Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts5 |
T |
A |
16: 85,684,702 (GRCm39) |
|
probably null |
Het |
Afg3l1 |
T |
A |
8: 124,228,746 (GRCm39) |
W771R |
probably damaging |
Het |
Braf |
A |
G |
6: 39,628,586 (GRCm39) |
S348P |
probably damaging |
Het |
Cd200 |
T |
C |
16: 45,217,419 (GRCm39) |
T112A |
possibly damaging |
Het |
Cep350 |
T |
C |
1: 155,828,993 (GRCm39) |
I304V |
probably benign |
Het |
Fcsk |
G |
T |
8: 111,617,108 (GRCm39) |
H388N |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,323,064 (GRCm39) |
T1072A |
probably damaging |
Het |
Fry |
A |
T |
5: 150,362,276 (GRCm39) |
|
probably null |
Het |
Gcdh |
C |
T |
8: 85,620,288 (GRCm39) |
G8D |
probably damaging |
Het |
Ivns1abp |
C |
A |
1: 151,237,294 (GRCm39) |
T486K |
possibly damaging |
Het |
Mat1a |
G |
A |
14: 40,831,436 (GRCm39) |
V55M |
probably damaging |
Het |
Or52p1 |
T |
C |
7: 104,266,928 (GRCm39) |
F22S |
probably damaging |
Het |
Pcnx3 |
C |
T |
19: 5,717,287 (GRCm39) |
|
probably benign |
Het |
Psrc1 |
C |
A |
3: 108,294,008 (GRCm39) |
S275Y |
possibly damaging |
Het |
Slc22a13b |
A |
C |
9: 119,049,994 (GRCm39) |
|
probably benign |
Het |
Slc35b1 |
T |
A |
11: 95,279,910 (GRCm39) |
M178K |
probably benign |
Het |
Slc6a11 |
A |
T |
6: 114,111,829 (GRCm39) |
Q132L |
possibly damaging |
Het |
Slc9a8 |
C |
T |
2: 167,266,086 (GRCm39) |
T21I |
possibly damaging |
Het |
Tox |
T |
C |
4: 6,688,430 (GRCm39) |
T526A |
probably damaging |
Het |
Ubr3 |
C |
T |
2: 69,850,828 (GRCm39) |
P1749S |
probably benign |
Het |
Wdfy3 |
C |
A |
5: 102,061,126 (GRCm39) |
A1363S |
probably damaging |
Het |
Zdhhc23 |
T |
A |
16: 43,793,843 (GRCm39) |
H277L |
probably damaging |
Het |
|
Other mutations in Ptpn21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Ptpn21
|
APN |
12 |
98,646,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00576:Ptpn21
|
APN |
12 |
98,699,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00577:Ptpn21
|
APN |
12 |
98,699,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00580:Ptpn21
|
APN |
12 |
98,699,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00583:Ptpn21
|
APN |
12 |
98,699,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00773:Ptpn21
|
APN |
12 |
98,654,572 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00780:Ptpn21
|
APN |
12 |
98,646,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Ptpn21
|
APN |
12 |
98,681,448 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01939:Ptpn21
|
APN |
12 |
98,655,420 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02237:Ptpn21
|
APN |
12 |
98,671,351 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02512:Ptpn21
|
APN |
12 |
98,645,651 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Ptpn21
|
APN |
12 |
98,681,454 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02894:Ptpn21
|
APN |
12 |
98,655,891 (GRCm39) |
splice site |
probably benign |
|
IGL03024:Ptpn21
|
APN |
12 |
98,646,315 (GRCm39) |
missense |
probably benign |
|
IGL03220:Ptpn21
|
APN |
12 |
98,644,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Ptpn21
|
UTSW |
12 |
98,654,868 (GRCm39) |
missense |
probably benign |
0.01 |
R0472:Ptpn21
|
UTSW |
12 |
98,670,499 (GRCm39) |
splice site |
probably benign |
|
R0675:Ptpn21
|
UTSW |
12 |
98,654,475 (GRCm39) |
missense |
probably benign |
0.16 |
R0771:Ptpn21
|
UTSW |
12 |
98,655,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Ptpn21
|
UTSW |
12 |
98,654,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ptpn21
|
UTSW |
12 |
98,654,735 (GRCm39) |
missense |
probably benign |
|
R1470:Ptpn21
|
UTSW |
12 |
98,654,735 (GRCm39) |
missense |
probably benign |
|
R1837:Ptpn21
|
UTSW |
12 |
98,699,885 (GRCm39) |
missense |
probably damaging |
0.99 |
R1897:Ptpn21
|
UTSW |
12 |
98,646,664 (GRCm39) |
splice site |
probably null |
|
R2048:Ptpn21
|
UTSW |
12 |
98,655,785 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2376:Ptpn21
|
UTSW |
12 |
98,654,573 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3709:Ptpn21
|
UTSW |
12 |
98,654,800 (GRCm39) |
missense |
probably benign |
|
R4197:Ptpn21
|
UTSW |
12 |
98,646,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R4283:Ptpn21
