Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add3 |
T |
A |
19: 53,215,038 (GRCm39) |
L71Q |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,535,070 (GRCm39) |
I5732F |
probably damaging |
Het |
Adss2 |
A |
T |
1: 177,598,788 (GRCm39) |
V330E |
probably benign |
Het |
Agps |
T |
A |
2: 75,739,979 (GRCm39) |
Y488N |
probably damaging |
Het |
Ap3s1 |
A |
T |
18: 46,891,106 (GRCm39) |
R66S |
probably damaging |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Atp2a2 |
C |
T |
5: 122,599,024 (GRCm39) |
V593I |
probably benign |
Het |
Chrna6 |
C |
T |
8: 27,897,014 (GRCm39) |
V288M |
probably damaging |
Het |
Col4a2 |
C |
T |
8: 11,491,296 (GRCm39) |
L1232F |
probably benign |
Het |
Dcaf1 |
A |
G |
9: 106,740,288 (GRCm39) |
N1225D |
probably damaging |
Het |
Degs1 |
A |
G |
1: 182,106,875 (GRCm39) |
I128T |
probably benign |
Het |
Dnaaf11 |
T |
C |
15: 66,341,824 (GRCm39) |
T91A |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,350,759 (GRCm39) |
T2594S |
probably damaging |
Het |
Dnah8 |
G |
T |
17: 30,974,093 (GRCm39) |
R2826L |
probably damaging |
Het |
Elf3 |
A |
G |
1: 135,184,875 (GRCm39) |
Y104H |
probably damaging |
Het |
Fam222b |
C |
A |
11: 78,044,718 (GRCm39) |
T93N |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,554,006 (GRCm39) |
I211T |
probably benign |
Het |
Fcho2 |
T |
C |
13: 98,871,594 (GRCm39) |
T541A |
probably benign |
Het |
Flg2 |
T |
C |
3: 93,109,738 (GRCm39) |
S589P |
unknown |
Het |
Foxj3 |
T |
A |
4: 119,483,597 (GRCm39) |
V589E |
unknown |
Het |
Gria1 |
A |
G |
11: 57,208,538 (GRCm39) |
Y742C |
probably damaging |
Het |
Inpp5d |
T |
C |
1: 87,642,860 (GRCm39) |
S672P |
probably damaging |
Het |
Lrrc19 |
A |
C |
4: 94,529,009 (GRCm39) |
F91C |
probably damaging |
Het |
Mppe1 |
A |
G |
18: 67,358,775 (GRCm39) |
*398R |
probably null |
Het |
Mroh3 |
T |
C |
1: 136,118,541 (GRCm39) |
I561V |
probably benign |
Het |
Myh11 |
C |
A |
16: 14,041,883 (GRCm39) |
Q720H |
probably damaging |
Het |
Nbea |
G |
T |
3: 55,998,444 (GRCm39) |
T121K |
possibly damaging |
Het |
Nbr1 |
A |
C |
11: 101,455,519 (GRCm39) |
D91A |
probably benign |
Het |
Ncam2 |
C |
A |
16: 81,231,789 (GRCm39) |
N84K |
probably benign |
Het |
Or4c35 |
T |
C |
2: 89,808,475 (GRCm39) |
Y118H |
probably damaging |
Het |
Or51ac3 |
A |
T |
7: 103,213,569 (GRCm39) |
C306S |
probably benign |
Het |
Or52z13 |
A |
G |
7: 103,246,928 (GRCm39) |
Y135C |
probably benign |
Het |
Or6b6 |
A |
G |
7: 106,571,323 (GRCm39) |
V76A |
probably benign |
Het |
Pdgfrb |
A |
T |
18: 61,194,585 (GRCm39) |
I121F |
probably damaging |
Het |
Peak1 |
A |
T |
9: 56,165,609 (GRCm39) |
I773N |
probably damaging |
Het |
Pfkfb4 |
G |
T |
9: 108,836,769 (GRCm39) |
V155F |
probably damaging |
Het |
Pkm |
C |
T |
9: 59,585,382 (GRCm39) |
R455* |
probably null |
Het |
Plbd2 |
C |
A |
5: 120,632,550 (GRCm39) |
E151* |
probably null |
Het |
Pld5 |
G |
A |
1: 175,812,025 (GRCm39) |
T353M |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,544 (GRCm39) |
D134E |
possibly damaging |
Het |
Rida |
T |
A |
15: 34,488,772 (GRCm39) |
D40V |
possibly damaging |
Het |
Rnf126 |
A |
T |
10: 79,595,068 (GRCm39) |
H265Q |
probably damaging |
Het |
Rock2 |
C |
A |
12: 16,978,967 (GRCm39) |
Q86K |
probably benign |
Het |
Serpinb1b |
A |
T |
13: 33,269,302 (GRCm39) |
T12S |
probably benign |
Het |
Slco6c1 |
T |
A |
1: 97,046,303 (GRCm39) |
Q277L |
probably benign |
Het |
Spmap2 |
A |
T |
10: 79,421,785 (GRCm39) |
Y144* |
probably null |
Het |
Sptlc2 |
T |
A |
12: 87,415,892 (GRCm39) |
H45L |
probably benign |
Het |
Srsf4 |
A |
G |
4: 131,627,641 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
G |
6: 48,454,719 (GRCm39) |
S2969G |
