Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat1 |
C |
A |
9: 53,493,946 (GRCm39) |
V392F |
probably damaging |
Het |
Ache |
C |
T |
5: 137,288,326 (GRCm39) |
P11S |
possibly damaging |
Het |
Ache |
T |
A |
5: 137,288,692 (GRCm39) |
|
probably null |
Het |
Acoxl |
A |
T |
2: 127,696,821 (GRCm39) |
H23L |
probably benign |
Het |
Adamtsl1 |
G |
A |
4: 86,306,650 (GRCm39) |
|
probably null |
Het |
Adar |
T |
A |
3: 89,646,519 (GRCm39) |
F45I |
probably benign |
Het |
Adgrf4 |
A |
C |
17: 42,978,104 (GRCm39) |
L413R |
probably damaging |
Het |
Atp6v1g3 |
A |
T |
1: 138,215,627 (GRCm39) |
I96F |
probably benign |
Het |
Brsk2 |
T |
C |
7: 141,554,594 (GRCm39) |
M653T |
probably benign |
Het |
Cacna1s |
G |
T |
1: 136,033,549 (GRCm39) |
V1275L |
probably benign |
Het |
Ces3b |
T |
C |
8: 105,815,264 (GRCm39) |
V5A |
possibly damaging |
Het |
Chpt1 |
A |
T |
10: 88,312,969 (GRCm39) |
I281N |
probably damaging |
Het |
Col10a1 |
A |
G |
10: 34,270,553 (GRCm39) |
E175G |
probably damaging |
Het |
Col27a1 |
T |
C |
4: 63,142,902 (GRCm39) |
S197P |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 15,960,471 (GRCm39) |
R3315W |
probably damaging |
Het |
Ctnna2 |
T |
C |
6: 77,091,914 (GRCm39) |
E443G |
probably damaging |
Het |
Dhx9 |
G |
T |
1: 153,356,969 (GRCm39) |
S93R |
probably benign |
Het |
Efcab8 |
A |
G |
2: 153,625,676 (GRCm39) |
H112R |
probably damaging |
Het |
Eif3d |
A |
T |
15: 77,843,887 (GRCm39) |
N486K |
probably damaging |
Het |
Esp8 |
C |
T |
17: 40,840,909 (GRCm39) |
R57* |
probably null |
Het |
Eya3 |
A |
T |
4: 132,417,090 (GRCm39) |
I130F |
probably damaging |
Het |
Fat2 |
G |
T |
11: 55,143,052 (GRCm39) |
L4266I |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,793,019 (GRCm39) |
D983E |
probably benign |
Het |
Gcc2 |
T |
C |
10: 58,106,791 (GRCm39) |
S640P |
probably damaging |
Het |
Gys2 |
C |
T |
6: 142,394,147 (GRCm39) |
G464R |
probably damaging |
Het |
Heatr5a |
G |
A |
12: 51,935,026 (GRCm39) |
T1659I |
probably damaging |
Het |
Il17ra |
A |
G |
6: 120,458,403 (GRCm39) |
D518G |
probably damaging |
Het |
Kcnk13 |
A |
G |
12: 100,027,510 (GRCm39) |
Y195C |
probably damaging |
Het |
Kmt2a |
T |
A |
9: 44,759,782 (GRCm39) |
H722L |
probably damaging |
Het |
Luzp1 |
C |
A |
4: 136,270,653 (GRCm39) |
Q959K |
possibly damaging |
Het |
Mep1b |
T |
A |
18: 21,219,306 (GRCm39) |
H153Q |
probably damaging |
Het |
Mfsd13b |
A |
T |
7: 120,599,346 (GRCm39) |
I381F |
probably benign |
Het |
Mvk |
A |
G |
5: 114,597,034 (GRCm39) |
T334A |
probably benign |
Het |
Naa30 |
T |
C |
14: 49,425,008 (GRCm39) |
V320A |
probably damaging |
Het |
Naip5 |
C |
T |
13: 100,382,254 (GRCm39) |
G152S |
possibly damaging |
Het |
Neb |
A |
C |
2: 52,185,384 (GRCm39) |
S949R |
probably damaging |
Het |
Nfya |
A |
T |
17: 48,699,046 (GRCm39) |
I214N |
possibly damaging |
Het |
Nsf |
G |
T |
11: 103,773,637 (GRCm39) |
N292K |
probably damaging |
Het |
Nup133 |
T |
C |
8: 124,653,945 (GRCm39) |
T505A |
probably benign |
Het |
Or4c1 |
A |
C |
2: 89,133,920 (GRCm39) |
S5R |
probably benign |
Het |
Or5h24 |
T |
A |
16: 58,919,067 (GRCm39) |
H96L |
unknown |
Het |
Or9s23 |
A |
T |
1: 92,501,546 (GRCm39) |
T218S |
probably benign |
Het |
P4ha3 |
A |
T |
7: 99,943,022 (GRCm39) |
R136W |
probably damaging |
Het |
Parp12 |
A |
G |
6: 39,067,142 (GRCm39) |
V550A |
probably damaging |
Het |
Phf11a |
T |
C |
14: 59,532,387 (GRCm39) |
