Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,659,570 (GRCm39) |
D341G |
probably damaging |
Het |
Abca17 |
T |
C |
17: 24,486,657 (GRCm39) |
T1457A |
probably damaging |
Het |
Acot8 |
A |
T |
2: 164,646,663 (GRCm39) |
S25R |
probably benign |
Het |
Ap2a2 |
T |
C |
7: 141,210,212 (GRCm39) |
V850A |
probably benign |
Het |
Baiap2l1 |
T |
A |
5: 144,214,487 (GRCm39) |
E402D |
probably benign |
Het |
Bptf |
T |
C |
11: 106,943,815 (GRCm39) |
K2689E |
probably damaging |
Het |
Cdh22 |
C |
A |
2: 164,954,098 (GRCm39) |
D808Y |
probably damaging |
Het |
Cilp |
G |
A |
9: 65,186,286 (GRCm39) |
G794S |
probably damaging |
Het |
Cipc |
A |
G |
12: 87,008,809 (GRCm39) |
T223A |
probably benign |
Het |
Crem |
G |
T |
18: 3,295,397 (GRCm39) |
T57K |
possibly damaging |
Het |
Cyp17a1 |
T |
A |
19: 46,656,516 (GRCm39) |
I393F |
probably benign |
Het |
Dgcr2 |
C |
T |
16: 17,676,242 (GRCm39) |
G176D |
probably benign |
Het |
Dock3 |
C |
A |
9: 106,790,371 (GRCm39) |
V1451L |
probably benign |
Het |
Dsg2 |
C |
T |
18: 20,708,121 (GRCm39) |
P74L |
probably benign |
Het |
Ece1 |
T |
C |
4: 137,664,075 (GRCm39) |
V224A |
probably damaging |
Het |
Flg |
A |
T |
3: 93,190,586 (GRCm39) |
S152C |
unknown |
Het |
Gcsam |
A |
T |
16: 45,430,902 (GRCm39) |
N3I |
probably damaging |
Het |
Gm10188 |
C |
T |
1: 132,157,310 (GRCm39) |
V19I |
unknown |
Het |
Gpr27 |
T |
C |
6: 99,670,217 (GRCm39) |
L193P |
probably damaging |
Het |
Grin2b |
A |
T |
6: 135,900,074 (GRCm39) |
V269E |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Kif14 |
A |
G |
1: 136,443,651 (GRCm39) |
I1275V |
possibly damaging |
Het |
Krt27 |
T |
C |
11: 99,239,862 (GRCm39) |
E234G |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,139,807 (GRCm39) |
|
probably null |
Het |
Matk |
T |
G |
10: 81,094,121 (GRCm39) |
S18A |
probably benign |
Het |
Mbd3l1 |
A |
G |
9: 18,395,886 (GRCm39) |
T4A |
probably benign |
Het |
Mettl23 |
G |
A |
11: 116,739,185 (GRCm39) |
|
probably null |
Het |
Ncam1 |
A |
T |
9: 49,479,817 (GRCm39) |
W54R |
probably damaging |
Het |
Olfm5 |
A |
G |
7: 103,803,606 (GRCm39) |
Y286H |
probably damaging |
Het |
Or10d5j |
T |
A |
9: 39,868,265 (GRCm39) |
M1L |
probably benign |
Het |
Or4c11c |
G |
A |
2: 88,661,633 (GRCm39) |
M57I |
possibly damaging |
Het |
Or4q3 |
T |
C |
14: 50,582,922 (GRCm39) |
I326V |
probably benign |
Het |
Pmch |
A |
G |
10: 87,927,614 (GRCm39) |
Y105C |
probably damaging |
Het |
Prg3 |
A |
G |
2: 84,819,676 (GRCm39) |
T57A |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,688,838 (GRCm39) |
E877G |
probably damaging |
Het |
Ptprt |
A |
G |
2: 161,769,566 (GRCm39) |
V433A |
probably benign |
Het |
Rufy1 |
A |
T |
11: 50,297,233 (GRCm39) |
D406E |
probably benign |
Het |
Scara5 |
C |
T |
14: 65,927,234 (GRCm39) |
R44W |
probably damaging |
Het |
Scg2 |
T |
G |
1: 79,414,576 (GRCm39) |
