Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
A |
T |
18: 61,988,288 (GRCm39) |
I145N |
probably benign |
Het |
Ankrd1 |
G |
A |
19: 36,096,713 (GRCm39) |
A38V |
probably benign |
Het |
Ankrd34b |
A |
G |
13: 92,576,268 (GRCm39) |
E500G |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,916,890 (GRCm39) |
T419A |
probably damaging |
Het |
B3galt2 |
A |
T |
1: 143,523,072 (GRCm39) |
N403Y |
possibly damaging |
Het |
Bbx |
C |
T |
16: 50,100,755 (GRCm39) |
E47K |
probably benign |
Het |
C4b |
G |
A |
17: 34,953,193 (GRCm39) |
|
probably benign |
Het |
Cacna1e |
A |
T |
1: 154,324,693 (GRCm39) |
|
probably null |
Het |
Cdh3 |
T |
C |
8: 107,237,857 (GRCm39) |
V17A |
probably benign |
Het |
Cog7 |
A |
T |
7: 121,550,387 (GRCm39) |
L379Q |
probably damaging |
Het |
Cul9 |
T |
C |
17: 46,837,336 (GRCm39) |
N1044S |
possibly damaging |
Het |
Cyp4b1 |
C |
T |
4: 115,493,071 (GRCm39) |
D258N |
probably damaging |
Het |
Ddx39a |
T |
C |
8: 84,447,179 (GRCm39) |
V113A |
probably benign |
Het |
Dennd4b |
A |
T |
3: 90,179,671 (GRCm39) |
H643L |
probably damaging |
Het |
Dpy19l3 |
T |
C |
7: 35,413,640 (GRCm39) |
T334A |
probably benign |
Het |
Dsg3 |
T |
C |
18: 20,669,882 (GRCm39) |
L632S |
probably damaging |
Het |
Dtx4 |
G |
A |
19: 12,463,846 (GRCm39) |
T312I |
probably damaging |
Het |
Dusp18 |
C |
T |
11: 3,847,243 (GRCm39) |
R78C |
probably benign |
Het |
Fes |
A |
C |
7: 80,033,643 (GRCm39) |
F203V |
probably benign |
Het |
Fhad1 |
C |
A |
4: 141,656,957 (GRCm39) |
|
probably benign |
Het |
Gjb2 |
T |
C |
14: 57,337,526 (GRCm39) |
|
silent |
Het |
Gm5828 |
T |
C |
1: 16,838,579 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma |
A |
C |
11: 98,557,080 (GRCm39) |
E65A |
probably damaging |
Het |
Hck |
T |
A |
2: 152,976,140 (GRCm39) |
|
probably null |
Het |
Henmt1 |
A |
T |
3: 108,861,118 (GRCm39) |
H47L |
probably damaging |
Het |
Hivep2 |
T |
C |
10: 14,005,099 (GRCm39) |
F566L |
probably damaging |
Het |
Hnrnpl |
T |
C |
7: 28,513,617 (GRCm39) |
|
probably benign |
Het |
Igsf3 |
T |
C |
3: 101,342,917 (GRCm39) |
I518T |
probably damaging |
Het |
Ireb2 |
T |
C |
9: 54,793,193 (GRCm39) |
F223L |
probably benign |
Het |
Isoc2a |
T |
C |
7: 4,894,331 (GRCm39) |
|
probably null |
Het |
Krt73 |
T |
A |
15: 101,709,208 (GRCm39) |
R200W |
probably damaging |
Het |
Lgals9 |
T |
A |
11: 78,854,361 (GRCm39) |
I308F |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,429,811 (GRCm39) |
F420L |
probably damaging |
Het |
Mep1b |
T |
C |
18: 21,228,164 (GRCm39) |
|
probably benign |
Het |
Mex3a |
G |
T |
3: 88,443,562 (GRCm39) |
A213S |
probably benign |
Het |
Mmp13 |
T |
C |
9: 7,276,558 (GRCm39) |
F218L |
probably damaging |
Het |
Ncf1 |
G |
T |
5: 134,255,991 (GRCm39) |
|
probably benign |
Het |
Notch2 |
A |
G |
3: 98,053,433 (GRCm39) |
D2032G |
probably damaging |
Het |
Or10h28 |
T |
C |
17: 33,488,471 (GRCm39) |
S258P |
probably damaging |
Het |
Or5p1 |
A |
G |
7: 107,916,202 (GRCm39) |
I34V |
probably benign |
Het |
Or9i1b |
A |
C |
19: 13,896,614 (GRCm39) |
I77L |
probably damaging |
Het |
Pex16 |
G |
A |
2: 92,210,802 (GRCm39) |
G312D |
probably damaging |
Het |
Pex5 |
A |
T |
6: 124,375,448 (GRCm39) |
W525R |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,818,131 (GRCm39) |
I799N |
probably damaging |
Het |
Poldip3 |
G |
A |
15: 83,012,144 (GRCm39) |
L372F |
probably damaging |
Het |
Polg2 |
C |
A |
11: 106,668,352 (GRCm39) |
V174L |
probably benign |
Het |
Prrt4 |
C |
G |
6: 29,170,670 (GRCm39) |
G594A |
probably damaging |
Het |
Prss1 |
A |
G |
6: 41,440,522 (GRCm39) |
