Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
T |
A |
1: 120,093,906 (GRCm39) |
|
probably benign |
Het |
Aadacl2fm3 |
T |
A |
3: 59,784,440 (GRCm39) |
N304K |
probably benign |
Het |
Abcf3 |
T |
A |
16: 20,378,918 (GRCm39) |
|
probably null |
Het |
Acadm |
C |
T |
3: 153,641,961 (GRCm39) |
M190I |
possibly damaging |
Het |
Adamtsl3 |
G |
A |
7: 82,206,032 (GRCm39) |
R739Q |
probably damaging |
Het |
Ank1 |
T |
A |
8: 23,578,941 (GRCm39) |
|
probably benign |
Het |
Ap3b1 |
T |
A |
13: 94,540,626 (GRCm39) |
|
probably benign |
Het |
Arhgdib |
A |
G |
6: 136,903,732 (GRCm39) |
V31A |
probably damaging |
Het |
Arid4a |
A |
G |
12: 71,119,406 (GRCm39) |
R342G |
probably damaging |
Het |
Asic3 |
C |
T |
5: 24,622,700 (GRCm39) |
L517F |
probably benign |
Het |
Atxn7l1 |
C |
T |
12: 33,392,150 (GRCm39) |
P242L |
possibly damaging |
Het |
AY761185 |
T |
A |
8: 21,434,616 (GRCm39) |
E37D |
possibly damaging |
Het |
Babam1 |
T |
A |
8: 71,851,050 (GRCm39) |
D104E |
probably damaging |
Het |
Batf |
A |
T |
12: 85,755,446 (GRCm39) |
T100S |
probably benign |
Het |
Blcap |
A |
T |
2: 157,399,897 (GRCm39) |
Y59* |
probably null |
Het |
Cacnb3 |
G |
A |
15: 98,540,440 (GRCm39) |
A350T |
probably damaging |
Het |
Cdk15 |
T |
A |
1: 59,349,965 (GRCm39) |
V319D |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,382,911 (GRCm39) |
H2661R |
probably benign |
Het |
Cenpq |
T |
C |
17: 41,240,941 (GRCm39) |
E106G |
probably damaging |
Het |
Cfap43 |
A |
G |
19: 47,785,642 (GRCm39) |
|
probably benign |
Het |
Cfb |
G |
A |
17: 35,079,362 (GRCm39) |
S778L |
possibly damaging |
Het |
Clec2m |
A |
T |
6: 129,302,571 (GRCm39) |
L152* |
probably null |
Het |
Clspn |
T |
A |
4: 126,467,029 (GRCm39) |
N631K |
probably damaging |
Het |
Cntn2 |
T |
A |
1: 132,449,462 (GRCm39) |
T660S |
probably damaging |
Het |
Cntrob |
T |
A |
11: 69,202,167 (GRCm39) |
H475L |
possibly damaging |
Het |
Ddx46 |
T |
C |
13: 55,821,917 (GRCm39) |
I863T |
probably benign |
Het |
Dnah11 |
G |
A |
12: 118,004,748 (GRCm39) |
T2191I |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,813,411 (GRCm39) |
T1703A |
probably benign |
Het |
Fam13c |
C |
T |
10: 70,380,343 (GRCm39) |
P424S |
probably benign |
Het |
Fan1 |
T |
C |
7: 63,998,619 (GRCm39) |
N968D |
probably benign |
Het |
Fbxl20 |
A |
T |
11: 97,989,329 (GRCm39) |
|
probably benign |
Het |
Fkbp1b |
A |
T |
12: 4,888,229 (GRCm39) |
|
probably benign |
Het |
G930045G22Rik |
T |
A |
6: 50,824,039 (GRCm39) |
|
noncoding transcript |
Het |
Gm28042 |
C |
A |
2: 119,872,073 (GRCm39) |
R1008S |
probably benign |
Het |
Gon4l |
G |
A |
3: 88,765,707 (GRCm39) |
S376N |
probably damaging |
Het |
Gstt3 |
C |
A |
10: 75,616,749 (GRCm39) |
R15L |
probably damaging |
Het |
Gtdc1 |
A |
T |
2: 44,642,186 (GRCm39) |
S73T |
possibly damaging |
Het |
Hhatl |
A |
G |
9: 121,613,786 (GRCm39) |
S419P |
probably benign |
Het |
Hirip3 |
T |
G |
7: 126,462,363 (GRCm39) |
S46R |
probably damaging |
Het |
Hsf2 |
A |
G |
10: 57,378,735 (GRCm39) |
T204A |
probably benign |
Het |
Impg2 |
G |
A |
16: 56,089,378 (GRCm39) |
E1108K |
possibly damaging |
Het |
Itgb2l |
G |
T |
16: 96,224,130 (GRCm39) |
|
probably benign |
Het |
Itih5 |
A |
T |
2: 10,256,075 (GRCm39) |
