Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot1 |
T |
A |
12: 84,017,361 (GRCm38) |
H414Q |
probably benign |
Het |
Actrt2 |
A |
T |
4: 154,667,036 (GRCm38) |
D214E |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 128,980,153 (GRCm38) |
T332A |
unknown |
Het |
Chd9 |
C |
T |
8: 90,933,224 (GRCm38) |
H271Y |
unknown |
Het |
Depdc5 |
T |
G |
5: 32,945,049 (GRCm38) |
D966E |
probably benign |
Het |
Dolpp1 |
A |
G |
2: 30,396,246 (GRCm38) |
Y119C |
probably benign |
Het |
Dscam |
G |
C |
16: 96,643,879 (GRCm38) |
D1537E |
probably benign |
Het |
Dusp16 |
A |
G |
6: 134,739,873 (GRCm38) |
I157T |
probably benign |
Het |
Dyrk2 |
T |
C |
10: 118,859,829 (GRCm38) |
D508G |
probably benign |
Het |
Endov |
T |
C |
11: 119,507,411 (GRCm38) |
V334A |
probably benign |
Het |
Ep400 |
A |
T |
5: 110,687,883 (GRCm38) |
V1956E |
unknown |
Het |
Erich3 |
A |
T |
3: 154,720,115 (GRCm38) |
Y83F |
possibly damaging |
Het |
Fbrsl1 |
T |
C |
5: 110,378,379 (GRCm38) |
|
probably null |
Het |
Gm1110 |
T |
C |
9: 26,920,661 (GRCm38) |
I65V |
probably damaging |
Het |
Gm28374 |
A |
G |
19: 6,082,200 (GRCm38) |
V19A |
|
Het |
Gm436 |
A |
T |
4: 144,670,669 (GRCm38) |
N164K |
probably benign |
Het |
Gpr107 |
C |
A |
2: 31,184,869 (GRCm38) |
H336Q |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,359,406 (GRCm38) |
Y355C |
|
Het |
Grm1 |
C |
A |
10: 10,720,132 (GRCm38) |
R584L |
probably benign |
Het |
Gse1 |
T |
C |
8: 120,229,810 (GRCm38) |
S347P |
unknown |
Het |
Ier3ip1 |
T |
A |
18: 76,940,525 (GRCm38) |
I69K |
possibly damaging |
Het |
Impact |
T |
G |
18: 12,984,331 (GRCm38) |
L154V |
probably benign |
Het |
Katnb1 |
T |
C |
8: 95,093,945 (GRCm38) |
F141S |
possibly damaging |
Het |
Kifap3 |
T |
A |
1: 163,797,362 (GRCm38) |
N162K |
probably damaging |
Het |
Klhl5 |
A |
G |
5: 65,148,587 (GRCm38) |
|
probably null |
Het |
Klre1 |
A |
G |
6: 129,584,222 (GRCm38) |
D182G |
probably benign |
Het |
Krt42 |
T |
A |
11: 100,266,957 (GRCm38) |
Y227F |
probably benign |
Het |
Lhcgr |
T |
A |
17: 88,742,050 (GRCm38) |
K683* |
probably null |
Het |
Lrrc37a |
G |
A |
11: 103,503,057 (GRCm38) |
S514F |
probably benign |
Het |
Lrrc9 |
G |
T |
12: 72,454,059 (GRCm38) |
L186F |
probably damaging |
Het |
Metrn |
A |
G |
17: 25,795,030 (GRCm38) |
V274A |
probably benign |
Het |
Mettl25 |
A |
T |
10: 105,823,179 (GRCm38) |
F414L |
possibly damaging |
Het |
Mixl1 |
A |
G |
1: 180,696,702 (GRCm38) |
V104A |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,348,342 (GRCm38) |
M1047K |
probably damaging |
Het |
Nbea |
G |
A |
3: 55,819,315 (GRCm38) |
A2081V |
probably benign |
Het |
Ndufs1 |
A |
T |
1: 63,150,012 (GRCm38) |
D551E |
possibly damaging |
Het |
Nectin3 |
T |
C |
16: 46,464,121 (GRCm38) |
T67A |
possibly damaging |
Het |
Nme8 |
C |
T |
13: 19,650,960 (GRCm38) |
V519I |
probably benign |
Het |
Npat |
G |
T |
9: 53,571,129 (GRCm38) |
G1379V |
probably benign |
Het |
Obscn |
T |
A |
11: 59,061,634 (GRCm38) |
T3870S |
probably benign |
Het |
Olfr1000 |
T |
C |
2: 85,608,749 (GRCm38) |
R54G |
possibly damaging |
Het |
Olfr1288 |
T |
C |
2: 111,479,234 (GRCm38) |
V150A |
possibly damaging |
Het |
Olfr379-ps1 |
T |
A |
11: 73,433,854 (GRCm38) |
H124L |
unknown |
Het |
Olfr871 |
T |
A |
9: 20,212,451 (GRCm38) |
M34K |
possibly damaging |
Het |
Olfr910 |
A |
G |
9: 38,539,410 (GRCm38) |
N172D |
probably damaging |
Het |
Parp8 |
A |
T |
13: 116,867,073 (GRCm38) |
Y769* |
probably null |
Het |
Pcnx |
C |
T |
12: 81,918,819 (GRCm38) |
R59* |
probably null |
Het |
Pdzd2 |
G |
A |
15: 12,373,506 (GRCm38) |
S2181L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,711,161 (GRCm38) |
E65G |
probably damaging |
Het |
Ppif |
C |
T |
14: 25,698,326 (GRCm38) |
T157M |
probably damaging |
Het |
Ppp3ca |
T |
A |
3: 136,932,225 (GRCm38) |
|
probably null |
Het |
Proser1 |
T |
A |
3: 53,472,088 (GRCm38) |
