Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
C |
T |
1: 179,620,016 (GRCm39) |
G220E |
possibly damaging |
Het |
Arhgef10l |
A |
G |
4: 140,321,504 (GRCm39) |
I101T |
probably benign |
Het |
Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
Camkk2 |
A |
T |
5: 122,902,298 (GRCm39) |
C4S |
probably damaging |
Het |
Ccdc174 |
T |
A |
6: 91,876,538 (GRCm39) |
D458E |
possibly damaging |
Het |
Cercam |
A |
G |
2: 29,770,686 (GRCm39) |
N419S |
probably benign |
Het |
Clca3a2 |
T |
C |
3: 144,512,083 (GRCm39) |
N551S |
probably damaging |
Het |
Cldn18 |
T |
A |
9: 99,580,988 (GRCm39) |
I87F |
probably damaging |
Het |
Ctso |
T |
A |
3: 81,848,836 (GRCm39) |
|
probably benign |
Het |
Ddhd2 |
C |
A |
8: 26,236,981 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
T |
A |
9: 45,359,094 (GRCm39) |
Y118N |
probably damaging |
Het |
Ece1 |
C |
T |
4: 137,666,044 (GRCm39) |
A296V |
probably benign |
Het |
Fbxo40 |
T |
A |
16: 36,790,766 (GRCm39) |
I115F |
possibly damaging |
Het |
Fkbp9 |
T |
A |
6: 56,827,609 (GRCm39) |
N143K |
probably damaging |
Het |
Foxk2 |
G |
T |
11: 121,190,402 (GRCm39) |
|
probably benign |
Het |
Ggnbp1 |
A |
G |
17: 27,248,529 (GRCm39) |
K33E |
probably benign |
Het |
Hace1 |
A |
T |
10: 45,547,530 (GRCm39) |
|
probably benign |
Het |
Hk3 |
A |
T |
13: 55,162,107 (GRCm39) |
C133S |
probably damaging |
Het |
Kbtbd3 |
C |
T |
9: 4,331,252 (GRCm39) |
A542V |
probably damaging |
Het |
Lrch2 |
A |
C |
X: 146,263,537 (GRCm39) |
V363G |
probably damaging |
Het |
Lrch2 |
C |
T |
X: 146,302,131 (GRCm39) |
C264Y |
probably damaging |
Het |
Lrrc56 |
C |
A |
7: 140,787,546 (GRCm39) |
|
probably benign |
Het |
Lrtm2 |
C |
T |
6: 119,294,199 (GRCm39) |
V311M |
probably damaging |
Het |
N4bp1 |
G |
T |
8: 87,587,529 (GRCm39) |
Q470K |
probably benign |
Het |
Naa15 |
A |
C |
3: 51,367,552 (GRCm39) |
D575A |
probably benign |
Het |
Ncaph |
A |
T |
2: 126,969,456 (GRCm39) |
V69D |
probably damaging |
Het |
Nlrp5 |
G |
A |
7: 23,123,489 (GRCm39) |
|
probably null |
Het |
Nmbr |
A |
G |
10: 14,636,331 (GRCm39) |
D100G |
probably damaging |
Het |
Ofcc1 |
C |
T |
13: 40,250,553 (GRCm39) |
V588M |
possibly damaging |
Het |
Or4b13 |
G |
T |
2: 90,082,849 (GRCm39) |
T161N |
probably damaging |
Het |
Osmr |
C |
A |
15: 6,871,475 (GRCm39) |
R314M |
probably damaging |
Het |
Pcdhb16 |
C |
T |
18: 37,611,270 (GRCm39) |
Q77* |
probably null |
Het |
Pglyrp4 |
G |
A |
3: 90,642,955 (GRCm39) |
|
probably null |
Het |
Ptprh |
A |
G |
7: 4,552,498 (GRCm39) |
F922S |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,418,673 (GRCm39) |
Q813L |
possibly damaging |
Het |
Sgtb |
A |
G |
13: 104,254,922 (GRCm39) |
N64S |
probably benign |
Het |
Slc5a12 |
T |
C |
2: 110,471,201 (GRCm39) |
V481A |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,149,349 (GRCm39) |
V454A |
probably benign |
Het |
Sntg2 |
C |
A |
12: 30,317,025 (GRCm39) |
|
