Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,610,757 (GRCm39) |
|
probably benign |
Het |
9030619P08Rik |
T |
A |
15: 75,303,267 (GRCm39) |
|
noncoding transcript |
Het |
Abcb5 |
T |
A |
12: 118,850,626 (GRCm39) |
|
probably benign |
Het |
Acox3 |
A |
G |
5: 35,747,080 (GRCm39) |
N166D |
probably damaging |
Het |
Actn1 |
T |
C |
12: 80,219,904 (GRCm39) |
I656V |
probably benign |
Het |
Arhgef15 |
A |
G |
11: 68,838,143 (GRCm39) |
V659A |
probably benign |
Het |
AW551984 |
T |
C |
9: 39,508,472 (GRCm39) |
E348G |
possibly damaging |
Het |
Bbs2 |
A |
T |
8: 94,807,435 (GRCm39) |
V453E |
probably damaging |
Het |
Caskin1 |
A |
T |
17: 24,726,135 (GRCm39) |
D1414V |
probably damaging |
Het |
Ccdc57 |
A |
T |
11: 120,751,978 (GRCm39) |
S868T |
probably benign |
Het |
Cdc34b |
A |
T |
11: 94,633,087 (GRCm39) |
I96F |
probably damaging |
Het |
Ctnnd1 |
A |
G |
2: 84,452,417 (GRCm39) |
F69L |
possibly damaging |
Het |
Cyld |
A |
G |
8: 89,468,929 (GRCm39) |
I567V |
possibly damaging |
Het |
Dact3 |
G |
C |
7: 16,620,013 (GRCm39) |
V503L |
unknown |
Het |
Dlg1 |
C |
T |
16: 31,573,626 (GRCm39) |
T9I |
probably benign |
Het |
Dnase1 |
T |
C |
16: 3,855,771 (GRCm39) |
|
probably benign |
Het |
Drc7 |
G |
A |
8: 95,798,224 (GRCm39) |
E490K |
probably benign |
Het |
Drd4 |
T |
C |
7: 140,873,690 (GRCm39) |
M114T |
probably damaging |
Het |
Exoc3l4 |
A |
G |
12: 111,395,155 (GRCm39) |
H591R |
probably benign |
Het |
Fgfr1 |
C |
A |
8: 26,062,461 (GRCm39) |
Y665* |
probably null |
Het |
G2e3 |
A |
G |
12: 51,418,413 (GRCm39) |
I603V |
probably benign |
Het |
Glp2r |
G |
T |
11: 67,648,419 (GRCm39) |
Y94* |
probably null |
Het |
Gnat1 |
A |
T |
9: 107,554,433 (GRCm39) |
M115K |
probably benign |
Het |
Gpr45 |
A |
G |
1: 43,072,280 (GRCm39) |
T308A |
probably benign |
Het |
Grm1 |
T |
A |
10: 10,595,409 (GRCm39) |
K740* |
probably null |
Het |
Gtsf2 |
T |
C |
15: 103,352,755 (GRCm39) |
E88G |
possibly damaging |
Het |
Hsh2d |
C |
T |
8: 72,947,372 (GRCm39) |
A23V |
probably benign |
Het |
Ino80c |
T |
C |
18: 24,239,702 (GRCm39) |
D153G |
probably damaging |
Het |
Ints11 |
T |
C |
4: 155,971,385 (GRCm39) |
F278L |
probably damaging |
Het |
Ints6 |
A |
G |
14: 62,939,911 (GRCm39) |
L593P |
probably damaging |
Het |
Map4k1 |
A |
T |
7: 28,682,427 (GRCm39) |
H16L |
probably benign |
Het |
Mipep |
G |
T |
14: 61,022,231 (GRCm39) |
R32L |
probably damaging |
Het |
Mon1a |
A |
G |
9: 107,779,850 (GRCm39) |
E473G |
probably damaging |
Het |
Myf5 |
A |
T |
10: 107,321,733 (GRCm39) |
C20* |
probably null |
Het |
Myh11 |
T |
C |
16: 14,023,818 (GRCm39) |
E1512G |
probably damaging |
Het |
Myo5c |
T |
C |
9: 75,176,878 (GRCm39) |
S608P |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,779,017 (GRCm39) |
D1591G |
probably benign |
Het |
Myof |
T |
A |
19: 37,924,300 (GRCm39) |
I1306F |
probably damaging |
Het |
Nlgn1 |
C |
T |
3: 25,974,401 (GRCm39) |
G165D |
possibly damaging |
Het |
Noc2l |
C |
G |
4: 156,330,368 (GRCm39) |
