Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
C |
T |
5: 114,383,198 (GRCm39) |
T2127M |
probably damaging |
Het |
Acp2 |
A |
G |
2: 91,036,606 (GRCm39) |
D175G |
possibly damaging |
Het |
Adamts12 |
T |
C |
15: 11,286,798 (GRCm39) |
L801P |
probably damaging |
Het |
Adcy10 |
T |
G |
1: 165,398,313 (GRCm39) |
V1470G |
possibly damaging |
Het |
Ankar |
T |
G |
1: 72,705,524 (GRCm39) |
K829Q |
probably benign |
Het |
Arhgef10l |
T |
C |
4: 140,274,318 (GRCm39) |
Y531C |
probably benign |
Het |
Atm |
T |
C |
9: 53,365,630 (GRCm39) |
I2590V |
probably benign |
Het |
Brme1 |
T |
A |
8: 84,886,137 (GRCm39) |
M31K |
probably benign |
Het |
Cblb |
T |
C |
16: 51,986,668 (GRCm39) |
L485P |
probably damaging |
Het |
Col4a1 |
T |
C |
8: 11,283,911 (GRCm39) |
|
probably benign |
Het |
Coprs |
T |
C |
8: 13,935,797 (GRCm39) |
K74R |
possibly damaging |
Het |
Cul3 |
A |
T |
1: 80,281,886 (GRCm39) |
L31M |
possibly damaging |
Het |
Cyp3a59 |
C |
A |
5: 146,033,463 (GRCm39) |
Q200K |
probably benign |
Het |
Ddx19b |
C |
A |
8: 111,735,456 (GRCm39) |
V402L |
probably damaging |
Het |
Disc1 |
T |
A |
8: 125,875,142 (GRCm39) |
|
probably benign |
Het |
Dsg4 |
C |
T |
18: 20,579,307 (GRCm39) |
|
probably benign |
Het |
Dspp |
A |
C |
5: 104,324,963 (GRCm39) |
Y442S |
probably damaging |
Het |
Dtl |
C |
T |
1: 191,290,172 (GRCm39) |
|
probably null |
Het |
Ezh1 |
A |
C |
11: 101,101,513 (GRCm39) |
V175G |
possibly damaging |
Het |
Hepacam2 |
C |
T |
6: 3,483,481 (GRCm39) |
G100D |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,340,764 (GRCm39) |
H1704Q |
possibly damaging |
Het |
Itprid2 |
G |
A |
2: 79,487,842 (GRCm39) |
E642K |
probably damaging |
Het |
Kif26a |
T |
C |
12: 112,140,177 (GRCm39) |
S469P |
probably damaging |
Het |
Lefty1 |
T |
C |
1: 180,765,242 (GRCm39) |
M270T |
probably benign |
Het |
Nap1l3 |
A |
T |
X: 121,305,752 (GRCm39) |
V322D |
probably damaging |
Het |
Ndufv2 |
A |
G |
17: 66,387,889 (GRCm39) |
|
probably benign |
Het |
Or14j5 |
A |
T |
17: 38,162,008 (GRCm39) |
H175L |
probably damaging |
Het |
Or4p18 |
G |
A |
2: 88,232,456 (GRCm39) |
T274I |
possibly damaging |
Het |
Or8b55 |
T |
C |
9: 38,726,901 (GRCm39) |
I34T |
possibly damaging |
Het |
Papolb |
G |
A |
5: 142,514,480 (GRCm39) |
H388Y |
probably benign |
Het |
Ppp1r10 |
A |
G |
17: 36,237,094 (GRCm39) |
E128G |
probably damaging |
Het |
Prss12 |
T |
A |
3: 123,280,669 (GRCm39) |
D451E |
probably damaging |
Het |
Psmc1 |
T |
C |
12: 100,081,087 (GRCm39) |
|
probably benign |
Het |
Pygo1 |
T |
A |
9: 72,833,222 (GRCm39) |
I10N |
probably benign |
Het |
Rab31 |
C |
T |
17: 66,028,998 (GRCm39) |
|
probably null |
Het |
Ret |
G |
A |
6: 118,158,860 (GRCm39) |
T184I |
probably damaging |
Het |
Rhd |
A |
T |
4: 134,611,481 (GRCm39) |
M214L |
possibly damaging |
Het |
Ripor3 |
C |
A |
