Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
T |
A |
5: 144,982,181 (GRCm39) |
Y255* |
probably null |
Het |
2310003L06Rik |
A |
T |
5: 88,112,455 (GRCm39) |
|
probably benign |
Het |
Abcb5 |
A |
G |
12: 118,904,067 (GRCm39) |
S213P |
probably damaging |
Het |
Agpat1 |
A |
G |
17: 34,829,551 (GRCm39) |
I42V |
probably benign |
Het |
Apoh |
A |
T |
11: 108,288,199 (GRCm39) |
I106F |
probably damaging |
Het |
BB014433 |
G |
T |
8: 15,092,540 (GRCm39) |
C104* |
probably null |
Het |
Bsn |
C |
T |
9: 107,989,045 (GRCm39) |
G2236S |
possibly damaging |
Het |
Casp9 |
A |
G |
4: 141,521,221 (GRCm39) |
E19G |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,055,163 (GRCm39) |
|
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,959,760 (GRCm39) |
M797L |
probably benign |
Het |
Col14a1 |
A |
G |
15: 55,271,264 (GRCm39) |
|
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,232,964 (GRCm39) |
|
probably null |
Het |
Col6a4 |
T |
A |
9: 105,874,345 (GRCm39) |
H2214L |
probably benign |
Het |
Ctu2 |
T |
G |
8: 123,204,932 (GRCm39) |
S72R |
probably damaging |
Het |
Cyp24a1 |
T |
A |
2: 170,333,619 (GRCm39) |
M245L |
possibly damaging |
Het |
Dgkb |
T |
A |
12: 38,266,030 (GRCm39) |
V503E |
probably benign |
Het |
Diaph3 |
T |
C |
14: 87,206,938 (GRCm39) |
R501G |
probably benign |
Het |
Dip2b |
A |
G |
15: 100,109,874 (GRCm39) |
D1453G |
probably damaging |
Het |
Dnah2 |
G |
A |
11: 69,420,357 (GRCm39) |
T119M |
probably benign |
Het |
F5 |
T |
G |
1: 164,007,018 (GRCm39) |
V274G |
probably damaging |
Het |
Farp1 |
A |
T |
14: 121,492,808 (GRCm39) |
|
probably benign |
Het |
Fcsk |
T |
C |
8: 111,619,891 (GRCm39) |
|
probably null |
Het |
Foxf1 |
T |
C |
8: 121,811,742 (GRCm39) |
V202A |
possibly damaging |
Het |
Fras1 |
G |
A |
5: 96,910,449 (GRCm39) |
V3293I |
probably damaging |
Het |
Furin |
C |
T |
7: 80,041,032 (GRCm39) |
G602D |
probably damaging |
Het |
Gclm |
T |
C |
3: 122,049,269 (GRCm39) |
|
probably benign |
Het |
Gemin4 |
G |
A |
11: 76,102,988 (GRCm39) |
T591M |
probably benign |
Het |
Glrx3 |
T |
C |
7: 137,055,214 (GRCm39) |
S119P |
possibly damaging |
Het |
Gm16485 |
G |
T |
9: 8,972,437 (GRCm39) |
|
probably benign |
Het |
Helq |
T |
C |
5: 100,938,066 (GRCm39) |
N460S |
probably benign |
Het |
Hs6st1 |
G |
A |
1: 36,108,266 (GRCm39) |
|
probably null |
Het |
Kpna2 |
A |
G |
11: 106,882,148 (GRCm39) |
L226S |
probably damaging |
Het |
Myom3 |
G |
A |
4: 135,505,454 (GRCm39) |
V448M |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,536,580 (GRCm39) |
S1224P |
probably damaging |
Het |
Or52n2 |
A |
T |
7: 104,542,521 (GRCm39) |
F105I |
probably damaging |
Het |
Or56b1b |
C |
T |
7: 108,164,721 (GRCm39) |
D94N |
probably benign |
Het |
Or7a38 |
A |
G |
10: 78,753,177 (GRCm39) |
T168A |
probably benign |
Het |
Plag1 |
C |
T |
4: 3,904,546 (GRCm39) |
C215Y |
probably damaging |
Het |
Plekha5 |
G |
A |
6: 140,537,473 (GRCm39) |
R646K |
possibly damaging |
Het |
Pot1a |
G |
A |
6: 25,771,679 (GRCm39) |
|
probably benign |
Het |
Ppfia1 |
T |
C |
7: 144,038,929 (GRCm39) |
D494G |
probably damaging |
Het |
Ppp1r1a |
T |
A |
15: 103,441,915 (GRCm39) |
D51V |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 22,973,175 (GRCm39) |
|
probably benign |
Het |
Rad51ap1 |
A |
T |
6: 126,911,704 (GRCm39) |
V61D |
probably damaging |
Het |
Reln |
G |
A |
5: 22,253,798 (GRCm39) |
L605F |
probably damaging |
Het |
Riok3 |
T |
C |
18: 12,282,006 (GRCm39) |
I325T |
probably damaging |
Het |
Sclt1 |
A |
T |
3: 41,616,005 (GRCm39) |
|
probably null |
Het |
Slc25a39 |
A |
G |
11: 102,297,395 (GRCm39) |
V24A |
possibly damaging |
Het |
Slc9a3 |
T |
G |
13: 74,305,726 (GRCm39) |
