Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agtpbp1 |
A |
G |
13: 59,660,312 (GRCm39) |
C305R |
probably damaging |
Het |
Anpep |
C |
A |
7: 79,488,946 (GRCm39) |
V381L |
probably damaging |
Het |
Ap5s1 |
T |
C |
2: 131,054,627 (GRCm39) |
L146P |
probably damaging |
Het |
Arhgef11 |
A |
G |
3: 87,629,690 (GRCm39) |
I599V |
probably damaging |
Het |
Arpc2 |
T |
C |
1: 74,302,973 (GRCm39) |
Y250H |
probably damaging |
Het |
Baz1b |
T |
A |
5: 135,246,582 (GRCm39) |
M677K |
probably damaging |
Het |
Begain |
C |
T |
12: 108,999,413 (GRCm39) |
A453T |
unknown |
Het |
C1ql4 |
T |
C |
15: 98,985,092 (GRCm39) |
D173G |
probably benign |
Het |
Card11 |
T |
G |
5: 140,881,781 (GRCm39) |
N461T |
probably benign |
Het |
Ccdc9 |
T |
C |
7: 16,018,287 (GRCm39) |
D7G |
probably damaging |
Het |
Ces2a |
T |
C |
8: 105,463,744 (GRCm39) |
V152A |
probably benign |
Het |
Chl1 |
G |
A |
6: 103,668,613 (GRCm39) |
A449T |
possibly damaging |
Het |
Col11a1 |
G |
T |
3: 113,907,385 (GRCm39) |
G638W |
unknown |
Het |
Cse1l |
A |
T |
2: 166,764,708 (GRCm39) |
T171S |
probably benign |
Het |
D2hgdh |
T |
A |
1: 93,766,687 (GRCm39) |
|
probably null |
Het |
Dlg4 |
T |
C |
11: 69,930,680 (GRCm39) |
Y432H |
possibly damaging |
Het |
Dmwd |
C |
T |
7: 18,814,660 (GRCm39) |
L437F |
probably damaging |
Het |
F11 |
T |
A |
8: 45,702,545 (GRCm39) |
Q251L |
probably damaging |
Het |
Gtf2f1 |
T |
A |
17: 57,312,458 (GRCm39) |
E195V |
possibly damaging |
Het |
Hap1 |
A |
T |
11: 100,242,374 (GRCm39) |
L376Q |
probably damaging |
Het |
Hars2 |
T |
A |
18: 36,921,289 (GRCm39) |
I234N |
probably damaging |
Het |
Hcfc2 |
T |
C |
10: 82,535,063 (GRCm39) |
V29A |
probably benign |
Het |
Hp |
C |
T |
8: 110,305,731 (GRCm39) |
|
probably benign |
Het |
Hrh1 |
T |
C |
6: 114,456,748 (GRCm39) |
S10P |
probably benign |
Het |
Kcnmb2 |
A |
G |
3: 32,252,465 (GRCm39) |
Y222C |
probably damaging |
Het |
Kdm3a |
A |
G |
6: 71,576,438 (GRCm39) |
V792A |
probably benign |
Het |
Kif13b |
G |
A |
14: 64,994,956 (GRCm39) |
V903I |
probably benign |
Het |
Lars2 |
G |
T |
9: 123,206,895 (GRCm39) |
|
probably null |
Het |
Med7 |
A |
G |
11: 46,331,687 (GRCm39) |
D94G |
possibly damaging |
Het |
Mier3 |
A |
G |
13: 111,841,846 (GRCm39) |
T136A |
probably benign |
Het |
Nin |
T |
C |
12: 70,124,956 (GRCm39) |
E122G |
|
Het |
Or5h18 |
G |
T |
16: 58,847,469 (GRCm39) |
T267K |
probably benign |
Het |
Or6k14 |
A |
G |
1: 173,927,042 (GRCm39) |
Q6R |
probably benign |
Het |
Oxsr1 |
T |
C |
9: 119,070,821 (GRCm39) |
I489V |
probably benign |
Het |
Pdcd6ip |
A |
T |
9: 113,516,763 (GRCm39) |
L216Q |
probably damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,553,364 (GRCm39) |
C379* |
probably null |
Het |
Pramel24 |
A |
T |
4: 143,453,284 (GRCm39) |
K131* |
probably null |
Het |
Ptpn13 |
T |
A |
5: 103,713,018 (GRCm39) |
C1714S |
probably benign |
Het |
Pum2 |
G |
A |
12: 8,778,922 (GRCm39) |
R498Q |
possibly damaging |
Het |
Sema3d |
T |
A |
5: 12,623,823 (GRCm39) |
Y577* |
probably null |
Het |
Slc29a3 |
G |
A |
10: 60,552,145 (GRCm39) |
P300S |
not run |
Het |
Slc5a4b |
A |
G |
10: 75,899,906 (GRCm39) |
V444A |
probably damaging |
Het |
Smad9 |
A |
G |
3: 54,696,685 (GRCm39) |
E250G |
probably damaging |
Het |
Srsf7 |
A |
G |
17: 80,514,703 (GRCm39) |
|
probably benign |
Het |
Triml2 |
C |
A |
8: 43,638,325 (GRCm39) |
Q98K |
probably damaging |
Het |
Txndc11 |
A |
T |
16: 10,902,099 (GRCm39) |
L705Q |
probably damaging |
Het |
Vmn1r22 |
A |
G |
6: 57,877,404 (GRCm39) |
M191T |
probably damaging |
Het |
Vmn2r89 |
A |
T |
14: 51,692,651 (GRCm39) |
K151N |
probably benign |
Het |
Vwa5a |
A |
G |
9: 38,646,125 (GRCm39) |
I498V |
probably damaging |
Het |
Zfp459 |
T |
C |
13: 67,556,615 (GRCm39) |
H156R |
probably damaging |
Het |
Zscan18 |
T |
A |
7: 12,503,532 (GRCm39) |
K676* |
probably null |
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 |
IGL02793:Thsd7b
|
APN |
1 |
129,879,130 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|