2: 167,834,682 (GRCm39) |
|
probably benign |
Het |
Sec16a |
A |
G |
2: 26,312,052 (GRCm39) |
L2036P |
probably benign |
Het |
Slc26a3 |
C |
A |
12: 31,507,051 (GRCm39) |
D335E |
possibly damaging |
Het |
Taf6 |
A |
G |
5: 138,182,756 (GRCm39) |
|
probably benign |
Het |
Tnk2 |
T |
C |
16: 32,494,408 (GRCm39) |
V442A |
probably benign |
Het |
Virma |
A |
G |
4: 11,527,029 (GRCm39) |
M1143V |
probably damaging |
Het |
Vmn2r77 |
A |
T |
7: 86,452,848 (GRCm39) |
R522* |
probably null |
Het |
Vmn2r-ps129 |
A |
G |
17: 23,227,393 (GRCm39) |
|
noncoding transcript |
Het |
Zfp473 |
A |
G |
7: 44,383,107 (GRCm39) |
C408R |
probably damaging |
Het |
|
Other mutations in Otol1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01551:Otol1
|
APN |
3 |
69,935,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01664:Otol1
|
APN |
3 |
69,935,130 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02205:Otol1
|
APN |
3 |
69,925,929 (GRCm39) |
missense |
probably benign |
|
IGL02674:Otol1
|
APN |
3 |
69,926,077 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03376:Otol1
|
APN |
3 |
69,934,845 (GRCm39) |
missense |
probably damaging |
0.96 |
R0094:Otol1
|
UTSW |
3 |
69,926,016 (GRCm39) |
missense |
probably benign |
0.03 |
R0492:Otol1
|
UTSW |
3 |
69,935,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Otol1
|
UTSW |
3 |
69,934,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Otol1
|
UTSW |
3 |
69,935,437 (GRCm39) |
missense |
probably benign |
0.01 |
R2049:Otol1
|
UTSW |
3 |
69,926,169 (GRCm39) |
missense |
probably benign |
0.06 |
R2321:Otol1
|
UTSW |
3 |
69,925,858 (GRCm39) |
nonsense |
probably null |
|
R4042:Otol1
|
UTSW |
3 |
69,935,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Otol1
|
UTSW |
3 |
69,935,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R4044:Otol1
|
UTSW |
3 |
69,935,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R4092:Otol1
|
UTSW |
3 |
69,935,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R4433:Otol1
|
UTSW |
3 |
69,925,881 (GRCm39) |
missense |
probably benign |
0.02 |
R4993:Otol1
|
UTSW |
3 |
69,926,211 (GRCm39) |
missense |
probably benign |
0.07 |
R6921:Otol1
|
UTSW |
3 |
69,935,433 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6983:Otol1
|
UTSW |
3 |
69,935,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Otol1
|
UTSW |
3 |
69,926,027 (GRCm39) |
missense |
probably benign |
0.00 |
R7619:Otol1
|
UTSW |
3 |
69,935,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R8368:Otol1
|
UTSW |
3 |
69,935,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8851:Otol1
|
UTSW |
3 |
69,935,299 (GRCm39) |
missense |
probably damaging |
1.00 |
RF019:Otol1
|
UTSW |
3 |
69,925,933 (GRCm39) |
missense |
probably benign |
0.00 |
X0062:Otol1
|
UTSW |
3 |
69,934,973 (GRCm39) |
missense |
probably damaging |
1.00 |
|