Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
A |
G |
12: 80,215,251 (GRCm39) |
Y842H |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,849,765 (GRCm39) |
|
probably benign |
Het |
Adgrg7 |
A |
T |
16: 56,550,661 (GRCm39) |
Y684N |
probably damaging |
Het |
Aoc1 |
A |
T |
6: 48,885,203 (GRCm39) |
N646I |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,869,054 (GRCm39) |
S37P |
probably benign |
Het |
Bhmt2 |
G |
A |
13: 93,799,839 (GRCm39) |
|
probably benign |
Het |
Bpifb1 |
A |
T |
2: 154,054,966 (GRCm39) |
D286V |
probably damaging |
Het |
Cadps |
T |
A |
14: 12,705,539 (GRCm38) |
E285D |
probably damaging |
Het |
Cap2 |
C |
T |
13: 46,791,317 (GRCm39) |
|
probably benign |
Het |
Clcn4 |
T |
G |
7: 7,293,427 (GRCm39) |
Y443S |
probably damaging |
Het |
Clcn6 |
T |
A |
4: 148,098,740 (GRCm39) |
T463S |
possibly damaging |
Het |
Cmip |
A |
G |
8: 118,174,155 (GRCm39) |
I412V |
possibly damaging |
Het |
Cndp1 |
T |
C |
18: 84,646,938 (GRCm39) |
D250G |
probably damaging |
Het |
Colec10 |
A |
G |
15: 54,325,947 (GRCm39) |
D259G |
probably damaging |
Het |
Ctnna2 |
A |
T |
6: 77,613,827 (GRCm39) |
D254E |
possibly damaging |
Het |
Dlec1 |
T |
C |
9: 118,966,408 (GRCm39) |
Y1126H |
probably damaging |
Het |
Dzank1 |
T |
C |
2: 144,324,147 (GRCm39) |
S565G |
probably benign |
Het |
Eef2k |
A |
G |
7: 120,457,821 (GRCm39) |
Y60C |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,377,074 (GRCm39) |
V170A |
possibly damaging |
Het |
Foxk2 |
T |
A |
11: 121,176,439 (GRCm39) |
I195N |
possibly damaging |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
Gpr6 |
G |
A |
10: 40,947,264 (GRCm39) |
T106M |
probably damaging |
Het |
Grk3 |
T |
A |
5: 113,062,850 (GRCm39) |
N666Y |
possibly damaging |
Het |
Hnmt |
T |
C |
2: 23,893,777 (GRCm39) |
D239G |
probably benign |
Het |
Igf2 |
A |
G |
7: 142,208,044 (GRCm39) |
V111A |
probably benign |
Het |
Lrriq4 |
T |
C |
3: 30,704,422 (GRCm39) |
V150A |
possibly damaging |
Het |
Mroh8 |
A |
G |
2: 157,098,272 (GRCm39) |
V292A |
probably benign |
Het |
Myo1e |
A |
G |
9: 70,232,157 (GRCm39) |
I229V |
probably benign |
Het |
Nisch |
A |
G |
14: 30,898,776 (GRCm39) |
|
probably benign |
Het |
Nkx2-2 |
T |
C |
2: 147,026,154 (GRCm39) |
T195A |
probably benign |
Het |
Or10aa3 |
C |
T |
1: 173,878,683 (GRCm39) |
T248I |
probably benign |
Het |
Or2t47 |
G |
A |
11: 58,442,222 (GRCm39) |
T281I |
possibly damaging |
Het |
Or5p63 |
A |
T |
7: 107,810,949 (GRCm39) |
Y262* |
probably null |
Het |
Or8w1 |
T |
A |
2: 87,465,499 (GRCm39) |
L197F |
probably damaging |
Het |
Plekhn1 |
A |
G |
4: 156,309,207 (GRCm39) |
V233A |
probably damaging |
Het |
Ppp3r1 |
T |
C |
11: 17,144,786 (GRCm39) |
V133A |
probably damaging |
Het |
Sash1 |
T |
C |
10: 8,605,681 (GRCm39) |
D903G |
probably benign |
Het |
Scn8a |
A |
G |
15: 100,937,674 (GRCm39) |
D1681G |
probably damaging |
Het |
Slk |
A |
G |
19: 47,610,809 (GRCm39) |
|
probably null |
Het |
Tasor2 |
T |
C |
13: 3,634,554 (GRCm39) |
D751G |
probably damaging |
Het |
Tlr11 |
C |
T |
14: 50,600,303 (GRCm39) |
T763I |
probably benign |
Het |
Ttbk2 |
T |
C |
2: 120,590,736 (GRCm39) |
T308A |
possibly damaging |
Het |
Tyk2 |
G |
A |
9: 21,027,215 (GRCm39) |
L552F |
probably damaging |
Het |
Ubp1 |
A |
G |
9: 113,773,951 (GRCm39) |
D50G |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ulk4 |
A |
T |
9: 120,873,915 (GRCm39) |
I1172N |
possibly damaging |
Het |
Usf3 |
T |
A |
16: 44,036,528 (GRCm39) |
V336E |
possibly damaging |
Het |
Vangl2 |
T |
C |
1: 171,835,608 (GRCm39) |
S355G |
probably benign |
