Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
T |
C |
9: 114,301,702 (GRCm38) |
|
noncoding transcript |
Het |
Apob |
A |
G |
12: 8,006,017 (GRCm38) |
K1500E |
probably benign |
Het |
Atp8b1 |
A |
T |
18: 64,573,262 (GRCm38) |
Y225* |
probably null |
Het |
Cdc25c |
A |
T |
18: 34,748,973 (GRCm38) |
|
probably benign |
Het |
Ceacam15 |
T |
C |
7: 16,672,075 (GRCm38) |
N184D |
probably benign |
Het |
Cntln |
T |
C |
4: 84,996,479 (GRCm38) |
S508P |
probably damaging |
Het |
Dhx34 |
A |
G |
7: 16,218,368 (GRCm38) |
S111P |
probably damaging |
Het |
Dst |
A |
G |
1: 34,164,167 (GRCm38) |
E759G |
probably damaging |
Het |
Fis1 |
G |
A |
5: 136,965,146 (GRCm38) |
A28T |
probably damaging |
Het |
Fsd1 |
T |
C |
17: 55,990,542 (GRCm38) |
|
probably null |
Het |
Gm15293 |
T |
A |
8: 21,202,433 (GRCm38) |
F90Y |
probably benign |
Het |
Grk6 |
T |
C |
13: 55,454,527 (GRCm38) |
|
probably null |
Het |
Il23r |
A |
T |
6: 67,473,810 (GRCm38) |
H228Q |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,752,338 (GRCm38) |
V368I |
possibly damaging |
Het |
Kdr |
T |
C |
5: 75,956,231 (GRCm38) |
E728G |
probably damaging |
Het |
Krt33a |
T |
A |
11: 100,015,937 (GRCm38) |
M71L |
probably benign |
Het |
Lrrc7 |
T |
G |
3: 158,161,143 (GRCm38) |
D987A |
probably damaging |
Het |
Naalad2 |
C |
T |
9: 18,347,506 (GRCm38) |
R491Q |
probably damaging |
Het |
Nedd4l |
A |
T |
18: 65,167,499 (GRCm38) |
|
probably benign |
Het |
Pramel7 |
A |
G |
2: 87,491,190 (GRCm38) |
L167S |
probably damaging |
Het |
Prkci |
A |
G |
3: 31,050,192 (GRCm38) |
D568G |
probably damaging |
Het |
Psg18 |
G |
A |
7: 18,351,075 (GRCm38) |
T32I |
possibly damaging |
Het |
Ric8b |
T |
A |
10: 84,970,717 (GRCm38) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,485,998 (GRCm38) |
|
probably benign |
Het |
Rttn |
T |
C |
18: 89,064,249 (GRCm38) |
V1433A |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 110,367,172 (GRCm38) |
|
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,838,646 (GRCm38) |
|
silent |
Het |
Sfta2 |
T |
C |
17: 35,650,127 (GRCm38) |
|
probably benign |
Het |
Slc17a1 |
T |
A |
13: 23,878,450 (GRCm38) |
|
probably benign |
Het |
Slc6a21 |
G |
A |
7: 45,288,202 (GRCm38) |
C314Y |
probably benign |
Het |
Smpd4 |
T |
C |
16: 17,623,969 (GRCm38) |
V35A |
probably damaging |
Het |
Sorl1 |
T |
C |
9: 42,014,490 (GRCm38) |
D1182G |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,042,035 (GRCm38) |
I5056V |
possibly damaging |
Het |
Tex14 |
T |
C |
11: 87,519,745 (GRCm38) |
|
probably benign |
Het |
Tex44 |
A |
G |
1: 86,427,055 (GRCm38) |
T229A |
probably benign |
Het |
Tfap2b |
T |
A |
1: 19,234,149 (GRCm38) |
C394* |
probably null |
Het |
Ttk |
T |
A |
9: 83,844,149 (GRCm38) |
|
probably benign |
Het |
Wac |
A |
G |
18: 7,921,916 (GRCm38) |
T553A |
probably damaging |
Het |
Wdcp |
T |
A |
12: 4,850,685 (GRCm38) |
H180Q |
probably damaging |
Het |
Wdr33 |
A |
G |
18: 31,835,461 (GRCm38) |
H235R |
probably benign |
