Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
A |
3: 121,920,527 (GRCm39) |
V1083M |
probably damaging |
Het |
Aco2 |
A |
G |
15: 81,791,736 (GRCm39) |
|
probably null |
Het |
AI661453 |
A |
T |
17: 47,747,752 (GRCm39) |
Q8L |
probably null |
Het |
Ankrd42 |
T |
C |
7: 92,261,980 (GRCm39) |
D295G |
possibly damaging |
Het |
Ccdc73 |
A |
T |
2: 104,821,442 (GRCm39) |
I464L |
probably benign |
Het |
Cdc5l |
A |
C |
17: 45,704,073 (GRCm39) |
M717R |
probably benign |
Het |
Col4a1 |
G |
A |
8: 11,271,015 (GRCm39) |
P809S |
probably damaging |
Het |
Dctn1 |
T |
C |
6: 83,167,459 (GRCm39) |
M358T |
possibly damaging |
Het |
Dgkz |
A |
G |
2: 91,765,456 (GRCm39) |
S799P |
probably benign |
Het |
Dna2 |
T |
C |
10: 62,805,561 (GRCm39) |
C933R |
probably damaging |
Het |
Dock6 |
T |
C |
9: 21,729,188 (GRCm39) |
N1275S |
probably benign |
Het |
Ect2l |
A |
G |
10: 18,017,652 (GRCm39) |
I659T |
probably benign |
Het |
Ets1 |
T |
A |
9: 32,645,357 (GRCm39) |
Y201* |
probably null |
Het |
Gle1 |
T |
A |
2: 29,848,462 (GRCm39) |
C679S |
probably benign |
Het |
Gm10118 |
T |
G |
10: 63,762,643 (GRCm39) |
|
probably benign |
Het |
Guk1 |
G |
A |
11: 59,075,921 (GRCm39) |
R146C |
probably damaging |
Het |
H2-Q7 |
A |
G |
17: 35,658,688 (GRCm39) |
S109G |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,882,418 (GRCm39) |
V2809A |
probably damaging |
Het |
Izumo1 |
T |
A |
7: 45,276,536 (GRCm39) |
D366E |
probably benign |
Het |
Kctd20 |
A |
T |
17: 29,176,872 (GRCm39) |
M1L |
possibly damaging |
Het |
Lct |
C |
T |
1: 128,214,346 (GRCm39) |
A1809T |
probably benign |
Het |
Manea |
T |
C |
4: 26,327,983 (GRCm39) |
I353V |
probably damaging |
Het |
Mybl2 |
T |
C |
2: 162,917,688 (GRCm39) |
Y65H |
probably benign |
Het |
Myh11 |
C |
T |
16: 14,021,042 (GRCm39) |
E1744K |
probably damaging |
Het |
Neb |
T |
C |
2: 52,167,560 (GRCm39) |
D1922G |
probably damaging |
Het |
Nepro |
C |
A |
16: 44,556,382 (GRCm39) |
D513E |
probably benign |
Het |
Nnt |
A |
T |
13: 119,531,192 (GRCm39) |
I185K |
possibly damaging |
Het |
Npat |
A |
T |
9: 53,456,480 (GRCm39) |
Q17L |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,175,071 (GRCm39) |
E956G |
possibly damaging |
Het |
Or1x6 |
A |
G |
11: 50,939,254 (GRCm39) |
I107V |
probably benign |
Het |
Or2a14 |
T |
A |
6: 43,130,558 (GRCm39) |
F106L |
probably benign |
Het |
Or4q3 |
A |
G |
14: 50,583,545 (GRCm39) |
V118A |
probably damaging |
Het |
Or8g18 |
A |
T |
9: 39,149,146 (GRCm39) |
N191K |
possibly damaging |
Het |
Or8g4 |
A |
T |
9: 39,661,687 (GRCm39) |
I2L |
probably benign |
Het |
Or9e1 |
G |
A |
11: 58,732,478 (GRCm39) |
M179I |
probably benign |
Het |
Pah |
T |
C |
10: 87,357,924 (GRCm39) |
S16P |
probably damaging |
Het |
Pcdh15 |
C |
A |
10: 74,462,614 (GRCm39) |
P1365Q |
probably null |
Het |
Pds5b |
G |
T |
5: 150,688,427 (GRCm39) |
V640F |
probably benign |
Het |
Pgam5 |
A |
T |
5: 110,414,996 (GRCm39) |
H72Q |
probably benign |
Het |
Plagl2 |
C |
A |
2: 153,074,461 (GRCm39) |
A147S |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,256,545 (GRCm39) |
L113Q |
probably null |
Het |
Ppp1r12a |
T |
C |
10: 108,034,722 (GRCm39) |
V89A |
probably damaging |
Het |
Ptprc |
A |
G |
1: 138,028,870 (GRCm39) |
Y443H |
possibly damaging |
Het |
Ralgapb |
T |
C |
2: 158,315,203 (GRCm39) |
|
probably null |
Het |
Rgsl1 |
A |
G |
1: 153,677,980 (GRCm39) |
|
probably null |
Het |
Rubcn |
A |
C |
16: 32,647,713 (GRCm39) |
