Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
A |
C |
15: 57,892,414 (GRCm39) |
H128Q |
possibly damaging |
Het |
Abcd2 |
T |
C |
15: 91,075,315 (GRCm39) |
Y166C |
possibly damaging |
Het |
Adamtsl4 |
C |
A |
3: 95,588,575 (GRCm39) |
V546F |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,723,755 (GRCm39) |
V717E |
probably damaging |
Het |
Atm |
A |
G |
9: 53,407,150 (GRCm39) |
|
probably null |
Het |
Atp2c1 |
C |
A |
9: 105,291,851 (GRCm39) |
E904* |
probably null |
Het |
Ccdc88c |
G |
A |
12: 100,889,474 (GRCm39) |
S1523F |
possibly damaging |
Het |
Cds1 |
A |
T |
5: 101,963,751 (GRCm39) |
I357F |
probably benign |
Het |
Cilp |
T |
A |
9: 65,174,451 (GRCm39) |
V13D |
possibly damaging |
Het |
Copz2 |
A |
G |
11: 96,748,386 (GRCm39) |
D180G |
possibly damaging |
Het |
Cpsf1 |
C |
T |
15: 76,484,992 (GRCm39) |
E546K |
probably benign |
Het |
Ctsm |
T |
C |
13: 61,684,413 (GRCm39) |
N320D |
probably damaging |
Het |
Fat3 |
G |
A |
9: 15,907,863 (GRCm39) |
T2713I |
probably benign |
Het |
Fcrl5 |
T |
A |
3: 87,343,195 (GRCm39) |
S2T |
probably benign |
Het |
Fgfr4 |
T |
C |
13: 55,315,974 (GRCm39) |
S796P |
unknown |
Het |
Flrt3 |
A |
G |
2: 140,502,159 (GRCm39) |
F490L |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,910,359 (GRCm39) |
I3263F |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,301,648 (GRCm39) |
D3793V |
probably damaging |
Het |
Kif5c |
T |
A |
2: 49,590,604 (GRCm39) |
L269* |
probably null |
Het |
Klhl32 |
A |
G |
4: 24,649,608 (GRCm39) |
V396A |
probably benign |
Het |
Krt1c |
C |
T |
15: 101,724,926 (GRCm39) |
R228Q |
probably benign |
Het |
Lcn9 |
T |
C |
2: 25,714,784 (GRCm39) |
|
probably null |
Het |
Lingo4 |
A |
C |
3: 94,310,676 (GRCm39) |
D538A |
probably benign |
Het |
Lonp1 |
G |
T |
17: 56,927,516 (GRCm39) |
Y299* |
probably null |
Het |
Mettl16 |
T |
A |
11: 74,708,127 (GRCm39) |
V442D |
possibly damaging |
Het |
Mettl25b |
G |
T |
3: 87,831,768 (GRCm39) |
Q397K |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,180,631 (GRCm39) |
V950A |
probably benign |
Het |
Mndal |
A |
T |
1: 173,690,274 (GRCm39) |
V352E |
probably damaging |
Het |
Mrpl55 |
T |
C |
11: 59,096,578 (GRCm39) |
V117A |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,226,738 (GRCm39) |
S1430C |
unknown |
Het |
Myh11 |
C |
A |
16: 14,087,120 (GRCm39) |
G119C |
|
Het |
Myorg |
T |
C |
4: 41,499,030 (GRCm39) |
D200G |
probably benign |
Het |
Neu1 |
A |
G |
17: 35,150,396 (GRCm39) |
D5G |
probably benign |
Het |
Nrcam |
T |
A |
12: 44,610,837 (GRCm39) |
D512E |
probably benign |
Het |
Nup214 |
T |
G |
2: 31,923,347 (GRCm39) |
V1292G |
possibly damaging |
Het |
Nwd1 |
T |
A |
8: 73,397,566 (GRCm39) |
L602M |
probably damaging |
Het |
Or6c3b |
C |
A |
10: 129,527,003 (GRCm39) |
L302F |
probably benign |
Het |
Pck2 |
G |
T |
14: 55,782,702 (GRCm39) |
G379W |
probably damaging |
Het |
Per2 |
C |
T |
1: 91,376,445 (GRCm39) |
V143M |
probably damaging |
Het |
Pfkl |
A |
T |
10: 77,825,489 (GRCm39) |
Y634N |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,100,281 (GRCm39) |
D183G |
possibly damaging |
Het |
Pkdrej |
T |
A |
15: 85,700,098 (GRCm39) |
Y1946F |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,139,018 (GRCm39) |
D1717N |
probably damaging |
Het |
Ppp1r14bl |
G |
T |
1: 23,141,275 (GRCm39) |
T13N |
probably benign |
Het |
Pramel23 |
T |
A |
4: 143,425,685 (GRCm39) |
D86V |
probably damaging |
Het |
Prdm16 |
A |
T |
4: 154,422,155 (GRCm39) |
V879E |
probably damaging |
Het |
Prr23a3 |
T |
C |
9: 98,747,298 (GRCm39) |
V84A |
probably benign |
Het |
Ptp4a1 |
A |
G |
1: 30,985,346 (GRCm39) |
|
probably benign |
Het |
Rhbdf1 |
T |
C |
11: 32,160,754 (GRCm39) |
H634R |
probably benign |
Het |
Rmi2 |
T |
C |
16: 10,653,089 (GRCm39) |
S46P |
probably benign |
Het |
Rsf1 |
A |
T |
7: 97,334,918 (GRCm39) |
E1350D |
|
Het |
Slc6a6 |
T |
A |
6: 91,716,952 (GRCm39) |
F276Y |
possibly damaging |
Het |
Sppl3 |
A |
G |
5: 115,221,532 (GRCm39) |
Y120C |
probably benign |
Het |
Stard13 |
G |
T |
5: 150,985,956 (GRCm39) |
A518E |
probably benign |
Het |
