Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf2 |
T |
C |
11: 94,453,737 (GRCm39) |
Y408C |
probably damaging |
Het |
Aox4 |
T |
C |
1: 58,293,477 (GRCm39) |
L943S |
probably damaging |
Het |
Ap1g1 |
G |
A |
8: 110,589,958 (GRCm39) |
|
probably benign |
Het |
Arsb |
T |
C |
13: 93,930,667 (GRCm39) |
S212P |
probably damaging |
Het |
Arsi |
A |
G |
18: 61,049,984 (GRCm39) |
N289S |
probably damaging |
Het |
Atp6v1h |
T |
A |
1: 5,165,865 (GRCm39) |
F72I |
probably damaging |
Het |
Atxn7 |
T |
C |
14: 14,090,063 (GRCm38) |
I336T |
probably benign |
Het |
Bak1 |
G |
A |
17: 27,241,722 (GRCm39) |
P65L |
possibly damaging |
Het |
Bcl6 |
A |
T |
16: 23,791,697 (GRCm39) |
M219K |
possibly damaging |
Het |
Brd3 |
T |
C |
2: 27,352,460 (GRCm39) |
K157E |
probably damaging |
Het |
Ccdc171 |
T |
G |
4: 83,581,892 (GRCm39) |
S674A |
possibly damaging |
Het |
Cfap43 |
A |
G |
19: 47,768,833 (GRCm39) |
I737T |
probably benign |
Het |
Cul9 |
A |
T |
17: 46,836,758 (GRCm39) |
V1089D |
possibly damaging |
Het |
Dffa |
C |
A |
4: 149,201,887 (GRCm39) |
A155E |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,352,416 (GRCm39) |
R2523Q |
probably damaging |
Het |
Efcab12 |
T |
A |
6: 115,800,451 (GRCm39) |
M191L |
probably benign |
Het |
Efl1 |
T |
C |
7: 82,421,707 (GRCm39) |
L1018P |
probably damaging |
Het |
Fcho1 |
A |
G |
8: 72,167,600 (GRCm39) |
|
probably benign |
Het |
Fndc3b |
T |
A |
3: 27,511,219 (GRCm39) |
T764S |
probably benign |
Het |
Gm29125 |
T |
C |
1: 80,361,948 (GRCm39) |
|
noncoding transcript |
Het |
Gm5108 |
A |
G |
5: 68,101,953 (GRCm39) |
|
probably benign |
Het |
Gm9949 |
T |
G |
18: 62,313,636 (GRCm39) |
|
probably benign |
Het |
Golgb1 |
T |
C |
16: 36,695,503 (GRCm39) |
|
probably benign |
Het |
Gpd2 |
T |
C |
2: 57,230,216 (GRCm39) |
Y323H |
probably damaging |
Het |
Grip1 |
T |
G |
10: 119,767,164 (GRCm39) |
D96E |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,532,492 (GRCm39) |
I3132V |
probably benign |
Het |
Hsd17b1 |
T |
C |
11: 100,971,024 (GRCm39) |
W327R |
possibly damaging |
Het |
Htra2 |
G |
A |
6: 83,031,223 (GRCm39) |
P62L |
probably benign |
Het |
Kdr |
A |
T |
5: 76,113,077 (GRCm39) |
|
probably null |
Het |
Kif14 |
T |
A |
1: 136,455,207 (GRCm39) |
C1626* |
probably null |
Het |
Kmt2a |
A |
T |
9: 44,731,543 (GRCm39) |
|
probably benign |
Het |
Krt15 |
T |
C |
11: 100,024,259 (GRCm39) |
T321A |
probably damaging |
Het |
Lactbl1 |
A |
T |
4: 136,358,356 (GRCm39) |
H109L |
probably benign |
Het |
Lilra6 |
T |
A |
7: 3,917,635 (GRCm39) |
H120L |
probably benign |
Het |
Lpcat2 |
G |
A |
8: 93,596,365 (GRCm39) |
S134N |
probably benign |
Het |
Mpp4 |
T |
C |
1: 59,164,742 (GRCm39) |
D465G |
probably benign |
Het |
Naip2 |
A |
T |
13: 100,325,859 (GRCm39) |
D16E |
probably damaging |
Het |
Nek5 |
C |
T |
8: 22,573,397 (GRCm39) |
A520T |
possibly damaging |
Het |
Nfatc2 |
A |
G |
2: 168,412,627 (GRCm39) |
F132L |
possibly damaging |
Het |
Nlrp3 |
C |
A |
11: 59,455,910 (GRCm39) |
T902N |
probably benign |
Het |
Or10d1b |
A |
T |
9: 39,613,172 (GRCm39) |
W298R |
probably benign |
Het |
Or4c123 |
A |
T |
2: 89,126,731 (GRCm39) |
H294Q |
probably benign |
Het |
Or8h7 |
T |
C |
2: 86,720,946 (GRCm39) |
D191G |
probably benign |
Het |
Pcdhb16 |
T |
C |
18: 37,613,142 (GRCm39) |
S701P |
possibly damaging |
Het |
Phf7 |
A |
G |
14: 30,969,994 (GRCm39) |
|
probably null |
Het |
Plpp4 |
G |
A |
7: 128,918,028 (GRCm39) |
V68M |
probably damaging |
Het |
Pnma2 |
A |
T |
14: 67,153,578 (GRCm39) |
M1L |
possibly damaging |
Het |
Pnma8b |
A |
T |
7: 16,679,901 (GRCm39) |
D295V |
probably damaging |
Het |
Rad21l |
T |
C |
2: 151,499,382 (GRCm39) |
D270G |