I681M |
probably damaging |
Het |
Scaf11 |
A |
G |
15: 96,321,434 (GRCm39) |
L169S |
probably damaging |
Het |
Scgb1b27 |
A |
G |
7: 33,721,276 (GRCm39) |
K55E |
probably benign |
Het |
Sos1 |
A |
T |
17: 80,741,159 (GRCm39) |
I542N |
probably damaging |
Het |
Syf2 |
T |
A |
4: 134,663,374 (GRCm39) |
V182D |
probably damaging |
Het |
Tapbp |
T |
C |
17: 34,144,717 (GRCm39) |
V271A |
probably benign |
Het |
Tmem33 |
T |
A |
5: 67,421,651 (GRCm39) |
L60Q |
probably damaging |
Het |
Tmf1 |
A |
G |
6: 97,153,284 (GRCm39) |
V263A |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,806,020 (GRCm39) |
V798A |
probably benign |
Het |
Zfp384 |
C |
A |
6: 125,013,631 (GRCm39) |
D550E |
probably benign |
Het |
|
Other mutations in Or1e35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01288:Or1e35
|
APN |
11 |
73,798,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01618:Or1e35
|
APN |
11 |
73,798,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01995:Or1e35
|
APN |
11 |
73,798,261 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02494:Or1e35
|
APN |
11 |
73,797,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02995:Or1e35
|
APN |
11 |
73,798,045 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03256:Or1e35
|
APN |
11 |
73,797,522 (GRCm39) |
missense |
probably benign |
0.07 |
R0018:Or1e35
|
UTSW |
11 |
73,797,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Or1e35
|
UTSW |
11 |
73,797,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1222:Or1e35
|
UTSW |
11 |
73,798,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Or1e35
|
UTSW |
11 |
73,797,911 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1819:Or1e35
|
UTSW |
11 |
73,797,505 (GRCm39) |
missense |
probably benign |
0.02 |
R2994:Or1e35
|
UTSW |
11 |
73,797,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Or1e35
|
UTSW |
11 |
73,797,484 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4622:Or1e35
|
UTSW |
11 |
73,797,737 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4753:Or1e35
|
UTSW |
11 |
73,797,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5137:Or1e35
|
UTSW |
11 |
73,797,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Or1e35
|
UTSW |
11 |
73,797,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Or1e35
|
UTSW |
11 |
73,797,853 (GRCm39) |
missense |
probably benign |
0.02 |
R5748:Or1e35
|
UTSW |
11 |
73,797,721 (GRCm39) |
missense |
probably damaging |
0.98 |
R5899:Or1e35
|
UTSW |
11 |
73,797,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Or1e35
|
UTSW |
11 |
73,797,447 (GRCm39) |
nonsense |
probably null |
|
R6388:Or1e35
|
UTSW |
11 |
73,798,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Or1e35
|
UTSW |
11 |
73,797,629 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7241:Or1e35
|
UTSW |
11 |
73,798,058 (GRCm39) |
missense |
probably benign |
0.05 |
R8870:Or1e35
|
UTSW |
11 |
73,797,725 (GRCm39) |
missense |
probably benign |
0.03 |
R9358:Or1e35
|
UTSW |
11 |
73,797,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Or1e35
|
UTSW |
11 |
73,797,637 (GRCm39) |
missense |
probably benign |
0.14 |
R9645:Or1e35
|
UTSW |
11 |
73,797,713 (GRCm39) |
missense |
probably benign |
|
R9667:Or1e35
|
UTSW |
11 |
73,798,097 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9707:Or1e35
|
UTSW |
11 |
73,798,090 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Or1e35
|
UTSW |
11 |
73,797,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|