|
probably null |
Het |
Reg3d |
T |
A |
6: 78,376,079 (GRCm38) |
K174* |
probably null |
Het |
Rubcn |
A |
T |
16: 32,856,950 (GRCm38) |
L55Q |
probably damaging |
Het |
Sec14l3 |
T |
C |
11: 4,066,198 (GRCm38) |
L39P |
probably damaging |
Het |
Ska3 |
A |
G |
14: 57,826,102 (GRCm38) |
I4T |
probably damaging |
Het |
Slc30a10 |
A |
G |
1: 185,464,154 (GRCm38) |
I338V |
possibly damaging |
Het |
Slc35g1 |
T |
A |
19: 38,402,831 (GRCm38) |
L187H |
probably damaging |
Het |
Slc35g1 |
C |
G |
19: 38,402,829 (GRCm38) |
S186R |
probably damaging |
Het |
Spata5 |
T |
C |
3: 37,431,782 (GRCm38) |
S218P |
probably benign |
Het |
Tbc1d5 |
T |
C |
17: 50,742,086 (GRCm38) |
I659V |
probably benign |
Het |
Tbl3 |
G |
T |
17: 24,700,916 (GRCm38) |
D751E |
probably benign |
Het |
Tdrd3 |
T |
A |
14: 87,486,266 (GRCm38) |
D311E |
possibly damaging |
Het |
Tenm4 |
T |
C |
7: 96,854,728 (GRCm38) |
F1335S |
probably benign |
Het |
Tm2d1 |
A |
T |
4: 98,375,023 (GRCm38) |
C83S |
probably damaging |
Het |
Tnfrsf22 |
A |
T |
7: 143,638,373 (GRCm38) |
V192D |
unknown |
Het |
Trpm6 |
A |
G |
19: 18,811,790 (GRCm38) |
T575A |
probably damaging |
Het |
Uri1 |
T |
C |
7: 37,981,673 (GRCm38) |
D102G |
possibly damaging |
Het |
Vmn2r1 |
T |
A |
3: 64,103,050 (GRCm38) |
C570S |
probably damaging |
Het |
Vps13a |
C |
T |
19: 16,640,787 (GRCm38) |
V2906I |
probably damaging |
Het |
Zfp472 |
T |
C |
17: 32,978,003 (GRCm38) |
Y351H |
possibly damaging |
Het |
Zfp874a |
G |
T |
13: 67,443,234 (GRCm38) |
Y110* |
probably null |
Het |
Zfp986 |
T |
A |
4: 145,899,305 (GRCm38) |
N178K |
probably benign |
Het |
|
Other mutations in Olfr177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02084:Olfr177
|
APN |
16 |
58,873,036 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02223:Olfr177
|
APN |
16 |
58,872,694 (GRCm38) |
missense |
probably damaging |
1.00 |
R0131:Olfr177
|
UTSW |
16 |
58,872,906 (GRCm38) |
missense |
probably benign |
0.01 |
R0131:Olfr177
|
UTSW |
16 |
58,872,906 (GRCm38) |
missense |
probably benign |
0.01 |
R0132:Olfr177
|
UTSW |
16 |
58,872,906 (GRCm38) |
missense |
probably benign |
0.01 |
R0245:Olfr177
|
UTSW |
16 |
58,872,866 (GRCm38) |
missense |
probably benign |
0.01 |
R0717:Olfr177
|
UTSW |
16 |
58,872,770 (GRCm38) |
missense |
probably damaging |
1.00 |
R0975:Olfr177
|
UTSW |
16 |
58,873,150 (GRCm38) |
splice site |
probably null |
|
R1037:Olfr177
|
UTSW |
16 |
58,872,970 (GRCm38) |
missense |
probably damaging |
1.00 |
R1256:Olfr177
|
UTSW |
16 |
58,872,843 (GRCm38) |
nonsense |
probably null |
|
R1278:Olfr177
|
UTSW |
16 |
58,872,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R1538:Olfr177
|
UTSW |
16 |
58,872,898 (GRCm38) |
missense |
probably damaging |
1.00 |
R1992:Olfr177
|
UTSW |
16 |
58,872,511 (GRCm38) |
missense |
probably benign |
0.43 |
R2173:Olfr177
|
UTSW |
16 |
58,872,619 (GRCm38) |
missense |
probably damaging |
0.99 |
R2392:Olfr177
|
UTSW |
16 |
58,872,434 (GRCm38) |
missense |
probably damaging |
1.00 |
R5651:Olfr177
|
UTSW |
16 |
58,872,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R5652:Olfr177
|
UTSW |
16 |
58,872,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R5653:Olfr177
|
UTSW |
16 |
58,872,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R8031:Olfr177
|
UTSW |
16 |
58,872,691 (GRCm38) |
missense |
probably benign |
0.03 |
R8531:Olfr177
|
UTSW |
16 |
58,872,653 (GRCm38) |
missense |
probably damaging |
1.00 |
R8833:Olfr177
|
UTSW |
16 |
58,872,596 (GRCm38) |
missense |
probably damaging |
0.99 |
R9150:Olfr177
|
UTSW |
16 |
58,872,642 (GRCm38) |
nonsense |
probably null |
|
R9318:Olfr177
|
UTSW |
16 |
58,872,385 (GRCm38) |
missense |
probably damaging |
1.00 |
R9389:Olfr177
|
UTSW |
16 |
58,872,613 (GRCm38) |
missense |
probably damaging |
1.00 |
V8831:Olfr177
|
UTSW |
16 |
58,873,075 (GRCm38) |
missense |
probably benign |
0.28 |
|