Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730071L15Rik |
A |
T |
11: 6,150,161 (GRCm39) |
|
probably benign |
Het |
Abca13 |
A |
T |
11: 9,283,310 (GRCm39) |
N3244I |
probably benign |
Het |
Adgrf5 |
A |
G |
17: 43,748,562 (GRCm39) |
T219A |
probably damaging |
Het |
Adgrg5 |
A |
T |
8: 95,660,649 (GRCm39) |
N92I |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,694 (GRCm39) |
V475G |
probably damaging |
Het |
Akap6 |
A |
G |
12: 52,934,061 (GRCm39) |
K518E |
possibly damaging |
Het |
Apoh |
T |
G |
11: 108,295,697 (GRCm39) |
D133E |
probably benign |
Het |
Axdnd1 |
T |
A |
1: 156,220,319 (GRCm39) |
M234L |
possibly damaging |
Het |
Cacna1d |
A |
G |
14: 29,804,468 (GRCm39) |
I1335T |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cfap206 |
T |
A |
4: 34,711,566 (GRCm39) |
K444* |
probably null |
Het |
Clasp2 |
A |
G |
9: 113,707,832 (GRCm39) |
I614M |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,940,275 (GRCm39) |
D1218E |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,230,753 (GRCm39) |
V1010A |
possibly damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
D130043K22Rik |
C |
T |
13: 25,067,874 (GRCm39) |
T870M |
probably damaging |
Het |
Dagla |
C |
A |
19: 10,225,516 (GRCm39) |
A883S |
probably benign |
Het |
Dhx30 |
A |
G |
9: 109,926,263 (GRCm39) |
V87A |
probably damaging |
Het |
Dtx1 |
C |
A |
5: 120,848,249 (GRCm39) |
V44L |
possibly damaging |
Het |
Ecm2 |
T |
A |
13: 49,683,605 (GRCm39) |
S528T |
possibly damaging |
Het |
Eeig2 |
T |
A |
3: 108,886,164 (GRCm39) |
N356I |
probably benign |
Het |
Egfem1 |
A |
T |
3: 29,637,080 (GRCm39) |
N172I |
probably damaging |
Het |
Fam13a |
T |
G |
6: 58,912,594 (GRCm39) |
R686S |
probably damaging |
Het |
Fam243 |
A |
G |
16: 92,118,207 (GRCm39) |
L27P |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,663,828 (GRCm39) |
I234L |
probably benign |
Het |
Foxj2 |
C |
T |
6: 122,805,331 (GRCm39) |
R68W |
probably damaging |
Het |
Foxo6 |
A |
T |
4: 120,125,961 (GRCm39) |
M278K |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,820,775 (GRCm39) |
S5503G |
probably benign |
Het |
Gdf5 |
C |
G |
2: 155,784,010 (GRCm39) |
R100G |
probably benign |
Het |
Il1b |
A |
T |
2: 129,209,242 (GRCm39) |
D129E |
probably damaging |
Het |
Klhl29 |
A |
G |
12: 5,141,350 (GRCm39) |
S545P |
probably damaging |
Het |
Krt87 |
G |
T |
15: 101,385,708 (GRCm39) |
R296S |
possibly damaging |
Het |
Llgl1 |
T |
G |
11: 60,599,638 (GRCm39) |
S509R |
probably damaging |
Het |
Lmod1 |
A |
T |
1: 135,291,702 (GRCm39) |
K186* |
probably null |
Het |
Lrpprc |
C |
T |
17: 85,034,077 (GRCm39) |
A973T |
probably damaging |
Het |
Marco |
T |
C |
1: 120,422,514 (GRCm39) |
H49R |
possibly damaging |
Het |
Mylk4 |
T |
C |
13: 32,906,001 (GRCm39) |
N394S |
probably null |
Het |
Myo5a |
A |
G |
9: 75,030,322 (GRCm39) |
Y147C |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,059,179 (GRCm39) |
V469A |
probably damaging |
Het |
Myot |
A |
G |
18: 44,470,283 (GRCm39) |
T87A |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,247,312 (GRCm39) |
H2154R |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,999,112 (GRCm38) |
E1037G |
possibly damaging |
Het |
Or1j13 |
T |
C |
2: 36,369,986 (GRCm39) |
D52G |
probably damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,878 (GRCm39) |
T142A |
probably benign |
Het |
Pitrm1 |
G |
T |
13: 6,625,128 (GRCm39) |
V869F |
probably benign |
Het |
Plekhm3 |
CCTGCTGCTGCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGCTGCTGCTGC |
1: 64,976,940 (GRCm39) |
|
probably benign |
Het |
Prdx1 |
T |
G |
4: 116,550,997 (GRCm39) |
I156S |
probably benign |
Het |
Rbks |
T |
A |
5: 31,823,096 (GRCm39) |
T107S |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,506,219 (GRCm39) |
R3468W |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,103,813 (GRCm39) |
D1805N |
probably damaging |
Het |
Sirpa |
T |
C |
2: 129,457,568 (GRCm39) |
V214A |
probably benign |
Het |
Slc35c1 |
T |
C |
2: 92,289,225 (GRCm39) |
N94D |
probably benign |
Het |
Sorbs2 |
A |
T |
8: 46,248,407 (GRCm39) |
K553* |