S248A |
probably damaging |
Het |
Slco6d1 |
T |
A |
1: 98,394,422 (GRCm39) |
C369S |
probably benign |
Het |
Spen |
T |
C |
4: 141,244,181 (GRCm39) |
S285G |
unknown |
Het |
Stxbp5l |
A |
G |
16: 37,036,440 (GRCm39) |
|
probably benign |
Het |
Tmed3 |
C |
T |
9: 89,581,842 (GRCm39) |
S207N |
possibly damaging |
Het |
Trerf1 |
G |
T |
17: 47,652,062 (GRCm39) |
|
noncoding transcript |
Het |
Triml1 |
A |
T |
8: 43,583,542 (GRCm39) |
V353E |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,549,401 (GRCm39) |
R31759C |
probably damaging |
Het |
Ugt2b37 |
T |
C |
5: 87,398,443 (GRCm39) |
Q331R |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,588,048 (GRCm39) |
I420T |
probably damaging |
Het |
Vmn1r68 |
A |
T |
7: 10,261,201 (GRCm39) |
L299Q |
probably damaging |
Het |
Vmn1r81 |
T |
A |
7: 11,993,877 (GRCm39) |
T244S |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,618,941 (GRCm39) |
F2875S |
probably damaging |
Het |
Wscd1 |
A |
G |
11: 71,657,692 (GRCm39) |
M166V |
probably damaging |
Het |
Zfp296 |
T |
C |
7: 19,313,864 (GRCm39) |
Y240H |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,013,689 (GRCm39) |
H737R |
probably damaging |
Het |
|
Other mutations in Thsd7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00562:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00563:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00753:Thsd7a
|
APN |
6 |
12,327,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00835:Thsd7a
|
APN |
6 |
12,554,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01486:Thsd7a
|
APN |
6 |
12,471,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Thsd7a
|
APN |
6 |
12,554,980 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01931:Thsd7a
|
APN |
6 |
12,504,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Thsd7a
|
APN |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01978:Thsd7a
|
APN |
6 |
12,331,005 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02233:Thsd7a
|
APN |
6 |
12,555,257 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02354:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02361:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02375:Thsd7a
|
APN |
6 |
12,343,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02468:Thsd7a
|
APN |
6 |
12,318,170 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02616:Thsd7a
|
APN |
6 |
12,408,984 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02820:Thsd7a
|
APN |
6 |
12,321,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Thsd7a
|
APN |
6 |
12,500,994 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03074:Thsd7a
|
APN |
6 |
12,324,680 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03234:Thsd7a
|
APN |
6 |
12,343,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:Thsd7a
|
APN |
6 |
12,504,167 (GRCm39) |
splice site |
probably benign |
|
IGL03337:Thsd7a
|
APN |
6 |
12,405,173 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4354001:Thsd7a
|
UTSW |
6 |
12,331,926 (GRCm39) |
critical splice donor site |
probably null |
|
R0095:Thsd7a
|
UTSW |
6 |
12,320,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R0127:Thsd7a
|
UTSW |
6 |
12,554,907 (GRCm39) |
missense |
probably benign |
0.01 |
R0142:Thsd7a
|
UTSW |
6 |
12,418,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Thsd7a
|
UTSW |
6 |
12,321,899 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0365:Thsd7a
|
UTSW |
6 |
12,321,886 (GRCm39) |
critical splice donor site |
probably null |
|
R0504:Thsd7a
|
UTSW |
6 |
12,379,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Thsd7a
|
UTSW |
6 |
12,379,604 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0540:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0577:Thsd7a
