Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,771,839 (GRCm39) |
S343P |
possibly damaging |
Het |
4930563M21Rik |
T |
A |
9: 55,916,568 (GRCm39) |
E36D |
unknown |
Het |
Abcc8 |
T |
G |
7: 45,756,092 (GRCm39) |
K1450T |
probably benign |
Het |
Aox1 |
A |
T |
1: 58,361,953 (GRCm39) |
N720Y |
possibly damaging |
Het |
BC034090 |
T |
C |
1: 155,101,518 (GRCm39) |
T249A |
probably benign |
Het |
Brf2 |
A |
T |
8: 27,614,021 (GRCm39) |
S388R |
probably damaging |
Het |
Ccdc180 |
A |
T |
4: 45,944,461 (GRCm39) |
Q1437L |
probably damaging |
Het |
Cdc42ep1 |
A |
C |
15: 78,734,025 (GRCm39) |
D375A |
probably benign |
Het |
Cep85l |
T |
C |
10: 53,174,282 (GRCm39) |
Y487C |
probably damaging |
Het |
Cfap299 |
C |
T |
5: 98,646,162 (GRCm39) |
A86V |
probably benign |
Het |
Chd3 |
C |
T |
11: 69,244,027 (GRCm39) |
R1346H |
possibly damaging |
Het |
Cltc |
T |
A |
11: 86,603,446 (GRCm39) |
R793S |
possibly damaging |
Het |
Crat |
A |
G |
2: 30,298,214 (GRCm39) |
F162L |
probably benign |
Het |
Cyp3a44 |
C |
A |
5: 145,711,187 (GRCm39) |
V495L |
probably benign |
Het |
Dchs2 |
C |
T |
3: 83,189,361 (GRCm39) |
T1575I |
possibly damaging |
Het |
Ddx60 |
A |
G |
8: 62,462,994 (GRCm39) |
T1292A |
possibly damaging |
Het |
Dnah12 |
C |
T |
14: 26,495,016 (GRCm39) |
A109V |
probably benign |
Het |
Foxo3 |
C |
T |
10: 42,073,021 (GRCm39) |
V499M |
probably damaging |
Het |
Fry |
T |
C |
5: 150,419,297 (GRCm39) |
S546P |
|
Het |
Hfe |
T |
C |
13: 23,890,792 (GRCm39) |
K204E |
probably benign |
Het |
Hibch |
T |
A |
1: 52,952,986 (GRCm39) |
Y329N |
probably damaging |
Het |
Irf9 |
T |
G |
14: 55,846,247 (GRCm39) |
I426S |
probably damaging |
Het |
Kif26a |
C |
A |
12: 112,112,835 (GRCm39) |
P13T |
probably damaging |
Het |
Lhx5 |
A |
C |
5: 120,570,451 (GRCm39) |
K36Q |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,707,579 (GRCm39) |
S1623P |
probably damaging |
Het |
Mre11a |
T |
C |
9: 14,710,884 (GRCm39) |
F193L |
probably damaging |
Het |
Mybl2 |
G |
A |
2: 162,910,135 (GRCm39) |
G187E |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,099,929 (GRCm39) |
Q613L |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,087,312 (GRCm39) |
M1056K |
probably benign |
Het |
Or1e16 |
T |
C |
11: 73,285,955 (GRCm39) |
K298E |
probably damaging |
Het |
Or4a27 |
G |
A |
2: 88,559,799 (GRCm39) |
T48I |
probably benign |
Het |
Or51ag1 |
C |
T |
7: 103,155,727 (GRCm39) |
R142H |
probably benign |
Het |
Pcdhga12 |
G |
A |
18: 37,900,940 (GRCm39) |
V591M |
probably damaging |
Het |
Phyhipl |
A |
G |
10: 70,401,116 (GRCm39) |
S161P |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,263,205 (GRCm39) |
T775A |
probably benign |
Het |
Pou3f3 |
T |
C |
1: 42,736,682 (GRCm39) |
V126A |
unknown |
Het |
Reg4 |
A |
C |
3: 98,143,631 (GRCm39) |
K142Q |
possibly damaging |
Het |
Rimoc1 |
T |
C |
15: 4,021,336 (GRCm39) |
D73G |
probably damaging |
Het |
Sec22c |
G |
T |
9: 121,517,314 (GRCm39) |
A199E |
probably damaging |
Het |
Sema3d |
C |
T |
5: 12,603,181 (GRCm39) |
P395S |
probably damaging |
Het |
Sh2b2 |
C |
T |
5: 136,260,893 (GRCm39) |
E108K |
possibly damaging |
Het |
Slfn3 |
A |
G |
11: 83,105,616 (GRCm39) |
K538E |
possibly damaging |
Het |
Spatc1l |
A |
T |
10: 76,405,200 (GRCm39) |
D194V |
probably damaging |
Het |
Stoml3 |
T |
C |
3: 53,408,185 (GRCm39) |
V77A |
possibly damaging |
Het |
Taco1 |
A |
G |
11: 105,963,930 (GRCm39) |
I230V |
probably benign |
Het |
Tfcp2 |
T |
C |
15: 100,411,934 (GRCm39) |
T346A |
probably benign |
Het |
Tmem8b |
C |
T |
4: 43,686,188 (GRCm39) |
T273M |
probably damaging |
Het |
Trav6-1 |
A |
G |
14: 52,876,299 (GRCm39) |
N73S |
probably benign |