N847I |
probably benign |
Het |
Kif1a |
T |
C |
1: 92,982,164 (GRCm39) |
|
probably benign |
Het |
Klhl1 |
T |
A |
14: 96,755,780 (GRCm39) |
|
probably benign |
Het |
Ktn1 |
T |
A |
14: 47,952,119 (GRCm39) |
D963E |
probably benign |
Het |
Lclat1 |
T |
A |
17: 73,547,022 (GRCm39) |
V313E |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,712,639 (GRCm39) |
S395G |
probably benign |
Het |
Macroh2a1 |
G |
A |
13: 56,243,927 (GRCm39) |
|
probably benign |
Het |
Mbtps1 |
G |
A |
8: 120,264,856 (GRCm39) |
|
probably benign |
Het |
Me1 |
A |
G |
9: 86,478,257 (GRCm39) |
|
probably benign |
Het |
Mov10 |
C |
A |
3: 104,702,721 (GRCm39) |
C948F |
probably benign |
Het |
Mterf1a |
G |
A |
5: 3,940,990 (GRCm39) |
Q293* |
probably null |
Het |
Nfkb2 |
A |
T |
19: 46,300,065 (GRCm39) |
M838L |
possibly damaging |
Het |
Nhlrc2 |
T |
A |
19: 56,540,302 (GRCm39) |
L97Q |
probably damaging |
Het |
Nr6a1 |
A |
T |
2: 38,629,032 (GRCm39) |
Y331N |
possibly damaging |
Het |
Nup214 |
C |
T |
2: 31,924,826 (GRCm39) |
A1785V |
probably damaging |
Het |
Ogg1 |
C |
T |
6: 113,306,217 (GRCm39) |
T138I |
probably benign |
Het |
Or5ac20 |
A |
G |
16: 59,104,116 (GRCm39) |
V248A |
probably damaging |
Het |
Or5b107 |
A |
G |
19: 13,143,251 (GRCm39) |
Y291C |
probably damaging |
Het |
Or5b124 |
A |
G |
19: 13,611,048 (GRCm39) |
Y191C |
probably damaging |
Het |
Or7g17 |
T |
A |
9: 18,768,127 (GRCm39) |
Y60N |
probably damaging |
Het |
Plod2 |
G |
T |
9: 92,466,574 (GRCm39) |
R178L |
probably benign |
Het |
Polr3b |
T |
A |
10: 84,554,339 (GRCm39) |
L1017Q |
probably benign |
Het |
Postn |
C |
A |
3: 54,291,971 (GRCm39) |
T724N |
probably damaging |
Het |
Ppm1l |
T |
G |
3: 69,225,309 (GRCm39) |
|
probably benign |
Het |
Prpf8 |
T |
G |
11: 75,396,075 (GRCm39) |
L1983R |
probably damaging |
Het |
Psma7 |
A |
G |
2: 179,681,193 (GRCm39) |
V59A |
probably benign |
Het |
Qser1 |
T |
A |
2: 104,619,306 (GRCm39) |
Y502F |
probably benign |
Het |
Rad50 |
T |
C |
11: 53,558,852 (GRCm39) |
D1129G |
probably damaging |
Het |
Rasal1 |
C |
A |
5: 120,812,794 (GRCm39) |
P606Q |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,180,463 (GRCm39) |
Y438C |
probably damaging |
Het |
Rnf180 |
A |
G |
13: 105,388,774 (GRCm39) |
C73R |
probably benign |
Het |
Rnf216 |
T |
A |
5: 143,065,996 (GRCm39) |
I474F |
possibly damaging |
Het |
Sdha |
A |
T |
13: 74,480,366 (GRCm39) |
L371Q |
probably damaging |
Het |
Sdk1 |
T |
G |
5: 142,070,321 (GRCm39) |
L1162R |
possibly damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,237,146 (GRCm39) |
I223T |
probably damaging |
Het |
Sirpb1a |
A |
G |
3: 15,475,587 (GRCm39) |
V316A |
probably damaging |
Het |
Slc12a4 |
A |
T |
8: 106,672,021 (GRCm39) |
I897N |
probably benign |
Het |
Slc35d1 |
A |
T |
4: 103,048,035 (GRCm39) |
V243E |
probably damaging |
Het |
Slc4a11 |
T |
A |
2: 130,532,852 (GRCm39) |
K200N |
possibly damaging |
Het |
Slc9a8 |
T |
A |
2: 167,293,216 (GRCm39) |
M188K |
probably damaging |
Het |
Slco1a8 |
T |
A |
6: 141,918,137 (GRCm39) |
I580F |
possibly damaging |
Het |
Snrnp200 |
T |
C |
2: 127,074,902 (GRCm39) |
S1492P |
probably damaging |
Het |
Sphk2 |
T |
C |
7: 45,360,149 (GRCm39) |
*618W |
probably null |
Het |
Tdpoz3 |
A |
G |
