Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,030,458 (GRCm39) |
Y763F |
probably benign |
Het |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Actl11 |
A |
G |
9: 107,808,682 (GRCm39) |
T1002A |
probably damaging |
Het |
Ampd1 |
T |
A |
3: 102,998,980 (GRCm39) |
N378K |
probably damaging |
Het |
Arhgap42 |
A |
G |
9: 9,033,587 (GRCm39) |
|
probably benign |
Het |
Arhgap6 |
C |
A |
X: 167,579,499 (GRCm39) |
P95T |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,798,102 (GRCm39) |
N87S |
probably benign |
Het |
Atp9b |
C |
T |
18: 80,805,353 (GRCm39) |
C735Y |
probably damaging |
Het |
Atp9b |
T |
A |
18: 80,822,122 (GRCm39) |
T110S |
probably benign |
Het |
Birc6 |
T |
G |
17: 74,919,314 (GRCm39) |
L221R |
probably damaging |
Het |
Ces1c |
A |
G |
8: 93,854,233 (GRCm39) |
F101L |
probably benign |
Het |
Cfap91 |
A |
G |
16: 38,141,762 (GRCm39) |
V390A |
probably damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,750 (GRCm39) |
Y662H |
probably damaging |
Het |
Cldn12 |
A |
T |
5: 5,557,900 (GRCm39) |
F176I |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,450,626 (GRCm39) |
S374P |
probably benign |
Het |
Col6a2 |
A |
T |
10: 76,439,544 (GRCm39) |
V740E |
probably damaging |
Het |
Cpne3 |
A |
T |
4: 19,526,336 (GRCm39) |
I401K |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,159,191 (GRCm39) |
|
probably null |
Het |
Ddn |
G |
A |
15: 98,704,647 (GRCm39) |
T215I |
possibly damaging |
Het |
Dync1i1 |
T |
C |
6: 5,769,799 (GRCm39) |
|
probably benign |
Het |
Dync2li1 |
T |
C |
17: 84,954,667 (GRCm39) |
|
probably benign |
Het |
Eif2a |
T |
A |
3: 58,445,005 (GRCm39) |
L50* |
probably null |
Het |
Elavl3 |
G |
A |
9: 21,929,875 (GRCm39) |
A343V |
probably damaging |
Het |
Fastkd1 |
T |
C |
2: 69,538,982 (GRCm39) |
|
probably null |
Het |
Fgf8 |
C |
A |
19: 45,730,786 (GRCm39) |
V80F |
possibly damaging |
Het |
Fras1 |
A |
T |
5: 96,891,046 (GRCm39) |
E2858D |
probably benign |
Het |
Fshr |
A |
T |
17: 89,293,529 (GRCm39) |
L383Q |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,246,171 (GRCm39) |
K74R |
probably benign |
Het |
Gmeb2 |
T |
G |
2: 180,897,019 (GRCm39) |
M290L |
probably benign |
Het |
Gnptg |
A |
G |
17: 25,454,828 (GRCm39) |
|
probably null |
Het |
Grik2 |
A |
C |
10: 49,008,871 (GRCm39) |
S739A |
probably damaging |
Het |
Grk2 |
T |
A |
19: 4,337,222 (GRCm39) |
Q659L |
probably benign |
Het |
Hdhd5 |
A |
G |
6: 120,491,473 (GRCm39) |
V210A |
probably damaging |
Het |
Hyal1 |
C |
T |
9: 107,455,091 (GRCm39) |
L134F |
probably damaging |
Het |
Itgb2 |
A |
T |
10: 77,381,987 (GRCm39) |
K18N |
possibly damaging |
Het |
Jam3 |
A |
T |
9: 27,017,701 (GRCm39) |
I29K |
possibly damaging |
Het |
Kcnh3 |
C |
A |
15: 99,137,796 (GRCm39) |
D830E |
probably benign |
Het |
Kcnmb4 |
T |
C |
10: 116,309,203 (GRCm39) |
D75G |
possibly damaging |
Het |
Kdm4b |
A |
G |
17: 56,707,025 (GRCm39) |
Y981C |
probably damaging |
Het |
Klk1b26 |
C |
A |
7: 43,665,810 (GRCm39) |
D207E |
probably benign |
Het |
Kmt2a |
G |
T |
9: 44,759,563 (GRCm39) |
T762N |
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,742,819 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
C |
10: 38,964,876 (GRCm39) |
S1414P |
possibly damaging |
Het |
Lce1f |
C |
G |
3: 92,626,276 (GRCm39) |
C127S |
unknown |
Het |
Map7d1 |
A |
G |
4: 126,128,558 (GRCm39) |
|
probably null |
Het |
Ninl |
T |
C |
2: 150,822,096 (GRCm39) |
D2G |
possibly damaging |
Het |
Or2w1b |
T |
A |
13: 21,300,303 (GRCm39) |
M147K |
probably benign |
Het |
Or5k3 |
A |
G |
16: 58,969,287 (GRCm39) |
T25A |
probably benign |
Het |
Or5m11b |
C |
T |
2: 85,806,372 (GRCm39) |
P262S |
possibly damaging |
Het |
Or8g18 |
G |
C |
9: 39,149,547 (GRCm39) |
P58A |
probably benign |
Het |
Pax8 |
A |
G |
2: 24,319,608 (GRCm39) |
Y381H |
possibly damaging |
Het |
Pde7a |
T |
C |
3: 19,314,408 (GRCm39) |
I63V |
possibly damaging |
Het |
Pgm3 |
A |
T |
9: 86,452,340 (GRCm39) |
F40Y |
probably benign |
Het |
