Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
A |
T |
4: 144,504,683 (GRCm39) |
I156N |
probably damaging |
Het |
Abca1 |
C |
A |
4: 53,042,381 (GRCm39) |
R1897L |
possibly damaging |
Het |
Ablim2 |
A |
G |
5: 36,015,170 (GRCm39) |
K461E |
probably damaging |
Het |
Acss3 |
A |
T |
10: 106,773,008 (GRCm39) |
Y659* |
probably null |
Het |
Actr8 |
T |
G |
14: 29,708,952 (GRCm39) |
L253R |
probably damaging |
Het |
Arid4b |
A |
G |
13: 14,362,281 (GRCm39) |
K915R |
probably damaging |
Het |
C3 |
T |
C |
17: 57,511,502 (GRCm39) |
E1560G |
probably benign |
Het |
Cacna1c |
A |
T |
6: 118,631,333 (GRCm39) |
I1013N |
probably damaging |
Het |
Cep83 |
G |
A |
10: 94,625,600 (GRCm39) |
R670H |
probably benign |
Het |
Col19a1 |
T |
A |
1: 24,332,193 (GRCm39) |
D870V |
probably damaging |
Het |
Ddr2 |
A |
G |
1: 169,832,298 (GRCm39) |
V164A |
possibly damaging |
Het |
Dnaaf10 |
A |
G |
11: 17,162,031 (GRCm39) |
D23G |
possibly damaging |
Het |
Donson |
A |
T |
16: 91,476,814 (GRCm39) |
V549E |
probably damaging |
Het |
Egflam |
C |
T |
15: 7,254,144 (GRCm39) |
G824R |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,292,075 (GRCm39) |
F916S |
probably damaging |
Het |
Fam110c |
A |
G |
12: 31,124,406 (GRCm39) |
M123V |
unknown |
Het |
G3bp1 |
A |
T |
11: 55,388,813 (GRCm39) |
I342F |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,720,870 (GRCm39) |
N409D |
probably benign |
Het |
Grin2b |
C |
T |
6: 135,713,304 (GRCm39) |
G859D |
probably damaging |
Het |
Hspb1 |
A |
T |
5: 135,918,186 (GRCm39) |
T178S |
probably benign |
Het |
Iigp1 |
A |
G |
18: 60,523,329 (GRCm39) |
Y149C |
probably damaging |
Het |
Il22 |
G |
T |
10: 118,045,366 (GRCm39) |
G159* |
probably null |
Het |
Jcad |
T |
C |
18: 4,675,790 (GRCm39) |
F1184S |
probably damaging |
Het |
Kcnj2 |
G |
T |
11: 110,963,057 (GRCm39) |
V150L |
probably damaging |
Het |
Kifc1 |
C |
T |
17: 34,105,639 (GRCm39) |
R56Q |
probably damaging |
Het |
Lce1h |
A |
G |
3: 92,671,027 (GRCm39) |
S42P |
unknown |
Het |
Lrp4 |
C |
A |
2: 91,327,418 (GRCm39) |
D1471E |
probably benign |
Het |
Lrrc3 |
C |
A |
10: 77,737,299 (GRCm39) |
V46L |
probably benign |
Het |
Mcf2l |
G |
A |
8: 12,976,646 (GRCm39) |
A2T |
possibly damaging |
Het |
Med12l |
G |
A |
3: 59,170,634 (GRCm39) |
C1673Y |
probably null |
Het |
Nckap1 |
T |
C |
2: 80,343,034 (GRCm39) |
E955G |
possibly damaging |
Het |
Ndufs3 |
T |
A |
2: 90,732,690 (GRCm39) |
|
probably null |
Het |
Nkx6-1 |
A |
G |
5: 101,809,698 (GRCm39) |
|
probably null |
Het |
Obscn |
C |
A |
11: 58,890,954 (GRCm39) |
E1713* |
probably null |
Het |
Or10ak12 |
G |
A |
4: 118,666,560 (GRCm39) |
T167I |
possibly damaging |
Het |
Or10g1b |
A |
G |
14: 52,627,582 (GRCm39) |
F216S |
probably damaging |
Het |
Or10n1 |
A |
G |
9: 39,524,916 (GRCm39) |
T18A |
probably benign |
Het |
Or2n1 |
T |
A |
17: 38,486,917 (GRCm39) |
|
probably null |
Het |
Or6n1 |
A |
G |
1: 173,917,541 (GRCm39) |
R312G |
probably benign |
Het |
Or7e165 |
A |
C |
9: 19,695,161 (GRCm39) |
H244P |
probably damaging |
Het |
Osbpl5 |
A |
G |
7: 143,295,433 (GRCm39) |
