Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524J17Rik |
A |
G |
8: 86,138,870 (GRCm39) |
I73T |
probably benign |
Het |
4930556J24Rik |
A |
G |
11: 3,926,192 (GRCm39) |
|
probably benign |
Het |
Ace |
A |
G |
11: 105,875,971 (GRCm39) |
T1010A |
probably benign |
Het |
Adam20 |
A |
T |
8: 41,248,865 (GRCm39) |
Y325F |
probably benign |
Het |
Aff4 |
A |
C |
11: 53,259,509 (GRCm39) |
N7H |
probably damaging |
Het |
Apob |
A |
T |
12: 8,057,830 (GRCm39) |
D2104V |
probably damaging |
Het |
Asap3 |
T |
C |
4: 135,965,722 (GRCm39) |
S411P |
probably benign |
Het |
Atxn1l |
C |
T |
8: 110,458,462 (GRCm39) |
G600D |
probably damaging |
Het |
Brd3 |
A |
T |
2: 27,352,558 (GRCm39) |
M124K |
probably benign |
Het |
Bsx |
A |
G |
9: 40,785,484 (GRCm39) |
N4S |
probably damaging |
Het |
Ccdc125 |
T |
C |
13: 100,814,552 (GRCm39) |
I44T |
probably benign |
Het |
Ccdc141 |
G |
A |
2: 76,879,963 (GRCm39) |
T620I |
probably benign |
Het |
Ccdc178 |
T |
A |
18: 22,157,809 (GRCm39) |
I550F |
probably benign |
Het |
Ccdc77 |
G |
T |
6: 120,318,962 (GRCm39) |
T163N |
probably damaging |
Het |
Cd55 |
A |
T |
1: 130,380,273 (GRCm39) |
I235K |
probably benign |
Het |
Cdc123 |
A |
T |
2: 5,826,174 (GRCm39) |
M118K |
possibly damaging |
Het |
Cep192 |
A |
T |
18: 67,951,958 (GRCm39) |
K378* |
probably null |
Het |
Chd7 |
C |
T |
4: 8,850,812 (GRCm39) |
R1733C |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,792,766 (GRCm39) |
S134C |
possibly damaging |
Het |
Cyp2d26 |
A |
G |
15: 82,676,907 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,085,299 (GRCm39) |
|
probably null |
Het |
Dyrk2 |
A |
T |
10: 118,696,922 (GRCm39) |
V112E |
probably benign |
Het |
Eppk1 |
A |
G |
15: 75,994,598 (GRCm39) |
L761P |
probably benign |
Het |
Evpl |
T |
C |
11: 116,114,489 (GRCm39) |
K1067R |
probably benign |
Het |
Fancm |
C |
A |
12: 65,171,947 (GRCm39) |
D1862E |
probably damaging |
Het |
Fhl2 |
A |
G |
1: 43,167,571 (GRCm39) |
V174A |
probably damaging |
Het |
Gemin4 |
A |
T |
11: 76,102,656 (GRCm39) |
C702S |
probably damaging |
Het |
Ggnbp2 |
T |
A |
11: 84,760,767 (GRCm39) |
D10V |
possibly damaging |
Het |
Glul |
T |
C |
1: 153,778,769 (GRCm39) |
V26A |
probably benign |
Het |
Gml2 |
A |
G |
15: 74,696,089 (GRCm39) |
N161S |
probably benign |
Het |
Gnao1 |
C |
A |
8: 94,682,795 (GRCm39) |
T327K |
probably damaging |
Het |
Gpr179 |
A |
G |
11: 97,227,124 (GRCm39) |
V1677A |
possibly damaging |
Het |
Greb1l |
A |
T |
18: 10,544,450 (GRCm39) |
H1348L |
probably benign |
Het |
Grm8 |
T |
C |
6: 28,126,030 (GRCm39) |
H32R |
probably benign |
Het |
Hk2 |
T |
A |
6: 82,716,627 (GRCm39) |
M302L |
probably benign |
Het |
Hnrnpm |
C |
A |
17: 33,877,884 (GRCm39) |
M333I |
probably benign |
Het |
Hsd3b1 |
A |
G |
3: 98,760,223 (GRCm39) |
