Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
A |
8: 111,767,361 (GRCm39) |
W156R |
probably damaging |
Het |
Acvr1 |
T |
A |
2: 58,364,286 (GRCm39) |
|
probably null |
Het |
Adamts2 |
G |
T |
11: 50,494,315 (GRCm39) |
V130L |
probably damaging |
Het |
Adcy4 |
C |
T |
14: 56,012,697 (GRCm39) |
V541I |
probably benign |
Het |
Adgrl2 |
C |
T |
3: 148,552,542 (GRCm39) |
V654I |
probably damaging |
Het |
Ago3 |
T |
A |
4: 126,270,721 (GRCm39) |
K258* |
probably null |
Het |
Akap11 |
A |
T |
14: 78,749,929 (GRCm39) |
S819R |
|
Het |
Alox5ap |
T |
C |
5: 149,224,419 (GRCm39) |
F121L |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,731,858 (GRCm39) |
M2060K |
probably damaging |
Het |
Bltp3b |
T |
C |
10: 89,627,281 (GRCm39) |
S449P |
probably benign |
Het |
C030005K15Rik |
T |
C |
10: 97,561,414 (GRCm39) |
I106V |
unknown |
Het |
Carmil2 |
T |
A |
8: 106,417,716 (GRCm39) |
S604T |
probably benign |
Het |
Ccdc121rt2 |
C |
T |
5: 112,598,653 (GRCm39) |
T400I |
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,813,935 (GRCm39) |
T164A |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,914,569 (GRCm39) |
E976G |
possibly damaging |
Het |
Dnah17 |
C |
T |
11: 118,005,021 (GRCm39) |
G788R |
probably benign |
Het |
Dus2 |
T |
C |
8: 106,722,645 (GRCm39) |
|
probably benign |
Het |
Etv6 |
T |
C |
6: 134,225,717 (GRCm39) |
V316A |
possibly damaging |
Het |
Fabp9 |
T |
G |
3: 10,259,085 (GRCm39) |
K107T |
possibly damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Gapdh |
A |
G |
6: 125,140,226 (GRCm39) |
V92A |
probably benign |
Het |
Gfy |
A |
G |
7: 44,826,019 (GRCm39) |
L453P |
probably damaging |
Het |
Gp2 |
C |
T |
7: 119,042,010 (GRCm39) |
C505Y |
probably benign |
Het |
Gtpbp8 |
T |
C |
16: 44,566,676 (GRCm39) |
R9G |
probably benign |
Het |
Hipk4 |
G |
T |
7: 27,223,033 (GRCm39) |
R31L |
probably damaging |
Het |
Htt |
T |
A |
5: 35,063,068 (GRCm39) |
M2900K |
probably damaging |
Het |
Ighv1-20 |
T |
C |
12: 114,687,810 (GRCm39) |
I6V |
probably benign |
Het |
Il17d |
C |
T |
14: 57,779,937 (GRCm39) |
T153I |
probably damaging |
Het |
Izumo3 |
T |
A |
4: 92,034,581 (GRCm39) |
N117I |
probably damaging |
Het |
Kcnh7 |
T |
C |
2: 62,680,879 (GRCm39) |
D236G |
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,750,478 (GRCm39) |
D2405G |
unknown |
Het |
Map4k2 |
T |
C |
19: 6,396,596 (GRCm39) |
W533R |
probably damaging |
Het |
Matn1 |
C |
A |
4: 130,673,300 (GRCm39) |
Y89* |
probably null |
Het |
Mettl18 |
T |
A |
1: 163,824,509 (GRCm39) |
Y277N |
probably damaging |
Het |
Muc5b |
G |
A |
7: 141,417,898 (GRCm39) |
G3615S |
probably benign |
Het |
Mycbp2 |
A |
C |
14: 103,398,111 (GRCm39) |
|
probably null |
Het |
Myh4 |
T |
A |
11: 67,143,390 (GRCm39) |
S1041T |
possibly damaging |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Naaladl1 |
T |
C |
19: 6,159,703 (GRCm39) |
V378A |
possibly damaging |
Het |
Nars1 |
T |
C |
18: 64,637,458 (GRCm39) |
D374G |
probably benign |
Het |
Neb |
C |
T |
2: 52,198,283 (GRCm39) |
|
probably null |
Het |
Neurl1b |
A |
G |
17: 26,650,965 (GRCm39) |
Y79C |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,101,248 (GRCm39) |
T306A |
probably benign |
Het |
Ola1 |
G |
T |
2: 73,029,745 (GRCm39) |
R125S |
probably damaging |
Het |
Or12d15 |
T |
A |
17: 37,694,122 (GRCm39) |
F221L |
probably benign |
Het |
Pak1ip1 |
C |
A |
13: 41,158,214 (GRCm39) |
T29K |
probably benign |
Het |
Podnl1 |
T |
A |
8: 84,857,402 (GRCm39) |
L337H |
|
Het |
Rictor |
T |
G |
15: 6,807,800 (GRCm39) |
|
probably null |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sel1l2 |
T |
C |
2: 140,072,753 (GRCm39) |
I627M |
probably benign |
Het |
Sh3rf2 |
T |
C |
18: 42,244,493 (GRCm39) |
S352P |
probably damaging |
Het |
Slc6a6 |
