Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
A |
T |
3: 36,136,324 (GRCm39) |
M370L |
probably benign |
Het |
Aimp1 |
A |
G |
3: 132,373,265 (GRCm39) |
M225T |
possibly damaging |
Het |
Atp8a1 |
T |
C |
5: 67,824,950 (GRCm39) |
I809V |
possibly damaging |
Het |
Bbs10 |
A |
G |
10: 111,135,622 (GRCm39) |
Y245C |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,520,157 (GRCm39) |
F1572Y |
probably damaging |
Het |
Cd79a |
A |
G |
7: 24,598,772 (GRCm39) |
N107S |
possibly damaging |
Het |
Cdc7 |
G |
A |
5: 107,130,925 (GRCm39) |
A428T |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,359,191 (GRCm39) |
T974A |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,829,120 (GRCm39) |
N261K |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,241,001 (GRCm39) |
D8V |
probably damaging |
Het |
Col6a4 |
T |
C |
9: 105,952,185 (GRCm39) |
D571G |
probably damaging |
Het |
Cpe |
A |
C |
8: 65,070,645 (GRCm39) |
V200G |
probably benign |
Het |
Ctnnd1 |
C |
T |
2: 84,444,231 (GRCm39) |
|
probably null |
Het |
D5Ertd579e |
A |
C |
5: 36,772,921 (GRCm39) |
C491W |
probably damaging |
Het |
Dek |
A |
G |
13: 47,252,856 (GRCm39) |
I183T |
probably damaging |
Het |
Dennd1a |
A |
T |
2: 37,742,453 (GRCm39) |
H437Q |
possibly damaging |
Het |
Dido1 |
C |
T |
2: 180,302,940 (GRCm39) |
A1655T |
probably benign |
Het |
Eva1b |
A |
G |
4: 126,043,278 (GRCm39) |
D106G |
probably damaging |
Het |
Evc2 |
G |
T |
5: 37,581,923 (GRCm39) |
S1189I |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,267,558 (GRCm39) |
L405Q |
probably damaging |
Het |
Fbxw15 |
T |
A |
9: 109,386,234 (GRCm39) |
M249L |
probably benign |
Het |
Gbp10 |
A |
T |
5: 105,366,326 (GRCm39) |
L526Q |
probably damaging |
Het |
Gm19402 |
A |
C |
10: 77,526,354 (GRCm39) |
|
probably benign |
Het |
Gm2244 |
A |
G |
14: 19,590,865 (GRCm39) |
Y141H |
probably damaging |
Het |
Gm4181 |
A |
T |
14: 51,870,666 (GRCm39) |
N98K |
probably damaging |
Het |
Golga4 |
C |
T |
9: 118,387,695 (GRCm39) |
R616* |
probably null |
Het |
Gpank1 |
T |
A |
17: 35,343,266 (GRCm39) |
S226T |
probably damaging |
Het |
Hipk3 |
T |
C |
2: 104,301,770 (GRCm39) |
M141V |
probably damaging |
Het |
Hoxc11 |
T |
C |
15: 102,863,178 (GRCm39) |
V73A |
probably benign |
Het |
Igf1r |
T |
G |
7: 67,653,885 (GRCm39) |
I141S |
possibly damaging |
Het |
Jak2 |
T |
A |
19: 29,273,059 (GRCm39) |
F628I |
probably benign |
Het |
Kcp |
C |
A |
6: 29,502,364 (GRCm39) |
V227L |
probably benign |
Het |
Knl1 |
T |
G |
2: 118,902,422 (GRCm39) |
C1374W |
probably damaging |
Het |
Larp6 |
A |
T |
9: 60,645,043 (GRCm39) |
R394S |
probably benign |
Het |
Lilra5 |
G |
A |
7: 4,245,114 (GRCm39) |
G253R |
probably damaging |
Het |
Map3k4 |
A |
G |
17: 12,482,945 (GRCm39) |
S591P |
probably damaging |
Het |
Mdfic2 |
T |
C |
6: 98,215,134 (GRCm39) |
D163G |
probably damaging |
Het |
Minar2 |
A |
G |
18: 59,205,296 (GRCm39) |
K28R |
probably benign |
Het |
Mrpl16 |
T |
A |
19: 11,750,332 (GRCm39) |
I72K |
probably damaging |
Het |
Nol11 |
C |
G |
11: 107,071,860 (GRCm39) |
R244S |
probably benign |
Het |
Nr2f1 |
T |
C |
13: 78,343,782 (GRCm39) |
T161A |
probably benign |
Het |
Nrdc |
G |
T |
4: 108,895,203 (GRCm39) |
V476F |
probably damaging |
Het |
Or10j7 |
G |
T |
1: 173,011,477 (GRCm39) |
H175N |
probably damaging |
Het |
Or10z1 |
A |
T |
1: 174,078,395 (GRCm39) |
S33T |
possibly damaging |
Het |
Or13a22 |
T |
A |
7: 140,072,626 (GRCm39) |
L25Q |
possibly damaging |
Het |
Or13m2-ps1 |
A |
T |
6: 42,777,843 (GRCm39) |
H56L |
probably benign |
Het |
P2rx1 |
A |
G |
11: 72,898,974 (GRCm39) |
I62V |
probably benign |
Het |
Pcdhgc5 |
A |
T |
18: 37,953,674 (GRCm39) |
Y316F |
probably benign |
Het |
Pecam1 |
T |
C |
11: 106,576,065 (GRCm39) |
D490G |
probably benign |
Het |
Pfkfb2 |
A |
T |
1: 130,635,299 (GRCm39) |
Y87* |
probably null |
Het |
Poldip2 |
A |
G |
11: 78,408,458 (GRCm39) |
