Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
G |
16: 4,667,521 (GRCm39) |
E304G |
unknown |
Het |
4933436I01Rik |
T |
A |
X: 66,964,689 (GRCm39) |
K57* |
probably null |
Het |
Aar2 |
T |
C |
2: 156,392,893 (GRCm39) |
V94A |
probably benign |
Het |
Abcb9 |
T |
C |
5: 124,228,176 (GRCm39) |
T22A |
possibly damaging |
Het |
Adam25 |
T |
C |
8: 41,206,911 (GRCm39) |
V59A |
probably damaging |
Het |
Ampd2 |
T |
C |
3: 107,987,616 (GRCm39) |
D103G |
probably damaging |
Het |
Ankrd12 |
A |
G |
17: 66,291,408 (GRCm39) |
S1342P |
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,730,571 (GRCm39) |
T739A |
probably benign |
Het |
Catsperg1 |
T |
A |
7: 28,894,885 (GRCm39) |
N571Y |
probably benign |
Het |
Cela3b |
A |
G |
4: 137,152,355 (GRCm39) |
I74T |
probably damaging |
Het |
Cfhr1 |
A |
G |
1: 139,485,293 (GRCm39) |
L51P |
probably benign |
Het |
Cfhr4 |
T |
A |
1: 139,682,044 (GRCm39) |
Y184F |
probably benign |
Het |
Ckap5 |
T |
A |
2: 91,396,100 (GRCm39) |
D534E |
probably benign |
Het |
Cstf3 |
C |
T |
2: 104,493,778 (GRCm39) |
P594L |
probably damaging |
Het |
Ctdp1 |
A |
G |
18: 80,492,689 (GRCm39) |
L602P |
probably damaging |
Het |
Defa24 |
A |
G |
8: 22,224,559 (GRCm39) |
T3A |
probably damaging |
Het |
Dmgdh |
A |
G |
13: 93,847,941 (GRCm39) |
H546R |
probably benign |
Het |
Dscam |
A |
G |
16: 96,517,263 (GRCm39) |
V882A |
possibly damaging |
Het |
Dydc2 |
A |
G |
14: 40,771,260 (GRCm39) |
*140Q |
probably null |
Het |
Ehd4 |
T |
C |
2: 119,921,708 (GRCm39) |
D516G |
possibly damaging |
Het |
En1 |
T |
C |
1: 120,534,893 (GRCm39) |
V394A |
unknown |
Het |
Erich3 |
T |
G |
3: 154,468,872 (GRCm39) |
L1108R |
unknown |
Het |
Erp27 |
A |
G |
6: 136,896,945 (GRCm39) |
S86P |
probably benign |
Het |
Esr1 |
A |
C |
10: 4,696,798 (GRCm39) |
S216R |
probably damaging |
Het |
Fbxo40 |
A |
T |
16: 36,789,286 (GRCm39) |
I608N |
probably damaging |
Het |
Fcna |
G |
A |
2: 25,517,782 (GRCm39) |
Q23* |
probably null |
Het |
Foxn4 |
C |
T |
5: 114,394,955 (GRCm39) |
R324Q |
probably benign |
Het |
Gata6 |
A |
G |
18: 11,054,520 (GRCm39) |
T150A |
probably damaging |
Het |
Gbp2b |
T |
A |
3: 142,317,178 (GRCm39) |
H511Q |
probably benign |
Het |
Gpr171 |
C |
A |
3: 59,005,362 (GRCm39) |
V138L |
probably damaging |
Het |
Grhl2 |
G |
A |
15: 37,344,904 (GRCm39) |
V509I |
probably benign |
Het |
Gzmd |
G |
A |
14: 56,367,869 (GRCm39) |
P135S |
probably damaging |
Het |
Hhatl |
C |
A |
9: 121,618,862 (GRCm39) |
C90F |
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,278,480 (GRCm39) |
K3050R |
probably benign |
Het |
Kcnh3 |
T |
C |
15: 99,130,786 (GRCm39) |
Y468H |
probably damaging |
Het |
Lhfpl6 |
A |
G |
3: 52,950,891 (GRCm39) |
H55R |
probably benign |
Het |
Lpgat1 |
T |
C |
1: 191,451,488 (GRCm39) |
V38A |
probably benign |
Het |
Lrrc49 |
A |
G |
9: 60,510,031 (GRCm39) |
I479T |
probably benign |
Het |
Map1b |
A |
T |
13: 99,567,570 (GRCm39) |
I1717N |
unknown |
Het |
Map3k20 |
G |
T |
2: 72,272,216 (GRCm39) |
R781S |
possibly damaging |
Het |
Mcm3ap |
A |
G |
10: 76,306,358 (GRCm39) |
E157G |
probably benign |
Het |
Mylk2 |
A |
G |
2: 152,755,370 (GRCm39) |
E178G |
probably damaging |
Het |
Naaladl2 |
A |
G |
3: 24,057,146 (GRCm39) |
L605P |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Nt5el |
