Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
A |
6: 121,645,575 (GRCm39) |
W1040* |
probably null |
Het |
Adgrv1 |
C |
A |
13: 81,627,789 (GRCm39) |
A3691S |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,295 (GRCm39) |
Y345* |
probably null |
Het |
Aplp2 |
A |
T |
9: 31,069,823 (GRCm39) |
Y496* |
probably null |
Het |
Ash1l |
T |
C |
3: 88,979,855 (GRCm39) |
V2793A |
probably damaging |
Het |
Bfsp1 |
A |
T |
2: 143,668,853 (GRCm39) |
D575E |
probably benign |
Het |
Ceacam20 |
G |
T |
7: 19,704,332 (GRCm39) |
V128F |
probably benign |
Het |
Cers4 |
A |
T |
8: 4,570,306 (GRCm39) |
K204* |
probably null |
Het |
Cog1 |
T |
C |
11: 113,544,852 (GRCm39) |
Y345H |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,312,272 (GRCm39) |
|
probably benign |
Het |
Col19a1 |
A |
T |
1: 24,351,453 (GRCm39) |
|
probably null |
Het |
Ctnnd2 |
T |
A |
15: 30,966,914 (GRCm39) |
M955K |
probably damaging |
Het |
Cyp3a16 |
A |
T |
5: 145,388,652 (GRCm39) |
M275K |
probably damaging |
Het |
Degs2 |
T |
G |
12: 108,658,254 (GRCm39) |
T242P |
probably damaging |
Het |
Elac2 |
T |
C |
11: 64,890,001 (GRCm39) |
V612A |
probably benign |
Het |
Elovl6 |
T |
A |
3: 129,398,733 (GRCm39) |
F45I |
probably damaging |
Het |
Exoc1 |
A |
C |
5: 76,693,193 (GRCm39) |
N360H |
probably damaging |
Het |
Fam221b |
A |
T |
4: 43,666,309 (GRCm39) |
S101T |
possibly damaging |
Het |
Garre1 |
A |
T |
7: 33,955,909 (GRCm39) |
N393K |
probably damaging |
Het |
Glyr1 |
A |
G |
16: 4,854,812 (GRCm39) |
F89L |
probably benign |
Het |
Herc4 |
C |
A |
10: 63,142,203 (GRCm39) |
T668K |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,525,874 (GRCm39) |
V259I |
possibly damaging |
Het |
Hp1bp3 |
T |
A |
4: 137,967,983 (GRCm39) |
D397E |
probably damaging |
Het |
Ift80 |
G |
T |
3: 68,805,869 (GRCm39) |
D724E |
probably benign |
Het |
Igkv3-10 |
T |
C |
6: 70,550,223 (GRCm39) |
|
probably benign |
Het |
Irf9 |
G |
T |
14: 55,842,678 (GRCm39) |
A75S |
possibly damaging |
Het |
Kif13a |
C |
T |
13: 46,938,769 (GRCm39) |
V76M |
probably damaging |
Het |
Krt4 |
T |
C |
15: 101,829,740 (GRCm39) |
I263V |
probably benign |
Het |
Lgals8 |
A |
G |
13: 12,469,699 (GRCm39) |
W87R |
probably benign |
Het |
Mccc2 |
G |
A |
13: 100,127,816 (GRCm39) |
P96L |
probably damaging |
Het |
Megf11 |
A |
C |
9: 64,587,531 (GRCm39) |
D443A |
probably damaging |
Het |
Nckap5l |
T |
C |
15: 99,321,008 (GRCm39) |
|
probably benign |
Het |
Ndor1 |
A |
G |
2: 25,139,281 (GRCm39) |
V230A |
probably benign |
Het |
Nif3l1 |
G |
T |
1: 58,496,956 (GRCm39) |
V294L |
possibly damaging |
Het |
Pcdhb13 |
T |
A |
18: 37,576,128 (GRCm39) |
Y169N |
probably damaging |
Het |
Peg3 |
A |
G |
7: 6,710,635 (GRCm39) |
I1529T |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,279,915 (GRCm39) |
I219F |
probably damaging |
Het |
Prpf38a |
G |
A |
4: 108,424,836 (GRCm39) |
R242W |
unknown |
Het |
Prrc2a |
A |
T |
17: 35,379,480 (GRCm39) |
D255E |
unknown |
Het |
Rapgef6 |
G |
T |
11: 54,567,181 (GRCm39) |
D1121Y |
possibly damaging |
