Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034E13Rik |
A |
G |
18: 52,796,654 (GRCm39) |
D64G |
possibly damaging |
Het |
Ano2 |
T |
A |
6: 126,016,242 (GRCm39) |
M925K |
possibly damaging |
Het |
Arnt2 |
T |
C |
7: 83,996,720 (GRCm39) |
T69A |
probably damaging |
Het |
Asap2 |
T |
A |
12: 21,262,810 (GRCm39) |
N229K |
possibly damaging |
Het |
Atp13a3 |
T |
A |
16: 30,181,552 (GRCm39) |
N23Y |
probably benign |
Het |
Cbr4 |
G |
A |
8: 61,943,627 (GRCm39) |
G91R |
possibly damaging |
Het |
Cdc27 |
A |
T |
11: 104,406,244 (GRCm39) |
C624S |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,360,845 (GRCm39) |
I201N |
probably damaging |
Het |
Cdh5 |
A |
G |
8: 104,869,209 (GRCm39) |
Y645C |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,321,259 (GRCm39) |
V518I |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,617,821 (GRCm39) |
T761A |
possibly damaging |
Het |
Cpne4 |
C |
A |
9: 104,802,969 (GRCm39) |
S204R |
probably damaging |
Het |
Dcaf1 |
T |
C |
9: 106,740,849 (GRCm39) |
W1279R |
probably damaging |
Het |
Dennd4a |
C |
T |
9: 64,819,037 (GRCm39) |
P1731S |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,004,051 (GRCm39) |
V892D |
possibly damaging |
Het |
Fam131b |
A |
G |
6: 42,298,182 (GRCm39) |
|
probably null |
Het |
Fam83b |
T |
A |
9: 76,399,132 (GRCm39) |
D657V |
possibly damaging |
Het |
Fam83e |
T |
A |
7: 45,371,787 (GRCm39) |
|
probably null |
Het |
Fbxo4 |
A |
T |
15: 4,007,301 (GRCm39) |
I121N |
probably damaging |
Het |
Gabrg2 |
A |
G |
11: 41,859,647 (GRCm39) |
S202P |
probably damaging |
Het |
Grid2 |
T |
A |
6: 64,640,146 (GRCm39) |
I788N |
probably damaging |
Het |
Grik4 |
T |
A |
9: 42,599,319 (GRCm39) |
N53Y |
probably damaging |
Het |
Hipk2 |
A |
C |
6: 38,707,802 (GRCm39) |
|
probably null |
Het |
Hps5 |
T |
C |
7: 46,438,620 (GRCm39) |
T38A |
probably damaging |
Het |
Hs1bp3 |
A |
G |
12: 8,391,843 (GRCm39) |
D315G |
possibly damaging |
Het |
Kdm4a |
C |
T |
4: 117,996,073 (GRCm39) |
M985I |
probably damaging |
Het |
Kdm5d |
A |
G |
Y: 900,525 (GRCm39) |
Y190C |
probably damaging |
Het |
Krt86 |
T |
C |
15: 101,374,491 (GRCm39) |
S295P |
probably damaging |
Het |
Matr3 |
T |
A |
18: 35,720,791 (GRCm39) |
D413E |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,164,657 (GRCm39) |
F319L |
probably damaging |
Het |
Mcoln1 |
T |
A |
8: 3,560,910 (GRCm39) |
Y411N |
probably damaging |
Het |
Mpdz |
C |
A |
4: 81,203,711 (GRCm39) |
E1863* |
probably null |
Het |
Mrps9 |
A |
G |
1: 42,934,538 (GRCm39) |
E173G |
probably damaging |
Het |
Or7a42 |
A |
T |
10: 78,791,191 (GRCm39) |
I51F |
probably benign |
Het |
Osmr |
T |
C |
15: 6,850,528 (GRCm39) |
T692A |
probably benign |
Het |
Pkhd1l1 |
A |
T |
15: 44,441,984 (GRCm39) |
H3641L |
possibly damaging |
Het |
Pml |
T |
C |
9: 58,140,465 (GRCm39) |
T421A |
possibly damaging |
Het |
Podxl |
A |
G |
6: 31,505,391 (GRCm39) |
|
probably null |
Het |
Ppargc1b |
C |
G |
18: 61,442,164 (GRCm39) |
D591H |
probably damaging |
Het |
Prkag3 |
A |
G |
1: 74,787,975 (GRCm39) |
|
probably benign |
Het |
Proz |
A |
G |
8: 13,123,448 (GRCm39) |
R240G |
probably benign |
Het |
Rbm5 |
T |
G |
9: 107,637,525 (GRCm39) |
K135N |
probably damaging |
Het |
Ska1 |
G |
A |
18: 74,330,599 (GRCm39) |
T201M |
probably damaging |
Het |
Slc35f5 |
A |
C |
1: 125,515,100 (GRCm39) |
|
probably null |
Het |
Slc9a3 |
T |
C |
13: 74,309,842 (GRCm39) |
L510P |
probably damaging |
Het |
Speer4a2 |
T |
C |
5: 26,289,716 (GRCm39) |
E237G |
probably damaging |
Het |
Svil |
A |
G |
18: 5,082,828 (GRCm39) |
K1231E |
probably damaging |
Het |
Tanc2 |
T |
C |
11: 105,813,439 (GRCm39) |