G |
A |
6: 91,703,224 (GRCm39) |
W199* |
probably null |
Het |
Smc2 |
T |
A |
4: 52,450,965 (GRCm39) |
V261E |
probably benign |
Het |
Sorcs3 |
G |
A |
19: 48,692,808 (GRCm39) |
|
probably null |
Het |
Spdye4a |
T |
A |
5: 143,211,562 (GRCm39) |
M1L |
probably benign |
Het |
Stag1 |
T |
C |
9: 100,639,819 (GRCm39) |
I125T |
possibly damaging |
Het |
Stx8 |
T |
A |
11: 67,911,814 (GRCm39) |
D177E |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,623,125 (GRCm39) |
Y71C |
probably damaging |
Het |
Tmed9 |
T |
C |
13: 55,742,617 (GRCm39) |
F129L |
probably benign |
Het |
Tmem216 |
T |
A |
19: 10,529,336 (GRCm39) |
T17S |
probably benign |
Het |
Tmpo |
A |
T |
10: 90,997,974 (GRCm39) |
N604K |
probably benign |
Het |
Tmprss11f |
T |
A |
5: 86,681,666 (GRCm39) |
I196F |
probably benign |
Het |
Tnks |
A |
G |
8: 35,301,738 (GRCm39) |
F1244L |
probably benign |
Het |
Tspan2 |
T |
C |
3: 102,676,226 (GRCm39) |
C212R |
probably damaging |
Het |
Tspan4 |
A |
G |
7: 141,071,718 (GRCm39) |
D155G |
probably damaging |
Het |
Ttc6 |
T |
C |
12: 57,707,282 (GRCm39) |
F730L |
possibly damaging |
Het |
Txnrd2 |
G |
A |
16: 18,245,291 (GRCm39) |
A33T |
unknown |
Het |
Wnk1 |
C |
T |
6: 119,940,454 (GRCm39) |
R761H |
probably damaging |
Het |
Zfp217 |
T |
C |
2: 169,962,024 (GRCm39) |
D101G |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,555,620 (GRCm39) |
F866S |
probably damaging |
Het |
|
Other mutations in Or51a43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01614:Or51a43
|
APN |
7 |
103,717,576 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02937:Or51a43
|
APN |
7 |
103,718,056 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03188:Or51a43
|
APN |
7 |
103,717,945 (GRCm39) |
missense |
possibly damaging |
0.89 |
FR4737:Or51a43
|
UTSW |
7 |
103,720,499 (GRCm39) |
start gained |
probably benign |
|
R0467:Or51a43
|
UTSW |
7 |
103,717,332 (GRCm39) |
missense |
probably benign |
0.07 |
R1310:Or51a43
|
UTSW |
7 |
103,717,805 (GRCm39) |
missense |
probably benign |
|
R1457:Or51a43
|
UTSW |
7 |
103,717,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Or51a43
|
UTSW |
7 |
103,717,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Or51a43
|
UTSW |
7 |
103,717,336 (GRCm39) |
missense |
probably null |
1.00 |
R2428:Or51a43
|
UTSW |
7 |
103,717,675 (GRCm39) |
nonsense |
probably null |
|
R2922:Or51a43
|
UTSW |
7 |
103,717,794 (GRCm39) |
missense |
probably benign |
0.09 |
R2923:Or51a43
|
UTSW |
7 |
103,717,794 (GRCm39) |
missense |
probably benign |
0.09 |
R3929:Or51a43
|
UTSW |
7 |
103,717,791 (GRCm39) |
missense |
probably benign |
0.06 |
R4500:Or51a43
|
UTSW |
7 |
103,717,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5035:Or51a43
|
UTSW |
7 |
103,717,614 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5303:Or51a43
|
UTSW |
7 |
103,718,239 (GRCm39) |
utr 5 prime |
probably benign |
|
R5464:Or51a43
|
UTSW |
7 |
103,717,674 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5722:Or51a43
|
UTSW |
7 |
103,717,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R5742:Or51a43
|
UTSW |
7 |
103,717,412 (GRCm39) |
missense |
probably damaging |
0.97 |
R6874:Or51a43
|
UTSW |
7 |
103,717,396 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6940:Or51a43
|
UTSW |
7 |
103,717,620 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7848:Or51a43
|
UTSW |
7 |
103,717,302 (GRCm39) |
missense |
probably benign |
|
R8714:Or51a43
|
UTSW |
7 |
103,717,483 (GRCm39) |
missense |
probably damaging |
0.97 |
R8866:Or51a43
|
UTSW |
7 |
103,718,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R8909:Or51a43
|
UTSW |
7 |
103,718,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Or51a43
|
UTSW |
7 |
103,718,139 (GRCm39) |
missense |
probably damaging |
1.00 |
|