Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,835,094 (GRCm39) |
T679A |
possibly damaging |
Het |
Ahr |
T |
C |
12: 35,558,193 (GRCm39) |
T276A |
probably benign |
Het |
Akap9 |
A |
T |
5: 4,114,136 (GRCm39) |
Q3138H |
probably damaging |
Het |
Armt1 |
T |
A |
10: 4,382,689 (GRCm39) |
F7I |
probably benign |
Het |
B3galt2 |
A |
G |
1: 143,521,878 (GRCm39) |
R5G |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,958,576 (GRCm39) |
N2750S |
probably benign |
Het |
Cadps2 |
T |
A |
6: 23,583,395 (GRCm39) |
E365V |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,778,080 (GRCm39) |
|
probably null |
Het |
Cemip2 |
T |
A |
19: 21,795,335 (GRCm39) |
S743T |
probably benign |
Het |
Cst7 |
T |
A |
2: 150,417,806 (GRCm39) |
|
probably benign |
Het |
Defb30 |
A |
T |
14: 63,287,212 (GRCm39) |
|
probably benign |
Het |
Dido1 |
C |
T |
2: 180,301,644 (GRCm39) |
G2087S |
probably benign |
Het |
Dio2 |
A |
G |
12: 90,704,845 (GRCm39) |
Y72H |
probably benign |
Het |
Dnah11 |
C |
T |
12: 117,951,204 (GRCm39) |
E3035K |
probably damaging |
Het |
Dnajb13 |
T |
C |
7: 100,152,456 (GRCm39) |
K287E |
possibly damaging |
Het |
Dnajc11 |
G |
A |
4: 152,058,085 (GRCm39) |
V244I |
possibly damaging |
Het |
Ect2 |
C |
T |
3: 27,193,801 (GRCm39) |
A226T |
probably damaging |
Het |
Ercc8 |
G |
A |
13: 108,310,595 (GRCm39) |
|
probably null |
Het |
Fam120b |
T |
A |
17: 15,623,189 (GRCm39) |
M389K |
probably benign |
Het |
Fam151a |
A |
G |
4: 106,605,128 (GRCm39) |
M497V |
probably benign |
Het |
Fam186b |
C |
A |
15: 99,178,009 (GRCm39) |
G439V |
probably benign |
Het |
Fank1 |
A |
G |
7: 133,478,494 (GRCm39) |
Y185C |
probably damaging |
Het |
Gart |
T |
C |
16: 91,427,490 (GRCm39) |
|
probably benign |
Het |
Glb1l |
T |
C |
1: 75,176,364 (GRCm39) |
Y572C |
probably damaging |
Het |
Gm11563 |
C |
T |
11: 99,549,263 (GRCm39) |
A164T |
unknown |
Het |
Gnb4 |
C |
T |
3: 32,645,356 (GRCm39) |
V112I |
probably benign |
Het |
Gsdmc3 |
T |
A |
15: 63,731,542 (GRCm39) |
D330V |
probably damaging |
Het |
H2-DMa |
C |
T |
17: 34,356,934 (GRCm39) |
T144M |
probably damaging |
Het |
Haus6 |
A |
T |
4: 86,501,751 (GRCm39) |
F707I |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,469,767 (GRCm39) |
T4971S |
probably benign |
Het |
Ints6 |
A |
T |
14: 62,934,208 (GRCm39) |
F766L |
probably benign |
Het |
Kdm5d |
T |
A |
Y: 927,330 (GRCm39) |
M650K |
probably damaging |
Het |
Kif21b |
T |
C |
1: 136,087,166 (GRCm39) |
F881S |
possibly damaging |
Het |
Klrk1 |
C |
A |
6: 129,591,598 (GRCm39) |
Q176H |
possibly damaging |
Het |
Ky |
T |
C |
9: 102,414,820 (GRCm39) |
V244A |
probably benign |
Het |
Mia2 |
T |
A |
12: 59,201,205 (GRCm39) |
L191M |
possibly damaging |
Het |
Miga2 |
T |
A |
2: 30,271,756 (GRCm39) |
|
probably benign |
Het |
Mtss2 |
C |
T |
8: 111,464,580 (GRCm39) |
P322S |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,536,553 (GRCm39) |
|
probably benign |
Het |
Ncbp3 |
T |
A |
11: 72,940,671 (GRCm39) |
|
probably benign |
Het |
Nprl3 |
G |
A |
11: 32,184,876 (GRCm39) |
L378F |
probably damaging |
Het |
Ntrk2 |
A |
T |
13: 58,994,635 (GRCm39) |
M184L |
probably benign |
Het |
Or11g1 |
G |
T |
14: 50,651,154 (GRCm39) |
C51F |
probably benign |
Het |
Or9e1 |
T |
G |
11: 58,732,269 (GRCm39) |
C110G |
probably damaging |
Het |
Osbpl9 |
T |
C |
4: 108,940,325 (GRCm39) |
E287G |
probably damaging |
Het |
Parva |
T |
C |
7: 112,175,618 (GRCm39) |
F250L |
probably damaging |
Het |
Pcdhb11 |
C |
T |
18: 37,554,864 (GRCm39) |
Q65* |
probably null |
Het |
Phtf1 |
A |
G |
3: 103,901,081 (GRCm39) |
T377A |
probably damaging |
Het |
Pkp4 |
G |
A |
2: 59,152,987 (GRCm39) |
V612I |
possibly damaging |
Het |
Plscr2 |
C |
A |
9: 92,169,707 (GRCm39) |
S52R |
probably benign |
Het |
