Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
C |
9: 44,198,627 (GRCm39) |
N42D |
probably damaging |
Het |
Adamdec1 |
G |
A |
14: 68,807,562 (GRCm39) |
T366I |
probably damaging |
Het |
Adamts7 |
C |
A |
9: 90,075,383 (GRCm39) |
H1038Q |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,666,209 (GRCm39) |
D5G |
possibly damaging |
Het |
Amhr2 |
A |
T |
15: 102,362,688 (GRCm39) |
D485V |
probably damaging |
Het |
Arhgap35 |
A |
T |
7: 16,298,663 (GRCm39) |
F134Y |
probably damaging |
Het |
Asxl3 |
A |
G |
18: 22,649,534 (GRCm39) |
T508A |
probably benign |
Het |
Atp10a |
TGGCGGCGGC |
TGGCGGC |
7: 58,308,248 (GRCm39) |
|
probably benign |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
Atp9a |
A |
G |
2: 168,479,592 (GRCm39) |
F928L |
possibly damaging |
Het |
BC034090 |
A |
T |
1: 155,108,221 (GRCm39) |
D13E |
probably damaging |
Het |
Bco1 |
A |
G |
8: 117,855,980 (GRCm39) |
E425G |
probably benign |
Het |
Brsk1 |
T |
C |
7: 4,710,298 (GRCm39) |
S436P |
possibly damaging |
Het |
C1s1 |
T |
C |
6: 124,513,449 (GRCm39) |
I193V |
probably benign |
Het |
Calb2 |
A |
G |
8: 110,894,709 (GRCm39) |
F21L |
probably benign |
Het |
Catsperz |
T |
G |
19: 6,902,171 (GRCm39) |
T108P |
probably benign |
Het |
Cep57l1 |
T |
A |
10: 41,595,767 (GRCm39) |
D329V |
possibly damaging |
Het |
Cfdp1 |
A |
G |
8: 112,557,577 (GRCm39) |
F188S |
probably benign |
Het |
Chrna2 |
G |
A |
14: 66,386,292 (GRCm39) |
G146D |
probably damaging |
Het |
Col6a1 |
A |
C |
10: 76,550,506 (GRCm39) |
F520V |
unknown |
Het |
Cyb5d2 |
C |
A |
11: 72,669,771 (GRCm39) |
V43L |
probably damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,775,290 (GRCm39) |
T321A |
probably benign |
Het |
Dnajc16 |
A |
C |
4: 141,490,859 (GRCm39) |
Y764D |
probably damaging |
Het |
Dsg1a |
G |
A |
18: 20,473,590 (GRCm39) |
V888M |
probably damaging |
Het |
F5 |
A |
C |
1: 164,012,489 (GRCm39) |
T468P |
probably damaging |
Het |
Faap24 |
A |
G |
7: 35,094,509 (GRCm39) |
M97T |
probably benign |
Het |
Fam227b |
A |
T |
2: 125,849,230 (GRCm39) |
I334N |
probably damaging |
Het |
Frem2 |
G |
T |
3: 53,562,864 (GRCm39) |
P548T |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,340,731 (GRCm39) |
E94G |
probably damaging |
Het |
Gm17606 |
A |
T |
14: 54,885,696 (GRCm39) |
|
probably benign |
Het |
Gnb2 |
A |
T |
5: 137,528,515 (GRCm39) |
M1K |
probably null |
Het |
Gys1 |
G |
A |
7: 45,104,258 (GRCm39) |
A544T |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,096,675 (GRCm39) |
Y230C |
probably damaging |
Het |
Hunk |
A |
T |
16: 90,244,196 (GRCm39) |
|
probably null |
Het |
Ifnl2 |
A |
G |
7: 28,209,635 (GRCm39) |
F51L |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,387,892 (GRCm39) |
|
probably null |
Het |
Kcnj1 |
A |
G |
9: 32,307,918 (GRCm39) |
Y114C |
probably benign |
Het |
Kdm4b |
T |
A |
17: 56,706,459 (GRCm39) |
S322T |
probably damaging |
Het |
Kif27 |
T |
C |
13: 58,471,730 (GRCm39) |
E786G |
probably damaging |
Het |
