Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
A |
G |
15: 11,310,904 (GRCm39) |
T1054A |
probably benign |
Het |
Ankfn1 |
A |
C |
11: 89,413,859 (GRCm39) |
I172S |
probably benign |
Het |
Ano3 |
T |
C |
2: 110,605,367 (GRCm39) |
T280A |
possibly damaging |
Het |
Arhgef37 |
T |
A |
18: 61,638,827 (GRCm39) |
E307D |
probably benign |
Het |
Bptf |
C |
T |
11: 107,001,709 (GRCm39) |
V468I |
probably benign |
Het |
Ces1b |
A |
G |
8: 93,786,987 (GRCm39) |
V464A |
probably benign |
Het |
Cmc2 |
A |
T |
8: 117,616,446 (GRCm39) |
L93* |
probably null |
Het |
Ddx60 |
A |
G |
8: 62,407,569 (GRCm39) |
D360G |
probably benign |
Het |
Dock6 |
C |
T |
9: 21,744,135 (GRCm39) |
|
probably null |
Het |
Erp44 |
A |
G |
4: 48,218,136 (GRCm39) |
F178L |
possibly damaging |
Het |
Fam47e |
T |
C |
5: 92,722,541 (GRCm39) |
V79A |
probably damaging |
Het |
Fancd2 |
T |
C |
6: 113,542,165 (GRCm39) |
S770P |
probably damaging |
Het |
Fcgr1 |
A |
G |
3: 96,191,897 (GRCm39) |
F304L |
probably benign |
Het |
Fkbp15 |
T |
C |
4: 62,230,538 (GRCm39) |
E725G |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,638,825 (GRCm39) |
I1971V |
probably benign |
Het |
Gdf6 |
A |
G |
4: 9,844,652 (GRCm39) |
S59G |
probably benign |
Het |
Gm5773 |
T |
A |
3: 93,680,373 (GRCm39) |
I15N |
possibly damaging |
Het |
Hesx1 |
T |
C |
14: 26,723,379 (GRCm39) |
S70P |
probably benign |
Het |
Htr5a |
T |
C |
5: 28,055,995 (GRCm39) |
S329P |
probably damaging |
Het |
Htt |
T |
C |
5: 34,987,225 (GRCm39) |
|
probably null |
Het |
Iba57 |
T |
A |
11: 59,052,288 (GRCm39) |
M118L |
unknown |
Het |
Ifi35 |
C |
T |
11: 101,348,307 (GRCm39) |
Q112* |
probably null |
Het |
Il12rb1 |
G |
T |
8: 71,265,233 (GRCm39) |
R183L |
possibly damaging |
Het |
Il12rb2 |
A |
T |
6: 67,328,311 (GRCm39) |
Y306* |
probably null |
Het |
Ints1 |
C |
G |
5: 139,742,282 (GRCm39) |
D1722H |
probably damaging |
Het |
Ipp |
T |
G |
4: 116,381,453 (GRCm39) |
D317E |
probably damaging |
Het |
Kif26a |
A |
G |
12: 112,142,481 (GRCm39) |
T912A |
probably benign |
Het |
Klhdc7a |
A |
G |
4: 139,693,045 (GRCm39) |
V634A |
probably damaging |
Het |
Klhl40 |
C |
A |
9: 121,607,748 (GRCm39) |
P303T |
probably damaging |
Het |
Krt13 |
T |
C |
11: 100,008,478 (GRCm39) |
T420A |
unknown |
Het |
Lpcat2 |
T |
C |
8: 93,582,186 (GRCm39) |
F35S |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,289,753 (GRCm39) |
V5470A |
probably damaging |
Het |
Mta2 |
T |
C |
19: 8,925,151 (GRCm39) |
|
probably null |
Het |
Muc16 |
G |
T |
9: 18,567,725 (GRCm39) |
T1598K |
unknown |
Het |
Nckap5 |
A |
T |
1: 125,954,547 (GRCm39) |
N668K |
probably damaging |
Het |
Nlrp4a |
A |
T |
7: 26,150,070 (GRCm39) |
D559V |
possibly damaging |
Het |
Npat |
T |
C |
9: 53,474,167 (GRCm39) |
L653P |
probably benign |
Het |
Oog1 |
G |
A |
12: 87,655,252 (GRCm39) |
V467I |
possibly damaging |
Het |
Or4c15b |
A |
G |
2: 89,113,082 (GRCm39) |
S132P |
probably benign |
Het |
Pdzph1 |
T |
A |
17: 59,186,105 (GRCm39) |
M1229L |
possibly damaging |
Het |
Piwil4 |
T |
A |
9: 14,614,445 (GRCm39) |
Q106L |
|
Het |
Plekha5 |
C |
A |
6: 140,472,267 (GRCm39) |
R65S |
probably damaging |
Het |
Ptger4 |
T |
C |
15: 5,264,381 (GRCm39) |
Y425C |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,951,465 (GRCm39) |
