Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
C |
2: 69,122,293 (GRCm39) |
I397V |
possibly damaging |
Het |
Bco2 |
A |
T |
9: 50,455,834 (GRCm39) |
V173E |
probably damaging |
Het |
Bdnf |
T |
C |
2: 109,554,196 (GRCm39) |
V150A |
probably damaging |
Het |
Cdh15 |
T |
A |
8: 123,587,721 (GRCm39) |
V215E |
probably damaging |
Het |
Col6a2 |
A |
T |
10: 76,432,144 (GRCm39) |
I1003N |
possibly damaging |
Het |
Daam2 |
A |
C |
17: 49,771,056 (GRCm39) |
I887S |
probably damaging |
Het |
Dnajb13 |
C |
T |
7: 100,156,648 (GRCm39) |
D143N |
probably damaging |
Het |
Fabp3-ps1 |
T |
A |
10: 86,567,943 (GRCm39) |
|
probably benign |
Het |
Gid4 |
G |
A |
11: 60,323,256 (GRCm39) |
R116Q |
probably benign |
Het |
Hectd2 |
A |
G |
19: 36,564,821 (GRCm39) |
E34G |
probably damaging |
Het |
Hyal6 |
A |
T |
6: 24,734,378 (GRCm39) |
K104* |
probably null |
Het |
Il1b |
A |
G |
2: 129,209,171 (GRCm39) |
I153T |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,962,072 (GRCm39) |
M1499V |
probably damaging |
Het |
Kntc1 |
C |
A |
5: 123,916,340 (GRCm39) |
|
probably null |
Het |
Lmbr1 |
A |
G |
5: 29,497,186 (GRCm39) |
S72P |
probably damaging |
Het |
Lrrc2 |
T |
C |
9: 110,808,695 (GRCm39) |
|
probably null |
Het |
Map2k5 |
T |
C |
9: 63,164,321 (GRCm39) |
I328V |
probably benign |
Het |
Mphosph9 |
T |
A |
5: 124,421,800 (GRCm39) |
|
probably null |
Het |
Mpp4 |
C |
T |
1: 59,175,993 (GRCm39) |
|
probably null |
Het |
Ndrg3 |
A |
G |
2: 156,791,952 (GRCm39) |
|
probably null |
Het |
Ndufa10 |
A |
C |
1: 92,397,639 (GRCm39) |
Y136D |
probably damaging |
Het |
Or10ak9 |
A |
T |
4: 118,726,794 (GRCm39) |
D271V |
probably damaging |
Het |
Or2b7 |
T |
A |
13: 21,740,172 (GRCm39) |
S7C |
probably damaging |
Het |
Or4a72 |
T |
C |
2: 89,405,896 (GRCm39) |
Y58C |
probably damaging |
Het |
Or8g34 |
A |
G |
9: 39,372,802 (GRCm39) |
E22G |
probably benign |
Het |
Rab18 |
T |
C |
18: 6,788,474 (GRCm39) |
|
probably benign |
Het |
Rad1 |
T |
C |
15: 10,493,365 (GRCm39) |
I264T |
probably benign |
Het |
Rhbdf1 |
A |
G |
11: 32,163,293 (GRCm39) |
V393A |
possibly damaging |
Het |
Rrp12 |
A |
G |
19: 41,860,005 (GRCm39) |
L1025P |
probably damaging |
Het |
Rtca |
A |
G |
3: 116,286,726 (GRCm39) |
F302S |
probably damaging |
Het |
Slc9b1 |
T |
A |
3: 135,080,167 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
T |
6: 48,464,828 (GRCm39) |
|
probably benign |
Het |
Ssrp1 |
T |
A |
2: 84,871,264 (GRCm39) |
I257N |
probably damaging |
Het |
Sval2 |
A |
C |
6: 41,838,795 (GRCm39) |
Y11S |
probably benign |
Het |
Tcl1b2 |
T |
C |
12: 105,120,358 (GRCm39) |
*118Q |
probably null |
Het |
Tlr4 |
A |
C |
4: 66,757,681 (GRCm39) |
H158P |
probably damaging |
Het |
Vmn2r42 |
T |
C |
7: 8,197,852 (GRCm39) |
T256A |
probably benign |
Het |
Xdh |
T |
C |
17: 74,207,576 (GRCm39) |
E927G |
probably damaging |
Het |
Yap1 |
T |
C |
9: 7,973,907 (GRCm39) |
N178S |
probably benign |
Het |
|
Other mutations in Thsd7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Thsd7b
|
APN |
1 |
129,523,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00850:Thsd7b
|
APN |
1 |
130,092,814 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00987:Thsd7b
|
APN |
1 |
129,541,016 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Thsd7b
|
APN |
1 |
129,523,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01091:Thsd7b
|
APN |
1 |
129,704,071 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01535:Thsd7b
|
APN |
1 |
129,605,954 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01560:Thsd7b
|
APN |
1 |
130,145,918 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01701:Thsd7b
|
APN |
1 |
129,358,665 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01775:Thsd7b
|
APN |
1 |
129,556,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02077:Thsd7b
|
APN |
1 |
129,744,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02338:Thsd7b
|
APN |
1 |
129,523,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Thsd7b
|
APN |
1 |
130,087,369 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02404:Thsd7b
|
APN |
1 |
129,540,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02519:Thsd7b
|
APN |
1 |
129,540,932 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02543:Thsd7b
|
APN |
1 |
130,092,840 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02740:Thsd7b
|
APN |
1 |
129,540,864 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02875:Thsd7b
