Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora3 |
T |
A |
3: 105,814,991 (GRCm39) |
L101* |
probably null |
Het |
Atf7ip2 |
T |
C |
16: 10,022,534 (GRCm39) |
I71T |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,322,512 (GRCm39) |
C206R |
probably damaging |
Het |
Cacna1d |
A |
G |
14: 29,845,411 (GRCm39) |
L606P |
probably damaging |
Het |
Cass4 |
T |
C |
2: 172,269,639 (GRCm39) |
F574L |
probably damaging |
Het |
Cdcp3 |
G |
A |
7: 130,846,601 (GRCm39) |
|
probably null |
Het |
Col17a1 |
C |
A |
19: 47,668,847 (GRCm39) |
E126* |
probably null |
Het |
Cxadr |
A |
C |
16: 78,122,147 (GRCm39) |
D49A |
probably damaging |
Het |
Dact1 |
T |
C |
12: 71,365,327 (GRCm39) |
S703P |
probably damaging |
Het |
Dchs2 |
T |
A |
3: 83,178,425 (GRCm39) |
H1159Q |
possibly damaging |
Het |
Dnmt3a |
T |
A |
12: 3,952,399 (GRCm39) |
F697I |
probably damaging |
Het |
Dnpep |
T |
A |
1: 75,292,022 (GRCm39) |
K199N |
probably benign |
Het |
Gnl2 |
A |
T |
4: 124,946,353 (GRCm39) |
I525F |
possibly damaging |
Het |
Hsph1 |
C |
A |
5: 149,542,441 (GRCm39) |
K692N |
probably damaging |
Het |
Itga6 |
T |
A |
2: 71,664,116 (GRCm39) |
C489S |
possibly damaging |
Het |
Kdm2b |
C |
T |
5: 123,018,254 (GRCm39) |
C1007Y |
probably damaging |
Het |
Ly6m |
T |
C |
15: 74,751,813 (GRCm39) |
T74A |
probably benign |
Het |
Mast4 |
T |
C |
13: 103,042,185 (GRCm39) |
S22G |
possibly damaging |
Het |
Ms4a12 |
A |
G |
19: 11,192,376 (GRCm39) |
*264Q |
probably null |
Het |
Myh8 |
G |
T |
11: 67,189,405 (GRCm39) |
A1194S |
probably benign |
Het |
Ncapd3 |
T |
A |
9: 26,955,805 (GRCm39) |
N131K |
probably damaging |
Het |
Or10g6 |
T |
C |
9: 39,933,824 (GRCm39) |
I45T |
probably damaging |
Het |
Or5w13 |
A |
T |
2: 87,523,872 (GRCm39) |
M118K |
probably damaging |
Het |
Rbm14 |
G |
T |
19: 4,853,191 (GRCm39) |
|
probably benign |
Het |
Rnf130 |
T |
A |
11: 49,986,617 (GRCm39) |
C320* |
probably null |
Het |
Rnf5 |
A |
G |
17: 34,821,101 (GRCm39) |
V77A |
possibly damaging |
Het |
Sh3pxd2a |
G |
T |
19: 47,258,366 (GRCm39) |
P418T |
probably damaging |
Het |
Shank3 |
G |
T |
15: 89,387,616 (GRCm39) |
V262F |
possibly damaging |
Het |
Six5 |
T |
A |
7: 18,830,696 (GRCm39) |
V441E |
probably damaging |
Het |
Tbc1d9b |
T |
A |
11: 50,037,155 (GRCm39) |
I268N |
probably benign |
Het |
Terb1 |
G |
A |
8: 105,212,078 (GRCm39) |
T301I |
possibly damaging |
Het |
Tnxb |
A |
C |
17: 34,936,891 (GRCm39) |
D2820A |
probably damaging |
Het |
Tram2 |
C |
T |
1: 21,074,457 (GRCm39) |
E242K |
possibly damaging |
Het |
Trps1 |
T |
C |
15: 50,694,793 (GRCm39) |
K210E |
probably damaging |
Het |
Tulp2 |
T |
A |
7: 45,168,012 (GRCm39) |
D141E |
probably benign |
Het |
Umodl1 |
C |
T |
17: 31,205,121 (GRCm39) |
T572I |
probably benign |
Het |
Upf2 |
C |
A |
2: 5,984,588 (GRCm39) |
A501E |
unknown |
Het |
Vmn2r102 |
A |
G |
17: 19,901,483 (GRCm39) |
T537A |
possibly damaging |
Het |
Wdr11 |
T |
A |
7: 129,208,242 (GRCm39) |
D332E |
possibly damaging |
Het |
Wdr38 |
A |
G |
2: 38,890,723 (GRCm39) |
N199S |
probably damaging |
Het |
Zfp672 |
T |
A |
11: 58,207,758 (GRCm39) |
I188F |
possibly damaging |
Het |
|
Other mutations in Ear2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01700:Ear2
|
APN |
14 |
44,340,716 (GRCm39) |
nonsense |
probably null |
|
IGL01729:Ear2
|
APN |
14 |
44,340,701 (GRCm39) |
nonsense |
probably null |
|
R0346:Ear2
|
UTSW |
14 |
44,340,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0458:Ear2
|
UTSW |
14 |
44,340,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1035:Ear2
|
UTSW |
14 |
44,340,344 (GRCm39) |
start codon destroyed |
possibly damaging |
0.59 |
R4920:Ear2
|
UTSW |
14 |
44,340,582 (GRCm39) |
missense |
probably damaging |
0.97 |
R5845:Ear2
|
UTSW |
14 |
44,340,618 (GRCm39) |
missense |
probably benign |
0.00 |
R6008:Ear2
|
UTSW |
14 |
44,340,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6720:Ear2
|
UTSW |
14 |
44,340,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7721:Ear2
|
UTSW |
14 |
44,340,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Ear2
|
UTSW |
14 |
44,340,477 (GRCm39) |
missense |
probably benign |
0.00 |
R8719:Ear2
|
UTSW |
14 |
44,340,734 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9659:Ear2
|
UTSW |
14 |
44,340,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Ear2
|
UTSW |
14 |
44,340,729 (GRCm39) |
missense |
probably benign |
0.02 |
R9788:Ear2
|
UTSW |
14 |
44,340,705 (GRCm39) |
missense |
probably damaging |
1.00 |
|