Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
A |
12: 118,832,404 (GRCm39) |
E1190V |
probably damaging |
Het |
Arhgef10 |
A |
G |
8: 15,029,998 (GRCm39) |
T928A |
probably benign |
Het |
Arhgef10l |
T |
A |
4: 140,242,762 (GRCm39) |
I836F |
probably benign |
Het |
Blm |
T |
A |
7: 80,152,610 (GRCm39) |
T446S |
probably benign |
Het |
Ccdc63 |
T |
A |
5: 122,260,813 (GRCm39) |
Q237L |
probably damaging |
Het |
Ccn5 |
A |
G |
2: 163,670,904 (GRCm39) |
D137G |
probably damaging |
Het |
Cep57l1 |
G |
T |
10: 41,605,356 (GRCm39) |
R130S |
probably damaging |
Het |
Clstn2 |
T |
G |
9: 97,339,613 (GRCm39) |
E786A |
possibly damaging |
Het |
Col16a1 |
C |
T |
4: 129,962,545 (GRCm39) |
P540L |
probably damaging |
Het |
Csf2 |
A |
G |
11: 54,140,159 (GRCm39) |
F61L |
probably damaging |
Het |
Ctr9 |
C |
T |
7: 110,654,750 (GRCm39) |
R1094C |
unknown |
Het |
Cyp3a41a |
A |
G |
5: 145,650,350 (GRCm39) |
C98R |
probably damaging |
Het |
Dthd1 |
T |
A |
5: 62,984,508 (GRCm39) |
C404* |
probably null |
Het |
Egfem1 |
A |
C |
3: 29,740,880 (GRCm39) |
H518P |
probably benign |
Het |
Elf3 |
T |
C |
1: 135,182,015 (GRCm39) |
S369G |
probably benign |
Het |
Eml6 |
C |
T |
11: 29,788,577 (GRCm39) |
V503M |
probably damaging |
Het |
Enthd1 |
T |
C |
15: 80,444,240 (GRCm39) |
D105G |
probably damaging |
Het |
Eral1 |
A |
G |
11: 77,966,428 (GRCm39) |
L250P |
probably damaging |
Het |
Gdf15 |
A |
T |
8: 71,082,605 (GRCm39) |
M167K |
probably benign |
Het |
Ggps1 |
T |
C |
13: 14,228,284 (GRCm39) |
K300E |
probably benign |
Het |
Gm8074 |
G |
A |
9: 78,229,618 (GRCm39) |
|
noncoding transcript |
Het |
Herc3 |
A |
G |
6: 58,853,822 (GRCm39) |
I623V |
probably damaging |
Het |
Mad1l1 |
A |
G |
5: 140,118,571 (GRCm39) |
S457P |
probably damaging |
Het |
Map1lc3a |
G |
T |
2: 155,119,462 (GRCm39) |
V91F |
possibly damaging |
Het |
Map4k3 |
A |
G |
17: 80,913,394 (GRCm39) |
V617A |
probably benign |
Het |
Mov10l1 |
T |
A |
15: 88,879,235 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
A |
G |
1: 88,186,386 (GRCm39) |
S64G |
probably benign |
Het |
Ncor1 |
G |
T |
11: 62,220,494 (GRCm39) |
|
probably null |
Het |
Nfe2 |
C |
T |
15: 103,159,364 (GRCm39) |
E36K |
possibly damaging |
Het |
Oprm1 |
G |
A |
10: 6,779,087 (GRCm39) |
V95I |
probably benign |
Het |
Or4a78 |
T |
C |
2: 89,498,006 (GRCm39) |
I75V |
probably benign |
Het |
Or4c107 |
A |
G |
2: 88,789,617 (GRCm39) |
K269R |
probably benign |
Het |
Or5d46 |
T |
C |
2: 88,174,144 (GRCm39) |
|
probably null |
Het |
Pcdha9 |
T |
A |
18: 37,130,995 (GRCm39) |
H21Q |
probably benign |
Het |
Pcolce2 |
A |
T |
9: 95,520,808 (GRCm39) |
I62F |
probably damaging |
Het |
Pfpl |
T |
A |
19: 12,407,053 (GRCm39) |
C435S |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,361,953 (GRCm39) |
C542Y |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,529,597 (GRCm39) |
S75P |
probably damaging |
Het |
Pphln1 |
C |
A |
15: 93,362,987 (GRCm39) |
A202E |
probably damaging |
Het |
Ppp1r1a |
A |
G |
15: 103,440,881 (GRCm39) |
L92P |
probably damaging |
Het |
Prokr2 |
T |
C |
2: 132,223,414 (GRCm39) |
T43A |
probably benign |
Het |
Rai14 |
T |
C |
15: 10,592,298 (GRCm39) |
N199S |
probably benign |
Het |
Rasgrp2 |
T |
C |
19: 6,454,757 (GRCm39) |
L199P |
probably damaging |
Het |
Rnf213 |
A |
C |
11: 119,373,274 (GRCm39) |
M4939L |
possibly damaging |
Het |
Slc23a2 |
C |
T |
2: 131,902,603 (GRCm39) |
