Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
T |
6: 128,527,746 (GRCm39) |
S1015T |
probably damaging |
Het |
Adamts10 |
T |
A |
17: 33,770,406 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
G |
A |
13: 81,711,685 (GRCm39) |
T1097I |
probably damaging |
Het |
Apeh |
T |
C |
9: 107,969,302 (GRCm39) |
Y274C |
possibly damaging |
Het |
Apobec3 |
A |
G |
15: 79,782,068 (GRCm39) |
D26G |
possibly damaging |
Het |
Arg2 |
C |
T |
12: 79,196,794 (GRCm39) |
Q172* |
probably null |
Het |
Asb18 |
C |
T |
1: 89,942,104 (GRCm39) |
V66I |
probably benign |
Het |
Cacna1i |
G |
A |
15: 80,243,132 (GRCm39) |
G430S |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,449,802 (GRCm38) |
S1136P |
possibly damaging |
Het |
Cadps |
A |
G |
14: 12,505,796 (GRCm38) |
V758A |
probably benign |
Het |
Calhm3 |
A |
G |
19: 47,140,539 (GRCm39) |
W185R |
probably damaging |
Het |
Car5b |
T |
C |
X: 162,774,369 (GRCm39) |
D146G |
probably damaging |
Het |
Card10 |
G |
A |
15: 78,664,714 (GRCm39) |
R747W |
probably damaging |
Het |
Cd300lg |
T |
G |
11: 101,932,430 (GRCm39) |
V5G |
probably damaging |
Het |
Cd46 |
C |
A |
1: 194,765,931 (GRCm39) |
G145C |
probably damaging |
Het |
Chit1 |
T |
C |
1: 134,078,988 (GRCm39) |
S433P |
probably damaging |
Het |
Cntrl |
G |
A |
2: 35,008,131 (GRCm39) |
E182K |
possibly damaging |
Het |
Col6a5 |
T |
A |
9: 105,817,400 (GRCm39) |
M304L |
unknown |
Het |
Cplane1 |
A |
G |
15: 8,258,077 (GRCm39) |
I2108V |
probably benign |
Het |
Cpxm2 |
C |
T |
7: 131,745,392 (GRCm39) |
|
probably null |
Het |
Dbf4 |
G |
A |
5: 8,447,375 (GRCm39) |
Q612* |
probably null |
Het |
Dnah11 |
G |
C |
12: 118,027,587 (GRCm39) |
Q1835E |
possibly damaging |
Het |
Ehbp1l1 |
A |
T |
19: 5,767,882 (GRCm39) |
N1140K |
probably benign |
Het |
Eps8l1 |
C |
A |
7: 4,468,359 (GRCm39) |
|
probably benign |
Het |
Fbxl21 |
A |
T |
13: 56,674,876 (GRCm39) |
I76L |
probably benign |
Het |
Gcnt2 |
A |
T |
13: 41,014,577 (GRCm39) |
K249N |
possibly damaging |
Het |
Gm5819 |
A |
G |
18: 8,694,179 (GRCm39) |
T35A |
probably benign |
Het |
Gm8180 |
T |
C |
14: 44,021,139 (GRCm39) |
E23G |
probably benign |
Het |
Gorab |
A |
G |
1: 163,231,131 (GRCm39) |
F8L |
probably damaging |
Het |
Hlf |
A |
G |
11: 90,231,652 (GRCm39) |
L274S |
probably damaging |
Het |
Il15ra |
T |
A |
2: 11,728,247 (GRCm39) |
S137T |
possibly damaging |
Het |
Krt78 |
A |
T |
15: 101,855,004 (GRCm39) |
C936S |
possibly damaging |
Het |
Lamb2 |
T |
C |
9: 108,358,583 (GRCm39) |
S207P |
probably benign |
Het |
Lce1a1 |
T |
C |
3: 92,554,118 (GRCm39) |
S119G |
unknown |
Het |
Lipo3 |
A |
G |
19: 33,762,092 (GRCm39) |
F135S |
probably damaging |
Het |
Lrp4 |
T |
A |
2: 91,328,708 (GRCm39) |
L1536Q |
probably benign |
Het |
Lrrc25 |
T |
C |
8: 71,070,596 (GRCm39) |
S126P |
possibly damaging |
Het |
Mbd3l2 |
T |
C |
9: 18,356,217 (GRCm39) |
S181P |
possibly damaging |
Het |
Msantd5f6 |
