Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
A |
1: 71,319,549 (GRCm39) |
M1778L |
probably benign |
Het |
Aldh6a1 |
C |
T |
12: 84,486,312 (GRCm39) |
C202Y |
probably damaging |
Het |
Ankrd36 |
A |
G |
11: 5,582,198 (GRCm39) |
T276A |
probably benign |
Het |
Ankrd55 |
T |
C |
13: 112,517,702 (GRCm39) |
I556T |
probably benign |
Het |
Aqp4 |
A |
G |
18: 15,532,922 (GRCm39) |
I57T |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,501,574 (GRCm39) |
D43G |
possibly damaging |
Het |
Cyld |
G |
A |
8: 89,433,727 (GRCm39) |
R172H |
probably damaging |
Het |
Efcab9 |
T |
C |
11: 32,477,451 (GRCm39) |
R24G |
probably damaging |
Het |
F7 |
C |
A |
8: 13,078,685 (GRCm39) |
Q39K |
probably benign |
Het |
Galntl6 |
A |
T |
8: 58,411,494 (GRCm39) |
|
probably benign |
Het |
Kcnj5 |
A |
G |
9: 32,233,925 (GRCm39) |
V130A |
probably damaging |
Het |
Magee2 |
A |
G |
X: 103,899,574 (GRCm39) |
I359T |
possibly damaging |
Het |
Myh1 |
T |
G |
11: 67,102,238 (GRCm39) |
I843S |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,065,762 (GRCm39) |
M98K |
probably damaging |
Het |
Nrip3 |
T |
A |
7: 109,361,074 (GRCm39) |
N200I |
possibly damaging |
Het |
Or6c219 |
A |
T |
10: 129,781,810 (GRCm39) |
N40K |
probably damaging |
Het |
Phkb |
A |
T |
8: 86,744,094 (GRCm39) |
Q581L |
probably benign |
Het |
Plxdc2 |
T |
C |
2: 16,516,926 (GRCm39) |
V69A |
probably benign |
Het |
Pou3f1 |
G |
T |
4: 124,552,650 (GRCm39) |
W384L |
probably damaging |
Het |
Prrc2a |
G |
A |
17: 35,369,643 (GRCm39) |
S1890L |
possibly damaging |
Het |
Psmc1 |
C |
A |
12: 100,079,337 (GRCm39) |
P27H |
probably damaging |
Het |
Pvr |
C |
A |
7: 19,643,157 (GRCm39) |
A359S |
probably benign |
Het |
Rasal1 |
A |
T |
5: 120,814,882 (GRCm39) |
I711F |
probably benign |
Het |
Ror1 |
C |
T |
4: 100,266,968 (GRCm39) |
A223V |
probably damaging |
Het |
Slc22a16 |
A |
T |
10: 40,479,904 (GRCm39) |
I638L |
unknown |
Het |
Slfn10-ps |
C |
T |
11: 82,919,938 (GRCm39) |
|
noncoding transcript |
Het |
Sptbn4 |
A |
G |
7: 27,103,693 (GRCm39) |
L1176P |
probably damaging |
Het |
Usp21 |
A |
T |
1: 171,110,975 (GRCm39) |
F421I |
probably damaging |
Het |
Utp25 |
G |
A |
1: 192,800,573 (GRCm39) |
P416S |
probably damaging |
Het |
Vmn1r61 |
T |
A |
7: 5,614,202 (GRCm39) |
R37S |
possibly damaging |
Het |
Vps13a |
G |
A |
19: 16,722,221 (GRCm39) |
R364* |
probably null |
Het |
Vps29 |
A |
G |
5: 122,500,930 (GRCm39) |
Y165C |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 32,742,195 (GRCm39) |
|
probably benign |
Het |
Wdr24 |
A |
G |
17: 26,044,802 (GRCm39) |
D219G |
probably damaging |
Het |
Xpo1 |
T |
C |
11: 23,226,422 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
C |
A |
2: 174,486,711 (GRCm39) |
T462K |
possibly damaging |
Het |
Zswim5 |
T |
C |
4: 116,843,658 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ear2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R6432:Ear2
|
UTSW |
14 |
44,340,660 (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 |
|