Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,654 (GRCm39) |
S161G |
probably benign |
Het |
Ankfy1 |
G |
A |
11: 72,621,308 (GRCm39) |
R198Q |
possibly damaging |
Het |
Ankrd11 |
A |
G |
8: 123,616,919 (GRCm39) |
V2290A |
probably benign |
Het |
Aox4 |
A |
G |
1: 58,252,212 (GRCm39) |
N29S |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,891,379 (GRCm39) |
R592G |
possibly damaging |
Het |
Caap1 |
A |
T |
4: 94,389,640 (GRCm39) |
D231E |
possibly damaging |
Het |
Cabp1 |
T |
A |
5: 115,307,193 (GRCm39) |
M165L |
possibly damaging |
Het |
Calhm4 |
T |
A |
10: 33,917,630 (GRCm39) |
R274* |
probably null |
Het |
Cep72 |
A |
T |
13: 74,206,582 (GRCm39) |
L73H |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,525,743 (GRCm39) |
S731G |
probably null |
Het |
Dsc2 |
T |
C |
18: 20,179,295 (GRCm39) |
I258V |
probably benign |
Het |
Dsg1c |
T |
G |
18: 20,407,687 (GRCm39) |
N344K |
probably benign |
Het |
Enah |
A |
G |
1: 181,841,920 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,225,591 (GRCm39) |
S554C |
probably damaging |
Het |
Fkrp |
C |
A |
7: 16,545,037 (GRCm39) |
R275L |
possibly damaging |
Het |
Gbp4 |
C |
T |
5: 105,270,986 (GRCm39) |
G215D |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,783,284 (GRCm39) |
L239F |
probably damaging |
Het |
Gpr146 |
A |
G |
5: 139,378,573 (GRCm39) |
D125G |
probably damaging |
Het |
Hectd4 |
C |
A |
5: 121,494,259 (GRCm39) |
|
probably null |
Het |
Invs |
G |
A |
4: 48,397,534 (GRCm39) |
V370I |
possibly damaging |
Het |
Kdm2b |
A |
G |
5: 123,018,302 (GRCm39) |
V1040A |
probably damaging |
Het |
Kidins220 |
T |
A |
12: 25,088,434 (GRCm39) |
V1059D |
possibly damaging |
Het |
Kif26a |
T |
A |
12: 112,141,926 (GRCm39) |
S727T |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,410,813 (GRCm39) |
|
probably null |
Het |
Klk1b27 |
A |
G |
7: 43,705,169 (GRCm39) |
H112R |
probably benign |
Het |
Krt72 |
T |
G |
15: 101,685,187 (GRCm39) |
|
probably null |
Het |
Lactb |
C |
T |
9: 66,878,172 (GRCm39) |
R219H |
probably damaging |
Het |
Lrig2 |
A |
T |
3: 104,373,045 (GRCm39) |
I612N |
probably damaging |
Het |
Meaf6 |
A |
C |
4: 124,983,697 (GRCm39) |
N51T |
probably damaging |
Het |
Mtap |
A |
G |
4: 89,066,498 (GRCm39) |
T36A |
possibly damaging |
Het |
Myo3a |
G |
A |
2: 22,412,143 (GRCm39) |
G713S |
probably damaging |
Het |
Nr4a3 |
C |
T |
4: 48,083,255 (GRCm39) |
T596I |
probably damaging |
Het |
Or4f14 |
C |
G |
2: 111,743,228 (GRCm39) |
G16R |
possibly damaging |
Het |
Pam |
A |
G |
1: 97,765,752 (GRCm39) |
V759A |
possibly damaging |
Het |
Pcare |
T |
A |
17: 72,051,701 (GRCm39) |
E1217V |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,772,944 (GRCm39) |
I1220F |
probably benign |
Het |
Phldb2 |
T |
A |
16: 45,568,240 (GRCm39) |
M1222L |
possibly damaging |
Het |
Phospho1 |
C |
T |
11: 95,721,513 (GRCm39) |
A61V |
possibly damaging |
Het |
Pnpla7 |
G |
A |
2: 24,906,550 (GRCm39) |
V638I |
possibly damaging |
Het |
Pramel34 |
C |
A |
5: 93,785,391 (GRCm39) |
|
probably null |
Het |
Ptf1a |
T |
A |
2: 19,451,848 (GRCm39) |
D282E |
probably damaging |
Het |
Ptgs2 |
A |
T |
1: 149,975,879 (GRCm39) |
|
probably benign |
Het |
Racgap1 |
T |
C |
15: 99,522,156 (GRCm39) |
R471G |
probably damaging |
Het |
Rptn |
T |
C |
3: 93,303,419 (GRCm39) |
S251P |
possibly damaging |
Het |
Shcbp1 |
T |
C |
8: 4,794,507 (GRCm39) |
M429V |
probably benign |
Het |
Shprh |
T |
C |
10: 11,062,637 (GRCm39) |
L1248P |
probably damaging |
Het |
Son |
T |
C |
16: 91,456,835 (GRCm39) |
|
probably benign |
Het |
Sppl3 |
T |
C |
5: 115,233,995 (GRCm39) |
L355P |
probably damaging |
