Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730013G03Rik |
T |
G |
1: 192,515,947 (GRCm39) |
|
noncoding transcript |
Het |
Abcb4 |
G |
A |
5: 9,000,678 (GRCm39) |
V1031M |
probably benign |
Het |
Abcc4 |
A |
G |
14: 118,836,797 (GRCm39) |
S655P |
probably damaging |
Het |
Actn1 |
T |
C |
12: 80,245,820 (GRCm39) |
K121R |
probably damaging |
Het |
Aldh1l2 |
T |
A |
10: 83,358,750 (GRCm39) |
R82* |
probably null |
Het |
Arhgap31 |
T |
A |
16: 38,422,601 (GRCm39) |
H1155L |
possibly damaging |
Het |
Atp8a1 |
G |
T |
5: 68,004,549 (GRCm39) |
P2Q |
probably damaging |
Het |
Bcs1l |
A |
G |
1: 74,631,174 (GRCm39) |
M401V |
possibly damaging |
Het |
Brca2 |
A |
T |
5: 150,465,855 (GRCm39) |
N1873I |
probably damaging |
Het |
Cenpj |
T |
C |
14: 56,789,757 (GRCm39) |
N764S |
probably benign |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Clk1 |
A |
T |
1: 58,452,611 (GRCm39) |
C359S |
possibly damaging |
Het |
Clk2 |
T |
A |
3: 89,083,818 (GRCm39) |
F479I |
probably damaging |
Het |
Cul4b |
T |
C |
X: 37,632,247 (GRCm39) |
M709V |
probably damaging |
Het |
D130052B06Rik |
G |
T |
11: 33,573,620 (GRCm39) |
|
probably null |
Het |
Dgkb |
T |
A |
12: 38,134,233 (GRCm39) |
N46K |
probably damaging |
Het |
Dnah9 |
C |
T |
11: 65,962,882 (GRCm39) |
R1811H |
probably damaging |
Het |
Dnajc18 |
T |
C |
18: 35,813,926 (GRCm39) |
N281S |
probably benign |
Het |
Galnt5 |
A |
T |
2: 57,915,405 (GRCm39) |
I654L |
probably benign |
Het |
Gm9989 |
T |
G |
3: 81,829,518 (GRCm39) |
|
noncoding transcript |
Het |
Gpr179 |
T |
C |
11: 97,228,237 (GRCm39) |
E1306G |
probably benign |
Het |
Gsc |
C |
A |
12: 104,437,864 (GRCm39) |
K219N |
probably damaging |
Het |
Gsx2 |
A |
T |
5: 75,236,452 (GRCm39) |
I11F |
probably damaging |
Het |
Igdcc4 |
A |
C |
9: 65,042,446 (GRCm39) |
E121A |
probably damaging |
Het |
Lama2 |
C |
T |
10: 27,084,425 (GRCm39) |
R915H |
probably benign |
Het |
Large2 |
A |
G |
2: 92,200,984 (GRCm39) |
L64P |
probably damaging |
Het |
Lztr1 |
C |
A |
16: 17,340,317 (GRCm39) |
Q136K |
probably damaging |
Het |
Mageb18 |
A |
G |
X: 91,163,430 (GRCm39) |
W271R |
possibly damaging |
Het |
Magoh |
A |
C |
4: 107,742,203 (GRCm39) |
|
probably benign |
Het |
Matcap2 |
A |
T |
9: 22,346,460 (GRCm39) |
H356L |
probably benign |
Het |
Mrgprx1 |
T |
C |
7: 47,671,234 (GRCm39) |
H171R |
probably benign |
Het |
Muc1 |
C |
A |
3: 89,138,061 (GRCm39) |
T301K |
probably benign |
Het |
Nbas |
C |
T |
12: 13,410,959 (GRCm39) |
L868F |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,963,872 (GRCm39) |
D1152G |
possibly damaging |
Het |
Or7d10 |
G |
A |
9: 19,832,245 (GRCm39) |
V247M |
possibly damaging |
Het |
Ovgp1 |
T |
A |
3: 105,893,488 (GRCm39) |
D420E |
possibly damaging |
Het |
Pacsin3 |
A |
G |
2: 91,094,121 (GRCm39) |
D350G |
probably benign |
Het |
Pcolce2 |
A |
T |
9: 95,574,976 (GRCm39) |
N309Y |
probably damaging |
Het |
Pim2 |
C |
A |
X: 7,744,661 (GRCm39) |
|
probably benign |
Het |
Plcb1 |
A |
G |
2: 134,655,579 (GRCm39) |
Y53C |
probably damaging |
Het |
Pogk |
T |
C |
1: 166,236,047 (GRCm39) |
E18G |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,051,936 (GRCm39) |
D704E |
probably damaging |
Het |
Rb1 |
C |
A |
14: 73,443,310 (GRCm39) |