Het |
Trav6d-5 |
A |
G |
14: 53,033,060 (GRCm39) |
D103G |
probably damaging |
Het |
Ttll5 |
T |
A |
12: 85,937,806 (GRCm39) |
L379Q |
probably damaging |
Het |
Ube3c |
T |
A |
5: 29,803,846 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
A |
C |
2: 69,727,769 (GRCm39) |
D44A |
probably benign |
Het |
Upp2 |
G |
T |
2: 58,457,443 (GRCm39) |
R5L |
unknown |
Het |
Vmn1r43 |
G |
A |
6: 89,846,877 (GRCm39) |
T203M |
probably damaging |
Het |
Vmn2r17 |
C |
T |
5: 109,600,712 (GRCm39) |
T670I |
probably damaging |
Het |
Zfp433 |
A |
T |
10: 81,556,122 (GRCm39) |
H208L |
probably damaging |
Het |
Zfp616 |
A |
T |
11: 73,974,744 (GRCm39) |
I429F |
possibly damaging |
Het |
|
Other mutations in Or8b3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00958:Or8b3b
|
APN |
9 |
38,584,320 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01388:Or8b3b
|
APN |
9 |
38,584,379 (GRCm39) |
nonsense |
probably null |
|
IGL01516:Or8b3b
|
APN |
9 |
38,584,159 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02121:Or8b3b
|
APN |
9 |
38,584,711 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02209:Or8b3b
|
APN |
9 |
38,584,342 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02256:Or8b3b
|
APN |
9 |
38,584,776 (GRCm39) |
start codon destroyed |
probably null |
|
IGL02517:Or8b3b
|
APN |
9 |
38,584,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Or8b3b
|
APN |
9 |
38,584,312 (GRCm39) |
missense |
probably benign |
|
IGL02747:Or8b3b
|
APN |
9 |
38,584,380 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02971:Or8b3b
|
APN |
9 |
38,584,564 (GRCm39) |
missense |
probably damaging |
0.96 |
E0370:Or8b3b
|
UTSW |
9 |
38,583,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R0616:Or8b3b
|
UTSW |
9 |
38,584,776 (GRCm39) |
start codon destroyed |
probably null |
|
R2173:Or8b3b
|
UTSW |
9 |
38,584,240 (GRCm39) |
missense |
probably benign |
0.03 |
R2989:Or8b3b
|
UTSW |
9 |
38,583,831 (GRCm39) |
missense |
probably benign |
|
R3430:Or8b3b
|
UTSW |
9 |
38,584,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Or8b3b
|
UTSW |
9 |
38,584,159 (GRCm39) |
missense |
probably benign |
0.09 |
R4688:Or8b3b
|
UTSW |
9 |
38,584,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R4702:Or8b3b
|
UTSW |
9 |
38,584,776 (GRCm39) |
start codon destroyed |
probably null |
|
R5548:Or8b3b
|
UTSW |
9 |
38,584,600 (GRCm39) |
missense |
probably benign |
0.00 |
R5590:Or8b3b
|
UTSW |
9 |
38,584,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R6082:Or8b3b
|
UTSW |
9 |
38,583,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6214:Or8b3b
|
UTSW |
9 |
38,584,510 (GRCm39) |
missense |
probably benign |
0.13 |
R6215:Or8b3b
|
UTSW |
9 |
38,584,510 (GRCm39) |
missense |
probably benign |
0.13 |
R6893:Or8b3b
|
UTSW |
9 |
38,584,355 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7215:Or8b3b
|
UTSW |
9 |
38,584,743 (GRCm39) |
missense |
probably benign |
0.05 |
R7624:Or8b3b
|
UTSW |
9 |
38,583,919 (GRCm39) |
missense |
probably benign |
0.18 |
R7862:Or8b3b
|
UTSW |
9 |
38,584,624 (GRCm39) |
missense |
probably benign |
0.01 |
R8116:Or8b3b
|
UTSW |
9 |
38,584,464 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8897:Or8b3b
|
UTSW |
9 |
38,584,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R8899:Or8b3b
|
UTSW |
9 |
38,584,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Or8b3b
|
UTSW |
9 |
38,583,892 (GRCm39) |
missense |
probably benign |
|
R9311:Or8b3b
|
UTSW |
9 |
38,583,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R9690:Or8b3b
|
UTSW |
9 |
38,584,477 (GRCm39) |
nonsense |
probably null |
|
R9734:Or8b3b
|
UTSW |
9 |
38,584,239 (GRCm39) |
missense |
probably benign |
|
|