Kif6 |
T |
C |
17: 50,060,909 (GRCm39) |
V414A |
probably benign |
Het |
L1td1 |
A |
G |
4: 98,621,861 (GRCm39) |
K141R |
possibly damaging |
Het |
Loxhd1 |
A |
G |
18: 77,490,581 (GRCm39) |
I1394V |
possibly damaging |
Het |
Lrfn5 |
A |
T |
12: 61,886,433 (GRCm39) |
M74L |
probably damaging |
Het |
Lrp6 |
C |
T |
6: 134,488,230 (GRCm39) |
D289N |
probably benign |
Het |
Mroh7 |
A |
G |
4: 106,548,710 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
C |
16: 32,589,651 (GRCm39) |
E2885A |
possibly damaging |
Het |
Myo18b |
G |
T |
5: 113,023,041 (GRCm39) |
|
probably benign |
Het |
Ncln |
G |
A |
10: 81,328,902 (GRCm39) |
A172V |
probably damaging |
Het |
Nek9 |
G |
A |
12: 85,367,666 (GRCm39) |
T335M |
possibly damaging |
Het |
Notch2 |
A |
G |
3: 98,042,829 (GRCm39) |
Y1398C |
probably damaging |
Het |
Or2d4 |
T |
A |
7: 106,544,074 (GRCm39) |
I45F |
probably damaging |
Het |
Or5p52 |
A |
T |
7: 107,502,188 (GRCm39) |
H88L |
probably benign |
Het |
Pax2 |
G |
A |
19: 44,749,376 (GRCm39) |
V40M |
probably damaging |
Het |
Pde6c |
A |
G |
19: 38,157,887 (GRCm39) |
Y637C |
probably damaging |
Het |
Plppr5 |
A |
G |
3: 117,414,618 (GRCm39) |
I80V |
probably damaging |
Het |
Pold1 |
G |
T |
7: 44,182,233 (GRCm39) |
P1100T |
probably damaging |
Het |
Prune2 |
T |
C |
19: 16,977,387 (GRCm39) |
Y41H |
probably damaging |
Het |
Rgl2 |
C |
T |
17: 34,152,200 (GRCm39) |
A329V |
possibly damaging |
Het |
Rilp |
T |
A |
11: 75,402,250 (GRCm39) |
Y250N |
probably damaging |
Het |
Rilpl1 |
A |
G |
5: 124,652,751 (GRCm39) |
V19A |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,519 (GRCm39) |
|
probably null |
Het |
Rufy4 |
A |
G |
1: 74,172,266 (GRCm39) |
K246E |
probably damaging |
Het |
Saraf |
C |
A |
8: 34,635,616 (GRCm39) |
A306E |
probably damaging |
Het |
Slc26a8 |
A |
T |
17: 28,857,658 (GRCm39) |
N828K |
probably benign |
Het |
Src |
C |
T |
2: 157,311,852 (GRCm39) |
P527S |
probably damaging |
Het |
Susd3 |
C |
T |
13: 49,384,778 (GRCm39) |
|
probably null |
Het |
Syngap1 |
T |
C |
17: 27,185,880 (GRCm39) |
L1270P |
probably damaging |
Het |
Taf1c |
G |
A |
8: 120,325,589 (GRCm39) |
P758S |
probably damaging |
Het |
Tenm2 |
A |
T |
11: 35,915,275 (GRCm39) |
N2087K |
probably damaging |
Het |
Tfrc |
A |
T |
16: 32,448,969 (GRCm39) |
I703F |
probably damaging |
Het |
Thap1 |
C |
G |
8: 26,650,874 (GRCm39) |
T48S |
probably benign |
Het |
Tspear |
T |
C |
10: 77,702,163 (GRCm39) |
F199L |
probably benign |
Het |
Usp17lc |
A |
T |
7: 103,067,797 (GRCm39) |
H364L |
probably benign |
Het |
Usp9x |
A |
G |
X: 12,989,747 (GRCm39) |
R776G |
possibly damaging |
Homo |
Vmn1r1 |
T |
C |
1: 181,984,789 (GRCm39) |
E292G |
possibly damaging |
Het |
Vmn1r125 |
T |
G |
7: 21,006,552 (GRCm39) |
V150G |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,117 (GRCm39) |
L300I |
probably damaging |
Het |
Vmn2r106 |
A |
C |
17: 20,487,885 (GRCm39) |
I838S |
probably benign |
Het |
Wdr64 |
A |
T |
1: 175,554,060 (GRCm39) |