Pnisr |
C |
T |
4: 21,874,092 (GRCm39) |
|
probably benign |
Het |
Pole2 |
A |
C |
12: 69,256,653 (GRCm39) |
S291A |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 46,994,944 (GRCm39) |
F586L |
probably benign |
Het |
Prrx1 |
G |
A |
1: 163,085,385 (GRCm39) |
R182C |
probably damaging |
Het |
Ptprs |
A |
G |
17: 56,736,103 (GRCm39) |
I110T |
possibly damaging |
Het |
Rasgrf2 |
G |
A |
13: 92,067,936 (GRCm39) |
|
probably benign |
Het |
Resf1 |
A |
T |
6: 149,229,873 (GRCm39) |
Q973L |
probably damaging |
Het |
Riox2 |
T |
C |
16: 59,312,255 (GRCm39) |
V464A |
probably benign |
Het |
Robo2 |
A |
G |
16: 73,764,690 (GRCm39) |
V646A |
possibly damaging |
Het |
Ros1 |
T |
A |
10: 51,994,444 (GRCm39) |
I1279F |
probably damaging |
Het |
Siglec1 |
G |
A |
2: 130,916,188 (GRCm39) |
T1254M |
probably benign |
Het |
Snx7 |
T |
C |
3: 117,640,324 (GRCm39) |
N62D |
probably damaging |
Het |
Sp100 |
G |
A |
1: 85,587,588 (GRCm39) |
|
probably null |
Het |
Stil |
A |
T |
4: 114,864,356 (GRCm39) |
I86L |
possibly damaging |
Het |
Tbc1d16 |
T |
A |
11: 119,099,864 (GRCm39) |
D170V |
probably benign |
Het |
Trhr |
T |
A |
15: 44,092,896 (GRCm39) |
S378T |
probably benign |
Het |
Ttc7b |
T |
C |
12: 100,466,332 (GRCm39) |
|
probably null |
Het |
Vegfc |
A |
T |
8: 54,610,174 (GRCm39) |
Y110F |
probably benign |
Het |
Vmn1r184 |
C |
A |
7: 25,966,602 (GRCm39) |
P116H |
possibly damaging |
Het |
Vmn2r5 |
A |
T |
3: 64,411,235 (GRCm39) |
C444* |
probably null |
Het |
Zfp341 |
A |
G |
2: 154,476,193 (GRCm39) |
E460G |
possibly damaging |
Het |
Zfp819 |
T |
A |
7: 43,265,868 (GRCm39) |
V41E |
probably benign |
Het |
|
Other mutations in Trappc13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00826:Trappc13
|
APN |
13 |
104,281,016 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01930:Trappc13
|
APN |
13 |
104,284,586 (GRCm39) |
splice site |
probably benign |
|
IGL02637:Trappc13
|
APN |
13 |
104,286,570 (GRCm39) |
missense |
probably benign |
0.00 |
R0470:Trappc13
|
UTSW |
13 |
104,297,512 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0628:Trappc13
|
UTSW |
13 |
104,291,424 (GRCm39) |
splice site |
probably benign |
|
R1402:Trappc13
|
UTSW |
13 |
104,286,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Trappc13
|
UTSW |
13 |
104,286,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1530:Trappc13
|
UTSW |
13 |
104,286,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Trappc13
|
UTSW |
13 |
104,306,327 (GRCm39) |
critical splice donor site |
probably null |
|
R1951:Trappc13
|
UTSW |
13 |
104,311,150 (GRCm39) |
missense |
probably benign |
0.43 |
R3755:Trappc13
|
UTSW |
13 |
104,305,068 (GRCm39) |
missense |
probably benign |
|
R3756:Trappc13
|
UTSW |
13 |
104,305,068 (GRCm39) |
missense |
probably benign |
|
R3918:Trappc13
|
UTSW |
13 |
104,297,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Trappc13
|
UTSW |
13 |
104,303,329 (GRCm39) |
intron |
probably benign |
|
R4916:Trappc13
|
UTSW |
13 |
104,290,802 (GRCm39) |
critical splice donor site |
probably null |
|
R5590:Trappc13
|
UTSW |
13 |
104,284,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Trappc13
|
UTSW |
13 |
104,286,606 (GRCm39) |
missense |
probably benign |
0.01 |
R6862:Trappc13
|
UTSW |
13 |
104,286,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7708:Trappc13
|
UTSW |
13 |
104,283,845 (GRCm39) |
missense |
probably benign |
0.06 |
R8049:Trappc13
|
UTSW |
13 |
104,281,052 (GRCm39) |
missense |
probably benign |
|
R8377:Trappc13
|
UTSW |
13 |
104,297,509 (GRCm39) |
missense |
probably benign |
0.40 |
R9280:Trappc13
|
UTSW |
13 |
104,290,809 (GRCm39) |
missense |
probably benign |
0.30 |
R9380:Trappc13
|
UTSW |
13 |
104,280,707 (GRCm39) |
missense |
probably damaging |
1.00 |
|