I256T |
probably damaging |
Het |
Irx5 |
G |
A |
8: 93,087,327 (GRCm39) |
G420R |
probably damaging |
Het |
Krt87 |
A |
G |
15: 101,331,901 (GRCm39) |
V279A |
probably benign |
Het |
Lamb2 |
G |
A |
9: 108,363,365 (GRCm39) |
S848N |
probably benign |
Het |
Lypd10 |
A |
T |
7: 24,413,203 (GRCm39) |
H174L |
probably benign |
Het |
Mc1r |
A |
T |
8: 124,135,116 (GRCm39) |
T290S |
probably benign |
Het |
Or10d4 |
A |
T |
9: 39,580,376 (GRCm39) |
T8S |
probably benign |
Het |
Or52n2c |
A |
T |
7: 104,574,146 (GRCm39) |
V275D |
probably benign |
Het |
Or52z1 |
A |
T |
7: 103,436,729 (GRCm39) |
C252S |
possibly damaging |
Het |
Pex6 |
T |
C |
17: 47,022,975 (GRCm39) |
S184P |
probably damaging |
Het |
Pglyrp3 |
A |
T |
3: 91,933,762 (GRCm39) |
S136C |
probably null |
Het |
Pik3r1 |
A |
G |
13: 101,894,062 (GRCm39) |
S36P |
probably benign |
Het |
Pomt2 |
G |
T |
12: 87,156,790 (GRCm39) |
T782K |
probably benign |
Het |
Ppfibp2 |
A |
G |
7: 107,285,063 (GRCm39) |
|
probably benign |
Het |
Prdm9 |
T |
C |
17: 15,765,019 (GRCm39) |
H587R |
probably damaging |
Het |
Prp2 |
A |
G |
6: 132,576,932 (GRCm39) |
Q73R |
unknown |
Het |
Psmb4 |
T |
C |
3: 94,793,435 (GRCm39) |
N149D |
probably benign |
Het |
Ptprj |
A |
T |
2: 90,301,481 (GRCm39) |
I217N |
possibly damaging |
Het |
Rasal3 |
A |
G |
17: 32,611,736 (GRCm39) |
F797S |
possibly damaging |
Het |
Rsrp1 |
T |
A |
4: 134,652,610 (GRCm39) |
M188K |
probably damaging |
Het |
Senp8 |
A |
G |
9: 59,644,499 (GRCm39) |
I219T |
probably damaging |
Het |
Serpinb10 |
A |
T |
1: 107,468,630 (GRCm39) |
N91I |
probably damaging |
Het |
Skint4 |
C |
T |
4: 111,975,264 (GRCm39) |
R75C |
probably damaging |
Het |
Slc25a48 |
C |
A |
13: 56,612,825 (GRCm39) |
A241E |
probably damaging |
Het |
Slc39a6 |
C |
A |
18: 24,736,811 (GRCm39) |
|
probably benign |
Het |
Smarcc1 |
G |
A |
9: 110,002,972 (GRCm39) |
R354H |
probably damaging |
Het |
Spata21 |
G |
C |
4: 140,838,755 (GRCm39) |
|
probably null |
Het |
Sptbn2 |
A |
G |
19: 4,796,724 (GRCm39) |
E1774G |
possibly damaging |
Het |
Tep1 |
A |
T |
14: 51,082,894 (GRCm39) |
F1038Y |
possibly damaging |
Het |
Thbs2 |
T |
A |
17: 14,899,963 (GRCm39) |
D638V |
probably benign |
Het |
Tmem161a |
G |
T |
8: 70,627,047 (GRCm39) |
C33F |
probably damaging |
Het |
Trim47 |
T |
C |
11: 116,000,926 (GRCm39) |
S41G |
probably benign |
Het |
Trim56 |
T |
A |
5: 137,143,429 (GRCm39) |
H29L |
probably benign |
Het |
Ugt2b35 |
T |
A |
5: 87,156,064 (GRCm39) |
H385Q |
probably damaging |
Het |
Ugt2b37 |
T |
A |
5: 87,390,243 (GRCm39) |
H401L |
probably benign |
Het |
Usp44 |
A |
C |
10: 93,682,365 (GRCm39) |
T272P |
probably damaging |
Het |
Usp46 |
C |
T |
5: 74,189,897 (GRCm39) |
E156K |
probably benign |
Het |
Vmn1r232 |
T |
C |
17: 21,134,109 (GRCm39) |
