Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
T |
A |
19: 55,279,592 (GRCm39) |
Y443* |
probably null |
Het |
Aox3 |
C |
T |
1: 58,185,667 (GRCm39) |
T331M |
probably damaging |
Het |
Arhgap32 |
G |
A |
9: 32,170,967 (GRCm39) |
R1598H |
probably damaging |
Het |
Atp1a2 |
A |
G |
1: 172,106,436 (GRCm39) |
|
probably null |
Het |
Brpf3 |
A |
T |
17: 29,029,536 (GRCm39) |
M499L |
probably benign |
Het |
Cacnb1 |
A |
T |
11: 97,909,097 (GRCm39) |
|
probably null |
Het |
Cep295 |
A |
G |
9: 15,238,029 (GRCm39) |
S1899P |
probably damaging |
Het |
Cntn2 |
A |
G |
1: 132,446,595 (GRCm39) |
Y748H |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 47,532,599 (GRCm39) |
Y2532F |
probably damaging |
Het |
Cstdc1 |
G |
T |
2: 148,625,298 (GRCm39) |
L77F |
probably damaging |
Het |
Dsg1a |
A |
G |
18: 20,474,011 (GRCm39) |
D1028G |
probably damaging |
Het |
Eif1ad16 |
A |
C |
12: 87,985,265 (GRCm39) |
L93V |
probably benign |
Het |
Elp1 |
A |
T |
4: 56,800,104 (GRCm39) |
H7Q |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Gabra5 |
C |
T |
7: 57,140,533 (GRCm39) |
G55R |
probably damaging |
Het |
Gdf9 |
T |
A |
11: 53,328,034 (GRCm39) |
F330Y |
probably benign |
Het |
Gimap8 |
T |
C |
6: 48,633,236 (GRCm39) |
S352P |
probably damaging |
Het |
Gm4952 |
A |
T |
19: 12,600,993 (GRCm39) |
H71L |
probably benign |
Het |
Gnaq |
G |
A |
19: 16,110,790 (GRCm39) |
R34H |
probably benign |
Het |
Hebp2 |
T |
C |
10: 18,420,055 (GRCm39) |
D126G |
probably benign |
Het |
Hectd4 |
A |
G |
5: 121,453,464 (GRCm39) |
D601G |
possibly damaging |
Het |
Hook2 |
T |
C |
8: 85,728,033 (GRCm39) |
Y577H |
probably damaging |
Het |
Igfals |
A |
G |
17: 25,099,067 (GRCm39) |
T53A |
probably benign |
Het |
Igsf9b |
A |
G |
9: 27,222,968 (GRCm39) |
D123G |
probably damaging |
Het |
Ilrun |
A |
T |
17: 28,013,020 (GRCm39) |
I59N |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Mdm4 |
A |
T |
1: 132,919,396 (GRCm39) |
*490K |
probably null |
Het |
Melk |
C |
T |
4: 44,363,730 (GRCm39) |
T592M |
probably damaging |
Het |
Neurl2 |
C |
A |
2: 164,675,021 (GRCm39) |
A114S |
probably damaging |
Het |
Nuggc |
A |
G |
14: 65,876,075 (GRCm39) |
T563A |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pdlim1 |
A |
T |
19: 40,218,993 (GRCm39) |
S213T |
probably damaging |
Het |
Pitx1 |
T |
C |
13: 55,976,291 (GRCm39) |
I123V |
probably damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,829,204 (GRCm39) |
N1013D |
probably benign |
Het |
Pla2g2c |
T |
A |
4: 138,461,656 (GRCm39) |
Y42N |
possibly damaging |
Het |
Polr2b |
G |
A |
5: 77,496,993 (GRCm39) |
A1168T |
possibly damaging |
Het |
Ppp2r2a |
G |
A |
14: 67,254,020 (GRCm39) |
R383* |
probably null |
Het |
Prl7a2 |
C |
T |
13: 27,843,143 (GRCm39) |
R220H |
probably benign |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rc3h2 |
A |
G |
2: 37,279,867 (GRCm39) |
V454A |
possibly damaging |
Het |
Robo1 |
A |
G |
16: 72,732,665 (GRCm39) |
T307A |
probably damaging |
Het |
Slc22a6 |
T |
