Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
T |
A |
1: 130,665,430 (GRCm39) |
|
probably benign |
Het |
Atp7b |
T |
C |
8: 22,517,842 (GRCm39) |
H332R |
probably benign |
Het |
Bace2 |
C |
T |
16: 97,158,141 (GRCm39) |
P47L |
possibly damaging |
Het |
Cyp2c39 |
A |
G |
19: 39,499,315 (GRCm39) |
M1V |
probably null |
Het |
Dcbld2 |
A |
G |
16: 58,275,610 (GRCm39) |
E442G |
probably damaging |
Het |
Gm14496 |
A |
G |
2: 181,642,308 (GRCm39) |
T660A |
probably damaging |
Het |
Gm4945 |
A |
C |
17: 47,353,796 (GRCm39) |
|
noncoding transcript |
Het |
Gm6729 |
T |
C |
10: 86,376,456 (GRCm39) |
|
noncoding transcript |
Het |
Golga1 |
G |
A |
2: 38,937,655 (GRCm39) |
R204W |
probably damaging |
Het |
Guf1 |
T |
C |
5: 69,723,729 (GRCm39) |
I348T |
probably damaging |
Het |
Htra4 |
T |
A |
8: 25,527,160 (GRCm39) |
I212L |
probably benign |
Het |
Itih5 |
G |
A |
2: 10,253,999 (GRCm39) |
R750Q |
probably benign |
Het |
Lgalsl2 |
T |
C |
7: 5,362,828 (GRCm39) |
I153T |
probably damaging |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Nsd1 |
T |
C |
13: 55,425,403 (GRCm39) |
V1520A |
probably benign |
Het |
Nuak1 |
C |
T |
10: 84,211,144 (GRCm39) |
V315I |
probably damaging |
Het |
Nup205 |
G |
T |
6: 35,213,827 (GRCm39) |
G1740C |
probably damaging |
Het |
Or1r1 |
G |
C |
11: 73,874,685 (GRCm39) |
L250V |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,726,700 (GRCm39) |
|
probably benign |
Het |
Pik3r6 |
T |
C |
11: 68,426,927 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,292,556 (GRCm39) |
F1336I |
probably damaging |
Het |
Pla2r1 |
A |
G |
2: 60,345,291 (GRCm39) |
I355T |
possibly damaging |
Het |
Rgs22 |
A |
T |
15: 36,104,048 (GRCm39) |
|
probably benign |
Het |
Sec63 |
T |
A |
10: 42,677,924 (GRCm39) |
M312K |
probably damaging |
Het |
Slc2a5 |
T |
C |
4: 150,227,287 (GRCm39) |
I401T |
probably benign |
Het |
Slc9a8 |
G |
T |
2: 167,276,787 (GRCm39) |
|
probably benign |
Het |
Stab1 |
T |
C |
14: 30,867,206 (GRCm39) |
E1718G |
probably benign |
Het |
Terb1 |
A |
T |
8: 105,179,268 (GRCm39) |
I640N |
probably damaging |
Het |
Tmem217 |
A |
G |
17: 29,745,490 (GRCm39) |
L80P |
probably damaging |
Het |
Topbp1 |
C |
T |
9: 103,205,792 (GRCm39) |
P810L |
probably benign |
Het |
Ttbk2 |
G |
A |
2: 120,614,262 (GRCm39) |
R151C |
probably damaging |
Het |
Vmn2r88 |
T |
G |
14: 51,655,666 (GRCm39) |
L626R |
probably damaging |
Het |
|
Other mutations in Lgr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02481:Lgr6
|
APN |
1 |
134,929,429 (GRCm39) |
splice site |
probably benign |
|
IGL02483:Lgr6
|
APN |
1 |
134,929,429 (GRCm39) |
splice site |
probably benign |
|
IGL03270:Lgr6
|
APN |
1 |
134,925,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0294:Lgr6
|
UTSW |
1 |
135,032,799 (GRCm39) |
missense |
unknown |
|
R0294:Lgr6
|
UTSW |
1 |
134,915,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R0361:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0742:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Lgr6
|
UTSW |
1 |
134,921,624 (GRCm39) |
missense |
probably benign |
0.04 |
R0903:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0904:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Lgr6
|
UTSW |
1 |
134,921,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1079:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1131:Lgr6
|
UTSW |
1 |
134,915,042 (GRCm39) |
missense |
probably damaging |
0.98 |
R1440:Lgr6
|
UTSW |
1 |
134,915,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Lgr6
|
UTSW |
1 |
135,032,670 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1728:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1728:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1728:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1729:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1729:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1739:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1739:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1739:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1762:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1762:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1762:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1782:Lgr6
|
UTSW |
1 |
134,915,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R1783:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1783:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1783:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1783:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1784:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1784:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1785:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1785:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1785:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R2020:Lgr6
|
UTSW |
1 |
135,003,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R3104:Lgr6
|
UTSW |
1 |
134,928,210 (GRCm39) |
splice site |
probably null |
|
R4629:Lgr6
|
UTSW |
1 |
135,032,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R4792:Lgr6
|
UTSW |
1 |
134,949,544 (GRCm39) |
missense |
probably benign |
0.03 |
R5001:Lgr6
|
UTSW |
1 |
134,918,370 (GRCm39) |
missense |
probably benign |
0.01 |
R5191:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5194:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5196:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5197:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Lgr6
|
UTSW |
1 |
135,037,010 (GRCm39) |
unclassified |
probably benign |
|
R5299:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5300:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5417:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5419:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5601:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5603:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Lgr6
|
UTSW |
1 |
134,914,816 (GRCm39) |
missense |
probably benign |
0.28 |
R5699:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5748:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5971:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6078:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6079:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6138:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6740:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6871:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Lgr6
|
UTSW |
1 |
134,915,740 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6986:Lgr6
|
UTSW |
1 |
134,921,694 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7233:Lgr6
|
UTSW |
1 |
134,928,214 (GRCm39) |
critical splice donor site |
probably null |
|
R7699:Lgr6
|
UTSW |
1 |
134,923,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Lgr6
|
UTSW |
1 |
134,923,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7734:Lgr6
|
UTSW |
1 |
134,930,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Lgr6
|
UTSW |
1 |
134,915,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7970:Lgr6
|
UTSW |
1 |
134,921,723 (GRCm39) |
missense |
probably benign |
|
R8068:Lgr6
|
UTSW |
1 |
134,991,402 (GRCm39) |
missense |
probably benign |
0.00 |
R8252:Lgr6
|
UTSW |
1 |
134,931,215 (GRCm39) |
missense |
probably null |
0.78 |
R8516:Lgr6
|
UTSW |
1 |
135,003,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R8771:Lgr6
|
UTSW |
1 |
134,933,429 (GRCm39) |
nonsense |
probably null |
|
R8858:Lgr6
|
UTSW |
1 |
134,923,849 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8885:Lgr6
|
UTSW |
1 |
134,915,342 (GRCm39) |
missense |
probably benign |
0.00 |
R9014:Lgr6
|
UTSW |
1 |
134,931,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Lgr6
|
UTSW |
1 |
134,915,217 (GRCm39) |
nonsense |
probably null |
|
R9660:Lgr6
|
UTSW |
1 |
134,915,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Lgr6
|
UTSW |
1 |
134,915,245 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lgr6
|
UTSW |
1 |
134,915,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1191:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|