K164E |
probably benign |
Het |
Zan |
T |
A |
5: 137,385,217 (GRCm39) |
N5072I |
unknown |
Het |
Zfp318 |
T |
C |
17: 46,723,576 (GRCm39) |
S1860P |
probably benign |
Het |
Zfp616 |
C |
T |
11: 73,975,710 (GRCm39) |
R660W |
probably benign |
Het |
Zfp870 |
C |
T |
17: 33,102,679 (GRCm39) |
V217I |
possibly damaging |
Het |
|
Other mutations in Or6c202 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02341:Or6c202
|
APN |
10 |
128,996,302 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02366:Or6c202
|
APN |
10 |
128,996,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Or6c202
|
APN |
10 |
128,996,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Or6c202
|
UTSW |
10 |
128,996,608 (GRCm39) |
missense |
probably benign |
0.10 |
R0081:Or6c202
|
UTSW |
10 |
128,996,707 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1179:Or6c202
|
UTSW |
10 |
128,995,927 (GRCm39) |
missense |
probably benign |
0.00 |
R1328:Or6c202
|
UTSW |
10 |
128,996,293 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1701:Or6c202
|
UTSW |
10 |
128,995,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Or6c202
|
UTSW |
10 |
128,996,383 (GRCm39) |
missense |
probably benign |
0.16 |
R4814:Or6c202
|
UTSW |
10 |
128,996,245 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5106:Or6c202
|
UTSW |
10 |
128,996,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5109:Or6c202
|
UTSW |
10 |
128,996,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5209:Or6c202
|
UTSW |
10 |
128,996,801 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5646:Or6c202
|
UTSW |
10 |
128,996,706 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6114:Or6c202
|
UTSW |
10 |
128,996,202 (GRCm39) |
missense |
probably benign |
|
R6133:Or6c202
|
UTSW |
10 |
128,996,752 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6879:Or6c202
|
UTSW |
10 |
128,996,848 (GRCm39) |
missense |
probably benign |
0.04 |
R7358:Or6c202
|
UTSW |
10 |
128,995,939 (GRCm39) |
missense |
probably benign |
|
R7426:Or6c202
|
UTSW |
10 |
128,996,620 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7699:Or6c202
|
UTSW |
10 |
128,995,924 (GRCm39) |
missense |
probably benign |
|
R7700:Or6c202
|
UTSW |
10 |
128,995,924 (GRCm39) |
missense |
probably benign |
|
R8232:Or6c202
|
UTSW |
10 |
128,996,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Or6c202
|
UTSW |
10 |
128,996,334 (GRCm39) |
missense |
probably benign |
0.00 |
R8959:Or6c202
|
UTSW |
10 |
128,996,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R9338:Or6c202
|
UTSW |
10 |
128,996,610 (GRCm39) |
missense |
probably benign |
0.02 |
R9497:Or6c202
|
UTSW |
10 |
128,996,464 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Or6c202
|
UTSW |
10 |
128,996,271 (GRCm39) |
missense |
probably benign |
0.07 |
|