probably null |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Thg1l |
A |
G |
11: 45,842,392 (GRCm39) |
V142A |
probably benign |
Het |
Tiparp |
T |
A |
3: 65,460,551 (GRCm39) |
Y513* |
probably null |
Het |
Tmc6 |
A |
G |
11: 117,663,646 (GRCm39) |
V522A |
probably benign |
Het |
Trim39 |
T |
A |
17: 36,580,056 (GRCm39) |
|
probably benign |
Het |
Trrap |
G |
A |
5: 144,780,179 (GRCm39) |
|
probably null |
Het |
Tulp3 |
C |
T |
6: 128,304,601 (GRCm39) |
V218I |
probably benign |
Het |
Vmn1r38 |
T |
A |
6: 66,753,955 (GRCm39) |
I54F |
probably benign |
Het |
Vmn2r23 |
T |
A |
6: 123,719,147 (GRCm39) |
Y833* |
probably null |
Het |
Zfp810 |
A |
T |
9: 22,190,534 (GRCm39) |
S125T |
probably benign |
Het |
|
Other mutations in Or5k17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01845:Or5k17
|
APN |
16 |
58,746,929 (GRCm39) |
missense |
probably benign |
|
IGL02477:Or5k17
|
APN |
16 |
58,746,126 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02545:Or5k17
|
APN |
16 |
58,746,833 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02690:Or5k17
|
APN |
16 |
58,746,214 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02718:Or5k17
|
APN |
16 |
58,746,459 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02945:Or5k17
|
APN |
16 |
58,746,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Or5k17
|
APN |
16 |
58,746,323 (GRCm39) |
missense |
probably benign |
0.00 |
B5639:Or5k17
|
UTSW |
16 |
58,746,889 (GRCm39) |
missense |
probably benign |
0.00 |
R0550:Or5k17
|
UTSW |
16 |
58,746,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0659:Or5k17
|
UTSW |
16 |
58,746,772 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1433:Or5k17
|
UTSW |
16 |
58,746,049 (GRCm39) |
missense |
probably benign |
|
R1957:Or5k17
|
UTSW |
16 |
58,746,530 (GRCm39) |
missense |
probably benign |
|
R2155:Or5k17
|
UTSW |
16 |
58,746,486 (GRCm39) |
missense |
probably benign |
0.01 |
R2404:Or5k17
|
UTSW |
16 |
58,745,998 (GRCm39) |
missense |
probably benign |
0.01 |
R4022:Or5k17
|
UTSW |
16 |
58,746,483 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4592:Or5k17
|
UTSW |
16 |
58,746,455 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Or5k17
|
UTSW |
16 |
58,746,053 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4880:Or5k17
|
UTSW |
16 |
58,746,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R5109:Or5k17
|
UTSW |
16 |
58,746,422 (GRCm39) |
missense |
probably benign |
0.10 |
R5231:Or5k17
|
UTSW |
16 |
58,746,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5291:Or5k17
|
UTSW |
16 |
58,746,764 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5477:Or5k17
|
UTSW |
16 |
58,746,393 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5524:Or5k17
|
UTSW |
16 |
58,746,172 (GRCm39) |
missense |
probably benign |
0.00 |
R5809:Or5k17
|
UTSW |
16 |
58,746,860 (GRCm39) |
missense |
probably benign |
|
R5830:Or5k17
|
UTSW |
16 |
58,746,457 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6119:Or5k17
|
UTSW |
16 |
58,746,895 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6217:Or5k17
|
UTSW |
16 |
58,746,877 (GRCm39) |
missense |
probably benign |
0.03 |
R6861:Or5k17
|
UTSW |
16 |
58,746,867 (GRCm39) |
missense |
probably benign |
|
R6939:Or5k17
|
UTSW |
16 |
58,746,648 (GRCm39) |
nonsense |
probably null |
|
R7376:Or5k17
|
UTSW |
16 |
58,746,121 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7650:Or5k17
|
UTSW |
16 |
58,746,416 (GRCm39) |
nonsense |
probably null |
|
R8153:Or5k17
|
UTSW |
16 |
58,746,149 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8947:Or5k17
|
UTSW |
16 |
58,746,433 (GRCm39) |
missense |
probably benign |
|
R9205:Or5k17
|
UTSW |
16 |
58,746,486 (GRCm39) |
missense |
probably benign |
0.01 |
R9205:Or5k17
|
UTSW |
16 |
58,746,485 (GRCm39) |
missense |
probably benign |
0.00 |
R9318:Or5k17
|
UTSW |
16 |
58,746,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9654:Or5k17
|
UTSW |
16 |
58,746,752 (GRCm39) |
missense |
probably benign |
0.00 |
R9678:Or5k17
|
UTSW |
16 |
58,746,640 (GRCm39) |
missense |
probably benign |
0.17 |
|