S781I |
probably damaging |
Het |
Rnpepl1 |
A |
G |
1: 92,843,621 (GRCm39) |
H247R |
possibly damaging |
Het |
Scube1 |
A |
T |
15: 83,497,771 (GRCm39) |
F697I |
probably damaging |
Het |
Sel1l3 |
G |
T |
5: 53,273,675 (GRCm39) |
H1064N |
probably damaging |
Het |
Serinc3 |
A |
G |
2: 163,478,831 (GRCm39) |
Y99H |
probably damaging |
Het |
Slc36a2 |
T |
A |
11: 55,060,673 (GRCm39) |
|
probably benign |
Het |
Smarcc1 |
A |
C |
9: 109,968,693 (GRCm39) |
E130A |
possibly damaging |
Het |
Strc |
A |
G |
2: 121,201,276 (GRCm39) |
M1273T |
probably benign |
Het |
Tmem116 |
A |
G |
5: 121,601,862 (GRCm39) |
I21V |
probably benign |
Het |
Tmem190 |
T |
C |
7: 4,787,025 (GRCm39) |
|
probably benign |
Het |
Trim63 |
C |
T |
4: 134,052,987 (GRCm39) |
A316V |
probably benign |
Het |
Ugt2b34 |
T |
C |
5: 87,049,062 (GRCm39) |
E321G |
probably damaging |
Het |
Zfat |
T |
A |
15: 67,982,353 (GRCm39) |
R1053S |
probably damaging |
Het |
|
Other mutations in Or5p68 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02087:Or5p68
|
APN |
7 |
107,946,173 (GRCm39) |
missense |
probably benign |
|
IGL02484:Or5p68
|
APN |
7 |
107,945,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Or5p68
|
APN |
7 |
107,945,334 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03379:Or5p68
|
APN |
7 |
107,946,196 (GRCm39) |
unclassified |
probably benign |
|
PIT4486001:Or5p68
|
UTSW |
7 |
107,945,529 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0281:Or5p68
|
UTSW |
7 |
107,946,121 (GRCm39) |
missense |
probably benign |
0.00 |
R0285:Or5p68
|
UTSW |
7 |
107,945,706 (GRCm39) |
missense |
probably benign |
0.02 |
R1222:Or5p68
|
UTSW |
7 |
107,945,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Or5p68
|
UTSW |
7 |
107,946,014 (GRCm39) |
missense |
probably damaging |
0.98 |
R4178:Or5p68
|
UTSW |
7 |
107,945,765 (GRCm39) |
missense |
probably benign |
0.00 |
R5239:Or5p68
|
UTSW |
7 |
107,945,853 (GRCm39) |
missense |
probably benign |
0.03 |
R5421:Or5p68
|
UTSW |
7 |
107,946,182 (GRCm39) |
missense |
probably benign |
0.00 |
R5452:Or5p68
|
UTSW |
7 |
107,945,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Or5p68
|
UTSW |
7 |
107,945,295 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7372:Or5p68
|
UTSW |
7 |
107,945,703 (GRCm39) |
missense |
probably benign |
0.00 |
R7374:Or5p68
|
UTSW |
7 |
107,946,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Or5p68
|
UTSW |
7 |
107,945,689 (GRCm39) |
missense |
probably benign |
0.00 |
R8232:Or5p68
|
UTSW |
7 |
107,945,495 (GRCm39) |
missense |
probably damaging |
0.97 |
R8354:Or5p68
|
UTSW |
7 |
107,945,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Or5p68
|
UTSW |
7 |
107,945,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8914:Or5p68
|
UTSW |
7 |
107,945,759 (GRCm39) |
missense |
probably benign |
0.01 |
R9087:Or5p68
|
UTSW |
7 |
107,945,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Or5p68
|
UTSW |
7 |
107,945,886 (GRCm39) |
missense |
probably benign |
0.21 |
R9608:Or5p68
|
UTSW |
7 |
107,945,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Or5p68
|
UTSW |
7 |
107,945,645 (GRCm39) |
missense |
probably benign |
0.02 |
X0025:Or5p68
|
UTSW |
7 |
107,945,808 (GRCm39) |
missense |
probably benign |
0.01 |
|