|
UTSW |
6 |
12,321,047 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0607:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0755:Thsd7a
|
UTSW |
6 |
12,555,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Thsd7a
|
UTSW |
6 |
12,327,576 (GRCm39) |
missense |
probably benign |
0.09 |
R0780:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0870:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0871:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0872:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0873:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Thsd7a
|
UTSW |
6 |
12,555,701 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1144:Thsd7a
|
UTSW |
6 |
12,471,026 (GRCm39) |
splice site |
probably benign |
|
R1265:Thsd7a
|
UTSW |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R1276:Thsd7a
|
UTSW |
6 |
12,418,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Thsd7a
|
UTSW |
6 |
12,555,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Thsd7a
|
UTSW |
6 |
12,338,621 (GRCm39) |
missense |
probably benign |
0.08 |
R1519:Thsd7a
|
UTSW |
6 |
12,471,174 (GRCm39) |
missense |
probably benign |
0.01 |
R1633:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R1659:Thsd7a
|
UTSW |
6 |
12,504,063 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1769:Thsd7a
|
UTSW |
6 |
12,555,714 (GRCm39) |
nonsense |
probably null |
|
R1824:Thsd7a
|
UTSW |
6 |
12,409,041 (GRCm39) |
splice site |
probably null |
|
R1840:Thsd7a
|
UTSW |
6 |
12,330,973 (GRCm39) |
missense |
probably benign |
0.03 |
R1845:Thsd7a
|
UTSW |
6 |
12,321,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Thsd7a
|
UTSW |
6 |
12,555,434 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2023:Thsd7a
|
UTSW |
6 |
12,327,535 (GRCm39) |
missense |
probably benign |
0.16 |
R2039:Thsd7a
|
UTSW |
6 |
12,408,922 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2058:Thsd7a
|
UTSW |
6 |
12,318,105 (GRCm39) |
splice site |
probably benign |
|
R2138:Thsd7a
|
UTSW |
6 |
12,471,072 (GRCm39) |
nonsense |
probably null |
|
R2155:Thsd7a
|
UTSW |
6 |
12,379,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R2175:Thsd7a
|
UTSW |
6 |
12,331,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2216:Thsd7a
|
UTSW |
6 |
12,337,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2318:Thsd7a
|
UTSW |
6 |
12,405,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Thsd7a
|
UTSW |
6 |
12,337,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3858:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3890:Thsd7a
|
UTSW |
6 |
12,418,336 (GRCm39) |
missense |
probably benign |
0.09 |
R3910:Thsd7a
|
UTSW |
6 |
12,331,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R3933:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R4369:Thsd7a
|
UTSW |
6 |
12,468,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Thsd7a
|
UTSW |
6 |
12,324,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R4664:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4664:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4665:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4665:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4666:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4666:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4668:Thsd7a
|
UTSW |
6 |
12,408,967 (GRCm39) |
missense |
probably damaging |
0.98 |
R4886:Thsd7a
|
UTSW |
6 |
12,327,659 (GRCm39) |
nonsense |
probably null |
|
R4918:Thsd7a
|
UTSW |
6 |
12,327,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4938:Thsd7a
|
UTSW |
6 |
12,330,991 (GRCm39) |
missense |
probably benign |
0.09 |
R5064:Thsd7a