Het |
|
Other mutations in Vmn2r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01070:Vmn2r26
|
APN |
6 |
124,061,607 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01370:Vmn2r26
|
APN |
6 |
124,061,756 (GRCm38) |
missense |
probably benign |
0.08 |
IGL01603:Vmn2r26
|
APN |
6 |
124,053,874 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01651:Vmn2r26
|
APN |
6 |
124,050,673 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02282:Vmn2r26
|
APN |
6 |
124,061,625 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02425:Vmn2r26
|
APN |
6 |
124,061,818 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02551:Vmn2r26
|
APN |
6 |
124,026,141 (GRCm38) |
missense |
probably benign |
0.11 |
IGL02690:Vmn2r26
|
APN |
6 |
124,026,132 (GRCm38) |
missense |
probably benign |
0.14 |
IGL03002:Vmn2r26
|
APN |
6 |
124,039,795 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL03270:Vmn2r26
|
APN |
6 |
124,050,819 (GRCm38) |
missense |
probably benign |
0.16 |
R0032:Vmn2r26
|
UTSW |
6 |
124,039,899 (GRCm38) |
missense |
possibly damaging |
0.72 |
R0052:Vmn2r26
|
UTSW |
6 |
124,062,033 (GRCm38) |
makesense |
probably null |
|
R0083:Vmn2r26
|
UTSW |
6 |
124,053,981 (GRCm38) |
splice site |
probably null |
|
R0682:Vmn2r26
|
UTSW |
6 |
124,061,170 (GRCm38) |
missense |
probably damaging |
0.97 |
R1061:Vmn2r26
|
UTSW |
6 |
124,061,644 (GRCm38) |
missense |
probably benign |
0.12 |
R1263:Vmn2r26
|
UTSW |
6 |
124,050,708 (GRCm38) |
missense |
probably benign |
|
R1579:Vmn2r26
|
UTSW |
6 |
124,039,747 (GRCm38) |
missense |
probably benign |
0.00 |
R1741:Vmn2r26
|
UTSW |
6 |
124,061,472 (GRCm38) |
missense |
probably damaging |
1.00 |
R1834:Vmn2r26
|
UTSW |
6 |
124,061,410 (GRCm38) |
missense |
possibly damaging |
0.54 |
R1838:Vmn2r26
|
UTSW |
6 |
124,024,771 (GRCm38) |
missense |
probably benign |
|
R1956:Vmn2r26
|
UTSW |
6 |
124,053,887 (GRCm38) |
missense |
probably damaging |
1.00 |
R1996:Vmn2r26
|
UTSW |
6 |
124,061,185 (GRCm38) |
missense |
probably damaging |
1.00 |
R2140:Vmn2r26
|
UTSW |
6 |
124,061,237 (GRCm38) |
missense |
probably benign |
0.01 |
R2327:Vmn2r26
|
UTSW |
6 |
124,039,749 (GRCm38) |
missense |
probably benign |
0.07 |
R2417:Vmn2r26
|
UTSW |
6 |
124,061,350 (GRCm38) |
missense |
probably damaging |
1.00 |
R3930:Vmn2r26
|
UTSW |
6 |
124,025,979 (GRCm38) |
missense |
probably benign |
|
R4490:Vmn2r26
|
UTSW |
6 |
124,050,738 (GRCm38) |
missense |
possibly damaging |
0.47 |
R4629:Vmn2r26
|
UTSW |
6 |
124,061,191 (GRCm38) |
missense |
possibly damaging |
0.50 |
R4655:Vmn2r26
|
UTSW |
6 |
124,061,416 (GRCm38) |
missense |
probably damaging |
1.00 |
R4709:Vmn2r26
|
UTSW |
6 |
124,053,965 (GRCm38) |
missense |
probably damaging |
1.00 |
R4992:Vmn2r26
|
UTSW |
6 |
124,026,111 (GRCm38) |
missense |
probably benign |
0.00 |
R5297:Vmn2r26
|
UTSW |
6 |
124,061,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R5482:Vmn2r26
|
UTSW |
6 |
124,061,326 (GRCm38) |
missense |
possibly damaging |
