Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
G |
8: 73,209,199 (GRCm39) |
E443G |
probably damaging |
Het |
2700049A03Rik |
A |
G |
12: 71,263,004 (GRCm39) |
|
probably null |
Het |
3110082I17Rik |
A |
G |
5: 139,349,738 (GRCm39) |
Y104H |
probably damaging |
Het |
Abcg4 |
T |
C |
9: 44,190,681 (GRCm39) |
K282E |
probably benign |
Het |
Adamts17 |
T |
C |
7: 66,770,758 (GRCm39) |
S956P |
probably damaging |
Het |
Adh1 |
T |
C |
3: 137,986,235 (GRCm39) |
V74A |
probably damaging |
Het |
Akt1 |
A |
T |
12: 112,626,083 (GRCm39) |
M63K |
probably benign |
Het |
Arfrp1 |
G |
A |
2: 181,001,344 (GRCm39) |
R177* |
probably null |
Het |
Arl11 |
A |
G |
14: 61,548,346 (GRCm39) |
E52G |
possibly damaging |
Het |
BC051019 |
T |
C |
7: 109,319,825 (GRCm39) |
S10G |
|
Het |
Bfsp2 |
T |
A |
9: 103,357,118 (GRCm39) |
E103V |
probably damaging |
Het |
Bms1 |
G |
T |
6: 118,380,122 (GRCm39) |
C728* |
probably null |
Het |
Cachd1 |
T |
G |
4: 100,775,263 (GRCm39) |
N159K |
probably null |
Het |
Cd38 |
A |
G |
5: 44,067,651 (GRCm39) |
N294S |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,852,433 (GRCm39) |
N891S |
probably benign |
Het |
Chsy3 |
A |
T |
18: 59,543,370 (GRCm39) |
H836L |
probably damaging |
Het |
Cldn16 |
A |
T |
16: 26,301,388 (GRCm39) |
D232V |
probably damaging |
Het |
Dhx33 |
A |
T |
11: 70,884,689 (GRCm39) |
I425N |
probably damaging |
Het |
Dock4 |
A |
G |
12: 40,878,878 (GRCm39) |
N1506D |
probably damaging |
Het |
Dok7 |
T |
C |
5: 35,236,392 (GRCm39) |
S227P |
probably damaging |
Het |
Elf2 |
T |
C |
3: 51,168,432 (GRCm39) |
R201G |
probably damaging |
Het |
Elp1 |
T |
C |
4: 56,787,944 (GRCm39) |
H329R |
probably damaging |
Het |
Etaa1 |
T |
C |
11: 17,890,339 (GRCm39) |
R841G |
possibly damaging |
Het |
Exoc4 |
T |
C |
6: 33,948,934 (GRCm39) |
Y926H |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,929,143 (GRCm39) |
H3849R |
probably benign |
Het |
Hapln3 |
C |
T |
7: 78,771,572 (GRCm39) |
G106R |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,452,961 (GRCm39) |
|
probably null |
Het |
Ifitm7 |
A |
T |
16: 13,801,600 (GRCm39) |
I53N |
possibly damaging |
Het |
Il6ra |
T |
C |
3: 89,778,554 (GRCm39) |
N433D |
probably damaging |
Het |
Iqch |
C |
T |
9: 63,329,191 (GRCm39) |
V1048I |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,765,588 (GRCm39) |
T862A |
probably benign |
Het |
Mcrs1 |
G |
A |
15: 99,146,609 (GRCm39) |
L141F |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,017 (GRCm39) |
S324P |
probably damaging |
Het |
Nmi |
A |
T |
2: 51,845,936 (GRCm39) |
|
probably null |
Het |
Nufip1 |
A |
G |
14: 76,372,325 (GRCm39) |
K480E |
possibly damaging |
Het |
Oit3 |
T |
A |
10: 59,264,166 (GRCm39) |
I323F |
probably damaging |
Het |
Or5b98 |
A |
T |
19: 12,931,478 (GRCm39) |
H175L |
possibly damaging |
Het |
Pcdha11 |
A |
G |
18: 37,140,291 (GRCm39) |
E640G |
probably benign |
Het |
Phip |
C |
T |
9: 82,759,353 (GRCm39) |
V1366I |
probably damaging |
Het |
Plin5 |
T |
C |
17: 56,422,174 (GRCm39) |
M162V |
probably null |
Het |
Podxl2 |
A |
G |
6: 88,820,487 (GRCm39) |
|
probably null |
Het |
Ptprb |
GAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT |
GAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACTGCAAAGACCCTCGGGAGCACT |
10: 116,119,582 (GRCm39) |
|
probably benign |
Het |
Rab4a |
A |
T |
8: 124,554,069 (GRCm39) |
D40V |
probably benign |
Het |
Scn7a |
A |