3: 93,734,231 (GRCm39) |
N302S |
probably benign |
Het |
Tdrd6 |
T |
C |
17: 43,935,199 (GRCm39) |
M1950V |
probably benign |
Het |
Tmem39a |
A |
G |
16: 38,384,675 (GRCm39) |
|
probably benign |
Het |
Trip4 |
A |
T |
9: 65,765,640 (GRCm39) |
I353K |
probably damaging |
Het |
Trip6 |
A |
T |
5: 137,311,103 (GRCm39) |
F204L |
probably benign |
Het |
Trpm4 |
T |
A |
7: 44,968,677 (GRCm39) |
I419F |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,775,140 (GRCm39) |
E1967D |
probably damaging |
Het |
Uba2 |
C |
T |
7: 33,850,281 (GRCm39) |
V391M |
possibly damaging |
Het |
Ubr4 |
T |
G |
4: 139,206,746 (GRCm39) |
|
probably benign |
Het |
Upf1 |
G |
A |
8: 70,788,295 (GRCm39) |
|
probably benign |
Het |
Vmn1r228 |
A |
C |
17: 20,996,858 (GRCm39) |
V220G |
possibly damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,652,594 (GRCm39) |
M429V |
probably benign |
Het |
Vps36 |
C |
T |
8: 22,700,472 (GRCm39) |
T210I |
possibly damaging |
Het |
Wdr17 |
C |
T |
8: 55,146,131 (GRCm39) |
A90T |
possibly damaging |
Het |
Ybx1 |
C |
T |
4: 119,138,788 (GRCm39) |
G126D |
probably benign |
Het |
Yipf5 |
C |
A |
18: 40,339,460 (GRCm39) |
|
probably benign |
Het |
Zbtb47 |
A |
G |
9: 121,596,641 (GRCm39) |
T666A |
probably benign |
Het |
Zdhhc5 |
A |
C |
2: 84,520,459 (GRCm39) |
S573A |
probably benign |
Het |
Zfp457 |
A |
T |
13: 67,441,991 (GRCm39) |
C99S |
probably damaging |
Het |
Zfp52 |
T |
A |
17: 21,781,564 (GRCm39) |
C471S |
probably damaging |
Het |
Zfp558 |
C |
T |
9: 18,379,252 (GRCm39) |
V71I |
probably damaging |
Het |
Zfp655 |
A |
G |
5: 145,181,267 (GRCm39) |
Y375C |
probably damaging |
Het |
Zfp882 |
A |
T |
8: 72,668,459 (GRCm39) |
T429S |
probably benign |
Het |
Zmym2 |
T |
C |
14: 57,187,141 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Sytl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Sytl2
|
APN |
7 |
90,022,113 (GRCm39) |
missense |
probably benign |
0.25 |
IGL00657:Sytl2
|
APN |
7 |
90,050,618 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00788:Sytl2
|
APN |
7 |
90,031,906 (GRCm39) |
intron |
probably benign |
|
IGL00834:Sytl2
|
APN |
7 |
90,031,844 (GRCm39) |
intron |
probably benign |
|
IGL01833:Sytl2
|
APN |
7 |
90,045,745 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01866:Sytl2
|
APN |
7 |
90,031,047 (GRCm39) |
intron |
probably benign |
|
IGL02215:Sytl2
|
APN |
7 |
90,030,422 (GRCm39) |
intron |
probably benign |
|
IGL02934:Sytl2
|
APN |
7 |
90,025,200 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03095:Sytl2
|
APN |
7 |
90,041,642 (GRCm39) |
missense |
probably damaging |
1.00 |
finder
|
UTSW |
7 |
90,024,860 (GRCm39) |
missense |
probably damaging |
1.00 |
keeper
|
UTSW |
7 |
90,007,432 (GRCm39) |
nonsense |
probably null |
|
R0126:Sytl2
|
UTSW |
7 |
90,045,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Sytl2
|
UTSW |
7 |
90,052,228 (GRCm39) |
splice site |
probably benign |
|
R0271:Sytl2
|
UTSW |
7 |
90,052,228 (GRCm39) |
splice site |
probably benign |
|
R0288:Sytl2
|
UTSW |
7 |
90,052,228 (GRCm39) |
splice site |
probably benign |
|
R0528:Sytl2
|
UTSW |
7 |
90,052,228 (GRCm39) |
splice site |
probably benign |
|
R0601:Sytl2
|
UTSW |
7 |
90,044,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Sytl2
