Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
A |
T |
10: 79,841,995 (GRCm39) |
T1043S |
probably benign |
Het |
Acadvl |
T |
A |
11: 69,902,554 (GRCm39) |
K410* |
probably null |
Het |
Adam8 |
C |
T |
7: 139,567,762 (GRCm39) |
G354D |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,590,175 (GRCm39) |
E1366G |
possibly damaging |
Het |
Bahcc1 |
C |
A |
11: 120,165,415 (GRCm39) |
Q949K |
probably benign |
Het |
Bsn |
G |
A |
9: 107,988,651 (GRCm39) |
A2367V |
probably benign |
Het |
Ccdc141 |
T |
A |
2: 76,889,894 (GRCm39) |
Y466F |
possibly damaging |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Cyp4a30b |
C |
A |
4: 115,314,972 (GRCm39) |
Q185K |
probably benign |
Het |
Dlx2 |
A |
T |
2: 71,375,882 (GRCm39) |
I147K |
possibly damaging |
Het |
Dnaaf6rt |
T |
A |
1: 31,262,349 (GRCm39) |
D110E |
probably damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,612,621 (GRCm39) |
L482S |
probably damaging |
Het |
Dnah8 |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
17: 30,979,841 (GRCm39) |
|
probably null |
Het |
Dock7 |
C |
A |
4: 98,971,266 (GRCm39) |
V100F |
|
Het |
Dspp |
C |
A |
5: 104,325,162 (GRCm39) |
D508E |
unknown |
Het |
Duox2 |
G |
T |
2: 122,128,636 (GRCm39) |
T4K |
probably benign |
Het |
Ear1 |
T |
C |
14: 44,056,704 (GRCm39) |
N55D |
probably damaging |
Het |
Echdc1 |
G |
C |
10: 29,210,242 (GRCm39) |
E179Q |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,046,109 (GRCm39) |
M547V |
possibly damaging |
Het |
Erbb2 |
A |
G |
11: 98,319,798 (GRCm39) |
N630S |
possibly damaging |
Het |
Fam227a |
G |
A |
15: 79,514,271 (GRCm39) |
S363L |
possibly damaging |
Het |
Fam98b |
A |
G |
2: 117,101,381 (GRCm39) |
R398G |
unknown |
Het |
Fsip2 |
G |
A |
2: 82,807,430 (GRCm39) |
D1250N |
probably benign |
Het |
Gdnf |
G |
T |
15: 7,864,134 (GRCm39) |
E182* |
probably null |
Het |
Gys2 |
T |
C |
6: 142,406,921 (GRCm39) |
H145R |
probably benign |
Het |
Hcls1 |
A |
G |
16: 36,767,003 (GRCm39) |
K69R |
probably benign |
Het |
Itih5 |
A |
G |
2: 10,239,869 (GRCm39) |
N332S |
probably benign |
Het |
Kcnb2 |
T |
A |
1: 15,382,934 (GRCm39) |
Y87N |
probably damaging |
Het |
Lsg1 |
A |
T |
16: 30,380,569 (GRCm39) |
W623R |
probably damaging |
Het |
Myo10 |
A |
G |
15: 25,725,158 (GRCm39) |
Y243C |
probably benign |
Het |
Nans |
T |
C |
4: 46,492,814 (GRCm39) |
Y81H |
probably damaging |
Het |
Nup54 |
T |
G |
5: 92,573,605 (GRCm39) |
N199T |
probably benign |
Het |
Or2h1 |
A |
G |
17: 37,404,664 (GRCm39) |
L34P |
probably damaging |
Het |
Or4c126 |
C |
T |
2: 89,824,348 (GRCm39) |
L204F |
probably benign |
Het |
Or4k15 |
T |
C |
14: 50,364,604 (GRCm39) |
I190T |
probably benign |
Het |
Or5w13 |
A |
T |
2: 87,524,088 (GRCm39) |
I46N |
probably damaging |
Het |
Or7d9 |
T |
A |
9: 20,197,337 (GRCm39) |
L122* |
probably null |
Het |
Pcnt |
G |
A |
10: 76,256,039 (GRCm39) |
R734W |
probably damaging |
Het |
Peg10 |
T |
C |
6: 4,755,462 (GRCm39) |
F13L |
possibly damaging |
Het |
Plcb1 |
T |
C |
2: 135,091,972 (GRCm39) |
|
probably null |
Het |
Ppfibp1 |
T |
C |
6: 146,902,448 (GRCm39) |
V285A |
possibly damaging |
Het |
Prpf39 |
T |
C |
12: 65,102,036 (GRCm39) |
V371A |
possibly damaging |
Het |
Psmb11 |
G |
A |
14: 54,863,013 (GRCm39) |
C77Y |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,797,053 (GRCm39) |
L1133P |
probably benign |
Het |
Slc16a1 |
G |
T |
3: 104,560,149 (GRCm39) |
M151I |
probably benign |
Het |
Tarm1 |
G |
T |
7: 3,546,037 (GRCm39) |
Q89K |
possibly damaging |
Het |
Tas2r116 |
T |
C |
6: 132,832,540 (GRCm39) |
I47T |
probably damaging |
Het |
Tmod3 |
T |
C |
9: 75,436,680 (GRCm39) |
D85G |
probably damaging |
Het |
Trbv14 |
T |
C |
6: 41,112,299 (GRCm39) |
L32P |
probably benign |
Het |
Trim16 |
T |
C |
11: 62,741,414 (GRCm39) |
L486P |
probably benign |
Het |
Trmt1l |
T |
G |
1: 151,325,727 (GRCm39) |
S391A |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,582,254 (GRCm39) |
N3772K |
probably damaging |
Het |
Vmn1r230 |
G |
T |
17: 21,066,870 (GRCm39) |
A20S |
probably benign |
Het |
Wdr76 |
A |
G |
2: 121,341,179 (GRCm39) |
N75D |
possibly damaging |
Het |
Zfp977 |
A |
G |
7: 42,230,102 (GRCm39) |
L141S |
probably benign |
Het |
Zfp988 |
A |
G |
4: 147,416,808 (GRCm39) |
D414G |
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 |
R4024:Lrriq3
|
UTSW |
3 |
154,893,939 (GRCm39) |
missense |
probably benign |
0.43 |
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 |
|
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 |
|
|