Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agfg2 |
C |
A |
5: 137,653,622 (GRCm39) |
V365F |
probably damaging |
Het |
Atxn7 |
A |
T |
14: 14,089,441 (GRCm38) |
N319I |
probably damaging |
Het |
AY074887 |
C |
T |
9: 54,858,087 (GRCm39) |
V13M |
unknown |
Het |
Boc |
T |
C |
16: 44,311,021 (GRCm39) |
T738A |
|
Het |
C2cd5 |
A |
G |
6: 143,027,127 (GRCm39) |
V126A |
possibly damaging |
Het |
Cdk9 |
A |
T |
2: 32,598,273 (GRCm39) |
L261Q |
possibly damaging |
Het |
Chi3l1 |
T |
C |
1: 134,115,685 (GRCm39) |
L231P |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,399,027 (GRCm39) |
C604S |
probably null |
Het |
Dop1a |
T |
C |
9: 86,415,027 (GRCm39) |
V1923A |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,546,018 (GRCm39) |
S230P |
probably benign |
Het |
Eps15l1 |
T |
C |
8: 73,095,274 (GRCm39) |
E892G |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,705,871 (GRCm39) |
T1133A |
probably benign |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,832,220 (GRCm39) |
I1518F |
possibly damaging |
Het |
Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,813,508 (GRCm39) |
C2580S |
probably damaging |
Het |
Ino80b |
T |
A |
6: 83,102,314 (GRCm39) |
|
probably benign |
Het |
Kdm2b |
T |
C |
5: 123,009,889 (GRCm39) |
R1274G |
probably damaging |
Het |
Lcn12 |
A |
G |
2: 25,382,273 (GRCm39) |
I144T |
possibly damaging |
Het |
Lrrc37 |
G |
T |
11: 103,509,859 (GRCm39) |
P703Q |
unknown |
Het |
Mroh5 |
T |
C |
15: 73,663,586 (GRCm39) |
N158S |
probably benign |
Het |
Mtpap |
G |
T |
18: 4,396,439 (GRCm39) |
G577V |
probably damaging |
Het |
Ncoa1 |
A |
G |
12: 4,325,177 (GRCm39) |
V967A |
possibly damaging |
Het |
Ndufa11 |
T |
C |
17: 57,028,112 (GRCm39) |
Y61H |
probably benign |
Het |
Nr2c2 |
T |
A |
6: 92,144,530 (GRCm39) |
N602K |
probably damaging |
Het |
Nubp1 |
C |
A |
16: 10,231,604 (GRCm39) |
T85K |
probably benign |
Het |
Oosp3 |
A |
G |
19: 11,676,753 (GRCm39) |
I37M |
probably damaging |
Het |
Optn |
A |
G |
2: 5,057,951 (GRCm39) |
S73P |
probably damaging |
Het |
Or10j3 |
T |
C |
1: 173,031,352 (GRCm39) |
I143T |
probably benign |
Het |
Or2y15 |
A |
G |
11: 49,350,529 (GRCm39) |
T8A |
probably benign |
Het |
Osmr |
T |
G |
15: 6,846,086 (GRCm39) |
I779L |
possibly damaging |
Het |
Pcdh20 |
T |
C |
14: 88,706,190 (GRCm39) |
D370G |
probably benign |
Het |
Pgap1 |
A |
G |
1: 54,550,570 (GRCm39) |
S571P |
probably benign |
Het |
Pgbd5 |
A |
G |
8: 125,106,930 (GRCm39) |
I204T |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,604,799 (GRCm39) |
I1172T |
possibly damaging |
Het |
Plch1 |
T |
A |
3: 63,606,412 (GRCm39) |
H1164L |
possibly damaging |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Rab38 |
T |
A |
7: 88,099,954 (GRCm39) |
F156L |
possibly damaging |
Het |
Rtl1 |
T |
C |
12: 109,561,017 (GRCm39) |
E274G |
possibly damaging |
Het |
Serpinb9 |
A |
G |
13: 33,199,479 (GRCm39) |
D258G |
probably benign |
Het |
Slco1a7 |
G |
T |
6: 141,686,153 (GRCm39) |
T229K |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,528,447 (GRCm39) |
T1568N |
probably damaging |
Het |
Ston2 |
T |
C |
12: 91,615,461 (GRCm39) |
T316A |
probably benign |
Het |
Tacc1 |
A |
T |
8: 25,672,634 (GRCm39) |
M198K |
probably benign |
Het |
Tspan33 |
T |
C |
6: 29,710,652 (GRCm39) |
F76S |
probably damaging |
Het |
Tspyl5 |
T |
C |
15: 33,687,082 (GRCm39) |
I288V |
possibly damaging |
Het |
Vmn2r50 |
G |
A |
7: 9,781,503 (GRCm39) |
S414F |
probably benign |
Het |
Zfp141 |
G |
A |
7: 42,125,111 (GRCm39) |
R454* |
probably null |
Het |
Zscan22 |
T |
A |
7: 12,641,075 (GRCm39) |
C440S |
probably damaging |
Het |
Zscan4-ps2 |
A |
T |
7: 11,251,339 (GRCm39) |
Q153L |
probably damaging |
Het |
|
Other mutations in Slc26a11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00941:Slc26a11
|
APN |
11 |
119,270,727 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01359:Slc26a11
|
APN |
11 |
119,254,257 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:Slc26a11
|
APN |
11 |
119,268,040 (GRCm39) |
missense |
probably benign |
|
R0193:Slc26a11
|
UTSW |
11 |
119,250,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Slc26a11
|
UTSW |
11 |
119,270,767 (GRCm39) |
splice site |
probably benign |
|
R0709:Slc26a11
|
UTSW |
11 |
119,265,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R1800:Slc26a11
|
UTSW |
11 |
119,263,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R1964:Slc26a11
|
UTSW |
11 |
119,271,020 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4762:Slc26a11
|
UTSW |
11 |
119,247,657 (GRCm39) |
unclassified |
probably benign |
|
R5153:Slc26a11
|
UTSW |
11 |
119,268,085 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5302:Slc26a11
|
UTSW |
11 |
119,254,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R5660:Slc26a11
|
UTSW |
11 |
119,248,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R5994:Slc26a11
|
UTSW |
11 |
119,270,738 (GRCm39) |
missense |
probably benign |
0.14 |
R6025:Slc26a11
|
UTSW |
11 |
119,265,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Slc26a11
|
UTSW |
11 |
119,250,125 (GRCm39) |
missense |
probably benign |
0.44 |
R6970:Slc26a11
|
UTSW |
11 |
119,247,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R6974:Slc26a11
|
UTSW |
11 |
119,248,844 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7466:Slc26a11
|
UTSW |
11 |
119,265,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R8210:Slc26a11
|
UTSW |
11 |
119,270,692 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8459:Slc26a11
|
UTSW |
11 |
119,259,643 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9324:Slc26a11
|
UTSW |
11 |
119,267,730 (GRCm39) |
missense |
probably benign |
0.00 |
R9393:Slc26a11
|
UTSW |
11 |
119,259,627 (GRCm39) |
missense |
probably benign |
|
X0026:Slc26a11
|
UTSW |
11 |
119,271,056 (GRCm39) |
missense |
probably benign |
|
X0028:Slc26a11
|
UTSW |
11 |
119,271,020 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Slc26a11
|
UTSW |
11 |
119,247,785 (GRCm39) |
missense |
not run |
|
|