S1628P |
possibly damaging |
Het |
Tm9sf3 |
T |
A |
19: 41,229,023 (GRCm39) |
D260V |
probably damaging |
Het |
Ttc9 |
G |
T |
12: 81,678,396 (GRCm39) |
R73L |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,917,207 (GRCm39) |
I3684V |
probably damaging |
Het |
Vps8 |
T |
C |
16: 21,280,189 (GRCm39) |
|
probably null |
Het |
Vwa3b |
T |
A |
1: 37,115,520 (GRCm39) |
I328N |
probably damaging |
Het |
Wdr1 |
C |
T |
5: 38,687,366 (GRCm39) |
V222M |
probably benign |
Het |
Xpnpep1 |
T |
A |
19: 52,985,439 (GRCm39) |
T530S |
probably damaging |
Het |
Zc3h6 |
C |
T |
2: 128,835,197 (GRCm39) |
S111F |
probably benign |
Het |
Zfp768 |
G |
A |
7: 126,943,718 (GRCm39) |
P137S |
probably benign |
Het |
|
Other mutations in Ptpn13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ptpn13
|
APN |
5 |
103,698,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00569:Ptpn13
|
APN |
5 |
103,738,872 (GRCm39) |
splice site |
probably benign |
|
IGL00764:Ptpn13
|
APN |
5 |
103,745,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00805:Ptpn13
|
APN |
5 |
103,702,595 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00922:Ptpn13
|
APN |
5 |
103,735,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00959:Ptpn13
|
APN |
5 |
103,665,437 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01090:Ptpn13
|
APN |
5 |
103,689,180 (GRCm39) |
missense |
probably null |
0.80 |
IGL01352:Ptpn13
|
APN |
5 |
103,634,641 (GRCm39) |
splice site |
probably null |
|
IGL01510:Ptpn13
|
APN |
5 |
103,710,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01515:Ptpn13
|
APN |
5 |
103,703,979 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01896:Ptpn13
|
APN |
5 |
103,649,389 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02094:Ptpn13
|
APN |
5 |
103,742,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02561:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Ptpn13
|
APN |
5 |
103,649,769 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02679:Ptpn13
|
APN |
5 |
103,717,320 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02981:Ptpn13
|
APN |
5 |
103,676,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Ptpn13
|
APN |
5 |
103,665,425 (GRCm39) |
missense |
probably benign |
|
IGL03136:Ptpn13
|
APN |
5 |
103,691,329 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03163:Ptpn13
|
APN |
5 |
103,739,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Ptpn13
|
APN |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Ptpn13
|
APN |
5 |
103,688,943 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03328:Ptpn13
|
APN |
5 |
103,664,214 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03343:Ptpn13
|
APN |
5 |
103,702,816 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02835:Ptpn13
|
UTSW |
5 |
103,707,891 (GRCm39) |
missense |
probably damaging |
0.98 |
P0021:Ptpn13
|
UTSW |
5 |
103,676,686 (GRCm39) |
missense |
probably benign |
0.39 |
R0017:Ptpn13
|
UTSW |
5 |
103,634,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0090:Ptpn13
|
UTSW |
5 |
103,717,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Ptpn13
|
UTSW |
5 |
103,728,629 (GRCm39) |
splice site |
probably benign |
|
R0183:Ptpn13
|
UTSW |
5 |
103,664,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0230:Ptpn13
|
UTSW |
5 |
103,674,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Ptpn13
|
UTSW |
5 |
103,713,091 (GRCm39) |
missense |
probably benign |
|
R0360:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Ptpn13
|
UTSW |
5 |
103,702,928 (GRCm39) |
missense |
probably benign |
0.31 |
R0504:Ptpn13
|
UTSW |
5 |