C |
T |
13: 105,246,114 (GRCm39) |
T225I |
probably benign |
Het |
Or10h28 |
T |
C |
17: 33,488,631 (GRCm39) |
V311A |
probably benign |
Het |
Or4a76 |
T |
C |
2: 89,460,555 (GRCm39) |
E229G |
probably damaging |
Het |
Padi3 |
A |
T |
4: 140,522,928 (GRCm39) |
I348N |
probably benign |
Het |
Pcdh18 |
T |
C |
3: 49,709,335 (GRCm39) |
D660G |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,355,635 (GRCm39) |
S1048R |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,452,949 (GRCm39) |
V3958A |
probably damaging |
Het |
Ppargc1b |
C |
A |
18: 61,456,267 (GRCm39) |
C80F |
probably damaging |
Het |
Rbm28 |
T |
C |
6: 29,128,674 (GRCm39) |
E590G |
probably benign |
Het |
Rbm47 |
T |
C |
5: 66,183,826 (GRCm39) |
E259G |
possibly damaging |
Het |
Rint1 |
A |
G |
5: 23,993,355 (GRCm39) |
*37W |
probably null |
Het |
Sacs |
G |
A |
14: 61,443,309 (GRCm39) |
R1785Q |
probably benign |
Het |
Samm50 |
T |
C |
15: 84,095,276 (GRCm39) |
C421R |
probably benign |
Het |
Scnn1b |
G |
T |
7: 121,511,254 (GRCm39) |
A314S |
probably damaging |
Het |
Sf3b3 |
C |
A |
8: 111,542,854 (GRCm39) |
V868L |
probably benign |
Het |
Sirt5 |
G |
T |
13: 43,530,327 (GRCm39) |
V136L |
probably benign |
Het |
Slc1a7 |
T |
C |
4: 107,850,237 (GRCm39) |
V116A |
probably damaging |
Het |
Slc24a4 |
G |
A |
12: 102,230,638 (GRCm39) |
V510M |
probably damaging |
Het |
Slc35f5 |
T |
C |
1: 125,517,628 (GRCm39) |
I116T |
probably benign |
Het |
Spata4 |
T |
C |
8: 55,053,899 (GRCm39) |
S22P |
probably benign |
Het |
Sqstm1 |
A |
G |
11: 50,091,725 (GRCm39) |
V324A |
probably benign |
Het |
Stmnd1 |
G |
A |
13: 46,453,079 (GRCm39) |
A252T |
probably benign |
Het |
Tbl1xr1 |
C |
A |
3: 22,258,150 (GRCm39) |
N470K |
possibly damaging |
Het |
Thap12 |
T |
C |
7: 98,364,323 (GRCm39) |
S164P |
possibly damaging |
Het |
Tnni2 |
C |
A |
7: 141,997,672 (GRCm39) |
D102E |
probably damaging |
Het |
Trav7n-4 |
A |
C |
14: 53,328,849 (GRCm39) |
N16T |
probably benign |
Het |
Trpm7 |
T |
C |
2: 126,665,906 (GRCm39) |
K900R |
probably benign |
Het |
Tspoap1 |
T |
A |
11: 87,668,839 (GRCm39) |
C1371S |
probably benign |
Het |
Tssk5 |
A |
G |
15: 76,257,156 (GRCm39) |
M242T |
possibly damaging |
Het |
Ubn2 |
A |
G |
6: 38,460,079 (GRCm39) |
I607V |
probably benign |
Het |
Ubr2 |
A |
T |
17: 47,284,865 (GRCm39) |
V551E |
probably benign |
Het |
Vipr2 |
A |
G |
12: 116,058,344 (GRCm39) |
N87S |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,485,132 (GRCm39) |
K787N |
probably damaging |
Het |
Wwc2 |
A |
T |
8: 48,353,859 (GRCm39) |
W92R |
probably damaging |
Het |
Zfp141 |
A |
G |
7: 42,125,639 (GRCm39) |
Y278H |
probably damaging |
Het |
Zfp827 |
T |
C |
8: 79,844,887 (GRCm39) |
S686P |
probably benign |
Het |
|
Other mutations in Thsd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01936:Thsd1
|
APN |
8 |
22,742,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Thsd1
|
APN |
8 |
22,749,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02517:Thsd1
|
APN |
8 |
22,733,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Thsd1
|
APN |
8 |
22,748,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03378:Thsd1
|
APN |
8 |
22,733,794 (GRCm39) |
missense |
probably benign |
0.13 |
R0137:Thsd1
|
UTSW |
8 |