|
APN |
1 |
129,879,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02986:Thsd7b
|
APN |
1 |
129,843,352 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03108:Thsd7b
|
APN |
1 |
130,138,013 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Thsd7b
|
APN |
1 |
130,116,288 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03195:Thsd7b
|
APN |
1 |
129,556,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Thsd7b
|
APN |
1 |
129,688,092 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03397:Thsd7b
|
APN |
1 |
129,523,901 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03399:Thsd7b
|
APN |
1 |
129,556,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Thsd7b
|
UTSW |
1 |
129,358,701 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Thsd7b
|
UTSW |
1 |
130,123,000 (GRCm39) |
missense |
probably benign |
0.00 |
R0526:Thsd7b
|
UTSW |
1 |
129,879,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Thsd7b
|
UTSW |
1 |
130,116,263 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0746:Thsd7b
|
UTSW |
1 |
130,116,268 (GRCm39) |
missense |
probably benign |
0.00 |
R0784:Thsd7b
|
UTSW |
1 |
129,523,096 (GRCm39) |
splice site |
probably benign |
|
R1158:Thsd7b
|
UTSW |
1 |
130,117,672 (GRCm39) |
splice site |
probably null |
|
R1267:Thsd7b
|
UTSW |
1 |
129,556,577 (GRCm39) |
splice site |
probably null |
|
R1375:Thsd7b
|
UTSW |
1 |
130,087,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Thsd7b
|
UTSW |
1 |
129,523,778 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1728:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1728:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1729:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1729:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1730:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1730:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1739:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1739:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1762:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1762:Thsd7b
|
UTSW |
1 |
130,030,813 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1762:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1783:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1783:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1784:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1784:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1785:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1785:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1812:Thsd7b
|
UTSW |
1 |
129,686,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Thsd7b
|
UTSW |
1 |
129,540,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Thsd7b
|
UTSW |
1 |
129,605,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R1996:Thsd7b
|
UTSW |
1 |
129,686,188 (GRCm39) |
nonsense |
probably null |
|
R2199:Thsd7b
|
UTSW |
1 |
130,145,895 (GRCm39) |
missense |
probably benign |
0.04 |
R2483:Thsd7b
|
UTSW |
1 |
130,030,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Thsd7b
|
UTSW |
1 |
130,117,587 (GRCm39) |
splice site |
probably benign |
|
R2935:Thsd7b
|
UTSW |
1 |
129,605,824 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3113:Thsd7b
|
UTSW |
1 |
129,977,599 (GRCm39) |
missense |
probably benign |
0.23 |
R3236:Thsd7b
|
UTSW |
1 |
130,145,855 (GRCm39) |
nonsense |
probably null |
|
R3745:Thsd7b
|
UTSW |
1 |
129,605,978 (GRCm39) |
missense |
probably benign |
0.04 |
R3877:Thsd7b
|
UTSW |
1 |
130,117,919 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3880:Thsd7b
|
UTSW |
1 |
129,523,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Thsd7b
|
UTSW |
1 |
130,044,356 (GRCm39) |
missense |
probably benign |
0.18 |
R4112:Thsd7b
|
UTSW |
1 |
130,044,356 (GRCm39) |
missense |
probably benign |
0.18 |
R4255:Thsd7b
|
UTSW |
1 |
129,688,024 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4621:Thsd7b
|
UTSW |
1 |
129,358,652 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4703:Thsd7b
|
UTSW |
1 |
129,977,646 (GRCm39) |
intron |
probably benign |
|
R4732:Thsd7b
|
UTSW |
1 |
129,540,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Thsd7b
|
UTSW |
1 |
129,540,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Thsd7b
|
UTSW |
1 |
130,138,001 (GRCm39) |
missense |
probably benign |
0.01 |
R4805:Thsd7b
|
UTSW |
1 |
130,116,276 (GRCm39) |