|
UTSW |
12 |
98,699,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R4368:Ptpn21
|
UTSW |
12 |
98,644,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R4397:Ptpn21
|
UTSW |
12 |
98,681,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R4397:Ptpn21
|
UTSW |
12 |
98,654,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R4703:Ptpn21
|
UTSW |
12 |
98,645,651 (GRCm39) |
missense |
probably benign |
0.00 |
R4737:Ptpn21
|
UTSW |
12 |
98,675,103 (GRCm39) |
missense |
probably benign |
0.03 |
R4829:Ptpn21
|
UTSW |
12 |
98,655,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R4926:Ptpn21
|
UTSW |
12 |
98,681,454 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4974:Ptpn21
|
UTSW |
12 |
98,646,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5022:Ptpn21
|
UTSW |
12 |
98,645,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Ptpn21
|
UTSW |
12 |
98,645,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Ptpn21
|
UTSW |
12 |
98,681,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Ptpn21
|
UTSW |
12 |
98,655,036 (GRCm39) |
missense |
probably benign |
0.00 |
R5741:Ptpn21
|
UTSW |
12 |
98,645,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5785:Ptpn21
|
UTSW |
12 |
98,648,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R5959:Ptpn21
|
UTSW |
12 |
98,675,148 (GRCm39) |
splice site |
probably null |
|
R5968:Ptpn21
|
UTSW |
12 |
98,677,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Ptpn21
|
UTSW |
12 |
98,655,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R6005:Ptpn21
|
UTSW |
12 |
98,644,811 (GRCm39) |
makesense |
probably null |
|
R6181:Ptpn21
|
UTSW |
12 |
98,666,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R6226:Ptpn21
|
UTSW |
12 |
98,681,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Ptpn21
|
UTSW |
12 |
98,646,375 (GRCm39) |
missense |
probably benign |
0.24 |
R6317:Ptpn21
|
UTSW |
12 |
98,655,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6370:Ptpn21
|
UTSW |
12 |
98,655,293 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6485:Ptpn21
|
UTSW |
12 |
98,665,131 (GRCm39) |
nonsense |
probably null |
|
R6894:Ptpn21
|
UTSW |
12 |
98,681,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R7122:Ptpn21
|
UTSW |
12 |
98,655,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R7232:Ptpn21
|
UTSW |
12 |
98,654,996 (GRCm39) |
missense |
probably benign |
0.17 |
R7289:Ptpn21
|
UTSW |
12 |
98,670,450 (GRCm39) |
missense |
probably benign |
0.35 |
R7327:Ptpn21
|
UTSW |
12 |
98,646,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Ptpn21
|
UTSW |
12 |
98,703,622 (GRCm39) |
critical splice donor site |
probably null |
|
R7748:Ptpn21
|
UTSW |
12 |
98,655,031 (GRCm39) |
missense |
probably benign |
0.01 |
R7816:Ptpn21
|
UTSW |
12 |
98,648,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7867:Ptpn21
|
UTSW |
12 |
98,671,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R7878:Ptpn21
|
UTSW |
12 |
98,681,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Ptpn21
|
UTSW |
12 |
98,655,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R8100:Ptpn21
|
UTSW |
12 |
98,648,881 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8199:Ptpn21
|
UTSW |
12 |
98,644,841 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8272:Ptpn21
|
UTSW |
12 |
98,654,789 (GRCm39) |
missense |
probably benign |
|
R8481:Ptpn21
|
UTSW |
12 |
98,655,153 (GRCm39) |
missense |
probably benign |
0.03 |
R8535:Ptpn21
|
UTSW |
12 |
98,646,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R8775:Ptpn21
|
UTSW |
12 |
98,649,001 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8775-TAIL:Ptpn21
|
UTSW |
12 |
98,649,001 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8929:Ptpn21
|
UTSW |
12 |
98,655,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R8969:Ptpn21
|
UTSW |
12 |
98,655,284 (GRCm39) |
missense |
probably benign |
0.39 |
R9189:Ptpn21
|
UTSW |
12 |
98,655,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Ptpn21
|
UTSW |
12 |
98,655,170 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ptpn21
|
UTSW |
12 |
98,654,717 (GRCm39) |
missense |
probably benign |
0.05 |
|