F10L |
possibly damaging |
Het |
Plvap |
A |
C |
8: 71,964,095 (GRCm39) |
I89S |
probably damaging |
Het |
Ppp2r2a |
A |
G |
14: 67,259,772 (GRCm39) |
V308A |
possibly damaging |
Het |
Ppp2r5e |
T |
C |
12: 75,540,250 (GRCm39) |
S132G |
probably benign |
Het |
Pum3 |
G |
T |
19: 27,389,659 (GRCm39) |
Q398K |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,184,430 (GRCm39) |
T1526A |
probably benign |
Het |
Sh3tc2 |
T |
A |
18: 62,122,704 (GRCm39) |
Y488* |
probably null |
Het |
Spmip7 |
A |
T |
11: 11,440,244 (GRCm39) |
R8S |
possibly damaging |
Het |
Sqle |
A |
G |
15: 59,202,753 (GRCm39) |
Y537C |
probably benign |
Het |
Sult2a8 |
T |
G |
7: 14,159,439 (GRCm39) |
K60T |
probably damaging |
Het |
Tex15 |
T |
C |
8: 34,064,199 (GRCm39) |
S1210P |
possibly damaging |
Het |
Thumpd3 |
A |
G |
6: 113,043,825 (GRCm39) |
|
silent |
Het |
Timeless |
A |
G |
10: 128,077,604 (GRCm39) |
D228G |
probably damaging |
Het |
Trim31 |
A |
T |
17: 37,216,797 (GRCm39) |
|
probably null |
Het |
Ttc39c |
A |
T |
18: 12,828,428 (GRCm39) |
D196V |
possibly damaging |
Het |
Wbp4 |
C |
A |
14: 79,709,837 (GRCm39) |
V133L |
possibly damaging |
Het |
Zfp354c |
G |
T |
11: 50,706,597 (GRCm39) |
D159E |
probably benign |
Het |
Zfp940 |
C |
A |
7: 29,544,858 (GRCm39) |
D350Y |
probably benign |
Het |
|
Other mutations in Or8c15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00331:Or8c15
|
APN |
9 |
38,120,534 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00914:Or8c15
|
APN |
9 |
38,121,095 (GRCm39) |
splice site |
probably null |
|
IGL01563:Or8c15
|
APN |
9 |
38,120,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01696:Or8c15
|
APN |
9 |
38,120,345 (GRCm39) |
unclassified |
probably benign |
|
IGL02064:Or8c15
|
APN |
9 |
38,120,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Or8c15
|
APN |
9 |
38,120,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R0415:Or8c15
|
UTSW |
9 |
38,121,269 (GRCm39) |
missense |
probably benign |
|
R0463:Or8c15
|
UTSW |
9 |
38,120,360 (GRCm39) |
missense |
probably benign |
0.00 |
R0843:Or8c15
|
UTSW |
9 |
38,120,579 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1441:Or8c15
|
UTSW |
9 |
38,120,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1939:Or8c15
|
UTSW |
9 |
38,120,725 (GRCm39) |
nonsense |
probably null |
|
R2512:Or8c15
|
UTSW |
9 |
38,120,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Or8c15
|
UTSW |
9 |
38,120,586 (GRCm39) |
missense |
probably benign |
0.00 |
R6918:Or8c15
|
UTSW |
9 |
38,120,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7621:Or8c15
|
UTSW |
9 |
38,120,447 (GRCm39) |
missense |
probably benign |
0.09 |
R7715:Or8c15
|
UTSW |
9 |
38,120,775 (GRCm39) |
missense |
probably benign |
0.30 |
R7940:Or8c15
|
UTSW |
9 |
38,120,496 (GRCm39) |
missense |
probably benign |
0.00 |
R8710:Or8c15
|
UTSW |
9 |
38,121,066 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8712:Or8c15
|
UTSW |
9 |
38,121,099 (GRCm39) |
missense |
probably benign |
0.39 |
R8882:Or8c15
|
UTSW |
9 |
38,120,461 (GRCm39) |
nonsense |
probably null |
|
|