probably null |
Het |
Synj1 |
C |
T |
16: 90,770,933 (GRCm39) |
V499I |
probably damaging |
Het |
Tmco1 |
T |
C |
1: 167,153,597 (GRCm39) |
|
probably benign |
Het |
Tmem38b |
T |
C |
4: 53,848,871 (GRCm39) |
I92T |
probably damaging |
Het |
Tmem9 |
T |
C |
1: 135,955,145 (GRCm39) |
V93A |
probably benign |
Het |
Ttn |
T |
A |
2: 76,625,582 (GRCm39) |
R15080S |
possibly damaging |
Het |
Ube2e3 |
T |
C |
2: 78,749,065 (GRCm39) |
I138T |
probably damaging |
Het |
Urgcp |
A |
G |
11: 5,665,752 (GRCm39) |
I862T |
possibly damaging |
Het |
Vmn1r68 |
A |
T |
7: 10,261,603 (GRCm39) |
I165N |
probably benign |
Het |
Washc4 |
G |
A |
10: 83,394,717 (GRCm39) |
V316I |
possibly damaging |
Het |
Zfp111 |
A |
T |
7: 23,899,113 (GRCm39) |
L166Q |
possibly damaging |
Het |
Zfyve1 |
A |
T |
12: 83,597,718 (GRCm39) |
|
probably benign |
Het |
Zscan18 |
A |
G |
7: 12,508,793 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or5p4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01472:Or5p4
|
APN |
7 |
107,680,411 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01570:Or5p4
|
APN |
7 |
107,680,480 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03175:Or5p4
|
APN |
7 |
107,680,925 (GRCm39) |
missense |
probably benign |
|
R0401:Or5p4
|
UTSW |
7 |
107,680,079 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0932:Or5p4
|
UTSW |
7 |
107,680,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R1679:Or5p4
|
UTSW |
7 |
107,680,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R2189:Or5p4
|
UTSW |
7 |
107,680,243 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3804:Or5p4
|
UTSW |
7 |
107,680,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R4532:Or5p4
|
UTSW |
7 |
107,680,756 (GRCm39) |
missense |
probably benign |
0.18 |
R4932:Or5p4
|
UTSW |
7 |
107,680,781 (GRCm39) |
missense |
probably damaging |
0.99 |
R5630:Or5p4
|
UTSW |
7 |
107,680,323 (GRCm39) |
missense |
probably benign |
0.05 |
R6155:Or5p4
|
UTSW |
7 |
107,680,493 (GRCm39) |
missense |
probably benign |
0.00 |
R6523:Or5p4
|
UTSW |
7 |
107,680,762 (GRCm39) |
missense |
probably benign |
0.34 |
R6987:Or5p4
|
UTSW |
7 |
107,680,338 (GRCm39) |
nonsense |
probably null |
|
R7378:Or5p4
|
UTSW |
7 |
107,680,399 (GRCm39) |
missense |
not run |
|
R7609:Or5p4
|
UTSW |
7 |
107,680,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R8293:Or5p4
|
UTSW |
7 |
107,680,269 (GRCm39) |
missense |
probably benign |
0.00 |
R9322:Or5p4
|
UTSW |
7 |
107,680,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Or5p4
|
UTSW |
7 |
107,680,040 (GRCm39) |
missense |
|
|
R9659:Or5p4
|
UTSW |
7 |
107,680,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9788:Or5p4
|
UTSW |
7 |
107,680,745 (GRCm39) |
missense |
probably damaging |
1.00 |
V8831:Or5p4
|
UTSW |
7 |
107,680,742 (GRCm39) |
missense |
probably benign |
0.24 |
Z1177:Or5p4
|
UTSW |
7 |
107,680,279 (GRCm39) |
missense |
probably benign |
0.03 |
|