103,649,362 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0558:Ptpn13
|
UTSW |
5 |
103,677,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R0562:Ptpn13
|
UTSW |
5 |
103,664,291 (GRCm39) |
critical splice donor site |
probably null |
|
R0568:Ptpn13
|
UTSW |
5 |
103,637,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Ptpn13
|
UTSW |
5 |
103,704,011 (GRCm39) |
missense |
probably benign |
|
R0669:Ptpn13
|
UTSW |
5 |
103,703,975 (GRCm39) |
missense |
probably benign |
|
R0739:Ptpn13
|
UTSW |
5 |
103,722,998 (GRCm39) |
missense |
probably benign |
|
R1006:Ptpn13
|
UTSW |
5 |
103,734,655 (GRCm39) |
missense |
probably benign |
0.04 |
R1164:Ptpn13
|
UTSW |
5 |
103,637,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1274:Ptpn13
|
UTSW |
5 |
103,698,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Ptpn13
|
UTSW |
5 |
103,664,230 (GRCm39) |
missense |
probably benign |
0.01 |
R1529:Ptpn13
|
UTSW |
5 |
103,711,998 (GRCm39) |
missense |
probably benign |
0.00 |
R1533:Ptpn13
|
UTSW |
5 |
103,704,044 (GRCm39) |
nonsense |
probably null |
|
R1613:Ptpn13
|
UTSW |
5 |
103,684,737 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1616:Ptpn13
|
UTSW |
5 |
103,713,103 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1830:Ptpn13
|
UTSW |
5 |
103,691,325 (GRCm39) |
missense |
probably benign |
0.00 |
R1892:Ptpn13
|
UTSW |
5 |
103,649,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1907:Ptpn13
|
UTSW |
5 |
103,728,575 (GRCm39) |
missense |
probably null |
0.45 |
R2143:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2145:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2151:Ptpn13
|
UTSW |
5 |
103,673,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptpn13
|
UTSW |
5 |
103,717,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:Ptpn13
|
UTSW |
5 |
103,637,527 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2313:Ptpn13
|
UTSW |
5 |
103,712,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Ptpn13
|
UTSW |
5 |
103,737,720 (GRCm39) |
splice site |
probably benign |
|
R3773:Ptpn13
|
UTSW |
5 |
103,624,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R3924:Ptpn13
|
UTSW |
5 |
103,698,607 (GRCm39) |
splice site |
probably benign |
|
R4289:Ptpn13
|
UTSW |
5 |
103,681,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Ptpn13
|
UTSW |
5 |
103,717,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Ptpn13
|
UTSW |
5 |
103,681,273 (GRCm39) |
splice site |
probably null |
|
R4526:Ptpn13
|
UTSW |
5 |
103,649,335 (GRCm39) |
missense |
probably benign |
0.32 |
R4557:Ptpn13
|
UTSW |
5 |
103,688,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Ptpn13
|
UTSW |
5 |
103,671,558 (GRCm39) |
missense |
probably benign |
0.06 |
R4632:Ptpn13
|
UTSW |
5 |
103,717,726 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4727:Ptpn13
|
UTSW |
5 |
103,717,721 (GRCm39) |
missense |
probably benign |
|
R4780:Ptpn13
|
UTSW |
5 |
103,734,639 (GRCm39) |
missense |
probably benign |
0.04 |
R4793:Ptpn13
|
UTSW |
5 |
103,730,644 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Ptpn13
|
UTSW |
5 |
103,671,481 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Ptpn13
|
UTSW |
5 |
103,665,335 (GRCm39) |
splice site |
probably null |
|
R4951:Ptpn13
|
UTSW |
5 |
103,735,912 (GRCm39) |
missense |
probably benign |
0.00 |
R5052:Ptpn13
|
UTSW |
5 |
103,709,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5148:Ptpn13
|
UTSW |
5 |
103,640,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Ptpn13
|
UTSW |
5 |
103,688,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Ptpn13
|
UTSW |
5 |
103,649,294 (GRCm39) |
missense |
probably benign |
0.03 |