|
probably null |
Het |
Ppp2r5b |
T |
A |
19: 6,280,566 (GRCm39) |
Q304L |
probably benign |
Het |
Pramel26 |
A |
G |
4: 143,542,609 (GRCm39) |
C4R |
probably damaging |
Het |
Psg26 |
A |
G |
7: 18,216,753 (GRCm39) |
F29L |
probably benign |
Het |
Ptprt |
A |
T |
2: 161,743,417 (GRCm39) |
I508N |
possibly damaging |
Het |
Rasgrp4 |
T |
C |
7: 28,847,808 (GRCm39) |
F406S |
probably damaging |
Het |
Rspo3 |
A |
G |
10: 29,375,926 (GRCm39) |
|
probably null |
Het |
Septin8 |
G |
T |
11: 53,425,594 (GRCm39) |
|
probably null |
Het |
Sirt2 |
A |
C |
7: 28,487,471 (GRCm39) |
T345P |
probably benign |
Het |
Slc6a20b |
T |
C |
9: 123,438,161 (GRCm39) |
E205G |
possibly damaging |
Het |
Sqstm1 |
G |
A |
11: 50,093,418 (GRCm39) |
Q327* |
probably null |
Het |
Susd3 |
T |
A |
13: 49,390,997 (GRCm39) |
S98C |
probably damaging |
Het |
Tada2b |
G |
A |
5: 36,634,186 (GRCm39) |
R56W |
probably damaging |
Het |
Tbc1d2 |
A |
T |
4: 46,615,045 (GRCm39) |
V546E |
possibly damaging |
Het |
Tbx6 |
A |
G |
7: 126,380,740 (GRCm39) |
Q21R |
possibly damaging |
Het |
Usp24 |
T |
G |
4: 106,231,297 (GRCm39) |
|
probably null |
Het |
Vinac1 |
T |
G |
2: 128,879,719 (GRCm39) |
T736P |
possibly damaging |
Het |
Vmn2r103 |
A |
G |
17: 20,032,406 (GRCm39) |
T727A |
probably benign |
Het |
Wdr48 |
C |
T |
9: 119,749,676 (GRCm39) |
T531M |
probably damaging |
Het |
|
Other mutations in Ptk6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Ptk6
|
APN |
2 |
180,837,611 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01630:Ptk6
|
APN |
2 |
180,838,859 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01862:Ptk6
|
APN |
2 |
180,841,433 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02231:Ptk6
|
APN |
2 |
180,838,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02965:Ptk6
|
APN |
2 |
180,840,861 (GRCm39) |
splice site |
probably benign |
|
R0115:Ptk6
|
UTSW |
2 |
180,844,320 (GRCm39) |
start gained |
probably benign |
|
R0139:Ptk6
|
UTSW |
2 |
180,838,724 (GRCm39) |
splice site |
probably benign |
|
R0245:Ptk6
|
UTSW |
2 |
180,844,284 (GRCm39) |
missense |
probably benign |
|
R0358:Ptk6
|
UTSW |
2 |
180,840,315 (GRCm39) |
missense |
probably benign |
0.01 |
R0416:Ptk6
|
UTSW |
2 |
180,844,101 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0454:Ptk6
|
UTSW |
2 |
180,844,075 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0470:Ptk6
|
UTSW |
2 |
180,837,732 (GRCm39) |
missense |
probably benign |
|
R0481:Ptk6
|
UTSW |
2 |
180,844,320 (GRCm39) |
start gained |
probably benign |
|
R1147:Ptk6
|
UTSW |
2 |
180,837,590 (GRCm39) |
missense |
probably benign |
0.23 |
R1147:Ptk6
|
UTSW |
2 |
180,837,590 (GRCm39) |
missense |
probably benign |
0.23 |
R1234:Ptk6
|
UTSW |
2 |
180,844,233 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2249:Ptk6
|
UTSW |
2 |
180,838,173 (GRCm39) |
missense |
probably benign |
0.03 |
R4842:Ptk6
|
UTSW |
2 |
180,838,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5568:Ptk6
|
UTSW |
2 |
180,841,488 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5806:Ptk6
|
UTSW |
2 |
180,841,523 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6017:Ptk6
|
UTSW |
2 |
180,837,605 (GRCm39) |
missense |
probably benign |
0.32 |
R6293:Ptk6
|
UTSW |
2 |
180,840,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Ptk6
|
UTSW |
2 |
180,840,895 (GRCm39) |
missense |
probably benign |
|
R7369:Ptk6
|
UTSW |
2 |
180,840,254 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8256:Ptk6
|
UTSW |
2 |
180,837,633 (GRCm39) |
nonsense |
probably null |
|
R9335:Ptk6
|
UTSW |
2 |
180,844,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Ptk6
|
UTSW |
2 |
180,840,206 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9500:Ptk6
|
UTSW |
2 |
180,837,566 (GRCm39) |
missense |
probably benign |
0.07 |
X0062:Ptk6
|
UTSW |
2 |
180,844,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|