Taf2 |
A |
T |
15: 54,929,409 (GRCm39) |
V49E |
possibly damaging |
Het |
Tas2r140 |
T |
A |
6: 40,468,592 (GRCm39) |
W141R |
probably damaging |
Het |
Tlx2 |
T |
A |
6: 83,047,035 (GRCm39) |
H9L |
unknown |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tmem132d |
G |
A |
5: 127,861,491 (GRCm39) |
Q877* |
probably null |
Het |
Unc5d |
A |
T |
8: 29,215,174 (GRCm39) |
|
probably null |
Het |
Upp1 |
A |
T |
11: 9,075,661 (GRCm39) |
T4S |
probably benign |
Het |
Uros |
A |
T |
7: 133,292,853 (GRCm39) |
I146N |
probably damaging |
Het |
Vsig10 |
A |
T |
5: 117,463,131 (GRCm39) |
D119V |
probably benign |
Het |
Washc2 |
C |
A |
6: 116,193,069 (GRCm39) |
Y138* |
probably null |
Het |
Ywhah |
T |
A |
5: 33,184,095 (GRCm39) |
D99E |
probably benign |
Het |
Zdbf2 |
G |
A |
1: 63,345,400 (GRCm39) |
G1260R |
probably damaging |
Het |
Zfp663 |
T |
C |
2: 165,195,974 (GRCm39) |
T82A |
probably benign |
Het |
Zfp831 |
T |
A |
2: 174,488,156 (GRCm39) |
C944S |
possibly damaging |
Het |
|
Other mutations in 4921509C19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01098:4921509C19Rik
|
APN |
2 |
151,315,453 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02117:4921509C19Rik
|
APN |
2 |
151,315,466 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02432:4921509C19Rik
|
APN |
2 |
151,314,481 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03025:4921509C19Rik
|
APN |
2 |
151,315,405 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0321:4921509C19Rik
|
UTSW |
2 |
151,314,620 (GRCm39) |
missense |
probably benign |
0.01 |
R0961:4921509C19Rik
|
UTSW |
2 |
151,314,686 (GRCm39) |
missense |
probably benign |
0.01 |
R1272:4921509C19Rik
|
UTSW |
2 |
151,313,977 (GRCm39) |
missense |
probably damaging |
0.98 |
R1455:4921509C19Rik
|
UTSW |
2 |
151,314,824 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3177:4921509C19Rik
|
UTSW |
2 |
151,314,020 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3277:4921509C19Rik
|
UTSW |
2 |
151,314,020 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4206:4921509C19Rik
|
UTSW |
2 |
151,315,435 (GRCm39) |
missense |
probably benign |
0.44 |
R4655:4921509C19Rik
|
UTSW |
2 |
151,314,778 (GRCm39) |
missense |
probably benign |
0.03 |
R4680:4921509C19Rik
|
UTSW |
2 |
151,315,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:4921509C19Rik
|
UTSW |
2 |
151,313,791 (GRCm39) |
missense |
unknown |
|
R4702:4921509C19Rik
|
UTSW |
2 |
151,314,509 (GRCm39) |
missense |
probably benign |
0.00 |
R4867:4921509C19Rik
|
UTSW |
2 |
151,314,742 (GRCm39) |
nonsense |
probably null |
|
R4962:4921509C19Rik
|
UTSW |
2 |
151,314,728 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5117:4921509C19Rik
|
UTSW |
2 |
151,314,460 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:4921509C19Rik
|
UTSW |
2 |
151,313,851 (GRCm39) |
missense |
probably benign |
|
R5602:4921509C19Rik
|
UTSW |
2 |
151,315,459 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6374:4921509C19Rik
|
UTSW |
2 |
151,314,800 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6894:4921509C19Rik
|
UTSW |
2 |
151,315,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R7079:4921509C19Rik
|
UTSW |
2 |
151,315,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7109:4921509C19Rik
|
UTSW |
2 |
151,315,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:4921509C19Rik
|
UTSW |
2 |
151,315,489 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7441:4921509C19Rik
|
UTSW |
2 |
151,314,845 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7845:4921509C19Rik
|
UTSW |
2 |
151,314,229 (GRCm39) |
missense |
probably damaging |
0.96 |
R7853:4921509C19Rik
|
UTSW |
2 |
151,315,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8773:4921509C19Rik
|
UTSW |
2 |
151,314,062 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8805:4921509C19Rik
|
UTSW |
2 |
151,313,285 (GRCm39) |
splice site |
probably benign |
|
R8983:4921509C19Rik
|
UTSW |
2 |
151,313,272 (GRCm39) |
missense |
unknown |
|
R9566:4921509C19Rik
|
UTSW |
2 |
151,314,226 (GRCm39) |
missense |
probably benign |
0.13 |
|