D513E |
probably damaging |
Het |
Nup205 |
G |
A |
6: 35,220,784 (GRCm39) |
R1862H |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,014,208 (GRCm39) |
H65R |
probably benign |
Het |
Or2y16 |
A |
G |
11: 49,334,945 (GRCm39) |
D89G |
possibly damaging |
Het |
Or9k7 |
A |
T |
10: 130,046,306 (GRCm39) |
M231K |
probably benign |
Het |
Pcmtd1 |
C |
A |
1: 7,231,233 (GRCm39) |
Y176* |
probably null |
Het |
Pde6h |
C |
T |
6: 136,938,201 (GRCm39) |
T58I |
possibly damaging |
Het |
Pkd1 |
T |
C |
17: 24,805,042 (GRCm39) |
|
probably null |
Het |
Polr1e |
G |
A |
4: 45,029,429 (GRCm39) |
A297T |
probably damaging |
Het |
Rbm34 |
T |
C |
8: 127,678,087 (GRCm39) |
D269G |
possibly damaging |
Het |
Rdx |
T |
C |
9: 51,986,309 (GRCm39) |
V372A |
probably benign |
Het |
Reep6 |
T |
A |
10: 80,169,633 (GRCm39) |
F107Y |
probably benign |
Het |
Rere |
G |
T |
4: 150,698,273 (GRCm39) |
|
probably benign |
Het |
Rmdn2 |
G |
T |
17: 79,974,304 (GRCm39) |
A266S |
probably damaging |
Het |
Rnf32 |
G |
A |
5: 29,403,576 (GRCm39) |
R7H |
probably benign |
Het |
Rnpepl1 |
A |
T |
1: 92,844,483 (GRCm39) |
N325I |
probably damaging |
Het |
Rps6ka5 |
T |
A |
12: 100,519,325 (GRCm39) |
M763L |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,729,497 (GRCm39) |
E2375G |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,848,878 (GRCm39) |
T361A |
probably benign |
Het |
Serpina3j |
T |
A |
12: 104,286,043 (GRCm39) |
C399* |
probably null |
Het |
Serpinb9 |
T |
A |
13: 33,192,847 (GRCm39) |
W135R |
probably damaging |
Het |
Sim2 |
T |
C |
16: 93,924,280 (GRCm39) |
V475A |
probably benign |
Het |
Slc24a5 |
G |
A |
2: 124,910,188 (GRCm39) |
V30I |
probably benign |
Het |
Snrnp25 |
A |
G |
11: 32,157,595 (GRCm39) |
K58E |
probably damaging |
Het |
Stx1b |
T |
C |
7: 127,407,093 (GRCm39) |
I55V |
probably damaging |
Het |
Tacc2 |
T |
C |
7: 130,330,507 (GRCm39) |
S264P |
probably damaging |
Het |
Tbc1d4 |
A |
T |
14: 101,695,610 (GRCm39) |
Y943N |
probably damaging |
Het |
Tlr5 |
T |
C |
1: 182,801,038 (GRCm39) |
I114T |
probably benign |
Het |
Tm2d3 |
A |
G |
7: 65,347,469 (GRCm39) |
N101S |
possibly damaging |
Het |
Tmem201 |
G |
T |
4: 149,803,144 (GRCm39) |
Q575K |
probably benign |
Het |
Tmem241 |
A |
G |
18: 12,237,176 (GRCm39) |
S87P |
probably damaging |
Het |
Trak2 |
G |
A |
1: 58,958,480 (GRCm39) |
T267I |
probably damaging |
Het |
Trmt2a |
T |
A |
16: 18,067,418 (GRCm39) |
C30* |
probably null |
Het |
Ttbk2 |
A |
T |
2: 120,603,758 (GRCm39) |
F258L |
possibly damaging |
Het |
Ttk |
T |
A |
9: 83,747,201 (GRCm39) |
I680N |
probably benign |
Het |
Ttn |
T |
C |
2: 76,785,380 (GRCm39) |
D665G |
probably damaging |
Het |
Tulp4 |
G |
A |
17: 6,249,088 (GRCm39) |
E36K |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,992,023 (GRCm39) |
|
probably null |
Het |
Uroc1 |
T |
C |
6: 90,322,376 (GRCm39) |
L300P |
probably damaging |
Het |
Vmn2r67 |
A |
T |
7: 84,785,593 (GRCm39) |
V804E |
probably damaging |
Het |
Wdr81 |
T |