|
UTSW |
6 |
12,330,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5153:Thsd7a
|
UTSW |
6 |
12,338,654 (GRCm39) |
missense |
probably benign |
0.00 |
R5177:Thsd7a
|
UTSW |
6 |
12,379,582 (GRCm39) |
nonsense |
probably null |
|
R5242:Thsd7a
|
UTSW |
6 |
12,327,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Thsd7a
|
UTSW |
6 |
12,379,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5442:Thsd7a
|
UTSW |
6 |
12,748,799 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Thsd7a
|
UTSW |
6 |
12,332,016 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5525:Thsd7a
|
UTSW |
6 |
12,332,006 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5544:Thsd7a
|
UTSW |
6 |
12,379,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5651:Thsd7a
|
UTSW |
6 |
12,343,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Thsd7a
|
UTSW |
6 |
12,343,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5848:Thsd7a
|
UTSW |
6 |
12,503,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Thsd7a
|
UTSW |
6 |
12,337,261 (GRCm39) |
missense |
probably benign |
0.02 |
R6012:Thsd7a
|
UTSW |
6 |
12,379,388 (GRCm39) |
splice site |
probably null |
|
R6139:Thsd7a
|
UTSW |
6 |
12,379,572 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6243:Thsd7a
|
UTSW |
6 |
12,327,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Thsd7a
|
UTSW |
6 |
12,408,987 (GRCm39) |
nonsense |
probably null |
|
R6273:Thsd7a
|
UTSW |
6 |
12,408,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R6300:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R6314:Thsd7a
|
UTSW |
6 |
12,554,996 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6392:Thsd7a
|
UTSW |
6 |
12,468,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R6418:Thsd7a
|
UTSW |
6 |
12,555,081 (GRCm39) |
nonsense |
probably null |
|
R6515:Thsd7a
|
UTSW |
6 |
12,501,085 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6725:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6742:Thsd7a
|
UTSW |
6 |
12,408,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Thsd7a
|
UTSW |
6 |
12,555,636 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6838:Thsd7a
|
UTSW |
6 |
12,504,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R7104:Thsd7a
|
UTSW |
6 |
12,379,429 (GRCm39) |
missense |
|
|
R7170:Thsd7a
|
UTSW |
6 |
12,352,090 (GRCm39) |
missense |
|
|
R7349:Thsd7a
|
UTSW |
6 |
12,352,067 (GRCm39) |
missense |
|
|
R7460:Thsd7a
|
UTSW |
6 |
12,554,933 (GRCm39) |
missense |
|
|
R7467:Thsd7a
|
UTSW |
6 |
12,331,584 (GRCm39) |
missense |
|
|
R7666:Thsd7a
|
UTSW |
6 |
12,379,437 (GRCm39) |
missense |
|
|
R7869:Thsd7a
|
UTSW |
6 |
12,471,123 (GRCm39) |
nonsense |
probably null |
|
R8032:Thsd7a
|
UTSW |
6 |
12,555,287 (GRCm39) |
missense |
|
|
R8165:Thsd7a
|
UTSW |
6 |
12,468,962 (GRCm39) |
missense |
|
|
R8167:Thsd7a
|
UTSW |
6 |
12,317,400 (GRCm39) |
nonsense |
probably null |
|
R8245:Thsd7a
|
UTSW |
6 |
12,379,592 (GRCm39) |
missense |
|
|
R8310:Thsd7a
|
UTSW |
6 |
12,396,612 (GRCm39) |
missense |
|
|
R8312:Thsd7a
|
UTSW |
6 |
12,471,181 (GRCm39) |
missense |
|
|
R8331:Thsd7a
|
UTSW |
6 |
12,471,157 (GRCm39) |
missense |
|
|
R8755:Thsd7a
|
UTSW |
6 |
12,408,851 (GRCm39) |
nonsense |
probably null |
|
R8843:Thsd7a
|
UTSW |
6 |
12,501,136 (GRCm39) |
missense |
|
|
R8867:Thsd7a
|
UTSW |
6 |
12,338,686 (GRCm39) |
missense |
|
|
R8952:Thsd7a
|
UTSW |
6 |
12,468,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R9036:Thsd7a
|
UTSW |
6 |
12,418,249 (GRCm39) |
missense |
|
|
R9299:Thsd7a
|
UTSW |
6 |
12,504,131 (GRCm39) |
missense |
|
|
R9366:Thsd7a
|
UTSW |
6 |
12,555,480 (GRCm39) |
missense |
|
|
R9489:Thsd7a
|
UTSW |
6 |
12,352,022 (GRCm39) |
missense |
|
|
|