R533Q |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,610,548 (GRCm39) |
|
probably null |
Het |
Snrpd2 |
T |
A |
7: 18,885,232 (GRCm39) |
V31E |
probably damaging |
Het |
Spire1 |
G |
T |
18: 67,662,101 (GRCm39) |
|
probably null |
Het |
Srsf4 |
T |
C |
4: 131,627,854 (GRCm39) |
|
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,737,630 (GRCm39) |
S1274P |
probably damaging |
Het |
Tcof1 |
C |
A |
18: 60,965,975 (GRCm39) |
A376S |
possibly damaging |
Het |
Thsd1 |
T |
A |
8: 22,733,180 (GRCm39) |
Y76N |
possibly damaging |
Het |
Timm44 |
A |
G |
8: 4,310,561 (GRCm39) |
V397A |
probably benign |
Het |
Tmc6 |
G |
A |
11: 117,669,087 (GRCm39) |
T89I |
possibly damaging |
Het |
Trbv31 |
C |
A |
6: 41,534,639 (GRCm39) |
C107F |
probably damaging |
Het |
Trim37 |
T |
A |
11: 87,031,429 (GRCm39) |
|
probably null |
Het |
Ttll5 |
T |
C |
12: 86,059,573 (GRCm39) |
V1226A |
probably benign |
Het |
Ube3b |
T |
C |
5: 114,550,931 (GRCm39) |
V865A |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,282,966 (GRCm39) |
M550K |
probably damaging |
Het |
Vps54 |
C |
A |
11: 21,250,183 (GRCm39) |
T373N |
probably benign |
Het |
Wdr64 |
T |
G |
1: 175,633,422 (GRCm39) |
I891S |
probably benign |
Het |
Zfhx4 |
C |
T |
3: 5,463,919 (GRCm39) |
S1384L |
probably damaging |
Het |
Zfp703 |
A |
G |
8: 27,469,113 (GRCm39) |
E259G |
possibly damaging |
Het |
Zfp933 |
T |
C |
4: 147,910,969 (GRCm39) |
H209R |
probably damaging |
Het |
Zfp980 |
A |
G |
4: 145,429,170 (GRCm39) |
H633R |
probably damaging |
Het |
|
Other mutations in Or52d3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01588:Or52d3
|
APN |
7 |
104,229,150 (GRCm39) |
missense |
probably damaging |
1.00 |
I2288:Or52d3
|
UTSW |
7 |
104,229,593 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Or52d3
|
UTSW |
7 |
104,229,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R0325:Or52d3
|
UTSW |
7 |
104,229,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R1599:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R1956:Or52d3
|
UTSW |
7 |
104,229,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Or52d3
|
UTSW |
7 |
104,228,848 (GRCm39) |
start gained |
probably benign |
|
R2418:Or52d3
|
UTSW |
7 |
104,229,141 (GRCm39) |
missense |
probably benign |
0.00 |
R2483:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R4757:Or52d3
|
UTSW |
7 |
104,229,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4828:Or52d3
|
UTSW |
7 |
104,229,180 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4842:Or52d3
|
UTSW |
7 |
104,229,422 (GRCm39) |
missense |
probably benign |
0.45 |
R5496:Or52d3
|
UTSW |
7 |
104,229,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Or52d3
|
UTSW |
7 |
104,229,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Or52d3
|
UTSW |
7 |
104,229,645 (GRCm39) |
nonsense |
probably null |
|
R7590:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7968:Or52d3
|
UTSW |
7 |
104,229,595 (GRCm39) |
nonsense |
probably null |
|
R8491:Or52d3
|
UTSW |
7 |
104,229,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R9306:Or52d3
|
UTSW |
7 |
104,229,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R9557:Or52d3
|
UTSW |
7 |
104,229,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9682:Or52d3
|
UTSW |
7 |
104,229,434 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Or52d3
|
UTSW |
7 |
104,229,497 (GRCm39) |
missense |
probably benign |
0.00 |
|