C |
19: 8,596,786 (GRCm39) |
L188P |
probably damaging |
Het |
Spag17 |
A |
G |
3: 100,016,726 (GRCm39) |
N2167S |
probably benign |
Het |
Spag5 |
G |
A |
11: 78,205,588 (GRCm39) |
E680K |
probably damaging |
Het |
Spata6 |
A |
G |
4: 111,680,026 (GRCm39) |
Y428C |
possibly damaging |
Het |
Tbc1d5 |
T |
C |
17: 51,291,660 (GRCm39) |
D47G |
probably benign |
Het |
Trp53 |
T |
C |
11: 69,479,566 (GRCm39) |
|
probably null |
Het |
Tsc22d1 |
TCAGCAGCAGCAGCAGCAGCAGCAGCA |
TCAGCAGCAGCAGCAGCAGCAGCA |
14: 76,654,707 (GRCm39) |
|
probably benign |
Het |
Ttc39b |
T |
C |
4: 83,180,084 (GRCm39) |
D103G |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,750,322 (GRCm39) |
W3576G |
probably benign |
Het |
Yeats2 |
T |
A |
16: 19,972,912 (GRCm39) |
M22K |
probably damaging |
Het |
|
Other mutations in Or8g32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01527:Or8g32
|
APN |
9 |
39,305,114 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01650:Or8g32
|
APN |
9 |
39,305,252 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02134:Or8g32
|
APN |
9 |
39,305,830 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03113:Or8g32
|
APN |
9 |
39,305,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Or8g32
|
UTSW |
9 |
39,305,238 (GRCm39) |
missense |
probably benign |
0.16 |
R1730:Or8g32
|
UTSW |
9 |
39,305,518 (GRCm39) |
missense |
probably benign |
0.01 |
R1783:Or8g32
|
UTSW |
9 |
39,305,518 (GRCm39) |
missense |
probably benign |
0.01 |
R1924:Or8g32
|
UTSW |
9 |
39,305,163 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3785:Or8g32
|
UTSW |
9 |
39,305,678 (GRCm39) |
missense |
probably benign |
0.07 |
R3787:Or8g32
|
UTSW |
9 |
39,305,678 (GRCm39) |
missense |
probably benign |
0.07 |
R4607:Or8g32
|
UTSW |
9 |
39,306,031 (GRCm39) |
makesense |
probably null |
|
R4803:Or8g32
|
UTSW |
9 |
39,305,932 (GRCm39) |
missense |
probably benign |
0.26 |
R5314:Or8g32
|
UTSW |
9 |
39,305,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R5338:Or8g32
|
UTSW |
9 |
39,305,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Or8g32
|
UTSW |
9 |
39,305,257 (GRCm39) |
missense |
probably benign |
0.33 |
R6590:Or8g32
|
UTSW |
9 |
39,305,845 (GRCm39) |
missense |
probably benign |
0.00 |
R6690:Or8g32
|
UTSW |
9 |
39,305,845 (GRCm39) |
missense |
probably benign |
0.00 |
R6925:Or8g32
|
UTSW |
9 |
39,305,157 (GRCm39) |
missense |
probably benign |
0.01 |
R6925:Or8g32
|
UTSW |
9 |
39,305,156 (GRCm39) |
missense |
probably benign |
0.32 |
R6982:Or8g32
|
UTSW |
9 |
39,305,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Or8g32
|
UTSW |
9 |
39,305,389 (GRCm39) |
missense |
probably benign |
0.01 |
R8074:Or8g32
|
UTSW |
9 |
39,305,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8389:Or8g32
|
UTSW |
9 |
39,305,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9444:Or8g32
|
UTSW |
9 |
39,305,365 (GRCm39) |
missense |
probably benign |
0.19 |
R9642:Or8g32
|
UTSW |
9 |
39,305,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|