M534T |
possibly damaging |
Het |
Rtkn2 |
C |
T |
10: 67,875,923 (GRCm39) |
P411S |
probably damaging |
Het |
Scand1 |
G |
A |
2: 156,154,232 (GRCm39) |
P13S |
unknown |
Het |
Scaper |
T |
C |
9: 55,765,438 (GRCm39) |
H550R |
probably benign |
Het |
Senp5 |
T |
A |
16: 31,796,514 (GRCm39) |
K617I |
probably damaging |
Het |
Shq1 |
A |
G |
6: 100,613,972 (GRCm39) |
L282P |
probably damaging |
Het |
Slc12a6 |
T |
A |
2: 112,166,256 (GRCm39) |
C227S |
probably damaging |
Het |
Slc5a9 |
T |
A |
4: 111,747,729 (GRCm39) |
T284S |
probably benign |
Het |
Stat2 |
T |
A |
10: 128,120,831 (GRCm39) |
F579L |
probably damaging |
Het |
Tes |
G |
T |
6: 17,096,242 (GRCm39) |
A77S |
possibly damaging |
Het |
Themis |
A |
T |
10: 28,637,342 (GRCm39) |
T149S |
probably benign |
Het |
Tmprss6 |
C |
T |
15: 78,326,664 (GRCm39) |
R653H |
probably benign |
Het |
Trmt6 |
G |
A |
2: 132,652,959 (GRCm39) |
L107F |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,792,714 (GRCm39) |
C713R |
probably damaging |
Het |
Trpm7 |
T |
C |
2: 126,667,454 (GRCm39) |
I820V |
probably benign |
Het |
Usp45 |
G |
A |
4: 21,824,543 (GRCm39) |
A432T |
probably benign |
Het |
Xab2 |
A |
T |
8: 3,668,622 (GRCm39) |
V82E |
possibly damaging |
Het |
Zfp938 |
T |
A |
10: 82,061,777 (GRCm39) |
Y281F |
possibly damaging |
Het |
|
Other mutations in Or4f56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Or4f56
|
APN |
2 |
111,703,295 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02198:Or4f56
|
APN |
2 |
111,703,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Or4f56
|
APN |
2 |
111,703,925 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02302:Or4f56
|
APN |
2 |
111,703,887 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03348:Or4f56
|
APN |
2 |
111,703,493 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4131001:Or4f56
|
UTSW |
2 |
111,703,649 (GRCm39) |
missense |
probably benign |
0.02 |
R2144:Or4f56
|
UTSW |
2 |
111,703,768 (GRCm39) |
missense |
probably damaging |
0.96 |
R2860:Or4f56
|
UTSW |
2 |
111,703,818 (GRCm39) |
nonsense |
probably null |
|
R2861:Or4f56
|
UTSW |
2 |
111,703,818 (GRCm39) |
nonsense |
probably null |
|
R3785:Or4f56
|
UTSW |
2 |
111,703,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R4474:Or4f56
|
UTSW |
2 |
111,703,784 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4508:Or4f56
|
UTSW |
2 |
111,703,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4540:Or4f56
|
UTSW |
2 |
111,703,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Or4f56
|
UTSW |
2 |
111,703,395 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4784:Or4f56
|
UTSW |
2 |
111,703,395 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4785:Or4f56
|
UTSW |
2 |
111,703,395 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5410:Or4f56
|
UTSW |
2 |
111,703,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5491:Or4f56
|
UTSW |
2 |
111,703,907 (GRCm39) |
missense |
probably benign |
0.44 |
R6875:Or4f56
|
UTSW |
2 |
111,703,306 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7185:Or4f56
|
UTSW |
2 |
111,704,167 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9100:Or4f56
|
UTSW |
2 |
111,703,606 (GRCm39) |
missense |
possibly damaging |
0.61 |
|