D199G |
probably damaging |
Het |
Rbms2 |
T |
A |
10: 127,973,823 (GRCm39) |
Q207L |
probably benign |
Het |
Retreg2 |
A |
G |
1: 75,123,074 (GRCm39) |
D334G |
possibly damaging |
Het |
Slc6a15 |
T |
G |
10: 103,253,929 (GRCm39) |
C622G |
probably benign |
Het |
Spdya |
T |
A |
17: 71,865,635 (GRCm39) |
D84E |
probably damaging |
Het |
Stat3 |
A |
T |
11: 100,785,982 (GRCm39) |
S432T |
possibly damaging |
Het |
Tiam1 |
A |
T |
16: 89,695,088 (GRCm39) |
V123E |
probably benign |
Het |
Tnpo3 |
A |
G |
6: 29,565,651 (GRCm39) |
|
probably benign |
Het |
Tnrc6c |
A |
C |
11: 117,643,811 (GRCm39) |
N1481H |
probably damaging |
Het |
Top3b |
T |
C |
16: 16,701,389 (GRCm39) |
S234P |
probably damaging |
Het |
Tpsab1 |
T |
A |
17: 25,562,418 (GRCm39) |
H303L |
probably benign |
Het |
Traf3 |
T |
A |
12: 111,228,010 (GRCm39) |
V407D |
probably damaging |
Het |
Trim33 |
T |
A |
3: 103,259,417 (GRCm39) |
D1035E |
probably benign |
Het |
Ttc38 |
T |
C |
15: 85,737,920 (GRCm39) |
V402A |
possibly damaging |
Het |
Ube4b |
C |
T |
4: 149,439,914 (GRCm39) |
R646H |
possibly damaging |
Het |
Usp8 |
C |
A |
2: 126,597,009 (GRCm39) |
|
probably benign |
Het |
Zdbf2 |
A |
T |
1: 63,347,233 (GRCm39) |
I1871F |
probably benign |
Het |
Zfp345 |
T |
A |
2: 150,314,475 (GRCm39) |
Q354L |
probably benign |
Het |
Zfp462 |
C |
A |
4: 55,023,402 (GRCm39) |
|
probably benign |
Het |
Zfp81 |
G |
A |
17: 33,554,095 (GRCm39) |
H240Y |
possibly damaging |
Het |
Zfp830 |
A |
G |
11: 82,655,994 (GRCm39) |
D266G |
possibly damaging |
Het |
|
Other mutations in Tor1aip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01812:Tor1aip2
|
APN |
1 |
155,935,285 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02175:Tor1aip2
|
APN |
1 |
155,940,752 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02328:Tor1aip2
|
APN |
1 |
155,940,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R1037:Tor1aip2
|
UTSW |
1 |
155,941,082 (GRCm39) |
missense |
probably benign |
0.00 |
R1146:Tor1aip2
|
UTSW |
1 |
155,940,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1146:Tor1aip2
|
UTSW |
1 |
155,940,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1694:Tor1aip2
|
UTSW |
1 |
155,941,031 (GRCm39) |
missense |
probably benign |
|
R1922:Tor1aip2
|
UTSW |
1 |
155,940,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Tor1aip2
|
UTSW |
1 |
155,927,588 (GRCm39) |
intron |
probably benign |
|
R2131:Tor1aip2
|
UTSW |
1 |
155,941,095 (GRCm39) |
missense |
probably damaging |
0.97 |
R3758:Tor1aip2
|
UTSW |
1 |
155,941,035 (GRCm39) |
missense |
probably damaging |
0.98 |
R4243:Tor1aip2
|
UTSW |
1 |
155,941,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R4583:Tor1aip2
|
UTSW |
1 |
155,940,888 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Tor1aip2
|
UTSW |
1 |
155,940,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R5564:Tor1aip2
|
UTSW |
1 |
155,939,307 (GRCm39) |
unclassified |
probably benign |
|
R6316:Tor1aip2
|
UTSW |
1 |
155,937,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R6713:Tor1aip2
|
UTSW |
1 |
155,941,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R6892:Tor1aip2
|
UTSW |
1 |
155,940,927 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7137:Tor1aip2
|
UTSW |
1 |
155,927,722 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8137:Tor1aip2
|
UTSW |
1 |
155,939,414 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9456:Tor1aip2
|
UTSW |
1 |
155,937,525 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1176:Tor1aip2
|
UTSW |
1 |
155,927,935 (GRCm39) |
missense |
possibly damaging |
0.66 |
|