22,733,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Thsd1
|
UTSW |
8 |
22,748,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R0854:Thsd1
|
UTSW |
8 |
22,748,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R1109:Thsd1
|
UTSW |
8 |
22,733,708 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1402:Thsd1
|
UTSW |
8 |
22,749,384 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1402:Thsd1
|
UTSW |
8 |
22,749,384 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1899:Thsd1
|
UTSW |
8 |
22,742,334 (GRCm39) |
splice site |
probably benign |
|
R1900:Thsd1
|
UTSW |
8 |
22,742,334 (GRCm39) |
splice site |
probably benign |
|
R2008:Thsd1
|
UTSW |
8 |
22,749,247 (GRCm39) |
missense |
probably benign |
0.23 |
R2048:Thsd1
|
UTSW |
8 |
22,749,333 (GRCm39) |
missense |
probably benign |
0.01 |
R2090:Thsd1
|
UTSW |
8 |
22,749,673 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2165:Thsd1
|
UTSW |
8 |
22,728,538 (GRCm39) |
intron |
probably benign |
|
R2209:Thsd1
|
UTSW |
8 |
22,748,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3831:Thsd1
|
UTSW |
8 |
22,733,132 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3833:Thsd1
|
UTSW |
8 |
22,733,132 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3847:Thsd1
|
UTSW |
8 |
22,749,427 (GRCm39) |
missense |
probably damaging |
0.97 |
R4049:Thsd1
|
UTSW |
8 |
22,733,180 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4454:Thsd1
|
UTSW |
8 |
22,733,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Thsd1
|
UTSW |
8 |
22,749,314 (GRCm39) |
nonsense |
probably null |
|
R4997:Thsd1
|
UTSW |
8 |
22,733,340 (GRCm39) |
missense |
probably damaging |
0.98 |
R6440:Thsd1
|
UTSW |
8 |
22,748,569 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6457:Thsd1
|
UTSW |
8 |
22,733,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R6488:Thsd1
|
UTSW |
8 |
22,733,733 (GRCm39) |
missense |
probably benign |
0.36 |
R6519:Thsd1
|
UTSW |
8 |
22,749,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R7267:Thsd1
|
UTSW |
8 |
22,733,597 (GRCm39) |
missense |
probably benign |
0.10 |
R7448:Thsd1
|
UTSW |
8 |
22,733,349 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7698:Thsd1
|
UTSW |
8 |
22,749,003 (GRCm39) |
nonsense |
probably null |
|
R7733:Thsd1
|
UTSW |
8 |
22,748,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Thsd1
|
UTSW |
8 |
22,733,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R7894:Thsd1
|
UTSW |
8 |
22,749,585 (GRCm39) |
missense |
probably damaging |
0.99 |
R8181:Thsd1
|
UTSW |
8 |
22,733,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R8192:Thsd1
|
UTSW |
8 |
22,733,918 (GRCm39) |
missense |
probably benign |
0.22 |
R8426:Thsd1
|
UTSW |
8 |
22,733,654 (GRCm39) |
missense |
probably benign |
0.01 |
R8775:Thsd1
|
UTSW |
8 |
22,749,643 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8775-TAIL:Thsd1
|
UTSW |
8 |
22,749,643 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9494:Thsd1
|
UTSW |
8 |
22,733,268 (GRCm39) |
missense |
probably benign |
0.00 |
R9550:Thsd1
|
UTSW |
8 |
22,733,026 (GRCm39) |
start gained |
probably benign |
|
X0023:Thsd1
|
UTSW |
8 |
22,749,583 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Thsd1
|
UTSW |
8 |
22,742,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|