Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
C |
A |
4: 86,166,302 (GRCm39) |
H394N |
probably benign |
Het |
Ahrr |
A |
G |
13: 74,361,826 (GRCm39) |
S558P |
probably benign |
Het |
Ankrd26 |
T |
C |
6: 118,499,919 (GRCm39) |
N1184S |
probably damaging |
Het |
Anpep |
A |
T |
7: 79,476,696 (GRCm39) |
C14* |
probably null |
Het |
Arhgap18 |
A |
G |
10: 26,736,718 (GRCm39) |
D187G |
possibly damaging |
Het |
Arhgef5 |
A |
G |
6: 43,250,337 (GRCm39) |
T363A |
probably benign |
Het |
Atxn1 |
A |
T |
13: 45,720,386 (GRCm39) |
L503Q |
possibly damaging |
Het |
Babam1 |
A |
G |
8: 71,852,277 (GRCm39) |
D155G |
possibly damaging |
Het |
Bbs9 |
A |
G |
9: 22,798,945 (GRCm39) |
T858A |
probably benign |
Het |
Cacna1g |
C |
A |
11: 94,334,157 (GRCm39) |
G828V |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,380,405 (GRCm39) |
T392A |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,289,689 (GRCm39) |
V469A |
possibly damaging |
Het |
Cdh23 |
G |
T |
10: 60,150,110 (GRCm39) |
N2576K |
probably damaging |
Het |
Coro2b |
A |
G |
9: 62,396,705 (GRCm39) |
Y18H |
probably damaging |
Het |
Crispld2 |
G |
T |
8: 120,750,311 (GRCm39) |
K238N |
probably benign |
Het |
Ctnnd2 |
T |
C |
15: 30,922,014 (GRCm39) |
I880T |
probably damaging |
Het |
Cubn |
C |
A |
2: 13,292,472 (GRCm39) |
C3237F |
probably damaging |
Het |
Ddx31 |
A |
G |
2: 28,771,171 (GRCm39) |
M519V |
probably benign |
Het |
Dhx32 |
A |
T |
7: 133,350,753 (GRCm39) |
C106S |
possibly damaging |
Het |
Diaph1 |
A |
G |
18: 38,029,146 (GRCm39) |
|
probably null |
Het |
Dnaaf1 |
T |
C |
8: 120,304,162 (GRCm39) |
F67L |
probably benign |
Het |
Duox1 |
T |
G |
2: 122,175,204 (GRCm39) |
L1334R |
probably damaging |
Het |
Dync1li2 |
A |
T |
8: 105,152,667 (GRCm39) |
I322N |
probably damaging |
Het |
Eml6 |
T |
C |
11: 29,742,256 (GRCm39) |
|
probably null |
Het |
Entpd6 |
A |
G |
2: 150,600,670 (GRCm39) |
Q126R |
probably benign |
Het |
Entpd7 |
C |
G |
19: 43,679,516 (GRCm39) |
P23R |
possibly damaging |
Het |
Epha3 |
T |
C |
16: 63,366,541 (GRCm39) |
I970V |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,861,855 (GRCm39) |
H2163L |
probably damaging |
Het |
Gse1 |
C |
G |
8: 121,294,949 (GRCm39) |
|
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,999,301 (GRCm39) |
V300A |
probably damaging |
Het |
Hsd3b1 |
T |
A |
3: 98,760,214 (GRCm39) |
D259V |
probably damaging |
Het |
Hspbap1 |
T |
C |
16: 35,645,673 (GRCm39) |
S453P |
probably damaging |
Het |
Ifnl3 |
A |
G |
7: 28,223,652 (GRCm39) |
T163A |
probably benign |
Het |
Igbp1b |
T |
A |
6: 138,635,442 (GRCm39) |
M1L |
possibly damaging |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Lpxn |
T |
C |
19: 12,781,456 (GRCm39) |
|
probably null |
Het |
Mast1 |
G |
A |
8: 85,655,238 (GRCm39) |
Q249* |
probably null |
Het |
Mink1 |
A |
G |
11: 70,492,833 (GRCm39) |
D153G |
probably null |
Het |
Mllt10 |
G |
A |
2: 18,097,646 (GRCm39) |
|
probably null |
Het |
Mpl |
C |
T |
4: 118,305,765 (GRCm39) |
G420E |
possibly damaging |
Het |
Ms4a1 |
T |
A |
19: 11,230,557 (GRCm39) |
T215S |
probably benign |
Het |
Ncapd3 |
C |
T |
9: 26,994,656 (GRCm39) |
Q1179* |
probably null |
Het |
Nr3c2 |
A |
G |
8: 77,635,733 (GRCm39) |
H278R |
probably damaging |
Het |
Or10v5 |
T |
C |
19: 11,805,983 (GRCm39) |
I136V |
probably benign |
Het |
Or5b102 |
A |
G |
19: 13,041,639 (GRCm39) |
Y288C |
probably damaging |
Het |
Os9 |
C |
T |
10: 126,934,771 (GRCm39) |
V353M |
probably damaging |
Het |
Osbpl5 |
A |
T |
7: 143,248,817 (GRCm39) |
M589K |
probably benign |
Het |
Phf20 |
G |
T |
2: 156,144,969 (GRCm39) |
G859V |
possibly damaging |
Het |
Pkhd1 |
G |
A |
1: 20,187,625 (GRCm39) |
T3561I |
probably benign |
Het |
Prss46 |
G |
A |
9: 110,679,236 (GRCm39) |
V146I |
probably benign |
Het |
Ptprk |
G |
A |
10: 28,461,626 (GRCm39) |
V1139M |
probably damaging |
Het |
Ranbp10 |
A |
G |
8: 106,500,963 (GRCm39) |
L396P |
probably benign |
Het |
Rb1cc1 |
A |
G |
1: 6,319,958 (GRCm39) |
T1126A |
probably benign |
Het |
Rbl2 |
G |
A |
8: 91,833,045 (GRCm39) |
A659T |
probably benign |
Het |
Rdm1 |
T |
C |
11: 101,524,643 (GRCm39) |
L192P |
probably damaging |
Het |
Reln |
A |
C |
5: 22,239,742 (GRCm39) |
W842G |
probably damaging |
Het |
Scn5a |
C |
T |
9: 119,362,913 (GRCm39) |
R569H |
probably damaging |
Het |
Sele |
A |
G |
1: 163,881,420 (GRCm39) |
K509R |
probably benign |