K49T |
probably benign |
Het |
Slc40a1 |
A |
G |
1: 45,950,180 (GRCm39) |
I424T |
probably benign |
Het |
Slc4a8 |
T |
A |
15: 100,693,735 (GRCm39) |
S479T |
probably damaging |
Het |
Sorl1 |
T |
C |
9: 41,929,456 (GRCm39) |
D1139G |
probably damaging |
Het |
Srcap |
A |
G |
7: 127,152,353 (GRCm39) |
I2206V |
possibly damaging |
Het |
Tpk1 |
T |
C |
6: 43,642,711 (GRCm39) |
E9G |
probably benign |
Het |
Ttn |
C |
T |
2: 76,642,645 (GRCm39) |
V13297I |
possibly damaging |
Het |
Uchl3 |
T |
C |
14: 101,932,655 (GRCm39) |
|
probably null |
Het |
Usp12 |
T |
C |
5: 146,688,751 (GRCm39) |
D201G |
probably damaging |
Het |
Vmn1r193 |
C |
T |
13: 22,403,146 (GRCm39) |
R282H |
probably benign |
Het |
Vmn2r104 |
T |
C |
17: 20,261,040 (GRCm39) |
D461G |
possibly damaging |
Het |
Zfp131 |
A |
G |
13: 120,244,440 (GRCm39) |
M80T |
possibly damaging |
Het |
Zfp457 |
A |
G |
13: 67,441,663 (GRCm39) |
L304P |
probably benign |
Het |
Zswim3 |
A |
G |
2: 164,663,566 (GRCm39) |
E682G |
probably damaging |
Het |
|
Other mutations in Or5ac15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01807:Or5ac15
|
APN |
16 |
58,939,936 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02098:Or5ac15
|
APN |
16 |
58,940,433 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02276:Or5ac15
|
APN |
16 |
58,940,378 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03122:Or5ac15
|
APN |
16 |
58,939,801 (GRCm39) |
missense |
probably benign |
0.00 |
R0781:Or5ac15
|
UTSW |
16 |
58,940,187 (GRCm39) |
missense |
probably damaging |
0.97 |
R1162:Or5ac15
|
UTSW |
16 |
58,939,735 (GRCm39) |
missense |
probably damaging |
0.99 |
R1526:Or5ac15
|
UTSW |
16 |
58,940,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Or5ac15
|
UTSW |
16 |
58,940,052 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4379:Or5ac15
|
UTSW |
16 |
58,940,027 (GRCm39) |
missense |
probably benign |
0.22 |
R4380:Or5ac15
|
UTSW |
16 |
58,940,027 (GRCm39) |
missense |
probably benign |
0.22 |
R5768:Or5ac15
|
UTSW |
16 |
58,940,335 (GRCm39) |
small deletion |
probably benign |
|
R5771:Or5ac15
|
UTSW |
16 |
58,940,335 (GRCm39) |
small deletion |
probably benign |
|
R5942:Or5ac15
|
UTSW |
16 |
58,940,039 (GRCm39) |
nonsense |
probably null |
|
R6131:Or5ac15
|
UTSW |
16 |
58,940,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R6539:Or5ac15
|
UTSW |
16 |
58,940,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R6621:Or5ac15
|
UTSW |
16 |
58,940,287 (GRCm39) |
missense |
probably benign |
0.19 |
R7642:Or5ac15
|
UTSW |
16 |
58,940,011 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8863:Or5ac15
|
UTSW |
16 |
58,939,712 (GRCm39) |
nonsense |
probably null |
|
RF009:Or5ac15
|
UTSW |
16 |
58,940,274 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Or5ac15
|
UTSW |
16 |
58,939,735 (GRCm39) |
nonsense |
probably null |
|
|