Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
A |
G |
18: 61,934,470 (GRCm39) |
S649P |
probably damaging |
Het |
Adam22 |
C |
A |
5: 8,140,182 (GRCm39) |
G202W |
probably damaging |
Het |
Adamts1 |
T |
A |
16: 85,599,496 (GRCm39) |
M35L |
probably benign |
Het |
Adgrg3 |
A |
T |
8: 95,762,556 (GRCm39) |
H202L |
probably damaging |
Het |
Anln |
G |
T |
9: 22,271,813 (GRCm39) |
R681S |
probably damaging |
Het |
Aprt |
A |
T |
8: 123,302,147 (GRCm39) |
M1K |
probably null |
Het |
Arid3b |
G |
T |
9: 57,702,320 (GRCm39) |
|
probably null |
Het |
Cbl |
A |
G |
9: 44,084,620 (GRCm39) |
F172L |
probably damaging |
Het |
Cd109 |
G |
T |
9: 78,617,521 (GRCm39) |
V1340L |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Chrm3 |
A |
G |
13: 9,928,593 (GRCm39) |
Y148H |
probably damaging |
Het |
Cog7 |
A |
C |
7: 121,540,470 (GRCm39) |
|
probably null |
Het |
Cpsf1 |
A |
T |
15: 76,486,771 (GRCm39) |
I255N |
probably damaging |
Het |
Crebzf |
G |
A |
7: 90,092,622 (GRCm39) |
G134R |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,849,661 (GRCm39) |
S1705G |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,726,082 (GRCm39) |
H1409Q |
probably benign |
Het |
Fank1 |
A |
G |
7: 133,478,632 (GRCm39) |
D232G |
probably damaging |
Het |
Fat1 |
G |
T |
8: 45,489,168 (GRCm39) |
V3480L |
probably benign |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
G |
T |
1: 174,330,572 (GRCm39) |
G321W |
unknown |
Het |
Greb1 |
A |
T |
12: 16,738,567 (GRCm39) |
Y1465* |
probably null |
Het |
Hdac9 |
G |
A |
12: 34,443,392 (GRCm39) |
Q330* |
probably null |
Het |
Kcnt2 |
C |
T |
1: 140,354,639 (GRCm39) |
T298I |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,901,464 (GRCm39) |
D1055G |
probably benign |
Het |
Mroh2b |
T |
C |
15: 4,946,660 (GRCm39) |
S487P |
probably damaging |
Het |
Naa38 |
G |
A |
11: 69,287,408 (GRCm39) |
V110I |
probably benign |
Het |
Nkd2 |
T |
C |
13: 73,969,557 (GRCm39) |
H303R |
probably damaging |
Het |
Nr1d2 |
A |
G |
14: 18,222,125 (GRCm38) |
C49R |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,844,099 (GRCm39) |
V103A |
probably benign |
Het |
Or52b2 |
A |
G |
7: 104,986,324 (GRCm39) |
Y200H |
probably damaging |
Het |
Ovch2 |
T |
A |
7: 107,393,631 (GRCm39) |
E165V |
probably damaging |
Het |
Phyh |
A |
T |
2: 4,947,012 (GRCm39) |
|
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,545,137 (GRCm39) |
|
probably null |
Het |
Ppip5k1 |
A |
C |
2: 121,142,201 (GRCm39) |
V1416G |
probably benign |
Het |
Ppm1b |
T |
C |
17: 85,301,537 (GRCm39) |
V139A |
probably benign |
Het |
Ppp1r12a |
T |
G |
10: 108,097,077 (GRCm39) |
|
probably null |
Het |
Pramel20 |
A |
G |
4: 143,297,807 (GRCm39) |
T76A |
probably benign |
Het |
Psmc5 |
G |
T |
11: 106,152,327 (GRCm39) |
A115S |
probably damaging |
Het |
Ptpn5 |
T |
A |
7: 46,731,642 (GRCm39) |
E409V |
probably benign |
Het |
Ptprg |
T |
A |
14: 11,554,235 (GRCm38) |
|
probably benign |
Het |
Qrich1 |
G |
T |
9: 108,422,164 (GRCm39) |
V593F |
probably damaging |
Het |
Rbbp9 |
T |
C |
2: 144,385,741 (GRCm39) |
I175V |
probably benign |
Het |
Selenot |
T |
C |
3: 58,493,387 (GRCm39) |
F88S |
possibly damaging |
Het |
Sp110 |
C |
T |
1: 85,516,841 (GRCm39) |
E219K |
possibly damaging |
Het |
Spred2 |
A |
G |
11: 19,968,155 (GRCm39) |
D208G |
possibly damaging |
Het |
Surf1 |
T |
C |
2: 26,804,204 (GRCm39) |
T197A |
probably benign |
Het |
Taco1 |
G |
A |
11: 105,963,539 (GRCm39) |
|
probably null |
Het |
Tpr |
C |
T |
1: 150,321,675 (GRCm39) |
R3C |
probably damaging |
Het |
Uggt2 |
A |
G |
14: 119,319,182 (GRCm39) |
I280T |
probably benign |
Het |
Yipf2 |
A |
G |
9: 21,503,228 (GRCm39) |
Y80H |
possibly damaging |
Het |
Zscan12 |
T |
C |
13: 21,548,178 (GRCm39) |
V120A |
possibly damaging |
Het |
|
Other mutations in Tas2r109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Tas2r109
|
APN |
6 |
132,956,986 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01837:Tas2r109
|
APN |
6 |
132,957,477 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02094:Tas2r109
|
APN |
6 |
132,957,202 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0788:Tas2r109
|
UTSW |
6 |
132,957,264 (GRCm39) |
missense |
probably benign |
0.01 |
R0849:Tas2r109
|
UTSW |
6 |
132,957,856 (GRCm39) |
missense |
probably benign |
0.00 |
R1542:Tas2r109
|
UTSW |
6 |
132,957,873 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1583:Tas2r109
|
UTSW |
6 |
132,957,389 (GRCm39) |
missense |
probably benign |
0.01 |
R2035:Tas2r109
|
UTSW |
6 |
132,957,423 (GRCm39) |
missense |
probably benign |
|
R3845:Tas2r109
|
UTSW |
6 |
132,957,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R4060:Tas2r109
|
UTSW |
6 |
132,957,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Tas2r109
|
UTSW |
6 |
132,957,144 (GRCm39) |
missense |
probably benign |
|
R5860:Tas2r109
|
UTSW |
6 |
132,957,664 (GRCm39) |
missense |
probably benign |
0.06 |
R6211:Tas2r109
|
UTSW |
6 |
132,957,587 (GRCm39) |
nonsense |
probably null |
|
R6378:Tas2r109
|
UTSW |
6 |
132,957,844 (GRCm39) |
missense |
probably benign |
0.00 |
R6861:Tas2r109
|
UTSW |
6 |
132,957,048 (GRCm39) |
missense |
probably benign |
0.43 |
R7319:Tas2r109
|
UTSW |
6 |
132,957,663 (GRCm39) |
missense |
probably benign |
0.33 |
R8553:Tas2r109
|
UTSW |
6 |
132,957,171 (GRCm39) |
missense |
probably benign |
0.33 |
R9447:Tas2r109
|
UTSW |
6 |
132,957,270 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Tas2r109
|
UTSW |
6 |
132,957,264 (GRCm39) |
missense |
probably benign |
0.07 |
|