D16G |
probably benign |
Het |
Pramel31 |
T |
A |
4: 144,088,207 (GRCm39) |
M1K |
probably null |
Het |
Rab3gap2 |
A |
G |
1: 185,009,342 (GRCm39) |
|
probably null |
Het |
Sco1 |
A |
G |
11: 66,954,784 (GRCm39) |
D263G |
probably damaging |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,103,384 (GRCm39) |
|
probably benign |
Homo |
Sfpq |
T |
A |
4: 126,915,516 (GRCm39) |
S103T |
unknown |
Het |
Shisa7 |
G |
A |
7: 4,832,975 (GRCm39) |
R263C |
probably damaging |
Het |
Ssc4d |
T |
A |
5: 135,992,254 (GRCm39) |
D144V |
probably benign |
Het |
Stxbp5l |
G |
A |
16: 36,950,213 (GRCm39) |
P1044L |
probably damaging |
Het |
Tgm6 |
G |
A |
2: 129,987,116 (GRCm39) |
R528Q |
probably benign |
Het |
Tlr3 |
A |
T |
8: 45,849,992 (GRCm39) |
H892Q |
probably benign |
Het |
Tmc2 |
A |
G |
2: 130,082,035 (GRCm39) |
H406R |
probably damaging |
Het |
Tmtc1 |
A |
T |
6: 148,345,397 (GRCm39) |
|
probably null |
Het |
Ttc19 |
A |
G |
11: 62,174,977 (GRCm39) |
I139M |
probably benign |
Het |
Utrn |
G |
A |
10: 12,524,929 (GRCm39) |
R2185C |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,681,959 (GRCm39) |
N3004S |
probably damaging |
Het |
Wdr3 |
C |
A |
3: 100,050,300 (GRCm39) |
G746W |
probably damaging |
Het |
Zfp335 |
T |
A |
2: 164,744,165 (GRCm39) |
Q500L |
probably damaging |
Het |
Zfp804b |
A |
T |
5: 6,820,071 (GRCm39) |
D961E |
probably benign |
Het |
Zkscan16 |
CTTCAGCTTTCA |
CTTCA |
4: 58,956,745 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or4p7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Or4p7
|
APN |
2 |
88,222,245 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02261:Or4p7
|
APN |
2 |
88,221,725 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03023:Or4p7
|
APN |
2 |
88,221,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Or4p7
|
APN |
2 |
88,221,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03168:Or4p7
|
APN |
2 |
88,221,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0432:Or4p7
|
UTSW |
2 |
88,222,377 (GRCm39) |
missense |
probably damaging |
0.98 |
R1738:Or4p7
|
UTSW |
2 |
88,221,671 (GRCm39) |
missense |
probably benign |
0.01 |
R2051:Or4p7
|
UTSW |
2 |
88,221,882 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2136:Or4p7
|
UTSW |
2 |
88,221,663 (GRCm39) |
missense |
probably benign |
0.24 |
R3236:Or4p7
|
UTSW |
2 |
88,221,750 (GRCm39) |
missense |
probably benign |
0.01 |
R4407:Or4p7
|
UTSW |
2 |
88,222,427 (GRCm39) |
missense |
probably benign |
0.37 |
R4930:Or4p7
|
UTSW |
2 |
88,222,284 (GRCm39) |
missense |
probably benign |
0.12 |
R4959:Or4p7
|
UTSW |
2 |
88,221,674 (GRCm39) |
missense |
probably benign |
0.37 |
R4973:Or4p7
|
UTSW |
2 |
88,221,674 (GRCm39) |
missense |
probably benign |
0.37 |
R5178:Or4p7
|
UTSW |
2 |
88,221,819 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6282:Or4p7
|
UTSW |
2 |
88,221,877 (GRCm39) |
nonsense |
probably null |
|
R7289:Or4p7
|
UTSW |
2 |
88,222,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R7493:Or4p7
|
UTSW |
2 |
88,222,224 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7591:Or4p7
|
UTSW |
2 |
88,222,220 (GRCm39) |
missense |
probably benign |
0.17 |
R8060:Or4p7
|
UTSW |
2 |
88,221,848 (GRCm39) |
missense |
probably benign |
0.00 |
R8242:Or4p7
|
UTSW |
2 |
88,222,418 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Or4p7
|
UTSW |
2 |
88,222,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|