A |
11: 75,336,775 (GRCm39) |
Q1538L |
probably benign |
Het |
Zfp457 |
T |
A |
13: 67,441,342 (GRCm39) |
H315L |
probably damaging |
Het |
Zfp518a |
T |
A |
19: 40,904,295 (GRCm39) |
V1408D |
possibly damaging |
Het |
Zfp712 |
C |
T |
13: 67,188,676 (GRCm39) |
C617Y |
probably damaging |
Het |
Zfp770 |
T |
C |
2: 114,027,868 (GRCm39) |
N67S |
probably benign |
Het |
Zmat4 |
T |
C |
8: 24,392,085 (GRCm39) |
S83P |
probably damaging |
Het |
|
Other mutations in Zfp52 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01752:Zfp52
|
APN |
17 |
21,780,412 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4449001:Zfp52
|
UTSW |
17 |
21,777,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Zfp52
|
UTSW |
17 |
21,781,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Zfp52
|
UTSW |
17 |
21,782,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1224:Zfp52
|
UTSW |
17 |
21,775,324 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1248:Zfp52
|
UTSW |
17 |
21,780,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R1622:Zfp52
|
UTSW |
17 |
21,781,833 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Zfp52
|
UTSW |
17 |
21,782,084 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1917:Zfp52
|
UTSW |
17 |
21,780,426 (GRCm39) |
missense |
probably benign |
|
R4272:Zfp52
|
UTSW |
17 |
21,780,459 (GRCm39) |
nonsense |
probably null |
|
R4273:Zfp52
|
UTSW |
17 |
21,780,459 (GRCm39) |
nonsense |
probably null |
|
R4278:Zfp52
|
UTSW |
17 |
21,782,132 (GRCm39) |
missense |
probably benign |
|
R4683:Zfp52
|
UTSW |
17 |
21,781,769 (GRCm39) |
missense |
probably benign |
0.31 |
R4865:Zfp52
|
UTSW |
17 |
21,781,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Zfp52
|
UTSW |
17 |
21,780,665 (GRCm39) |
missense |
probably benign |
0.04 |
R5430:Zfp52
|
UTSW |
17 |
21,775,329 (GRCm39) |
missense |
probably benign |
0.01 |
R5685:Zfp52
|
UTSW |
17 |
21,782,013 (GRCm39) |
missense |
probably benign |
0.15 |
R6133:Zfp52
|
UTSW |
17 |
21,780,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Zfp52
|
UTSW |
17 |
21,775,309 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R7083:Zfp52
|
UTSW |
17 |
21,780,392 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7439:Zfp52
|
UTSW |
17 |
21,781,132 (GRCm39) |
nonsense |
probably null |
|
R7456:Zfp52
|
UTSW |
17 |
21,781,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Zfp52
|
UTSW |
17 |
21,781,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8196:Zfp52
|
UTSW |
17 |
21,782,156 (GRCm39) |
missense |
possibly damaging |
0.45 |
R8930:Zfp52
|
UTSW |
17 |
21,780,692 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8932:Zfp52
|
UTSW |
17 |
21,780,692 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9033:Zfp52
|
UTSW |
17 |
21,780,655 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9510:Zfp52
|
UTSW |
17 |
21,782,218 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9645:Zfp52
|
UTSW |
17 |
21,781,937 (GRCm39) |
missense |
possibly damaging |
0.92 |
|