Het |
Vmn1r216 |
A |
G |
13: 23,284,061 (GRCm39) |
D248G |
probably damaging |
Het |
Vmn1r34 |
T |
A |
6: 66,614,688 (GRCm39) |
M17L |
probably benign |
Het |
Vmn2r120 |
T |
A |
17: 57,843,718 (GRCm39) |
D42V |
possibly damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,445,671 (GRCm39) |
S685T |
possibly damaging |
Het |
Vsig10l |
T |
C |
7: 43,117,510 (GRCm39) |
V701A |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,071,961 (GRCm39) |
|
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,319,544 (GRCm39) |
C258S |
possibly damaging |
Het |
Zfp988 |
A |
C |
4: 147,417,242 (GRCm39) |
K559Q |
probably benign |
Het |
|
Other mutations in Lrriq3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Lrriq3
|
APN |
3 |
154,806,698 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00468:Lrriq3
|
APN |
3 |
154,806,816 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03272:Lrriq3
|
APN |
3 |
154,806,695 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT1430001:Lrriq3
|
UTSW |
3 |
154,804,507 (GRCm39) |
missense |
probably benign |
0.36 |
R0526:Lrriq3
|
UTSW |
3 |
154,893,934 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Lrriq3
|
UTSW |
3 |
154,893,373 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1420:Lrriq3
|
UTSW |
3 |
154,893,349 (GRCm39) |
missense |
probably benign |
|
R2313:Lrriq3
|
UTSW |
3 |
154,869,660 (GRCm39) |
missense |
probably benign |
0.00 |
R4659:Lrriq3
|
UTSW |
3 |
154,835,090 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4801:Lrriq3
|
UTSW |
3 |
154,893,607 (GRCm39) |
missense |
probably benign |
|
R4802:Lrriq3
|
UTSW |
3 |
154,893,607 (GRCm39) |
missense |
probably benign |
|
R4864:Lrriq3
|
UTSW |
3 |
154,893,447 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4998:Lrriq3
|
UTSW |
3 |
154,893,695 (GRCm39) |
missense |
probably benign |
0.13 |
R5120:Lrriq3
|
UTSW |
3 |
154,835,021 (GRCm39) |
missense |
probably benign |
0.14 |
R5319:Lrriq3
|
UTSW |
3 |
154,835,108 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5406:Lrriq3
|
UTSW |
3 |
154,835,138 (GRCm39) |
critical splice donor site |
probably null |
|
R5943:Lrriq3
|
UTSW |
3 |
154,869,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R6184:Lrriq3
|
UTSW |
3 |
154,835,039 (GRCm39) |
missense |
probably benign |
0.09 |
R6572:Lrriq3
|
UTSW |
3 |
154,887,312 (GRCm39) |
missense |
probably benign |
0.01 |
R7389:Lrriq3
|
UTSW |
3 |
154,893,741 (GRCm39) |
missense |
probably benign |
0.00 |
R7537:Lrriq3
|
UTSW |
3 |
154,806,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R7636:Lrriq3
|
UTSW |
3 |
154,893,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R7806:Lrriq3
|
UTSW |
3 |
154,804,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R8038:Lrriq3
|
UTSW |
3 |
154,869,638 (GRCm39) |
missense |
probably benign |
0.03 |
R8361:Lrriq3
|
UTSW |
3 |
154,806,855 (GRCm39) |
nonsense |
probably null |
|
R8439:Lrriq3
|
UTSW |
3 |
154,893,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R8771:Lrriq3
|
UTSW |
3 |
154,899,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Lrriq3
|
UTSW |
3 |
154,893,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Lrriq3
|
UTSW |
3 |
154,893,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9134:Lrriq3
|
UTSW |
3 |
154,820,183 (GRCm39) |
critical splice donor site |
probably null |
|
R9792:Lrriq3
|
UTSW |
3 |
154,893,313 (GRCm39) |
missense |
probably benign |
|
R9793:Lrriq3
|
UTSW |
3 |
154,893,313 (GRCm39) |
missense |
probably benign |
|
R9795:Lrriq3
|
UTSW |
3 |
154,893,313 (GRCm39) |
missense |
probably benign |
|
|