|
UTSW |
7 |
90,030,061 (GRCm39) |
intron |
probably benign |
|
R1634:Sytl2
|
UTSW |
7 |
90,044,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Sytl2
|
UTSW |
7 |
90,052,260 (GRCm39) |
missense |
probably benign |
0.25 |
R2040:Sytl2
|
UTSW |
7 |
90,031,069 (GRCm39) |
intron |
probably benign |
|
R3788:Sytl2
|
UTSW |
7 |
90,025,289 (GRCm39) |
missense |
probably benign |
0.00 |
R3843:Sytl2
|
UTSW |
7 |
90,009,367 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3952:Sytl2
|
UTSW |
7 |
90,030,700 (GRCm39) |
intron |
probably benign |
|
R4082:Sytl2
|
UTSW |
7 |
90,057,635 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4600:Sytl2
|
UTSW |
7 |
90,024,977 (GRCm39) |
missense |
probably benign |
0.11 |
R4651:Sytl2
|
UTSW |
7 |
90,024,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Sytl2
|
UTSW |
7 |
89,998,000 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4730:Sytl2
|
UTSW |
7 |
90,030,457 (GRCm39) |
intron |
probably benign |
|
R4870:Sytl2
|
UTSW |
7 |
90,038,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Sytl2
|
UTSW |
7 |
90,025,245 (GRCm39) |
missense |
probably damaging |
0.97 |
R4995:Sytl2
|
UTSW |
7 |
90,031,465 (GRCm39) |
intron |
probably benign |
|
R5009:Sytl2
|
UTSW |
7 |
90,030,523 (GRCm39) |
intron |
probably benign |
|
R5096:Sytl2
|
UTSW |
7 |
90,025,290 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5191:Sytl2
|
UTSW |
7 |
90,024,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R5305:Sytl2
|
UTSW |
7 |
90,031,071 (GRCm39) |
intron |
probably benign |
|
R5538:Sytl2
|
UTSW |
7 |
90,038,114 (GRCm39) |
missense |
probably benign |
0.03 |
R5792:Sytl2
|
UTSW |
7 |
90,024,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R6378:Sytl2
|
UTSW |
7 |
90,007,432 (GRCm39) |
nonsense |
probably null |
|
R6982:Sytl2
|
UTSW |
7 |
90,045,772 (GRCm39) |
missense |
probably damaging |
0.96 |
R7456:Sytl2
|
UTSW |
7 |
89,998,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Sytl2
|
UTSW |
7 |
90,025,352 (GRCm39) |
missense |
probably benign |
0.00 |
R8127:Sytl2
|
UTSW |
7 |
90,024,798 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8171:Sytl2
|
UTSW |
7 |
90,058,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8225:Sytl2
|
UTSW |
7 |
90,024,725 (GRCm39) |
missense |
probably benign |
0.36 |
R8297:Sytl2
|
UTSW |
7 |
90,034,283 (GRCm39) |
missense |
probably benign |
|
R8843:Sytl2
|
UTSW |
7 |
90,025,334 (GRCm39) |
missense |
probably benign |
0.03 |
R8929:Sytl2
|
UTSW |
7 |
90,024,810 (GRCm39) |
missense |
probably benign |
0.20 |
R9027:Sytl2
|
UTSW |
7 |
90,028,748 (GRCm39) |
missense |
probably benign |
0.00 |
R9222:Sytl2
|
UTSW |
7 |
90,050,633 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9246:Sytl2
|
UTSW |
7 |
90,007,384 (GRCm39) |
missense |
probably benign |
0.31 |
R9268:Sytl2
|
UTSW |
7 |
90,034,359 (GRCm39) |
missense |
probably benign |
0.00 |
R9399:Sytl2
|
UTSW |
7 |
90,041,658 (GRCm39) |
missense |
probably benign |
0.23 |
R9480:Sytl2
|
UTSW |
7 |
90,020,718 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9573:Sytl2
|
UTSW |
7 |
90,057,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Sytl2
|
UTSW |
7 |
90,024,800 (GRCm39) |
missense |
probably benign |
0.02 |
|