Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
T |
A |
3: 59,944,737 (GRCm39) |
D136E |
probably damaging |
Het |
Agrn |
C |
T |
4: 156,263,675 (GRCm39) |
G173R |
probably damaging |
Het |
Apob |
T |
C |
12: 8,065,475 (GRCm39) |
F4115S |
possibly damaging |
Het |
Bsn |
T |
A |
9: 107,992,323 (GRCm39) |
D1143V |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,390,479 (GRCm39) |
V317A |
probably damaging |
Het |
Cdh1 |
G |
A |
8: 107,388,635 (GRCm39) |
V564I |
probably benign |
Het |
Cep250 |
T |
C |
2: 155,818,090 (GRCm39) |
V814A |
probably benign |
Het |
Ces2a |
A |
T |
8: 105,466,822 (GRCm39) |
I65F |
probably benign |
Het |
Commd8 |
A |
G |
5: 72,322,765 (GRCm39) |
W51R |
probably damaging |
Het |
Cyb561d1 |
A |
T |
3: 108,106,720 (GRCm39) |
H166Q |
probably damaging |
Het |
Dcun1d4 |
T |
A |
5: 73,638,618 (GRCm39) |
|
probably benign |
Het |
Dgkd |
A |
G |
1: 87,855,540 (GRCm39) |
|
probably benign |
Het |
Dipk2b |
A |
G |
X: 18,289,926 (GRCm39) |
S179P |
possibly damaging |
Het |
Dnajc28 |
T |
C |
16: 91,413,200 (GRCm39) |
N372S |
probably benign |
Het |
Ecpas |
A |
T |
4: 58,830,332 (GRCm39) |
|
probably null |
Het |
Eid1 |
A |
G |
2: 125,515,344 (GRCm39) |
D78G |
possibly damaging |
Het |
Emid1 |
T |
A |
11: 5,094,331 (GRCm39) |
Q60L |
probably damaging |
Het |
Fam135a |
A |
T |
1: 24,067,878 (GRCm39) |
V801E |
probably benign |
Het |
Foxh1 |
A |
G |
15: 76,552,820 (GRCm39) |
V298A |
probably benign |
Het |
Foxn4 |
T |
C |
5: 114,393,662 (GRCm39) |
T486A |
probably damaging |
Het |
Gpc6 |
A |
T |
14: 118,125,932 (GRCm39) |
|
probably null |
Het |
Grid2ip |
C |
T |
5: 143,371,847 (GRCm39) |
P690L |
probably benign |
Het |
H2bc9 |
T |
C |
13: 23,727,162 (GRCm39) |
K121E |
possibly damaging |
Het |
Hdhd2 |
C |
T |
18: 77,052,866 (GRCm39) |
T172M |
probably benign |
Het |
Hr |
A |
T |
14: 70,795,547 (GRCm39) |
D393V |
probably benign |
Het |
Ido2 |
T |
C |
8: 25,025,268 (GRCm39) |
Y253C |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Klre1 |
A |
G |
6: 129,562,593 (GRCm39) |
K206R |
probably benign |
Het |
Lama2 |
T |
C |
10: 26,862,793 (GRCm39) |
D2990G |
probably benign |
Het |
Magi3 |
G |
A |
3: 103,928,382 (GRCm39) |
|
probably benign |
Het |
Mamdc2 |
A |
T |
19: 23,281,267 (GRCm39) |
|
probably benign |
Het |
Med23 |
T |
G |
10: 24,750,499 (GRCm39) |
S109A |
probably benign |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mtss2 |
A |
G |
8: 111,455,362 (GRCm39) |
K92E |
possibly damaging |
Het |
Mybphl |
A |
G |
3: 108,272,317 (GRCm39) |
E2G |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,420,067 (GRCm39) |
V1401A |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,393,296 (GRCm39) |
E500G |
probably damaging |
Het |
Nlrp12 |
T |
C |
7: 3,282,575 (GRCm39) |
I775V |
probably benign |
Het |
Nr4a2 |
T |
A |
2: 57,002,018 (GRCm39) |
D145V |
possibly damaging |
Het |
Ntmt1 |
C |
A |
2: 30,710,472 (GRCm39) |
N58K |
probably benign |
Het |
P2ry13 |
T |
C |
3: 59,117,449 (GRCm39) |
M110V |
probably damaging |
Het |
P2ry14 |
T |
C |
3: 59,022,992 (GRCm39) |
N165S |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,077,461 (GRCm39) |
E423G |
probably benign |
Het |
Polq |
C |
A |
16: 36,882,515 (GRCm39) |
Q1560K |
possibly damaging |
Het |
Prrc1 |
G |
T |
18: 57,514,718 (GRCm39) |
D312Y |
probably damaging |
Het |
Ptprm |
A |
T |
17: 67,032,846 (GRCm39) |
|
probably null |
Het |
Ripk2 |
A |
T |
4: 16,152,011 (GRCm39) |
S183T |
possibly damaging |
Het |
Robo1 |
T |
A |
16: 72,775,660 (GRCm39) |
F728L |
probably benign |
Het |
Rttn |
A |
G |
18: 89,082,295 (GRCm39) |
N1407S |
probably benign |
Het |
Sec14l1 |
A |
T |
11: 117,047,314 (GRCm39) |
H664L |
probably damaging |
Het |
Slc10a7 |
G |
A |
8: 79,236,264 (GRCm39) |
G21S |
probably benign |
Het |
Slc35a3 |
T |
C |
3: 116,467,285 (GRCm39) |
K325E |
possibly damaging |