Phrf1 |
G |
T |
7: 140,836,564 (GRCm39) |
D78Y |
probably damaging |
Het |
Plekhg1 |
C |
T |
10: 3,890,538 (GRCm39) |
|
probably benign |
Het |
Prss59 |
A |
T |
6: 40,898,652 (GRCm39) |
S199T |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,446,567 (GRCm39) |
S209P |
probably damaging |
Het |
Qtrt2 |
A |
T |
16: 43,689,337 (GRCm39) |
F220L |
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,159,747 (GRCm39) |
|
probably null |
Het |
Rin3 |
A |
G |
12: 102,335,018 (GRCm39) |
T230A |
unknown |
Het |
Ros1 |
A |
T |
10: 51,974,773 (GRCm39) |
V1604E |
possibly damaging |
Het |
Rpp14 |
A |
G |
14: 8,090,528 (GRCm38) |
M151V |
probably benign |
Het |
Sacs |
T |
A |
14: 61,451,153 (GRCm39) |
F4400I |
possibly damaging |
Het |
Scamp1 |
C |
T |
13: 94,361,437 (GRCm39) |
V148I |
probably benign |
Het |
Slc13a5 |
A |
G |
11: 72,141,557 (GRCm39) |
C428R |
probably damaging |
Het |
Slc43a2 |
T |
G |
11: 75,453,733 (GRCm39) |
|
probably null |
Het |
Smarcc2 |
T |
A |
10: 128,299,741 (GRCm39) |
N135K |
probably damaging |
Het |
Snx15 |
G |
C |
19: 6,172,094 (GRCm39) |
S116R |
probably damaging |
Het |
Stag1 |
A |
G |
9: 100,737,885 (GRCm39) |
E414G |
possibly damaging |
Het |
Stag1 |
A |
T |
9: 100,769,426 (GRCm39) |
|
probably benign |
Het |
Tmem106a |
T |
A |
11: 101,481,263 (GRCm39) |
L257Q |
possibly damaging |
Het |
Tnc |
C |
T |
4: 63,882,991 (GRCm39) |
D1968N |
probably benign |
Het |
Trim42 |
A |
G |
9: 97,248,138 (GRCm39) |
L186P |
possibly damaging |
Het |
Tshb |
T |
A |
3: 102,685,624 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,584,484 (GRCm39) |
D13881V |
probably damaging |
Het |
Uqcrc2 |
T |
C |
7: 120,239,506 (GRCm39) |
V56A |
probably benign |
Het |
Uty |
G |
A |
Y: 1,197,228 (GRCm39) |
T113I |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,864,787 (GRCm39) |
E3032G |
probably benign |
Het |
Wfdc9 |
T |
G |
2: 164,493,729 (GRCm39) |
|
probably benign |
Het |
Zc3h7a |
G |
A |
16: 10,980,520 (GRCm39) |
T31I |
probably damaging |
Het |
Zfp462 |
T |
C |
4: 55,060,046 (GRCm39) |
S1191P |
probably damaging |
Het |
|
Other mutations in Or6n1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01626:Or6n1
|
APN |
1 |
173,917,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01868:Or6n1
|
APN |
1 |
173,916,936 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01972:Or6n1
|
APN |
1 |
173,916,987 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02412:Or6n1
|
APN |
1 |
173,916,809 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02628:Or6n1
|
APN |
1 |
173,916,756 (GRCm39) |
missense |
probably benign |
|
IGL02861:Or6n1
|
APN |
1 |
173,916,602 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03404:Or6n1
|
APN |
1 |
173,917,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0267:Or6n1
|
UTSW |
1 |
173,916,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R0357:Or6n1
|
UTSW |
1 |
173,916,675 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2051:Or6n1
|
UTSW |
1 |
173,916,785 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4706:Or6n1
|
UTSW |
1 |
173,917,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Or6n1
|
UTSW |
1 |
173,916,742 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5439:Or6n1
|
UTSW |
1 |
173,917,541 (GRCm39) |
missense |
probably benign |
0.01 |
R5538:Or6n1
|
UTSW |
1 |
173,917,544 (GRCm39) |
makesense |
probably null |
|
R5907:Or6n1
|
UTSW |
1 |
173,916,785 (GRCm39) |
missense |
probably benign |
0.08 |
R6932:Or6n1
|
UTSW |
1 |
173,917,316 (GRCm39) |
missense |
probably damaging |
0.96 |
R7808:Or6n1
|
UTSW |
1 |
173,917,417 (GRCm39) |
nonsense |
probably null |
|
R8040:Or6n1
|
UTSW |
1 |
173,916,723 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8467:Or6n1
|
UTSW |
1 |
173,917,007 (GRCm39) |
missense |
probably benign |
0.00 |
R9124:Or6n1
|
UTSW |
1 |
173,917,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Or6n1
|
UTSW |
1 |
173,917,356 (GRCm39) |
missense |
possibly damaging |
0.65 |
|