Het |
Ryr3 |
T |
A |
2: 112,585,303 (GRCm39) |
H2761L |
probably damaging |
Het |
Sel1l |
A |
T |
12: 91,810,042 (GRCm39) |
|
probably benign |
Het |
Slc30a9 |
A |
G |
5: 67,510,065 (GRCm39) |
D539G |
probably damaging |
Het |
Slc38a9 |
A |
G |
13: 112,826,777 (GRCm39) |
S172G |
probably benign |
Het |
Slfn2 |
C |
A |
11: 82,960,402 (GRCm39) |
T127K |
probably benign |
Het |
Smurf1 |
A |
T |
5: 144,821,534 (GRCm39) |
M496K |
probably damaging |
Het |
Srgap2 |
A |
T |
1: 131,247,340 (GRCm39) |
V564D |
probably damaging |
Het |
Stk32a |
T |
C |
18: 43,430,576 (GRCm39) |
I162T |
probably benign |
Het |
Tchhl1 |
A |
T |
3: 93,378,634 (GRCm39) |
N446I |
possibly damaging |
Het |
Tmem64 |
T |
A |
4: 15,266,584 (GRCm39) |
H211Q |
probably damaging |
Het |
Trim3 |
T |
C |
7: 105,262,218 (GRCm39) |
N586S |
probably benign |
Het |
Trpm1 |
A |
G |
7: 63,868,869 (GRCm39) |
E507G |
probably damaging |
Het |
Tyk2 |
G |
T |
9: 21,020,523 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
A |
T |
15: 9,365,316 (GRCm39) |
K310* |
probably null |
Het |
Unc13a |
T |
A |
8: 72,101,586 (GRCm39) |
N1022Y |
probably damaging |
Het |
Vmn1r172 |
A |
T |
7: 23,359,228 (GRCm39) |
N38Y |
probably damaging |
Het |
Vmn2r100 |
A |
T |
17: 19,741,770 (GRCm39) |
I161F |
probably damaging |
Het |
Zcchc17 |
A |
G |
4: 130,243,108 (GRCm39) |
M25T |
probably benign |
Het |
Zfp563 |
G |
A |
17: 33,323,795 (GRCm39) |
R130Q |
probably benign |
Het |
Zhx2 |
A |
G |
15: 57,686,802 (GRCm39) |
S724G |
probably benign |
Het |
|
Other mutations in Or4k39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01328:Or4k39
|
APN |
2 |
111,239,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01819:Or4k39
|
APN |
2 |
111,239,078 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02109:Or4k39
|
APN |
2 |
111,238,838 (GRCm39) |
exon |
noncoding transcript |
|
R0054:Or4k39
|
UTSW |
2 |
111,239,140 (GRCm39) |
missense |
probably benign |
0.00 |
R1665:Or4k39
|
UTSW |
2 |
111,239,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Or4k39
|
UTSW |
2 |
111,239,534 (GRCm39) |
missense |
probably benign |
0.36 |
R3876:Or4k39
|
UTSW |
2 |
111,238,967 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4260:Or4k39
|
UTSW |
2 |
111,238,850 (GRCm39) |
exon |
noncoding transcript |
|
R4439:Or4k39
|
UTSW |
2 |
111,239,653 (GRCm39) |
exon |
noncoding transcript |
|
R4762:Or4k39
|
UTSW |
2 |
111,239,225 (GRCm39) |
exon |
noncoding transcript |
|
R4821:Or4k39
|
UTSW |
2 |
111,239,570 (GRCm39) |
exon |
noncoding transcript |
|
R5120:Or4k39
|
UTSW |
2 |
111,239,585 (GRCm39) |
exon |
noncoding transcript |
|
R5215:Or4k39
|
UTSW |
2 |
111,239,631 (GRCm39) |
exon |
noncoding transcript |
|
R5244:Or4k39
|
UTSW |
2 |
111,238,899 (GRCm39) |
exon |
noncoding transcript |
|
R5667:Or4k39
|
UTSW |
2 |
111,238,818 (GRCm39) |
exon |
noncoding transcript |
|
R5671:Or4k39
|
UTSW |
2 |
111,238,818 (GRCm39) |
exon |
noncoding transcript |
|
R5687:Or4k39
|
UTSW |
2 |
111,239,033 (GRCm39) |
exon |
noncoding transcript |
|
|