Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankdd1a |
C |
T |
9: 65,409,466 (GRCm39) |
|
probably null |
Het |
Ankrd31 |
A |
G |
13: 96,968,562 (GRCm39) |
E733G |
possibly damaging |
Het |
Cars2 |
C |
T |
8: 11,580,321 (GRCm39) |
W239* |
probably null |
Het |
Catsperz |
A |
T |
19: 6,899,929 (GRCm39) |
L192* |
probably null |
Het |
Ccdc168 |
G |
A |
1: 44,099,173 (GRCm39) |
R642W |
probably benign |
Het |
Cdh3 |
T |
C |
8: 107,237,975 (GRCm39) |
|
probably null |
Het |
Cfh |
C |
T |
1: 140,075,459 (GRCm39) |
V260M |
probably damaging |
Het |
Clcn4 |
T |
A |
7: 7,296,958 (GRCm39) |
S227C |
probably benign |
Het |
Cntn3 |
A |
T |
6: 102,397,388 (GRCm39) |
W62R |
probably damaging |
Het |
Col27a1 |
C |
A |
4: 63,143,278 (GRCm39) |
A322D |
probably damaging |
Het |
Egflam |
C |
T |
15: 7,238,082 (GRCm39) |
G934S |
probably damaging |
Het |
Eloa |
A |
G |
4: 135,734,510 (GRCm39) |
V665A |
probably damaging |
Het |
Epg5 |
A |
G |
18: 78,073,275 (GRCm39) |
T2433A |
probably benign |
Het |
Ercc5 |
A |
G |
1: 44,215,011 (GRCm39) |
N848S |
possibly damaging |
Het |
Fbrsl1 |
A |
C |
5: 110,526,020 (GRCm39) |
F61V |
probably damaging |
Het |
Fry |
T |
C |
5: 150,349,683 (GRCm39) |
Y1595H |
probably damaging |
Het |
Fstl4 |
A |
G |
11: 52,963,256 (GRCm39) |
N213D |
probably benign |
Het |
Gab2 |
C |
T |
7: 96,950,645 (GRCm39) |
P446L |
probably damaging |
Het |
Ganab |
A |
T |
19: 8,888,716 (GRCm39) |
Y552F |
possibly damaging |
Het |
Gfy |
C |
T |
7: 44,826,962 (GRCm39) |
R378Q |
probably damaging |
Het |
Gm3285 |
T |
C |
10: 77,697,875 (GRCm39) |
V8A |
unknown |
Het |
Grip1 |
A |
T |
10: 119,913,043 (GRCm39) |
|
probably null |
Het |
Gtf3c3 |
A |
G |
1: 54,442,752 (GRCm39) |
L764P |
probably damaging |
Het |
Igfbp2 |
A |
T |
1: 72,888,307 (GRCm39) |
M150L |
probably benign |
Het |
Jakmip2 |
C |
T |
18: 43,673,676 (GRCm39) |
R796Q |
probably damaging |
Het |
Jpt1 |
T |
A |
11: 115,389,021 (GRCm39) |
R141W |
probably damaging |
Het |
Junb |
T |
C |
8: 85,704,802 (GRCm39) |
E86G |
probably damaging |
Het |
Klhl41 |
A |
T |
2: 69,505,068 (GRCm39) |
D457V |
probably benign |
Het |
Lama2 |
T |
C |
10: 26,977,389 (GRCm39) |
Y1930C |
probably benign |
Het |
Med13 |
A |
T |
11: 86,161,828 (GRCm39) |
I2167N |
probably damaging |
Het |
Msh3 |
A |
G |
13: 92,485,840 (GRCm39) |
|
probably benign |
Het |
Myo1b |
A |
C |
1: 51,817,483 (GRCm39) |
I593S |
probably damaging |
Het |
Myo1c |
A |
T |
11: 75,548,345 (GRCm39) |
T16S |
possibly damaging |
Het |
Ndufaf4 |
C |
T |
4: 24,901,829 (GRCm39) |
L126F |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,256,721 (GRCm39) |
N113I |
possibly damaging |
Het |
Or5d43 |
T |
A |
2: 88,104,794 (GRCm39) |
I200F |
probably damaging |
Het |
Or5g23 |
G |
C |
2: 85,438,528 (GRCm39) |
S242C |
probably damaging |
Het |
Or5p6 |
T |
A |
7: 107,631,128 (GRCm39) |
T141S |
probably benign |
Het |
Pabpc6 |
A |
T |
17: 9,887,611 (GRCm39) |
D313E |
probably damaging |
Het |
Pcdhb2 |
G |
T |
18: 37,428,857 (GRCm39) |
G277* |
probably null |
Het |
Phkb |
T |
G |
8: 86,756,226 (GRCm39) |
V840G |
probably damaging |
Het |
Pip4k2c |
A |
G |
10: 127,034,955 (GRCm39) |
F415S |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,179,779 (GRCm39) |
E1112G |
probably damaging |
Het |
Pum2 |
A |
G |
12: 8,797,206 (GRCm39) |
D847G |
probably damaging |
Het |
Qrich2 |
C |
T |
11: 116,346,450 (GRCm39) |
R1458H |
probably benign |
Het |
Rdh11 |
T |
C |
12: 79,231,957 (GRCm39) |
Y199C |
probably damaging |
Het |
Resf1 |
A |
T |
6: 149,228,291 (GRCm39) |
N446Y |
possibly damaging |
Het |
Scamp3 |
A |
G |
3: 89,087,673 (GRCm39) |
Y171C |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,223,743 (GRCm39) |
S312P |
probably damaging |
Het |
Slain2 |
G |
A |
5: 73,123,165 (GRCm39) |
S461N |
probably benign |
Het |
Slc23a1 |
G |
A |
18: 35,758,891 (GRCm39) |
T100I |
probably damaging |
Het |
Spata31d1b |
T |
A |
13: 59,866,194 (GRCm39) |
I1114N |