A |
T |
4: 73,320,037 (GRCm39) |
Y247* |
probably null |
Het |
Mss51 |
C |
T |
14: 20,534,936 (GRCm39) |
R278H |
probably damaging |
Het |
Myom3 |
G |
A |
4: 135,505,348 (GRCm39) |
M412I |
probably benign |
Het |
Naa25 |
T |
C |
5: 121,573,611 (GRCm39) |
V780A |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,437,067 (GRCm39) |
F485L |
probably benign |
Het |
Notch1 |
T |
C |
2: 26,359,962 (GRCm39) |
Y1251C |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,115,609 (GRCm39) |
N826D |
probably damaging |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Or2t47 |
T |
C |
11: 58,442,849 (GRCm39) |
Y72C |
probably benign |
Het |
Or4a74 |
A |
T |
2: 89,440,053 (GRCm39) |
L131* |
probably null |
Het |
Or4c35 |
A |
T |
2: 89,808,754 (GRCm39) |
I211F |
probably benign |
Het |
Or5p57 |
A |
C |
7: 107,665,932 (GRCm39) |
Y24* |
probably null |
Het |
Or8c8 |
T |
G |
9: 38,165,016 (GRCm39) |
M101R |
probably damaging |
Het |
Or8s16 |
G |
T |
15: 98,211,372 (GRCm39) |
Q20K |
probably benign |
Het |
Osbpl6 |
G |
A |
2: 76,415,402 (GRCm39) |
R588H |
probably damaging |
Het |
Pcdhb17 |
A |
T |
18: 37,619,164 (GRCm39) |
D318V |
probably benign |
Het |
Pcnx2 |
T |
A |
8: 126,545,525 (GRCm39) |
E1162V |
probably damaging |
Het |
Pde2a |
G |
A |
7: 101,160,361 (GRCm39) |
R845H |
probably damaging |
Het |
Pkhd1 |
G |
T |
1: 20,621,244 (GRCm39) |
R805S |
probably benign |
Het |
Ppl |
T |
C |
16: 4,905,844 (GRCm39) |
K1484E |
possibly damaging |
Het |
Pramel7 |
T |
C |
2: 87,321,675 (GRCm39) |
E120G |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,336,420 (GRCm39) |
D60V |
probably damaging |
Het |
Prpf6 |
T |
A |
2: 181,249,967 (GRCm39) |
D42E |
possibly damaging |
Het |
Rbm5 |
C |
T |
9: 107,627,718 (GRCm39) |
V408I |
possibly damaging |
Het |
Rsrp1 |
G |
T |
4: 134,651,388 (GRCm39) |
D51Y |
unknown |
Het |
Sec22a |
A |
G |
16: 35,168,088 (GRCm39) |
M141T |
probably damaging |
Het |
Spryd3 |
A |
G |
15: 102,026,094 (GRCm39) |
S417P |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,782,713 (GRCm39) |
M550V |
possibly damaging |
Het |
Sugt1 |
C |
T |
14: 79,846,434 (GRCm39) |
T157I |
probably damaging |
Het |
Syne4 |
T |
C |
7: 30,016,308 (GRCm39) |
V168A |
probably benign |
Het |
Tas2r122 |
A |
T |
6: 132,688,065 (GRCm39) |
L276* |
probably null |
Het |
Tbc1d14 |
G |
A |
5: 36,665,037 (GRCm39) |
S231F |
probably damaging |
Het |
Tenm3 |
T |
A |
8: 48,729,381 (GRCm39) |
I1526F |
probably benign |
Het |
Tgm2 |
C |
T |
2: 157,966,139 (GRCm39) |
C505Y |
probably damaging |
Het |
Thop1 |
T |
C |
10: 80,909,151 (GRCm39) |
Y61H |
probably damaging |
Het |
Ticam1 |
G |
A |
17: 56,578,436 (GRCm39) |
H220Y |
probably damaging |
Het |
Tle6 |
T |
C |
10: 81,427,755 (GRCm39) |
D500G |
possibly damaging |
Het |
Tm6sf2 |
T |
A |
8: 70,532,375 (GRCm39) |
L345Q |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,889,848 (GRCm39) |
C114R |
probably damaging |
