW |
6 |
71,115,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R7988:Thnsl2
|
UTSW |
6 |
71,118,303 (GRCm39) |
missense |
probably benign |
0.38 |
R8170:Thnsl2
|
UTSW |
6 |
71,106,317 (GRCm39) |
missense |
probably benign |
0.05 |
R8917:Thnsl2
|
UTSW |
6 |
71,116,927 (GRCm39) |
missense |
probably benign |
|
R9547:Thnsl2
|
UTSW |
6 |
71,116,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Thnsl2
|
UTSW |
6 |
71,108,930 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0021:Thnsl2
|
UTSW |
6 |
71,105,688 (GRCm39) |
missense |
probably benign |
0.02 |
X0066:Thnsl2
|
UTSW |
6 |
71,116,821 (GRCm39) |
nonsense |
probably null |
|
Z1177:Thnsl2
|
UTSW |
6 |
71,105,825 (GRCm39) |
missense |
probably damaging |
0.98 |
|