Het |
Tbc1d31 |
A |
T |
15: 57,818,778 (GRCm39) |
R794W |
probably damaging |
Het |
Telo2 |
T |
C |
17: 25,320,386 (GRCm39) |
Y766C |
probably damaging |
Het |
Tfr2 |
A |
G |
5: 137,572,793 (GRCm39) |
|
probably null |
Het |
Tle4 |
T |
C |
19: 14,429,056 (GRCm39) |
D722G |
probably damaging |
Het |
Tprg1l |
A |
G |
4: 154,243,862 (GRCm39) |
V98A |
probably benign |
Het |
Trak1 |
C |
T |
9: 121,272,822 (GRCm39) |
R237C |
probably benign |
Het |
Vmn2r113 |
T |
C |
17: 23,177,715 (GRCm39) |
I833T |
probably damaging |
Het |
Vmn2r118 |
T |
A |
17: 55,915,093 (GRCm39) |
S518C |
probably damaging |
Het |
Vmn2r49 |
A |
G |
7: 9,710,524 (GRCm39) |
I736T |
probably damaging |
Het |
Wdr38 |
T |
A |
2: 38,889,970 (GRCm39) |
|
probably null |
Het |
Wee2 |
A |
G |
6: 40,429,553 (GRCm39) |
E180G |
probably benign |
Het |
Zbtb1 |
T |
C |
12: 76,432,604 (GRCm39) |
S197P |
possibly damaging |
Het |
Zc3h7a |
T |
C |
16: 10,976,629 (GRCm39) |
|
probably null |
Het |
Zfp516 |
T |
A |
18: 82,973,835 (GRCm39) |
L11Q |
probably damaging |
Het |
Zfp623 |
G |
A |
15: 75,819,317 (GRCm39) |
R91H |
probably benign |
Het |
Zkscan7 |
G |
A |
9: 122,725,170 (GRCm39) |
R713Q |
probably benign |
Het |
|
Other mutations in Or10ak14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01092:Or10ak14
|
APN |
4 |
118,610,959 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02726:Or10ak14
|
APN |
4 |
118,610,961 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02928:Or10ak14
|
APN |
4 |
118,611,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03102:Or10ak14
|
APN |
4 |
118,611,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0062:Or10ak14
|
UTSW |
4 |
118,611,100 (GRCm39) |
missense |
probably benign |
0.00 |
R0062:Or10ak14
|
UTSW |
4 |
118,611,100 (GRCm39) |
missense |
probably benign |
0.00 |
R0299:Or10ak14
|
UTSW |
4 |
118,611,732 (GRCm39) |
start codon destroyed |
probably null |
0.82 |
R0501:Or10ak14
|
UTSW |
4 |
118,611,027 (GRCm39) |
missense |
probably benign |
0.00 |
R1301:Or10ak14
|
UTSW |
4 |
118,610,816 (GRCm39) |
missense |
probably benign |
|
R1719:Or10ak14
|
UTSW |
4 |
118,610,797 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2327:Or10ak14
|
UTSW |
4 |
118,611,331 (GRCm39) |
missense |
probably benign |
0.13 |
R3110:Or10ak14
|
UTSW |
4 |
118,611,421 (GRCm39) |
missense |
probably damaging |
0.99 |
R3112:Or10ak14
|
UTSW |
4 |
118,611,421 (GRCm39) |
missense |
probably damaging |
0.99 |
R4582:Or10ak14
|
UTSW |
4 |
118,611,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R4615:Or10ak14
|
UTSW |
4 |
118,611,334 (GRCm39) |
missense |
probably benign |
0.34 |
R5640:Or10ak14
|
UTSW |
4 |
118,610,986 (GRCm39) |
missense |
probably benign |
0.07 |
R6889:Or10ak14
|
UTSW |
4 |
118,611,504 (GRCm39) |
missense |
probably damaging |
0.99 |
R7157:Or10ak14
|
UTSW |
4 |
118,611,615 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7168:Or10ak14
|
UTSW |
4 |
118,611,048 (GRCm39) |
missense |
probably damaging |
0.98 |
R7378:Or10ak14
|
UTSW |
4 |
118,611,372 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7451:Or10ak14
|
UTSW |
4 |
118,610,884 (GRCm39) |
missense |
probably benign |
0.03 |
R7770:Or10ak14
|
UTSW |
4 |
118,611,254 (GRCm39) |
missense |
probably benign |
0.04 |
R7847:Or10ak14
|
UTSW |
4 |
118,611,565 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8839:Or10ak14
|
UTSW |
4 |
118,611,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R8942:Or10ak14
|
UTSW |
4 |
118,611,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9274:Or10ak14
|
UTSW |
4 |
118,610,883 (GRCm39) |
missense |
probably benign |
0.03 |
|