probably damaging |
Het |
Steap1 |
C |
T |
5: 5,786,664 (GRCm39) |
G258R |
probably damaging |
Het |
Stk19 |
A |
T |
17: 35,055,851 (GRCm39) |
M1K |
probably null |
Het |
Stk-ps2 |
C |
A |
1: 46,069,049 (GRCm39) |
|
noncoding transcript |
Het |
Taf1c |
C |
T |
8: 120,327,726 (GRCm39) |
R332H |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,891,743 (GRCm39) |
T791S |
probably damaging |
Het |
Tjap1 |
A |
G |
17: 46,574,652 (GRCm39) |
L21P |
probably damaging |
Het |
Tmem145 |
A |
G |
7: 25,007,268 (GRCm39) |
Y148C |
probably damaging |
Het |
Tmem267 |
T |
A |
13: 120,070,810 (GRCm39) |
V155E |
probably benign |
Het |
Tns1 |
T |
A |
1: 73,956,076 (GRCm39) |
H549L |
possibly damaging |
Het |
Tyro3 |
T |
G |
2: 119,632,182 (GRCm39) |
I83S |
probably benign |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Vmn1r53 |
A |
T |
6: 90,200,413 (GRCm39) |
C304S |
probably benign |
Het |
Vwf |
G |
A |
6: 125,622,917 (GRCm39) |
M1761I |
probably benign |
Het |
Zfp276 |
T |
C |
8: 123,991,786 (GRCm39) |
Y445H |
probably damaging |
Het |
Zfp407 |
A |
T |
18: 84,578,536 (GRCm39) |
I859N |
probably damaging |
Het |
|
Other mutations in Or52h9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Or52h9
|
APN |
7 |
104,202,299 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01120:Or52h9
|
APN |
7 |
104,202,552 (GRCm39) |
missense |
probably benign |
|
IGL01325:Or52h9
|
APN |
7 |
104,202,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01590:Or52h9
|
APN |
7 |
104,202,782 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02625:Or52h9
|
APN |
7 |
104,202,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Or52h9
|
APN |
7 |
104,202,357 (GRCm39) |
missense |
probably benign |
0.35 |
P0157:Or52h9
|
UTSW |
7 |
104,202,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Or52h9
|
UTSW |
7 |
104,202,576 (GRCm39) |
missense |
probably benign |
0.05 |
R0547:Or52h9
|
UTSW |
7 |
104,202,563 (GRCm39) |
missense |
probably benign |
0.01 |
R0630:Or52h9
|
UTSW |
7 |
104,202,998 (GRCm39) |
missense |
probably benign |
0.27 |
R1014:Or52h9
|
UTSW |
7 |
104,202,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1127:Or52h9
|
UTSW |
7 |
104,202,293 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1724:Or52h9
|
UTSW |
7 |
104,202,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R2473:Or52h9
|
UTSW |
7 |
104,202,146 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3115:Or52h9
|
UTSW |
7 |
104,202,295 (GRCm39) |
missense |
probably benign |
0.13 |
R3116:Or52h9
|
UTSW |
7 |
104,202,295 (GRCm39) |
missense |
probably benign |
0.13 |
R3834:Or52h9
|
UTSW |
7 |
104,202,552 (GRCm39) |
missense |
probably benign |
0.43 |
R4027:Or52h9
|
UTSW |
7 |
104,202,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4423:Or52h9
|
UTSW |
7 |
104,202,552 (GRCm39) |
missense |
probably benign |
|
R4907:Or52h9
|
UTSW |
7 |
104,202,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R4984:Or52h9
|
UTSW |
7 |
104,202,228 (GRCm39) |
missense |
probably benign |
0.38 |
R5266:Or52h9
|
UTSW |
7 |
104,203,026 (GRCm39) |
missense |
probably benign |
0.00 |
R5592:Or52h9
|
UTSW |
7 |
104,202,938 (GRCm39) |
missense |
probably benign |
0.28 |
R6441:Or52h9
|
UTSW |
7 |
104,202,542 (GRCm39) |
nonsense |
probably null |
|
R7463:Or52h9
|
UTSW |
7 |
104,202,689 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7647:Or52h9
|
UTSW |
7 |
104,202,893 (GRCm39) |
missense |
probably benign |
0.00 |
R8276:Or52h9
|
UTSW |
7 |
104,202,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9752:Or52h9
|
UTSW |
7 |
104,202,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0067:Or52h9
|
UTSW |
7 |
104,202,594 (GRCm39) |
missense |
probably damaging |
0.97 |
|