missense |
probably benign |
0.04 |
R4840:Thsd7b
|
UTSW |
1 |
129,523,581 (GRCm39) |
missense |
probably benign |
0.00 |
R4879:Thsd7b
|
UTSW |
1 |
130,116,236 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4936:Thsd7b
|
UTSW |
1 |
129,605,882 (GRCm39) |
missense |
probably benign |
0.00 |
R4972:Thsd7b
|
UTSW |
1 |
130,116,309 (GRCm39) |
missense |
probably damaging |
0.97 |
R5304:Thsd7b
|
UTSW |
1 |
129,605,980 (GRCm39) |
nonsense |
probably null |
|
R5422:Thsd7b
|
UTSW |
1 |
129,849,071 (GRCm39) |
missense |
probably benign |
0.41 |
R5495:Thsd7b
|
UTSW |
1 |
129,523,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5598:Thsd7b
|
UTSW |
1 |
129,523,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Thsd7b
|
UTSW |
1 |
130,090,673 (GRCm39) |
critical splice donor site |
probably null |
|
R5638:Thsd7b
|
UTSW |
1 |
129,523,270 (GRCm39) |
missense |
probably benign |
0.00 |
R5640:Thsd7b
|
UTSW |
1 |
130,044,408 (GRCm39) |
nonsense |
probably null |
|
R5655:Thsd7b
|
UTSW |
1 |
129,556,671 (GRCm39) |
splice site |
probably null |
|
R5711:Thsd7b
|
UTSW |
1 |
129,688,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5823:Thsd7b
|
UTSW |
1 |
129,605,821 (GRCm39) |
missense |
probably benign |
0.00 |
R5888:Thsd7b
|
UTSW |
1 |
130,138,057 (GRCm39) |
nonsense |
probably null |
|
R5932:Thsd7b
|
UTSW |
1 |
129,358,575 (GRCm39) |
missense |
probably benign |
|
R6243:Thsd7b
|
UTSW |
1 |
130,090,599 (GRCm39) |
missense |
probably benign |
0.21 |
R6258:Thsd7b
|
UTSW |
1 |
129,595,655 (GRCm39) |
missense |
probably benign |
|
R6260:Thsd7b
|
UTSW |
1 |
129,595,655 (GRCm39) |
missense |
probably benign |
|
R6399:Thsd7b
|
UTSW |
1 |
129,744,385 (GRCm39) |
missense |
probably benign |
0.13 |
R6437:Thsd7b
|
UTSW |
1 |
129,744,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6719:Thsd7b
|
UTSW |
1 |
130,087,451 (GRCm39) |
splice site |
probably null |
|
R6785:Thsd7b
|
UTSW |
1 |
129,358,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R7304:Thsd7b
|
UTSW |
1 |
130,030,890 (GRCm39) |
missense |
probably benign |
0.01 |
R7334:Thsd7b
|
UTSW |
1 |
130,123,012 (GRCm39) |
missense |
probably benign |
0.00 |
R7414:Thsd7b
|
UTSW |
1 |
129,556,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R7673:Thsd7b
|
UTSW |
1 |
129,843,487 (GRCm39) |
splice site |
probably null |
|
R7683:Thsd7b
|
UTSW |
1 |
129,523,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7861:Thsd7b
|
UTSW |
1 |
130,087,435 (GRCm39) |
missense |
probably benign |
0.00 |
R8145:Thsd7b
|
UTSW |
1 |
129,688,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R8241:Thsd7b
|
UTSW |
1 |
130,117,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Thsd7b
|
UTSW |
1 |
129,523,193 (GRCm39) |
missense |
probably benign |
0.01 |
R8355:Thsd7b
|
UTSW |
1 |
129,523,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Thsd7b
|
UTSW |
1 |
129,605,790 (GRCm39) |
missense |
probably benign |
0.21 |
R8520:Thsd7b
|
UTSW |
1 |
129,849,157 (GRCm39) |
missense |
probably benign |
0.07 |
R8555:Thsd7b
|
UTSW |
1 |
129,523,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Thsd7b
|
UTSW |
1 |
129,688,011 (GRCm39) |
nonsense |
probably null |
|
R8981:Thsd7b
|
UTSW |
1 |
129,523,187 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9029:Thsd7b
|
UTSW |
1 |
130,087,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9133:Thsd7b
|
UTSW |
1 |
129,843,382 (GRCm39) |
missense |
probably benign |
0.18 |
R9194:Thsd7b
|
UTSW |
1 |
129,843,371 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9229:Thsd7b
|
UTSW |
1 |
129,849,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Thsd7b
|
UTSW |
1 |
130,087,453 (GRCm39) |
critical splice donor site |
probably null |
|
R9460:Thsd7b
|
UTSW |
1 |
130,090,674 (GRCm39) |
critical splice donor site |
probably null |
|
R9466:Thsd7b
|
UTSW |
1 |
130,122,866 (GRCm39) |
missense |
probably benign |
|
R9588:Thsd7b
|
UTSW |
1 |
130,108,223 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Thsd7b
|
UTSW |
1 |
129,523,809 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Thsd7b
|
UTSW |
1 |
129,556,648 (GRCm39) |
missense |
probably benign |
0.17 |
Z1176:Thsd7b
|
UTSW |
1 |
129,523,397 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Thsd7b
|
UTSW |
1 |
129,523,253 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Thsd7b
|
UTSW |
1 |
130,108,161 (GRCm39) |
missense |
possibly damaging |
0.79 |
|