Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,772,272 (GRCm39) |
E487G |
probably benign |
Het |
2610021A01Rik |
A |
T |
7: 41,276,009 (GRCm39) |
K571* |
probably null |
Het |
A2m |
T |
C |
6: 121,651,766 (GRCm39) |
V1278A |
probably damaging |
Het |
Abcc2 |
T |
C |
19: 43,806,589 (GRCm39) |
V801A |
probably damaging |
Het |
Acod1 |
T |
A |
14: 103,292,731 (GRCm39) |
D418E |
possibly damaging |
Het |
Bsn |
G |
A |
9: 107,982,572 (GRCm39) |
A3727V |
unknown |
Het |
Cmah |
T |
G |
13: 24,648,267 (GRCm39) |
F501V |
probably damaging |
Het |
Csf2rb2 |
T |
A |
15: 78,176,952 (GRCm39) |
I173L |
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,491,942 (GRCm39) |
W1126R |
probably damaging |
Het |
Dock5 |
G |
T |
14: 68,000,633 (GRCm39) |
A1690E |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,598,472 (GRCm39) |
L1879P |
probably damaging |
Het |
Eif3j2 |
A |
T |
18: 43,610,647 (GRCm39) |
D55E |
probably benign |
Het |
Fus |
G |
A |
7: 127,568,969 (GRCm39) |
G40D |
unknown |
Het |
Glrp1 |
GTGCTGCTGCTGCTGCTGCTGCTGCTG |
GTGCTGCTGCTGCTGCTGCTGCTG |
1: 88,430,997 (GRCm39) |
|
probably benign |
Het |
Gxylt2 |
T |
C |
6: 100,781,576 (GRCm39) |
V417A |
probably damaging |
Het |
Hhipl1 |
G |
A |
12: 108,278,437 (GRCm39) |
R255H |
probably damaging |
Het |
Ints8 |
A |
T |
4: 11,216,477 (GRCm39) |
I838N |
possibly damaging |
Het |
Lama5 |
C |
A |
2: 179,833,097 (GRCm39) |
C1579F |
probably damaging |
Het |
Med13 |
C |
T |
11: 86,210,705 (GRCm39) |
R479H |
probably damaging |
Het |
Or51ag1 |
A |
T |
7: 103,155,309 (GRCm39) |
Y281* |
probably null |
Het |
Or5b113 |
G |
T |
19: 13,342,429 (GRCm39) |
G146C |
possibly damaging |
Het |
Or5k15 |
G |
T |
16: 58,710,381 (GRCm39) |
N67K |
probably damaging |
Het |
Or6e1 |
T |
A |
14: 54,520,155 (GRCm39) |
M66L |
probably benign |
Het |
Or9g3 |
T |
A |
2: 85,589,967 (GRCm39) |
Y251F |
probably benign |
Het |
Pak6 |
A |
G |
2: 118,523,784 (GRCm39) |
E313G |
probably benign |
Het |
Pigs |
T |
A |
11: 78,224,549 (GRCm39) |
Y145N |
probably damaging |
Het |
Pla2g2f |
T |
A |
4: 138,479,662 (GRCm39) |
D165V |
probably benign |
Het |
Plbd1 |
C |
T |
6: 136,618,154 (GRCm39) |
V133M |
probably benign |
Het |
Ppp1r14bl |
C |
T |
1: 23,141,183 (GRCm39) |
G44R |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,675,056 (GRCm39) |
Y1352C |
probably damaging |
Het |
Scamp1 |
C |
T |
13: 94,368,615 (GRCm39) |
R51H |
probably damaging |
Het |
Skic3 |
G |
A |
13: 76,295,886 (GRCm39) |
E1050K |
possibly damaging |
Het |
Slc2a2 |
G |
A |
3: 28,762,756 (GRCm39) |
V100M |
probably damaging |
Het |
Slc38a10 |
C |
G |
11: 119,995,888 (GRCm39) |
A1062P |
probably damaging |
Het |
Snai1 |
T |
C |
2: 167,380,888 (GRCm39) |
I127T |
probably benign |
Het |
Stat4 |
G |
A |
1: 52,144,395 (GRCm39) |
G692D |
probably damaging |
Het |
Stc1 |
A |
T |
14: 69,269,048 (GRCm39) |
D72V |
probably damaging |
Het |
Tmc1 |
T |
C |
19: 20,804,024 (GRCm39) |
N351S |
probably damaging |
Het |
Trim28 |
A |
G |
7: 12,759,275 (GRCm39) |
I130V |
probably benign |
Het |
Trim39 |
A |
G |
17: 36,571,382 (GRCm39) |
Y459H |
probably damaging |
Het |
Ugt1a6b |
C |
A |
1: 88,035,170 (GRCm39) |
Y169* |
probably null |
Het |
Vasp |
T |
C |
7: 18,992,780 (GRCm39) |
|
probably benign |
Het |
Vmn2r99 |
G |
T |
17: 19,598,868 (GRCm39) |
G184V |
probably benign |
Het |
Xrcc1 |
C |
T |
7: 24,266,988 (GRCm39) |
T358I |
probably damaging |
Het |
Zfp219 |
A |
G |
14: 52,247,022 (GRCm39) |
V35A |
probably benign |
Het |
|
Other mutations in Fam83f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02971:Fam83f
|
APN |
15 |
80,556,350 (GRCm39) |
missense |
probably benign |
|
R0212:Fam83f
|
UTSW |
15 |
80,574,779 (GRCm39) |
missense |
probably benign |
0.00 |
R0347:Fam83f
|
UTSW |
15 |
80,556,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R0976:Fam83f
|
UTSW |
15 |
80,576,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1725:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1741:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1796:Fam83f
|
UTSW |
15 |
80,574,283 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1870:Fam83f
|
UTSW |
15 |
80,574,113 (GRCm39) |
splice site |
probably benign |
|
R1899:Fam83f
|
UTSW |
15 |
80,576,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2114:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2115:Fam83f
|
UTSW |
15 |
80,576,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4090:Fam83f
|
UTSW |
15 |
80,576,393 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4865:Fam83f
|
UTSW |
15 |
80,576,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Fam83f
|
UTSW |
15 |
80,576,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Fam83f
|
UTSW |
15 |
80,576,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Fam83f
|
UTSW |
15 |
80,576,312 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7838:Fam83f
|
UTSW |
15 |
80,576,704 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8070:Fam83f
|
UTSW |
15 |
80,556,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Fam83f
|
UTSW |
15 |
80,574,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R9071:Fam83f
|
UTSW |
15 |
80,576,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R9711:Fam83f
|
UTSW |
15 |
80,574,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|