Het |
Topors |
G |
T |
4: 40,262,149 (GRCm39) |
C378* |
probably null |
Het |
Ttc6 |
G |
A |
12: 57,760,881 (GRCm39) |
G1544R |
probably benign |
Het |
Vmn2r4 |
A |
T |
3: 64,314,410 (GRCm39) |
N190K |
probably benign |
Het |
Wdr70 |
C |
A |
15: 7,950,054 (GRCm39) |
V447F |
probably benign |
Het |
Xpa |
A |
G |
4: 46,155,730 (GRCm39) |
|
probably benign |
Het |
Xrcc1 |
T |
C |
7: 24,270,000 (GRCm39) |
S474P |
possibly damaging |
Het |
Zfp658 |
T |
G |
7: 43,223,323 (GRCm39) |
F533V |
possibly damaging |
Het |
Zfp799 |
G |
A |
17: 33,038,374 (GRCm39) |
H631Y |
probably damaging |
Het |
|
Other mutations in Or6c66 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01093:Or6c66
|
APN |
10 |
129,461,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02866:Or6c66
|
APN |
10 |
129,461,575 (GRCm39) |
nonsense |
probably null |
|
BB009:Or6c66
|
UTSW |
10 |
129,461,094 (GRCm39) |
missense |
probably damaging |
0.97 |
BB019:Or6c66
|
UTSW |
10 |
129,461,094 (GRCm39) |
missense |
probably damaging |
0.97 |
R0743:Or6c66
|
UTSW |
10 |
129,461,712 (GRCm39) |
missense |
probably benign |
0.03 |
R1163:Or6c66
|
UTSW |
10 |
129,461,516 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1192:Or6c66
|
UTSW |
10 |
129,461,906 (GRCm39) |
missense |
probably benign |
|
R1867:Or6c66
|
UTSW |
10 |
129,461,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Or6c66
|
UTSW |
10 |
129,461,784 (GRCm39) |
missense |
probably benign |
|
R4898:Or6c66
|
UTSW |
10 |
129,461,468 (GRCm39) |
missense |
probably benign |
0.12 |
R4910:Or6c66
|
UTSW |
10 |
129,461,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R4988:Or6c66
|
UTSW |
10 |
129,461,930 (GRCm39) |
splice site |
probably null |
|
R5361:Or6c66
|
UTSW |
10 |
129,461,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Or6c66
|
UTSW |
10 |
129,461,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R5589:Or6c66
|
UTSW |
10 |
129,461,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Or6c66
|
UTSW |
10 |
129,461,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R5790:Or6c66
|
UTSW |
10 |
129,461,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Or6c66
|
UTSW |
10 |
129,461,633 (GRCm39) |
missense |
probably benign |
0.17 |
R7041:Or6c66
|
UTSW |
10 |
129,461,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Or6c66
|
UTSW |
10 |
129,461,634 (GRCm39) |
missense |
probably benign |
0.07 |
R7932:Or6c66
|
UTSW |
10 |
129,461,094 (GRCm39) |
missense |
probably damaging |
0.97 |
R7977:Or6c66
|
UTSW |
10 |
129,461,838 (GRCm39) |
missense |
probably benign |
|
R7987:Or6c66
|
UTSW |
10 |
129,461,838 (GRCm39) |
missense |
probably benign |
|
R8299:Or6c66
|
UTSW |
10 |
129,461,829 (GRCm39) |
missense |
probably benign |
0.00 |
R8487:Or6c66
|
UTSW |
10 |
129,461,114 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9110:Or6c66
|
UTSW |
10 |
129,461,820 (GRCm39) |
missense |
possibly damaging |
0.88 |
|