Het |
Spag17 |
C |
A |
3: 99,969,182 (GRCm39) |
|
probably null |
Het |
Spesp1 |
A |
T |
9: 62,180,834 (GRCm39) |
L25M |
probably damaging |
Het |
St6galnac1 |
G |
A |
11: 116,658,673 (GRCm39) |
Q264* |
probably null |
Het |
Tbc1d14 |
A |
G |
5: 36,700,561 (GRCm39) |
L269P |
possibly damaging |
Het |
Tgfbr3l |
A |
G |
8: 4,300,506 (GRCm39) |
E228G |
probably benign |
Het |
Tlr5 |
T |
A |
1: 182,802,600 (GRCm39) |
S635T |
possibly damaging |
Het |
Tmem233 |
G |
C |
5: 116,189,517 (GRCm39) |
|
probably benign |
Het |
Tnfsf13b |
A |
T |
8: 10,057,306 (GRCm39) |
R125S |
probably benign |
Het |
Tymp |
A |
T |
15: 89,258,011 (GRCm39) |
V378D |
probably damaging |
Het |
Vmn1r38 |
G |
T |
6: 66,753,433 (GRCm39) |
Q228K |
probably benign |
Het |
Vmn2r18 |
T |
C |
5: 151,510,127 (GRCm39) |
E82G |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,828,229 (GRCm39) |
V1461A |
possibly damaging |
Het |
Xrn1 |
A |
G |
9: 95,888,765 (GRCm39) |
D948G |
possibly damaging |
Het |
Zfp280d |
C |
A |
9: 72,209,052 (GRCm39) |
|
probably benign |
Het |
Zfp418 |
G |
A |
7: 7,185,807 (GRCm39) |
R590K |
probably benign |
Het |
|
Other mutations in Klra10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01505:Klra10
|
APN |
6 |
130,249,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02060:Klra10
|
APN |
6 |
130,249,688 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02249:Klra10
|
APN |
6 |
130,256,367 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02681:Klra10
|
APN |
6 |
130,256,382 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02684:Klra10
|
APN |
6 |
130,258,845 (GRCm39) |
missense |
possibly damaging |
0.85 |
FR4342:Klra10
|
UTSW |
6 |
130,249,710 (GRCm39) |
missense |
probably benign |
0.01 |
R0324:Klra10
|
UTSW |
6 |
130,249,613 (GRCm39) |
splice site |
probably null |
|
R1072:Klra10
|
UTSW |
6 |
130,258,811 (GRCm39) |
missense |
probably benign |
0.11 |
R1466:Klra10
|
UTSW |
6 |
130,256,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Klra10
|
UTSW |
6 |
130,256,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Klra10
|
UTSW |
6 |
130,256,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Klra10
|
UTSW |
6 |
130,256,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Klra10
|
UTSW |
6 |
130,256,241 (GRCm39) |
missense |
probably damaging |
0.98 |
R2427:Klra10
|
UTSW |
6 |
130,256,298 (GRCm39) |
missense |
probably benign |
0.00 |
R4260:Klra10
|
UTSW |
6 |
130,249,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Klra10
|
UTSW |
6 |
130,256,311 (GRCm39) |
missense |
probably benign |
0.00 |
R5897:Klra10
|
UTSW |
6 |
130,258,792 (GRCm39) |
nonsense |
probably null |
|
R6123:Klra10
|
UTSW |
6 |
130,256,339 (GRCm39) |
missense |
probably benign |
0.04 |
R6221:Klra10
|
UTSW |
6 |
130,246,235 (GRCm39) |
missense |
probably benign |
|
R6478:Klra10
|
UTSW |
6 |
130,249,507 (GRCm39) |
splice site |
probably null |
|
R6520:Klra10
|
UTSW |
6 |
130,252,755 (GRCm39) |
missense |
probably benign |
0.03 |
R6551:Klra10
|
UTSW |
6 |
130,252,718 (GRCm39) |
missense |
probably benign |
0.36 |
R7445:Klra10
|
UTSW |
6 |
130,252,819 (GRCm39) |
missense |
probably benign |
0.38 |
R7453:Klra10
|
UTSW |
6 |
130,257,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R7744:Klra10
|
UTSW |
6 |
130,249,724 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8079:Klra10
|
UTSW |
6 |
130,252,738 (GRCm39) |
missense |
probably benign |
|
R8320:Klra10
|
UTSW |
6 |
130,246,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Klra10
|
UTSW |
6 |
130,249,617 (GRCm39) |
critical splice donor site |
probably null |
|
R9419:Klra10
|
UTSW |
6 |
130,256,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9725:Klra10
|
UTSW |
6 |
130,252,849 (GRCm39) |
missense |
probably benign |
|
RF060:Klra10
|
UTSW |
6 |
130,252,784 (GRCm39) |
small deletion |
probably benign |
|
|