Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,381,861 (GRCm39) |
I3838V |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,414,537 (GRCm39) |
D1231E |
unknown |
Het |
Atxn1 |
A |
T |
13: 45,710,730 (GRCm39) |
I734K |
probably benign |
Het |
Axin1 |
A |
G |
17: 26,392,708 (GRCm39) |
S330G |
probably damaging |
Het |
Bend3 |
G |
A |
10: 43,369,686 (GRCm39) |
|
probably null |
Het |
Chodl |
C |
T |
16: 78,738,296 (GRCm39) |
T88I |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dst |
A |
G |
1: 34,174,173 (GRCm39) |
I179M |
probably damaging |
Het |
Ehmt2 |
C |
T |
17: 35,118,067 (GRCm39) |
R40* |
probably null |
Het |
Exoc2 |
A |
T |
13: 31,055,901 (GRCm39) |
|
probably null |
Het |
Grk2 |
T |
C |
19: 4,342,799 (GRCm39) |
E45G |
probably damaging |
Het |
Ift81 |
T |
C |
5: 122,745,119 (GRCm39) |
Y144C |
probably damaging |
Het |
Ighv1-15 |
T |
C |
12: 114,620,998 (GRCm39) |
D109G |
probably damaging |
Het |
Igtp |
T |
C |
11: 58,097,959 (GRCm39) |
W377R |
possibly damaging |
Het |
Map2k6 |
A |
G |
11: 110,383,789 (GRCm39) |
D145G |
probably benign |
Het |
Mcph1 |
T |
C |
8: 18,702,596 (GRCm39) |
|
probably benign |
Het |
Mdfi |
A |
G |
17: 48,131,759 (GRCm39) |
V95A |
possibly damaging |
Het |
Mical3 |
A |
G |
6: 120,936,473 (GRCm39) |
L1351P |
possibly damaging |
Het |
Nbas |
C |
T |
12: 13,491,926 (GRCm39) |
Q1506* |
probably null |
Het |
Nelfb |
A |
G |
2: 25,100,757 (GRCm39) |
V128A |
probably benign |
Het |
Otog |
A |
G |
7: 45,938,275 (GRCm39) |
T1995A |
probably benign |
Het |
Ppp1r7 |
A |
T |
1: 93,280,348 (GRCm39) |
I139L |
probably benign |
Het |
Ppp2r1b |
A |
G |
9: 50,768,340 (GRCm39) |
D19G |
probably benign |
Het |
Proca1 |
T |
C |
11: 78,096,078 (GRCm39) |
S150P |
probably damaging |
Het |
Rhof |
A |
G |
5: 123,258,611 (GRCm39) |
V100A |
probably damaging |
Het |
Rsbn1 |
G |
C |
3: 103,821,806 (GRCm39) |
G14R |
probably benign |
Het |
Serinc1 |
A |
G |
10: 57,399,147 (GRCm39) |
I252T |
probably damaging |
Het |
Skint4 |
A |
T |
4: 111,993,203 (GRCm39) |
I309F |
possibly damaging |
Het |
Slc12a3 |
A |
G |
8: 95,078,417 (GRCm39) |
Y815C |
probably damaging |
Het |
Slc25a24 |
A |
G |
3: 109,073,668 (GRCm39) |
S424G |
probably benign |
Het |
Spint2 |
G |
A |
7: 28,963,151 (GRCm39) |
A49V |
probably damaging |
Het |
Traf3ip3 |
T |
A |
1: 192,860,483 (GRCm39) |
K480* |
probably null |
Het |
Ube2g2 |
T |
C |
10: 77,480,379 (GRCm39) |
S162P |
possibly damaging |
Het |
Ubxn8 |
C |
A |
8: 34,131,947 (GRCm39) |
V7L |
possibly damaging |
Het |
Vmn1r200 |
T |
A |
13: 22,579,945 (GRCm39) |
C249* |
probably null |
Het |
Vmn1r38 |
T |
A |
6: 66,753,682 (GRCm39) |
T145S |
probably benign |
Het |
Wapl |
G |
A |
14: 34,455,765 (GRCm39) |
|
probably null |
Het |
Wfdc6a |
T |
C |
2: 164,422,311 (GRCm39) |
N96S |
possibly damaging |
Het |
Zfp503 |
A |
G |
14: 22,035,507 (GRCm39) |
S470P |
probably benign |
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 |
R0906: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 |
|
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 |
|