probably damaging |
Het |
Spinkl |
A |
G |
18: 44,307,656 (GRCm39) |
S2P |
probably damaging |
Het |
Srrt |
T |
C |
5: 137,300,457 (GRCm39) |
N173S |
probably damaging |
Het |
Stk24 |
C |
T |
14: 121,539,699 (GRCm39) |
A166T |
probably damaging |
Het |
Supt16 |
A |
T |
14: 52,411,013 (GRCm39) |
V697E |
probably damaging |
Het |
Taf6l |
C |
T |
19: 8,761,210 (GRCm39) |
E53K |
probably damaging |
Het |
Tmem81 |
A |
T |
1: 132,435,511 (GRCm39) |
I106F |
probably damaging |
Het |
Tnxb |
C |
A |
17: 34,935,382 (GRCm39) |
L2561I |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,652,085 (GRCm39) |
S1463T |
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Tubal3 |
A |
C |
13: 3,978,198 (GRCm39) |
D38A |
possibly damaging |
Het |
Vps13a |
T |
A |
19: 16,624,962 (GRCm39) |
I2766F |
probably benign |
Het |
Wwc1 |
A |
T |
11: 35,735,022 (GRCm39) |
V951E |
possibly damaging |
Het |
Zfp777 |
A |
T |
6: 48,006,152 (GRCm39) |
M414K |
probably benign |
Het |
|
Other mutations in Top3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00823:Top3b
|
APN |
16 |
16,705,486 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01512:Top3b
|
APN |
16 |
16,709,286 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL01552:Top3b
|
APN |
16 |
16,705,687 (GRCm39) |
splice site |
probably benign |
|
IGL01738:Top3b
|
APN |
16 |
16,698,468 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02090:Top3b
|
APN |
16 |
16,709,334 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0143:Top3b
|
UTSW |
16 |
16,701,389 (GRCm39) |
missense |
probably damaging |
0.97 |
R0883:Top3b
|
UTSW |
16 |
16,697,301 (GRCm39) |
splice site |
probably benign |
|
R1386:Top3b
|
UTSW |
16 |
16,698,493 (GRCm39) |
missense |
probably benign |
0.29 |
R1440:Top3b
|
UTSW |
16 |
16,710,641 (GRCm39) |
nonsense |
probably null |
|
R1958:Top3b
|
UTSW |
16 |
16,702,166 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1970:Top3b
|
UTSW |
16 |
16,701,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Top3b
|
UTSW |
16 |
16,700,396 (GRCm39) |
splice site |
probably null |
|
R4292:Top3b
|
UTSW |
16 |
16,701,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4307:Top3b
|
UTSW |
16 |
16,707,481 (GRCm39) |
splice site |
probably benign |
|
R4832:Top3b
|
UTSW |
16 |
16,708,526 (GRCm39) |
nonsense |
probably null |
|
R5047:Top3b
|
UTSW |
16 |
16,709,282 (GRCm39) |
missense |
probably benign |
0.00 |
R5364:Top3b
|
UTSW |
16 |
16,704,834 (GRCm39) |
missense |
probably benign |
0.00 |
R5590:Top3b
|
UTSW |
16 |
16,709,441 (GRCm39) |
intron |
probably benign |
|
R5604:Top3b
|
UTSW |
16 |
16,707,399 (GRCm39) |
nonsense |
probably null |
|
R5719:Top3b
|
UTSW |
16 |
16,703,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5969:Top3b
|
UTSW |
16 |
16,701,429 (GRCm39) |
critical splice donor site |
probably null |
|
R6018:Top3b
|
UTSW |
16 |
16,710,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6144:Top3b
|
UTSW |
16 |
16,697,005 (GRCm39) |
splice site |
probably null |
|
R6155:Top3b
|
UTSW |
16 |
16,709,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Top3b
|
UTSW |
16 |
16,696,935 (GRCm39) |
missense |
probably damaging |
0.98 |
R6700:Top3b
|
UTSW |
16 |
16,710,533 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7417:Top3b
|
UTSW |
16 |
16,695,714 (GRCm39) |
start gained |
probably benign |
|
R7747:Top3b
|
UTSW |
16 |
16,705,585 (GRCm39) |
missense |
probably benign |
0.17 |
R8382:Top3b
|
UTSW |
16 |
16,705,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R8438:Top3b
|
UTSW |
16 |
16,709,364 (GRCm39) |
missense |
probably benign |
0.04 |
R9142:Top3b
|
UTSW |
16 |
16,701,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9311:Top3b
|
UTSW |
16 |
16,700,563 (GRCm39) |
critical splice donor site |
probably null |
|
R9630:Top3b
|
UTSW |
16 |
16,710,354 (GRCm39) |
missense |
probably benign |
0.03 |
X0011:Top3b
|
UTSW |
16 |
16,708,053 (GRCm39) |
missense |
probably benign |
0.00 |
|