Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
A |
C |
11: 84,333,400 (GRCm39) |
D503E |
possibly damaging |
Het |
Bsn |
C |
T |
9: 107,990,208 (GRCm39) |
R1848Q |
possibly damaging |
Het |
Cacna1d |
C |
T |
14: 29,825,692 (GRCm39) |
V1001I |
probably damaging |
Het |
Calhm3 |
T |
C |
19: 47,140,516 (GRCm39) |
I192M |
probably damaging |
Het |
Cep44 |
A |
G |
8: 57,000,457 (GRCm39) |
S19P |
possibly damaging |
Het |
Cxcl15 |
T |
A |
5: 90,949,225 (GRCm39) |
I130K |
unknown |
Het |
Cxcl3 |
C |
T |
5: 90,934,175 (GRCm39) |
|
probably benign |
Het |
Emc1 |
T |
G |
4: 139,084,931 (GRCm39) |
H167Q |
probably benign |
Het |
Epb41l3 |
T |
G |
17: 69,566,066 (GRCm39) |
Y416D |
probably damaging |
Het |
Erbb2 |
G |
A |
11: 98,326,397 (GRCm39) |
R1007H |
probably damaging |
Het |
Esr1 |
A |
G |
10: 4,916,245 (GRCm39) |
|
probably benign |
Het |
Fat4 |
G |
A |
3: 39,005,388 (GRCm39) |
R1929Q |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,807,835 (GRCm39) |
C1385S |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,256,891 (GRCm39) |
I777T |
probably damaging |
Het |
Gm16092 |
T |
G |
1: 85,440,689 (GRCm39) |
|
noncoding transcript |
Het |
Greb1 |
T |
A |
12: 16,767,259 (GRCm39) |
K314N |
probably damaging |
Het |
Iigp1c |
C |
A |
18: 60,378,724 (GRCm39) |
N86K |
probably damaging |
Het |
Ipcef1 |
A |
G |
10: 6,858,029 (GRCm39) |
|
probably benign |
Het |
Iqank1 |
G |
A |
15: 75,917,281 (GRCm39) |
E305K |
possibly damaging |
Het |
Mgat4a |
C |
A |
1: 37,491,344 (GRCm39) |
L292F |
probably damaging |
Het |
Mill1 |
A |
G |
7: 17,996,613 (GRCm39) |
N143S |
probably benign |
Het |
Mindy1 |
A |
G |
3: 95,201,067 (GRCm39) |
T324A |
probably benign |
Het |
Mpdz |
T |
A |
4: 81,202,851 (GRCm39) |
H1882L |
probably damaging |
Het |
Ncapg2 |
T |
A |
12: 116,393,277 (GRCm39) |
W494R |
probably damaging |
Het |
Oas1c |
A |
T |
5: 120,943,598 (GRCm39) |
H180Q |
probably benign |
Het |
Or2q1 |
T |
A |
6: 42,794,701 (GRCm39) |
C99S |
probably damaging |
Het |
Or4c108 |
T |
C |
2: 88,803,357 (GRCm39) |
M293V |
probably benign |
Het |
Or4k49 |
A |
G |
2: 111,494,708 (GRCm39) |
M46V |
probably benign |
Het |
Or5ak20 |
A |
T |
2: 85,183,620 (GRCm39) |
S217T |
probably damaging |
Het |
Pelp1 |
A |
G |
11: 70,285,693 (GRCm39) |
V725A |
probably damaging |
Het |
Plxna4 |
T |
C |
6: 32,211,541 (GRCm39) |
E666G |
probably benign |
Het |
Pprc1 |
ATCCTCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTC |
19: 46,059,755 (GRCm39) |
|
probably benign |
Het |
Prdm16 |
T |
C |
4: 154,432,411 (GRCm39) |
D285G |
probably damaging |
Het |
Rasa2 |
A |
G |
9: 96,493,442 (GRCm39) |
S81P |
possibly damaging |
Het |
Rhd |
T |
A |
4: 134,623,287 (GRCm39) |
F418Y |
probably benign |
Het |
Rnf207 |
T |
C |
4: 152,402,385 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
C |
T |
7: 97,334,766 (GRCm39) |
R1300C |
probably damaging |
Het |
Ryr1 |
A |
C |
7: 28,746,290 (GRCm39) |
L3830R |
probably damaging |
Het |
Sgsh |
A |
G |
11: 119,237,625 (GRCm39) |
Y330H |
probably benign |
Het |
Sh3bp5 |
T |
C |
14: 31,109,791 (GRCm39) |
E130G |
possibly damaging |
Het |
Slc29a3 |