probably benign |
Het |
Ralgapa2 |
C |
A |
2: 146,230,406 (GRCm39) |
|
probably null |
Het |
Rasal3 |
A |
T |
17: 32,615,764 (GRCm39) |
L334Q |
probably damaging |
Het |
Rfx4 |
G |
T |
10: 84,699,114 (GRCm39) |
R240L |
probably damaging |
Het |
Rnf19b |
T |
A |
4: 128,977,713 (GRCm39) |
C642* |
probably null |
Het |
Slc28a2 |
G |
A |
2: 122,288,675 (GRCm39) |
E594K |
probably benign |
Het |
Spata31 |
G |
T |
13: 65,065,340 (GRCm39) |
W15L |
possibly damaging |
Het |
Spink5 |
T |
C |
18: 44,148,711 (GRCm39) |
S925P |
probably damaging |
Het |
Svep1 |
C |
T |
4: 58,084,534 (GRCm39) |
G1865S |
probably damaging |
Het |
Tg |
T |
C |
15: 66,645,323 (GRCm39) |
L791P |
probably damaging |
Het |
Thbs4 |
A |
C |
13: 92,911,675 (GRCm39) |
V247G |
probably damaging |
Het |
Tpcn2 |
A |
T |
7: 144,809,191 (GRCm39) |
F705Y |
probably damaging |
Het |
Try10 |
A |
T |
6: 41,333,483 (GRCm39) |
H76L |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,769,565 (GRCm39) |
V2695I |
probably damaging |
Het |
Tut1 |
C |
A |
19: 8,932,814 (GRCm39) |
T49N |
probably benign |
Het |
Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
Xdh |
G |
A |
17: 74,232,006 (GRCm39) |
R235C |
probably damaging |
Het |
Yipf4 |
A |
G |
17: 74,799,470 (GRCm39) |
D70G |
probably null |
Het |
Zfp108 |
G |
T |
7: 23,960,163 (GRCm39) |
K251N |
probably benign |
Het |
|
Other mutations in Or7e165 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01461:Or7e165
|
APN |
9 |
19,695,245 (GRCm39) |
splice site |
probably null |
|
IGL01815:Or7e165
|
APN |
9 |
19,695,311 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Or7e165
|
APN |
9 |
19,694,711 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02644:Or7e165
|
APN |
9 |
19,695,010 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03243:Or7e165
|
APN |
9 |
19,694,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R0603:Or7e165
|
UTSW |
9 |
19,695,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Or7e165
|
UTSW |
9 |
19,694,892 (GRCm39) |
missense |
probably benign |
0.00 |
R2570:Or7e165
|
UTSW |
9 |
19,695,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R3890:Or7e165
|
UTSW |
9 |
19,695,011 (GRCm39) |
missense |
probably benign |
0.03 |
R3892:Or7e165
|
UTSW |
9 |
19,695,011 (GRCm39) |
missense |
probably benign |
0.03 |
R4163:Or7e165
|
UTSW |
9 |
19,695,086 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4610:Or7e165
|
UTSW |
9 |
19,694,442 (GRCm39) |
nonsense |
probably null |
|
R4691:Or7e165
|
UTSW |
9 |
19,694,678 (GRCm39) |
missense |
probably benign |
0.33 |
R4707:Or7e165
|
UTSW |
9 |
19,694,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Or7e165
|
UTSW |
9 |
19,694,872 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4950:Or7e165
|
UTSW |
9 |
19,695,027 (GRCm39) |
missense |
probably benign |
|
R5202:Or7e165
|
UTSW |
9 |
19,694,514 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5439:Or7e165
|
UTSW |
9 |
19,695,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R5669:Or7e165
|
UTSW |
9 |
19,695,053 (GRCm39) |
missense |
probably benign |
0.02 |
R5672:Or7e165
|
UTSW |
9 |
19,694,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6038:Or7e165
|
UTSW |
9 |
19,694,858 (GRCm39) |
missense |
probably benign |
|
R6038:Or7e165
|
UTSW |
9 |
19,694,858 (GRCm39) |
missense |
probably benign |
|
R6212:Or7e165
|
UTSW |
9 |
19,694,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Or7e165
|
UTSW |
9 |
19,695,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R7385:Or7e165
|
UTSW |
9 |
19,694,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7669:Or7e165
|
UTSW |
9 |
19,694,839 (GRCm39) |
missense |
possibly damaging |
0.79 |
|