Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adad2 |
T |
C |
8: 120,342,708 (GRCm39) |
V418A |
probably benign |
Het |
Adamts16 |
T |
C |
13: 70,901,345 (GRCm39) |
T911A |
probably benign |
Het |
Adgra1 |
T |
C |
7: 139,427,619 (GRCm39) |
F62S |
possibly damaging |
Het |
Adgra3 |
A |
G |
5: 50,159,272 (GRCm39) |
V326A |
probably damaging |
Het |
Adgrg6 |
A |
G |
10: 14,316,114 (GRCm39) |
F569S |
probably benign |
Het |
Alcam |
T |
C |
16: 52,130,261 (GRCm39) |
T30A |
probably null |
Het |
Arnt2 |
G |
A |
7: 83,924,655 (GRCm39) |
R391W |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,576,196 (GRCm39) |
V817A |
probably damaging |
Het |
Atp13a4 |
G |
T |
16: 29,232,567 (GRCm39) |
T923K |
probably damaging |
Het |
Atp5po |
C |
T |
16: 91,725,794 (GRCm39) |
R64H |
probably damaging |
Het |
Ccdc185 |
T |
G |
1: 182,576,313 (GRCm39) |
Q125H |
possibly damaging |
Het |
Ccdc88a |
T |
A |
11: 29,436,006 (GRCm39) |
C10S |
probably damaging |
Het |
Cct2 |
T |
C |
10: 116,897,968 (GRCm39) |
N73S |
probably benign |
Het |
Clock |
G |
A |
5: 76,377,401 (GRCm39) |
Q633* |
probably null |
Het |
Col6a2 |
T |
C |
10: 76,439,193 (GRCm39) |
I826V |
probably benign |
Het |
Cpsf1 |
G |
T |
15: 76,485,981 (GRCm39) |
Y396* |
probably null |
Het |
Dnah1 |
A |
T |
14: 30,991,774 (GRCm39) |
M3076K |
possibly damaging |
Het |
Dxo |
A |
G |
17: 35,057,825 (GRCm39) |
N177D |
probably damaging |
Het |
Fbxw28 |
A |
T |
9: 109,167,472 (GRCm39) |
V95E |
possibly damaging |
Het |
Galnt6 |
T |
C |
15: 100,597,018 (GRCm39) |
N383D |
probably damaging |
Het |
Gpat2 |
G |
A |
2: 127,270,211 (GRCm39) |
V75M |
probably damaging |
Het |
Grik5 |
T |
C |
7: 24,762,397 (GRCm39) |
D198G |
probably benign |
Het |
Gsdmc4 |
A |
G |
15: 63,763,895 (GRCm39) |
S401P |
probably benign |
Het |
Gspt1 |
A |
T |
16: 11,047,109 (GRCm39) |
D435E |
probably damaging |
Het |
Hsf2 |
T |
C |
10: 57,381,378 (GRCm39) |
S266P |
probably damaging |
Het |
Jade2 |
T |
C |
11: 51,708,050 (GRCm39) |
D721G |
probably benign |
Het |
Klhl7 |
G |
T |
5: 24,343,319 (GRCm39) |
V212L |
probably damaging |
Het |
Klra17 |
T |
A |
6: 129,851,809 (GRCm39) |
N21I |
probably damaging |
Het |
L3mbtl3 |
T |
C |
10: 26,215,197 (GRCm39) |
N196S |
unknown |
Het |
Lama3 |
G |
C |
18: 12,546,915 (GRCm39) |
|
probably null |
Het |
Mcm5 |
T |
C |
8: 75,848,272 (GRCm39) |
M507T |
possibly damaging |
Het |
Mycbp2 |
T |
C |
14: 103,372,553 (GRCm39) |
R814G |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,449,456 (GRCm39) |
E186G |
probably damaging |
Het |
Nlrp4c |
A |
G |
7: 6,095,569 (GRCm39) |
K816E |
possibly damaging |
Het |
Nod1 |
G |
T |
6: 54,921,902 (GRCm39) |
R139S |
probably benign |
Het |
Nudcd1 |
T |
C |
15: 44,284,207 (GRCm39) |
M60V |
probably benign |
Het |
Or5b101 |
G |
C |
19: 13,005,411 (GRCm39) |
A94G |
probably benign |
Het |
Or5p63 |
G |
A |
7: 107,811,490 (GRCm39) |
P82L |
possibly damaging |
Het |
Or8g28 |
G |
T |
9: 39,169,897 (GRCm39) |
Q24K |
possibly damaging |
Het |
Ovol2 |
A |
G |
2: 144,159,796 (GRCm39) |
S82P |
probably benign |
Het |
Ppl |
T |
C |
16: 4,925,381 (GRCm39) |
E86G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ripk4 |
T |
C |
16: 97,545,157 (GRCm39) |
T497A |
probably benign |
Het |
Scml4 |
A |
G |