S197C |
probably damaging |
Het |
Zfp248 |
A |
T |
6: 118,410,268 (GRCm39) |
V47E |
possibly damaging |
Het |
|
Other mutations in Or10g6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01481:Or10g6
|
APN |
9 |
39,934,574 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02089:Or10g6
|
APN |
9 |
39,934,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R0722:Or10g6
|
UTSW |
9 |
39,934,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1117:Or10g6
|
UTSW |
9 |
39,934,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R1781:Or10g6
|
UTSW |
9 |
39,934,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Or10g6
|
UTSW |
9 |
39,934,151 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1893:Or10g6
|
UTSW |
9 |
39,934,270 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1942:Or10g6
|
UTSW |
9 |
39,934,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Or10g6
|
UTSW |
9 |
39,934,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Or10g6
|
UTSW |
9 |
39,933,985 (GRCm39) |
missense |
probably benign |
|
R2000:Or10g6
|
UTSW |
9 |
39,933,985 (GRCm39) |
missense |
probably benign |
|
R2173:Or10g6
|
UTSW |
9 |
39,934,550 (GRCm39) |
missense |
probably damaging |
0.97 |
R2760:Or10g6
|
UTSW |
9 |
39,933,692 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R4300:Or10g6
|
UTSW |
9 |
39,934,435 (GRCm39) |
missense |
probably benign |
0.02 |
R4530:Or10g6
|
UTSW |
9 |
39,934,589 (GRCm39) |
missense |
probably benign |
|
R4614:Or10g6
|
UTSW |
9 |
39,934,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Or10g6
|
UTSW |
9 |
39,933,994 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5017:Or10g6
|
UTSW |
9 |
39,933,672 (GRCm39) |
start gained |
probably benign |
|
R5065:Or10g6
|
UTSW |
9 |
39,934,546 (GRCm39) |
missense |
probably benign |
0.44 |
R5467:Or10g6
|
UTSW |
9 |
39,933,733 (GRCm39) |
missense |
probably benign |
0.00 |
R5668:Or10g6
|
UTSW |
9 |
39,933,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Or10g6
|
UTSW |
9 |
39,933,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6432:Or10g6
|
UTSW |
9 |
39,933,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6620:Or10g6
|
UTSW |
9 |
39,934,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Or10g6
|
UTSW |
9 |
39,933,896 (GRCm39) |
nonsense |
probably null |
|
R7156:Or10g6
|
UTSW |
9 |
39,934,526 (GRCm39) |
missense |
probably benign |
0.23 |
R7250:Or10g6
|
UTSW |
9 |
39,934,050 (GRCm39) |
nonsense |
probably null |
|
R7273:Or10g6
|
UTSW |
9 |
39,933,961 (GRCm39) |
missense |
probably benign |
0.04 |
R8006:Or10g6
|
UTSW |
9 |
39,933,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R8701:Or10g6
|
UTSW |
9 |
39,933,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8835:Or10g6
|
UTSW |
9 |
39,934,171 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9497:Or10g6
|
UTSW |
9 |
39,934,616 (GRCm39) |
missense |
probably benign |
|
R9733:Or10g6
|
UTSW |
9 |
39,934,171 (GRCm39) |
missense |
probably benign |
0.00 |
|