A |
G |
10: 60,588,563 (GRCm39) |
|
probably benign |
Het |
Slco1a5 |
A |
G |
6: 142,194,443 (GRCm39) |
L400P |
probably damaging |
Het |
Snd1 |
A |
G |
6: 28,874,858 (GRCm39) |
|
probably null |
Het |
Sox15 |
C |
T |
11: 69,546,556 (GRCm39) |
R120C |
probably damaging |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
Tas2r110 |
A |
T |
6: 132,845,016 (GRCm39) |
I16L |
probably benign |
Het |
Tmx3 |
T |
A |
18: 90,546,058 (GRCm39) |
V213D |
possibly damaging |
Het |
Uba2 |
A |
T |
7: 33,864,915 (GRCm39) |
|
probably null |
Het |
Wfikkn1 |
T |
A |
17: 26,097,886 (GRCm39) |
D112V |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,467,198 (GRCm39) |
N2452S |
probably damaging |
Het |
|
Other mutations in Or6c88 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01867:Or6c88
|
APN |
10 |
129,406,696 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02157:Or6c88
|
APN |
10 |
129,407,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Or6c88
|
APN |
10 |
129,407,306 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02833:Or6c88
|
APN |
10 |
129,406,619 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02930:Or6c88
|
APN |
10 |
129,407,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03038:Or6c88
|
APN |
10 |
129,406,790 (GRCm39) |
missense |
probably benign |
0.07 |
G4846:Or6c88
|
UTSW |
10 |
129,407,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Or6c88
|
UTSW |
10 |
129,406,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R1737:Or6c88
|
UTSW |
10 |
129,406,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Or6c88
|
UTSW |
10 |
129,407,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Or6c88
|
UTSW |
10 |
129,406,915 (GRCm39) |
nonsense |
probably null |
|
R3086:Or6c88
|
UTSW |
10 |
129,407,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Or6c88
|
UTSW |
10 |
129,406,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Or6c88
|
UTSW |
10 |
129,406,571 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6598:Or6c88
|
UTSW |
10 |
129,407,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Or6c88
|
UTSW |
10 |
129,406,941 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7066:Or6c88
|
UTSW |
10 |
129,407,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7226:Or6c88
|
UTSW |
10 |
129,406,584 (GRCm39) |
missense |
probably benign |
0.01 |
R7324:Or6c88
|
UTSW |
10 |
129,406,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R7408:Or6c88
|
UTSW |
10 |
129,406,493 (GRCm39) |
start gained |
probably benign |
|
R7779:Or6c88
|
UTSW |
10 |
129,407,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R8733:Or6c88
|
UTSW |
10 |
129,406,579 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8891:Or6c88
|
UTSW |
10 |
129,407,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R8931:Or6c88
|
UTSW |
10 |
129,406,550 (GRCm39) |
missense |
probably benign |
0.09 |
R9310:Or6c88
|
UTSW |
10 |
129,406,687 (GRCm39) |
missense |
probably benign |
0.00 |
R9681:Or6c88
|
UTSW |
10 |
129,406,664 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or6c88
|
UTSW |
10 |
129,407,105 (GRCm39) |
nonsense |
probably null |
|
|