G |
2: 66,530,537 (GRCm39) |
F603L |
probably benign |
Het |
Slfn5 |
A |
T |
11: 82,851,976 (GRCm39) |
K701* |
probably null |
Het |
Speer4f2 |
A |
G |
5: 17,582,446 (GRCm39) |
D223G |
|
Het |
Stip1 |
C |
T |
19: 6,999,178 (GRCm39) |
G467S |
possibly damaging |
Het |
Tas2r117 |
A |
T |
6: 132,780,350 (GRCm39) |
T163S |
probably benign |
Het |
Tecta |
T |
C |
9: 42,259,287 (GRCm39) |
D1532G |
probably damaging |
Het |
Tmem63a |
T |
C |
1: 180,782,441 (GRCm39) |
I146T |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,646,515 (GRCm39) |
G12844W |
probably damaging |
Het |
Usp22 |
T |
C |
11: 61,053,775 (GRCm39) |
I190V |
probably damaging |
Het |
Usp24 |
T |
C |
4: 106,219,412 (GRCm39) |
I536T |
probably damaging |
Het |
Vmn1r23 |
A |
G |
6: 57,903,061 (GRCm39) |
V239A |
possibly damaging |
Het |
Vmn1r9 |
A |
C |
6: 57,048,611 (GRCm39) |
T229P |
probably damaging |
Het |
Zbtb21 |
AGCTGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGC |
AGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGC |
16: 97,752,887 (GRCm39) |
|
probably benign |
Het |
Zbtb8a |
G |
C |
4: 129,254,188 (GRCm39) |
A102G |
probably damaging |
Het |
Zfp51 |
T |
C |
17: 21,681,971 (GRCm39) |
W57R |
probably damaging |
Het |
|
Other mutations in Or2ag17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Or2ag17
|
APN |
7 |
106,389,796 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02093:Or2ag17
|
APN |
7 |
106,390,030 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02404:Or2ag17
|
APN |
7 |
106,389,566 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03214:Or2ag17
|
APN |
7 |
106,389,552 (GRCm39) |
missense |
probably benign |
|
IGL03230:Or2ag17
|
APN |
7 |
106,389,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Or2ag17
|
UTSW |
7 |
106,390,030 (GRCm39) |
missense |
probably benign |
0.12 |
R0523:Or2ag17
|
UTSW |
7 |
106,389,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Or2ag17
|
UTSW |
7 |
106,389,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1373:Or2ag17
|
UTSW |
7 |
106,389,963 (GRCm39) |
missense |
probably benign |
0.01 |
R1482:Or2ag17
|
UTSW |
7 |
106,389,540 (GRCm39) |
missense |
probably benign |
0.00 |
R1498:Or2ag17
|
UTSW |
7 |
106,389,623 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1500:Or2ag17
|
UTSW |
7 |
106,390,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Or2ag17
|
UTSW |
7 |
106,389,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R4163:Or2ag17
|
UTSW |
7 |
106,389,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4638:Or2ag17
|
UTSW |
7 |
106,390,205 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5104:Or2ag17
|
UTSW |
7 |
106,389,539 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6216:Or2ag17
|
UTSW |
7 |
106,389,665 (GRCm39) |
missense |
probably benign |
0.23 |
R6976:Or2ag17
|
UTSW |
7 |
106,389,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R7130:Or2ag17
|
UTSW |
7 |
106,389,389 (GRCm39) |
missense |
probably benign |
0.35 |
R8104:Or2ag17
|
UTSW |
7 |
106,390,338 (GRCm39) |
start gained |
probably benign |
|
R8104:Or2ag17
|
UTSW |
7 |
106,390,337 (GRCm39) |
start gained |
probably benign |
|
R9057:Or2ag17
|
UTSW |
7 |
106,389,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R9445:Or2ag17
|
UTSW |
7 |
106,389,464 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or2ag17
|
UTSW |
7 |
106,389,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|