Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd3 |
T |
A |
18: 10,647,869 (GRCm39) |
D300V |
possibly damaging |
Het |
Agap1 |
A |
G |
1: 89,591,518 (GRCm39) |
|
probably benign |
Het |
Best3 |
A |
G |
10: 116,840,446 (GRCm39) |
|
probably benign |
Het |
Cfap43 |
T |
G |
19: 47,818,914 (GRCm39) |
I125L |
probably benign |
Het |
Cntn1 |
A |
G |
15: 92,148,758 (GRCm39) |
E335G |
possibly damaging |
Het |
Csmd3 |
A |
T |
15: 48,150,891 (GRCm39) |
S396T |
possibly damaging |
Het |
Cxxc5 |
T |
G |
18: 35,993,745 (GRCm39) |
*318G |
probably null |
Het |
Dpep3 |
T |
C |
8: 106,705,779 (GRCm39) |
T49A |
probably benign |
Het |
Elf1 |
T |
A |
14: 79,817,789 (GRCm39) |
M436K |
possibly damaging |
Het |
Ephx2 |
T |
G |
14: 66,330,286 (GRCm39) |
I310L |
probably benign |
Het |
Fancm |
A |
G |
12: 65,122,510 (GRCm39) |
T11A |
possibly damaging |
Het |
Ganab |
G |
T |
19: 8,879,959 (GRCm39) |
A73S |
probably benign |
Het |
Glp1r |
T |
G |
17: 31,120,891 (GRCm39) |
L14R |
possibly damaging |
Het |
Kif14 |
G |
A |
1: 136,396,756 (GRCm39) |
S354N |
probably benign |
Het |
Krtap9-1 |
C |
T |
11: 99,764,680 (GRCm39) |
P139S |
unknown |
Het |
L2hgdh |
T |
C |
12: 69,748,208 (GRCm39) |
D306G |
possibly damaging |
Het |
Liat1 |
T |
C |
11: 75,894,192 (GRCm39) |
S190P |
probably benign |
Het |
Lrriq4 |
A |
G |
3: 30,705,104 (GRCm39) |
|
probably null |
Het |
Mbd3 |
T |
G |
10: 80,229,717 (GRCm39) |
|
probably benign |
Het |
Men1 |
G |
A |
19: 6,387,237 (GRCm39) |
|
probably null |
Het |
Mug1 |
T |
C |
6: 121,842,768 (GRCm39) |
S585P |
probably damaging |
Het |
Nat8f4 |
C |
A |
6: 85,877,969 (GRCm39) |
A185S |
probably benign |
Het |
Nlrc5 |
C |
T |
8: 95,228,839 (GRCm39) |
|
probably benign |
Het |
Or8b12 |
T |
A |
9: 37,657,685 (GRCm39) |
I85N |
possibly damaging |
Het |
Peg3 |
T |
A |
7: 6,713,273 (GRCm39) |
I650F |
probably benign |
Het |
Prom1 |
A |
T |
5: 44,213,279 (GRCm39) |
N142K |
probably damaging |
Het |
Qser1 |
T |
A |
2: 104,596,401 (GRCm39) |
D1537V |
probably damaging |
Het |
Rbm44 |
T |
A |
1: 91,084,831 (GRCm39) |
D684E |
probably benign |
Het |
Rnf19a |
A |
C |
15: 36,265,948 (GRCm39) |
S50A |
probably damaging |
Het |
Rnf31 |
A |
G |
14: 55,829,776 (GRCm39) |
|
probably null |
Het |
Rspry1 |
A |
G |
8: 95,349,614 (GRCm39) |
M1V |
probably null |
Het |
Rspry1 |
A |
T |
8: 95,349,608 (GRCm39) |
|
probably benign |
Het |
Sap130 |
C |
A |
18: 31,831,819 (GRCm39) |
P769T |
probably benign |
Het |
Slc22a16 |
T |
A |
10: 40,471,278 (GRCm39) |
M483K |
probably damaging |
Het |
Slc27a1 |
T |
C |
8: 72,037,416 (GRCm39) |
|
probably null |
Het |
Slc35a5 |
A |
T |
16: 44,972,971 (GRCm39) |
C65* |
probably null |
Het |
Sox4 |
C |
A |
13: 29,136,956 (GRCm39) |
G17W |
probably damaging |
Het |
Ubqlnl |
T |
C |
7: 103,798,372 (GRCm39) |
E375G |
probably benign |
Het |
Uggt2 |
G |
A |
14: 119,286,688 (GRCm39) |
T692I |
possibly damaging |
Het |
Vmn1r211 |
A |
T |
13: 23,036,272 (GRCm39) |
C132S |
probably benign |
Het |
Vmn2r61 |
A |
T |
7: 41,950,175 (GRCm39) |
N865I |
possibly damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,506,795 (GRCm39) |
M839K |
|
Het |
Xrn2 |
T |
A |
2: 146,878,670 (GRCm39) |
S455R |
probably benign |
Het |
Zan |
T |
A |
5: 137,452,519 (GRCm39) |
T1521S |
unknown |
Het |
Zfp326 |
A |
G |
5: 106,054,911 (GRCm39) |
M361V |
possibly damaging |
Het |
Zfp472 |
A |
G |
17: 33,196,498 (GRCm39) |
Y191C |
possibly damaging |
Het |
|
Other mutations in Or8g23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01387:Or8g23
|
APN |
9 |
38,971,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01775:Or8g23
|
APN |
9 |
38,971,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02076:Or8g23
|
APN |
9 |
38,971,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Or8g23
|
APN |
9 |
38,971,585 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03115:Or8g23
|
APN |
9 |
38,971,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R0121:Or8g23
|
UTSW |
9 |
38,971,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:Or8g23
|
UTSW |
9 |
38,971,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R1559:Or8g23
|
UTSW |
9 |
38,971,437 (GRCm39) |
missense |
probably benign |
0.20 |
R2006:Or8g23
|
UTSW |
9 |
38,971,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R2010:Or8g23
|
UTSW |
9 |
38,971,395 (GRCm39) |
missense |
probably benign |
0.05 |
R2191:Or8g23
|
UTSW |
9 |
38,971,701 (GRCm39) |
missense |
probably benign |
|
R3874:Or8g23
|
UTSW |
9 |
38,971,470 (GRCm39) |
missense |
probably benign |
0.00 |
R4970:Or8g23
|
UTSW |
9 |
38,971,827 (GRCm39) |
missense |
probably benign |
0.12 |
R5217:Or8g23
|
UTSW |
9 |
38,971,065 (GRCm39) |
missense |
probably benign |
0.00 |
R5836:Or8g23
|
UTSW |
9 |
38,971,918 (GRCm39) |
missense |
probably benign |
|
R5886:Or8g23
|
UTSW |
9 |
38,971,678 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Or8g23
|
UTSW |
9 |
38,971,492 (GRCm39) |
missense |
probably benign |
0.23 |
R7261:Or8g23
|
UTSW |
9 |
38,971,504 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7328:Or8g23
|
UTSW |
9 |
38,971,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Or8g23
|
UTSW |
9 |
38,971,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Or8g23
|
UTSW |
9 |
38,971,465 (GRCm39) |
missense |
probably benign |
0.00 |
R9624:Or8g23
|
UTSW |
9 |
38,971,453 (GRCm39) |
missense |
probably benign |
0.40 |
X0022:Or8g23
|
UTSW |
9 |
38,971,713 (GRCm39) |
missense |
probably benign |
0.12 |
|