Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,244,175 (GRCm39) |
T2013S |
probably benign |
Het |
Ablim3 |
A |
G |
18: 61,938,135 (GRCm39) |
|
probably null |
Het |
Acvrl1 |
T |
A |
15: 101,034,104 (GRCm39) |
C206* |
probably null |
Het |
Adamts15 |
C |
A |
9: 30,817,454 (GRCm39) |
R541S |
probably damaging |
Het |
Add3 |
A |
G |
19: 53,221,577 (GRCm39) |
I230V |
probably benign |
Het |
Ankrd27 |
A |
G |
7: 35,327,871 (GRCm39) |
D742G |
possibly damaging |
Het |
Asxl3 |
A |
G |
18: 22,650,597 (GRCm39) |
E862G |
probably damaging |
Het |
Asxl3 |
A |
T |
18: 22,544,556 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
G |
A |
6: 113,742,693 (GRCm39) |
T798M |
possibly damaging |
Het |
Car12 |
T |
C |
9: 66,659,599 (GRCm39) |
I208T |
probably damaging |
Het |
Cgn |
T |
A |
3: 94,680,502 (GRCm39) |
Q600L |
probably damaging |
Het |
Cgnl1 |
C |
T |
9: 71,539,927 (GRCm39) |
A1106T |
probably benign |
Het |
Cmtr2 |
T |
C |
8: 110,949,178 (GRCm39) |
V496A |
probably benign |
Het |
Cplx4 |
C |
A |
18: 66,090,123 (GRCm39) |
D99Y |
probably damaging |
Het |
Cyfip2 |
T |
C |
11: 46,114,963 (GRCm39) |
T915A |
probably benign |
Het |
Cyp4a32 |
T |
C |
4: 115,466,894 (GRCm39) |
L193P |
probably damaging |
Het |
Dennd5b |
C |
T |
6: 148,946,102 (GRCm39) |
R503Q |
probably damaging |
Het |
Depdc5 |
C |
A |
5: 33,059,209 (GRCm39) |
Q303K |
possibly damaging |
Het |
Dlx1 |
T |
A |
2: 71,362,840 (GRCm39) |
M249K |
possibly damaging |
Het |
Dnah10 |
A |
T |
5: 124,890,892 (GRCm39) |
E3218V |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,856,473 (GRCm39) |
D2896G |
probably damaging |
Het |
Dtx4 |
C |
A |
19: 12,447,022 (GRCm39) |
G557* |
probably null |
Het |
Eps8l2 |
A |
G |
7: 140,940,305 (GRCm39) |
N512D |
probably damaging |
Het |
Fam20a |
T |
C |
11: 109,612,201 (GRCm39) |
D114G |
possibly damaging |
Het |
Fbln1 |
T |
C |
15: 85,090,353 (GRCm39) |
S7P |
unknown |
Het |
Fli1 |
T |
C |
9: 32,335,484 (GRCm39) |
E316G |
probably damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Haus8 |
G |
A |
8: 71,705,781 (GRCm39) |
T302I |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,514,627 (GRCm39) |
I3582V |
probably benign |
Het |
Hnrnpul1 |
G |
A |
7: 25,447,842 (GRCm39) |
Q161* |
probably null |
Het |
Hsf4 |
C |
T |
8: 105,998,779 (GRCm39) |
A223V |
probably damaging |
Het |
Ighg2c |
A |
G |
12: 113,251,636 (GRCm39) |
W164R |
|
Het |
Isl1 |
A |
G |
13: 116,439,826 (GRCm39) |
V174A |
probably benign |
Het |
Itih4 |
A |
T |
14: 30,618,571 (GRCm39) |
I661F |
probably benign |
Het |
Klhl14 |
A |
T |
18: 21,785,193 (GRCm39) |
L78Q |
probably damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,215,180 (GRCm39) |
I177F |
unknown |
Het |
Lingo3 |
T |
A |
10: 80,670,938 (GRCm39) |
T331S |
possibly damaging |
Het |
Lrrc36 |
T |
C |
8: 106,187,689 (GRCm39) |
V535A |
possibly damaging |
Het |
Mapk8ip2 |
T |
G |
15: 89,342,279 (GRCm39) |
S497A |
probably benign |
Het |
Mbip |
A |
G |
12: 56,384,547 (GRCm39) |
|
probably null |
Het |
Nelfa |
C |
T |
5: 34,056,169 (GRCm39) |
G498D |
probably damaging |
Het |
Nherf2 |
C |
T |
17: 24,869,078 (GRCm39) |
R16H |
probably damaging |
Het |
Nlrc5 |
T |
A |
8: 95,248,433 (GRCm39) |
|
probably null |
Het |
Or2ag2b |
A |
T |
7: 106,417,650 (GRCm39) |
Y120F |
probably damaging |
Het |
Or4f59 |
A |
T |
2: 111,872,711 (GRCm39) |
V222D |
probably damaging |
Het |
Or7e171-ps1 |
T |
A |
9: 19,852,855 (GRCm39) |
T294S |
unknown |
Het |
Pde2a |
A |
G |
7: 101,155,160 (GRCm39) |
Y567C |
probably damaging |
Het |
Pdia4 |
A |
T |
6: 47,777,891 (GRCm39) |
F367Y |
probably benign |
Het |
Pkdrej |
C |
A |
15: 85,700,389 (GRCm39) |
C1849F |
possibly damaging |
Het |
Plekhj1 |
T |
G |
10: 80,633,492 (GRCm39) |
T52P |
probably damaging |
Het |
Ppp2r5d |
A |
T |
17: 46,994,986 (GRCm39) |
Y572N |
probably benign |
Het |
Prkcq |
T |
A |
2: 11,295,262 (GRCm39) |
Y570* |
probably null |
Het |
Ptpn3 |
T |
A |
4: 57,245,062 (GRCm39) |
D226V |
probably damaging |
Het |
Rab1b |
A |
G |
19: 5,155,229 (GRCm39) |
S22P |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,650,976 (GRCm39) |