10: 42,833,667 (GRCm39) |
Y327C |
probably damaging |
Het |
Serpina3n |
A |
G |
12: 104,377,536 (GRCm39) |
E263G |
possibly damaging |
Het |
Six4 |
A |
G |
12: 73,159,657 (GRCm39) |
F101S |
probably damaging |
Het |
Sltm |
T |
G |
9: 70,493,240 (GRCm39) |
L728V |
probably damaging |
Het |
Sptb |
T |
G |
12: 76,657,589 (GRCm39) |
K1311Q |
possibly damaging |
Het |
Sycp1 |
T |
C |
3: 102,748,357 (GRCm39) |
K812E |
possibly damaging |
Het |
Tenm4 |
T |
C |
7: 96,501,737 (GRCm39) |
Y1314H |
probably damaging |
Het |
Tmem67 |
A |
T |
4: 12,073,952 (GRCm39) |
M288K |
probably benign |
Het |
Toporsl |
T |
C |
4: 52,610,970 (GRCm39) |
S288P |
probably benign |
Het |
Ttn |
A |
C |
2: 76,772,749 (GRCm39) |
N2415K |
possibly damaging |
Het |
Vmn2r65 |
T |
C |
7: 84,595,896 (GRCm39) |
I263V |
probably benign |
Het |
Vmn2r89 |
A |
T |
14: 51,693,628 (GRCm39) |
E326V |
probably damaging |
Het |
Wdr81 |
A |
G |
11: 75,343,758 (GRCm39) |
I503T |
probably damaging |
Het |
|
Other mutations in Or5p69 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Or5p69
|
APN |
7 |
107,967,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Or5p69
|
APN |
7 |
107,967,368 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Or5p69
|
APN |
7 |
107,966,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Or5p69
|
APN |
7 |
107,967,261 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02902:Or5p69
|
APN |
7 |
107,967,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Or5p69
|
UTSW |
7 |
107,967,576 (GRCm39) |
missense |
probably damaging |
0.98 |
R0523:Or5p69
|
UTSW |
7 |
107,967,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Or5p69
|
UTSW |
7 |
107,966,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1268:Or5p69
|
UTSW |
7 |
107,967,002 (GRCm39) |
missense |
probably benign |
0.06 |
R2036:Or5p69
|
UTSW |
7 |
107,966,947 (GRCm39) |
missense |
probably benign |
0.00 |
R2162:Or5p69
|
UTSW |
7 |
107,966,769 (GRCm39) |
missense |
probably benign |
0.08 |
R2278:Or5p69
|
UTSW |
7 |
107,967,288 (GRCm39) |
missense |
probably benign |
0.01 |
R2368:Or5p69
|
UTSW |
7 |
107,967,576 (GRCm39) |
missense |
probably damaging |
0.98 |
R3411:Or5p69
|
UTSW |
7 |
107,967,551 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3834:Or5p69
|
UTSW |
7 |
107,967,279 (GRCm39) |
missense |
probably damaging |
0.98 |
R4322:Or5p69
|
UTSW |
7 |
107,967,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Or5p69
|
UTSW |
7 |
107,966,895 (GRCm39) |
missense |
probably damaging |
0.98 |
R4724:Or5p69
|
UTSW |
7 |
107,967,205 (GRCm39) |
missense |
probably benign |
|
R4843:Or5p69
|
UTSW |
7 |
107,967,350 (GRCm39) |
missense |
probably benign |
0.01 |
R5525:Or5p69
|
UTSW |
7 |
107,967,206 (GRCm39) |
missense |
probably benign |
|
R5954:Or5p69
|
UTSW |
7 |
107,966,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R7027:Or5p69
|
UTSW |
7 |
107,967,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R8041:Or5p69
|
UTSW |
7 |
107,966,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Or5p69
|
UTSW |
7 |
107,967,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R9566:Or5p69
|
UTSW |
7 |
107,966,783 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Or5p69
|
UTSW |
7 |
107,967,468 (GRCm39) |
missense |
probably damaging |
1.00 |
|