0.88 |
R5517:Vmn2r26
|
UTSW |
6 |
124,050,717 (GRCm38) |
missense |
probably damaging |
1.00 |
R5737:Vmn2r26
|
UTSW |
6 |
124,039,449 (GRCm38) |
missense |
probably benign |
0.00 |
R5739:Vmn2r26
|
UTSW |
6 |
124,025,966 (GRCm38) |
missense |
probably benign |
0.00 |
R5873:Vmn2r26
|
UTSW |
6 |
124,061,674 (GRCm38) |
missense |
probably benign |
0.01 |
R5907:Vmn2r26
|
UTSW |
6 |
124,039,871 (GRCm38) |
missense |
probably benign |
0.00 |
R6086:Vmn2r26
|
UTSW |
6 |
124,039,560 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6134:Vmn2r26
|
UTSW |
6 |
124,061,485 (GRCm38) |
missense |
probably damaging |
0.97 |
R6391:Vmn2r26
|
UTSW |
6 |
124,061,389 (GRCm38) |
missense |
probably damaging |
1.00 |
R6428:Vmn2r26
|
UTSW |
6 |
124,026,080 (GRCm38) |
missense |
probably benign |
0.17 |
R6637:Vmn2r26
|
UTSW |
6 |
124,061,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R6927:Vmn2r26
|
UTSW |
6 |
124,039,098 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6953:Vmn2r26
|
UTSW |
6 |
124,039,782 (GRCm38) |
missense |
probably benign |
0.00 |
R7173:Vmn2r26
|
UTSW |
6 |
124,061,296 (GRCm38) |
missense |
probably benign |
0.16 |
R7206:Vmn2r26
|
UTSW |
6 |
124,039,768 (GRCm38) |
missense |
probably benign |
0.17 |
R7208:Vmn2r26
|
UTSW |
6 |
124,061,989 (GRCm38) |
missense |
probably damaging |
1.00 |
R7283:Vmn2r26
|
UTSW |
6 |
124,025,955 (GRCm38) |
missense |
probably damaging |
0.97 |
R7506:Vmn2r26
|
UTSW |
6 |
124,039,741 (GRCm38) |
missense |
probably benign |
0.00 |
R7672:Vmn2r26
|
UTSW |
6 |
124,039,647 (GRCm38) |
missense |
probably benign |
0.25 |
R7674:Vmn2r26
|
UTSW |
6 |
124,039,362 (GRCm38) |
missense |
probably benign |
|
R7696:Vmn2r26
|
UTSW |
6 |
124,061,535 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7716:Vmn2r26
|
UTSW |
6 |
124,061,745 (GRCm38) |
missense |
probably damaging |
1.00 |
R7831:Vmn2r26
|
UTSW |
6 |
124,039,799 (GRCm38) |
nonsense |
probably null |
|
R8063:Vmn2r26
|
UTSW |
6 |
124,024,955 (GRCm38) |
missense |
probably benign |
0.00 |
R8331:Vmn2r26
|
UTSW |
6 |
124,061,928 (GRCm38) |
missense |
probably benign |
0.22 |
R8352:Vmn2r26
|
UTSW |
6 |
124,039,618 (GRCm38) |
missense |
probably benign |
0.09 |
R8445:Vmn2r26
|
UTSW |
6 |
124,026,036 (GRCm38) |
missense |
probably damaging |
0.97 |
R8452:Vmn2r26
|
UTSW |
6 |
124,039,618 (GRCm38) |
missense |
probably benign |
0.09 |
R8681:Vmn2r26
|
UTSW |
6 |
124,024,918 (GRCm38) |
missense |
probably benign |
0.00 |
R8914:Vmn2r26
|
UTSW |
6 |
124,062,024 (GRCm38) |
missense |
probably benign |
|
R9333:Vmn2r26
|
UTSW |
6 |
124,026,050 (GRCm38) |
missense |
probably benign |
0.13 |
R9351:Vmn2r26
|
UTSW |
6 |
124,039,374 (GRCm38) |
missense |
probably benign |
|
R9436:Vmn2r26
|
UTSW |
6 |
124,025,867 (GRCm38) |
missense |
probably damaging |
1.00 |
R9515:Vmn2r26
|
UTSW |
6 |
124,061,178 (GRCm38) |
missense |
probably damaging |
1.00 |
RF010:Vmn2r26
|
UTSW |
6 |
124,039,489 (GRCm38) |
missense |
possibly damaging |
0.90 |
|