S2060P |
probably damaging |
Het |
Rnf148 |
G |
T |
6: 23,654,890 (GRCm39) |
S35R |
probably benign |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Samd15 |
T |
A |
12: 87,247,818 (GRCm39) |
S168T |
possibly damaging |
Het |
Slc26a4 |
T |
A |
12: 31,597,945 (GRCm39) |
N167I |
probably damaging |
Het |
Slc39a1 |
C |
A |
3: 90,159,097 (GRCm39) |
H141Q |
probably benign |
Het |
Snx21 |
T |
C |
2: 164,628,121 (GRCm39) |
S46P |
probably benign |
Het |
Strip2 |
A |
G |
6: 29,944,486 (GRCm39) |
S657G |
probably damaging |
Het |
Stxbp3 |
G |
A |
3: 108,708,125 (GRCm39) |
P392L |
probably damaging |
Het |
Suclg1 |
G |
A |
6: 73,240,954 (GRCm39) |
R161H |
probably benign |
Het |
Tas1r3 |
T |
C |
4: 155,947,283 (GRCm39) |
Y134C |
probably damaging |
Het |
Tgif1 |
T |
A |
17: 71,153,168 (GRCm39) |
Q114L |
probably damaging |
Het |
Tll2 |
A |
G |
19: 41,074,673 (GRCm39) |
F964L |
probably benign |
Het |
Tmem181a |
T |
C |
17: 6,348,195 (GRCm39) |
S247P |
possibly damaging |
Het |
Trav23 |
A |
T |
14: 54,215,025 (GRCm39) |
R79S |
probably damaging |
Het |
Trf |
C |
A |
9: 103,102,347 (GRCm39) |
C177F |
probably damaging |
Het |
Triml1 |
T |
C |
8: 43,589,408 (GRCm39) |
Y260C |
probably benign |
Het |
Tulp4 |
T |
C |
17: 6,286,510 (GRCm39) |
F1513L |
probably benign |
Het |
Umodl1 |
G |
A |
17: 31,205,090 (GRCm39) |
V562I |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,491,960 (GRCm39) |
K3083R |
possibly damaging |
Het |
Vmn1r74 |
A |
T |
7: 11,580,888 (GRCm39) |
I63F |
probably benign |
Het |
Vmn2r38 |
C |
T |
7: 9,100,637 (GRCm39) |
C43Y |
possibly damaging |
Het |
Vmn2r50 |
A |
T |
7: 9,787,010 (GRCm39) |
N32K |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,784,032 (GRCm39) |
V3914A |
|
Het |
Vwa5b2 |
A |
G |
16: 20,422,878 (GRCm39) |
T984A |
probably benign |
Het |
Zc3h3 |
C |
T |
15: 75,712,231 (GRCm39) |
V77M |
probably damaging |
Het |
Zfp397 |
A |
T |
18: 24,093,415 (GRCm39) |
H300L |
probably damaging |
Het |
Zfp950 |
G |
A |
19: 61,107,650 (GRCm39) |
R478C |
probably benign |
Het |
|
Other mutations in Or56a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02247:Or56a3
|
APN |
7 |
104,735,530 (GRCm39) |
nonsense |
probably null |
|
IGL02505:Or56a3
|
APN |
7 |
104,735,540 (GRCm39) |
missense |
probably benign |
|
IGL03160:Or56a3
|
APN |
7 |
104,735,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0079:Or56a3
|
UTSW |
7 |
104,735,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Or56a3
|
UTSW |
7 |
104,735,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Or56a3
|
UTSW |
7 |
104,735,509 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3122:Or56a3
|
UTSW |
7 |
104,735,385 (GRCm39) |
missense |
probably benign |
0.00 |
R3828:Or56a3
|
UTSW |
7 |
104,735,504 (GRCm39) |
missense |
probably benign |
0.00 |
R4235:Or56a3
|
UTSW |
7 |
104,734,994 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4360:Or56a3
|
UTSW |
7 |
104,735,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R4485:Or56a3
|
UTSW |
7 |
104,735,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Or56a3
|
UTSW |
7 |
104,735,844 (GRCm39) |
unclassified |
probably benign |
|
R5542:Or56a3
|
UTSW |
7 |
104,735,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Or56a3
|
UTSW |
7 |
104,735,757 (GRCm39) |
splice site |
probably null |
|
R5723:Or56a3
|
UTSW |
7 |
104,740,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R5770:Or56a3
|
UTSW |
7 |
104,740,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R5871:Or56a3
|
UTSW |
7 |
104,735,511 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7593:Or56a3
|
UTSW |
7 |
104,735,372 (GRCm39) |
missense |
probably benign |
|
R7881:Or56a3
|
UTSW |
7 |
104,735,780 (GRCm39) |
missense |
probably damaging |
0.98 |
R8878:Or56a3
|
UTSW |
7 |
104,735,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Or56a3
|
UTSW |
7 |
104,735,329 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9576:Or56a3
|
UTSW |
7 |
104,735,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R9684:Or56a3
|
UTSW |
7 |
104,735,589 (GRCm39) |
missense |
|
|
|