R5545:Ptpn13
|
UTSW |
5 |
103,709,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Ptpn13
|
UTSW |
5 |
103,702,625 (GRCm39) |
missense |
probably benign |
0.20 |
R5735:Ptpn13
|
UTSW |
5 |
103,702,686 (GRCm39) |
missense |
probably benign |
0.03 |
R5815:Ptpn13
|
UTSW |
5 |
103,745,556 (GRCm39) |
splice site |
probably null |
|
R5878:Ptpn13
|
UTSW |
5 |
103,624,984 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6366:Ptpn13
|
UTSW |
5 |
103,698,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Ptpn13
|
UTSW |
5 |
103,689,150 (GRCm39) |
missense |
probably benign |
0.00 |
R6492:Ptpn13
|
UTSW |
5 |
103,649,478 (GRCm39) |
missense |
probably benign |
0.02 |
R6709:Ptpn13
|
UTSW |
5 |
103,734,622 (GRCm39) |
missense |
probably benign |
0.18 |
R6759:Ptpn13
|
UTSW |
5 |
103,713,121 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6944:Ptpn13
|
UTSW |
5 |
103,624,857 (GRCm39) |
missense |
probably null |
1.00 |
R7079:Ptpn13
|
UTSW |
5 |
103,649,752 (GRCm39) |
missense |
probably benign |
0.00 |
R7253:Ptpn13
|
UTSW |
5 |
103,713,150 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7254:Ptpn13
|
UTSW |
5 |
103,742,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Ptpn13
|
UTSW |
5 |
103,688,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Ptpn13
|
UTSW |
5 |
103,674,961 (GRCm39) |
missense |
probably benign |
0.16 |
R7614:Ptpn13
|
UTSW |
5 |
103,649,331 (GRCm39) |
missense |
probably benign |
0.13 |
R7652:Ptpn13
|
UTSW |
5 |
103,677,578 (GRCm39) |
missense |
probably benign |
0.12 |
R7655:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7656:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7683:Ptpn13
|
UTSW |
5 |
103,713,018 (GRCm39) |
missense |
probably benign |
0.01 |
R7734:Ptpn13
|
UTSW |
5 |
103,709,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Ptpn13
|
UTSW |
5 |
103,640,090 (GRCm39) |
missense |
probably benign |
0.06 |
R7834:Ptpn13
|
UTSW |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Ptpn13
|
UTSW |
5 |
103,688,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Ptpn13
|
UTSW |
5 |
103,707,803 (GRCm39) |
nonsense |
probably null |
|
R8308:Ptpn13
|
UTSW |
5 |
103,688,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R8493:Ptpn13
|
UTSW |
5 |
103,717,671 (GRCm39) |
missense |
probably benign |
0.01 |
R8493:Ptpn13
|
UTSW |
5 |
103,712,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Ptpn13
|
UTSW |
5 |
103,705,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Ptpn13
|
UTSW |
5 |
103,707,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Ptpn13
|
UTSW |
5 |
103,739,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Ptpn13
|
UTSW |
5 |
103,727,671 (GRCm39) |
missense |
probably benign |
0.00 |
R8958:Ptpn13
|
UTSW |
5 |
103,698,973 (GRCm39) |
missense |
probably benign |
0.15 |
R8975:Ptpn13
|
UTSW |
5 |
103,649,266 (GRCm39) |
missense |
probably benign |
0.32 |
R9080:Ptpn13
|
UTSW |
5 |
103,637,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R9091:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9219:Ptpn13
|
UTSW |
5 |
103,745,632 (GRCm39) |
missense |
probably benign |
0.16 |
R9270:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9577:Ptpn13
|
UTSW |
5 |
103,676,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9593:Ptpn13
|
UTSW |
5 |
103,674,998 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9705:Ptpn13
|
UTSW |
5 |
103,681,221 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF017:Ptpn13
|
UTSW |
5 |
103,741,446 (GRCm39) |
missense |
probably benign |
0.45 |
Z1177:Ptpn13
|
UTSW |
5 |
103,717,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|