Het |
Slc15a1 |
A |
T |
14: 121,713,396 (GRCm39) |
I377N |
possibly damaging |
Het |
Slc17a3 |
G |
A |
13: 24,040,483 (GRCm39) |
G269D |
probably damaging |
Het |
Slc35a5 |
T |
C |
16: 44,971,920 (GRCm39) |
T115A |
probably benign |
Het |
Slc5a12 |
T |
G |
2: 110,440,483 (GRCm39) |
N157K |
possibly damaging |
Het |
Sphkap |
A |
G |
1: 83,234,924 (GRCm39) |
V1634A |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,074,919 (GRCm39) |
S2382P |
probably damaging |
Het |
Synj2 |
C |
A |
17: 6,084,194 (GRCm39) |
S1100R |
probably benign |
Het |
Tcf23 |
A |
G |
5: 31,130,901 (GRCm39) |
T180A |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,929,804 (GRCm39) |
V2846A |
probably damaging |
Het |
Tpr |
T |
A |
1: 150,293,751 (GRCm39) |
I915K |
probably damaging |
Het |
Uba1y |
C |
T |
Y: 828,862 (GRCm39) |
H557Y |
probably benign |
Het |
Unc45b |
T |
A |
11: 82,827,700 (GRCm39) |
D730E |
probably benign |
Het |
Unc5b |
A |
T |
10: 60,605,011 (GRCm39) |
L734Q |
probably damaging |
Het |
Vmn1r167 |
G |
T |
7: 23,204,204 (GRCm39) |
H271N |
probably benign |
Het |
Vmn2r76 |
A |
G |
7: 85,879,454 (GRCm39) |
V282A |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,344,283 (GRCm39) |
K2175E |
probably benign |
Het |
|
Other mutations in Or52e18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00978:Or52e18
|
APN |
7 |
104,609,923 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01100:Or52e18
|
APN |
7 |
104,609,202 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01351:Or52e18
|
APN |
7 |
104,609,946 (GRCm39) |
start gained |
probably benign |
|
IGL01478:Or52e18
|
APN |
7 |
104,609,555 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01835:Or52e18
|
APN |
7 |
104,609,669 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02326:Or52e18
|
APN |
7 |
104,609,853 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02434:Or52e18
|
APN |
7 |
104,609,281 (GRCm39) |
nonsense |
probably null |
|
IGL02434:Or52e18
|
APN |
7 |
104,609,279 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02968:Or52e18
|
APN |
7 |
104,609,451 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0055:Or52e18
|
UTSW |
7 |
104,609,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0055:Or52e18
|
UTSW |
7 |
104,609,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0345:Or52e18
|
UTSW |
7 |
104,609,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Or52e18
|
UTSW |
7 |
104,609,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Or52e18
|
UTSW |
7 |
104,609,018 (GRCm39) |
missense |
probably benign |
0.02 |
R1493:Or52e18
|
UTSW |
7 |
104,609,709 (GRCm39) |
missense |
probably damaging |
0.97 |
R1557:Or52e18
|
UTSW |
7 |
104,609,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R4072:Or52e18
|
UTSW |
7 |
104,609,923 (GRCm39) |
missense |
probably damaging |
0.96 |
R4074:Or52e18
|
UTSW |
7 |
104,609,923 (GRCm39) |
missense |
probably damaging |
0.96 |
R4075:Or52e18
|
UTSW |
7 |
104,609,923 (GRCm39) |
missense |
probably damaging |
0.96 |
R4076:Or52e18
|
UTSW |
7 |
104,609,923 (GRCm39) |
missense |
probably damaging |
0.96 |
R4229:Or52e18
|
UTSW |
7 |
104,609,801 (GRCm39) |
missense |
probably benign |
0.18 |
R4230:Or52e18
|
UTSW |
7 |
104,609,801 (GRCm39) |
missense |
probably benign |
0.18 |
R5374:Or52e18
|
UTSW |
7 |
104,609,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6006:Or52e18
|
UTSW |
7 |
104,609,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R6891:Or52e18
|
UTSW |
7 |
104,609,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7465:Or52e18
|
UTSW |
7 |
104,609,124 (GRCm39) |
missense |
probably benign |
0.23 |
R8105:Or52e18
|
UTSW |
7 |
104,609,629 (GRCm39) |
missense |
probably benign |
0.15 |
R8117:Or52e18
|
UTSW |
7 |
104,609,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Or52e18
|
UTSW |
7 |
104,609,934 (GRCm39) |
missense |
probably benign |
0.00 |
R8510:Or52e18
|
UTSW |
7 |
104,609,321 (GRCm39) |
nonsense |
probably null |
|
R9145:Or52e18
|
UTSW |
7 |
104,609,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Or52e18
|
UTSW |
7 |
104,609,001 (GRCm39) |
makesense |
probably null |
|
R9234:Or52e18
|
UTSW |
7 |
104,609,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9706:Or52e18
|
UTSW |
7 |
104,609,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Or52e18
|
UTSW |
7 |
104,609,657 (GRCm39) |
missense |
probably damaging |
0.97 |
|