Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
A |
12: 71,236,187 (GRCm39) |
M1179I |
probably benign |
Het |
4930402F06Rik |
T |
C |
2: 35,266,349 (GRCm39) |
Y107C |
probably damaging |
Het |
Aff4 |
T |
C |
11: 53,289,206 (GRCm39) |
S452P |
probably damaging |
Het |
Astn2 |
T |
C |
4: 65,712,795 (GRCm39) |
D615G |
probably damaging |
Het |
Begain |
A |
G |
12: 109,018,802 (GRCm39) |
L215P |
probably benign |
Het |
Carf |
T |
A |
1: 60,187,214 (GRCm39) |
S606T |
probably benign |
Het |
Cngb3 |
A |
T |
4: 19,461,684 (GRCm39) |
T522S |
probably benign |
Het |
Cubn |
G |
A |
2: 13,284,889 (GRCm39) |
T3509I |
probably benign |
Het |
Dmrta1 |
T |
C |
4: 89,580,170 (GRCm39) |
S377P |
probably benign |
Het |
Dnmbp |
G |
A |
19: 43,838,525 (GRCm39) |
A659V |
probably benign |
Het |
Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,326,227 (GRCm39) |
|
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,015,490 (GRCm39) |
D3598G |
probably benign |
Het |
Elp1 |
T |
C |
4: 56,774,552 (GRCm39) |
N779S |
possibly damaging |
Het |
Flot2 |
T |
C |
11: 77,940,339 (GRCm39) |
F29L |
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,849,003 (GRCm39) |
I367K |
possibly damaging |
Het |
Ivl |
T |
A |
3: 92,479,317 (GRCm39) |
K249N |
probably damaging |
Het |
Khnyn |
A |
G |
14: 56,125,425 (GRCm39) |
T503A |
probably damaging |
Het |
Mbd4 |
T |
A |
6: 115,821,546 (GRCm39) |
I490F |
probably damaging |
Het |
Mlip |
T |
C |
9: 77,136,838 (GRCm39) |
T690A |
probably benign |
Het |
Mmp1a |
T |
A |
9: 7,467,005 (GRCm39) |
D227E |
possibly damaging |
Het |
Mrgprf |
T |
C |
7: 144,862,380 (GRCm39) |
L314P |
probably damaging |
Het |
Ndufb9 |
T |
G |
15: 58,808,255 (GRCm39) |
Y80* |
probably null |
Het |
Neto2 |
C |
T |
8: 86,396,285 (GRCm39) |
R155H |
probably damaging |
Het |
Npat |
T |
A |
9: 53,470,470 (GRCm39) |
N365K |
possibly damaging |
Het |
Nsl1 |
G |
A |
1: 190,795,380 (GRCm39) |
V49M |
probably benign |
Het |
Nudt21 |
T |
A |
8: 94,749,493 (GRCm39) |
Y191F |
probably benign |
Het |
Or2w25 |
A |
G |
11: 59,504,467 (GRCm39) |
R226G |
probably damaging |
Het |
Or8b54 |
T |
G |
9: 38,687,073 (GRCm39) |
I174S |
possibly damaging |
Het |
Pcdh18 |
T |
C |
3: 49,709,278 (GRCm39) |
Y679C |
possibly damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,356,798 (GRCm39) |
D741G |
possibly damaging |
Het |
Pkhd1 |
T |
C |
1: 20,617,717 (GRCm39) |
D956G |
probably damaging |
Het |
Poglut2 |
T |
C |
1: 44,157,733 (GRCm39) |
|
probably benign |
Het |
Pparg |
C |
T |
6: 115,440,067 (GRCm39) |
P214S |
probably damaging |
Het |
Ppargc1a |
T |
A |
5: 51,630,883 (GRCm39) |
Y582F |
unknown |
Het |
Prdm9 |
C |
T |
17: 15,765,226 (GRCm39) |
C518Y |
probably damaging |
Het |
Rangrf |
T |
A |
11: 68,864,540 (GRCm39) |
E2V |
probably damaging |
Het |
Rpl19 |
T |
C |
11: 97,919,193 (GRCm39) |
I45T |
probably benign |
Het |
Rtn4rl2 |
T |
C |
2: 84,702,807 (GRCm39) |
D255G |
possibly damaging |
Het |
Shld2 |
T |
C |
14: 33,970,847 (GRCm39) |
K627E |
probably damaging |
Het |
Sirt3 |
T |
C |
7: 140,457,963 (GRCm39) |
D62G |
|
Het |
Slc22a30 |
T |
C |
19: 8,314,133 (GRCm39) |
T518A |
probably damaging |
Het |
Slc40a1 |
T |
C |
1: 45,950,466 (GRCm39) |
T329A |
probably damaging |
Het |
Slc6a17 |
C |
T |
3: 107,381,671 (GRCm39) |
G470D |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,044,181 (GRCm39) |
I3923L |
probably benign |
Het |
Tiam2 |
C |
T |
17: 3,471,591 (GRCm39) |
S411L |
probably benign |
Het |
Ticam1 |
A |
G |
17: 56,577,182 (GRCm39) |
C638R |
unknown |
Het |
Tnrc6c |
A |
G |
11: 117,648,912 (GRCm39) |
T1528A |
probably benign |
Het |
Ufl1 |
A |
G |
4: 25,262,274 (GRCm39) |
I404T |
probably benign |
Het |
Usp43 |
A |
T |
11: 67,782,294 (GRCm39) |
S375T |
possibly damaging |
Het |
Vmn2r88 |
C |
G |
14: 51,650,503 (GRCm39) |
A72G |
probably benign |
Het |
Vmn2r91 |
A |
T |
17: 18,330,311 (GRCm39) |
I532F |
possibly damaging |
Het |
Vmn2r95 |
T |
C |
17: 18,644,367 (GRCm39) |
M1T |
probably null |
Het |
Xirp2 |
T |
C |
2: 67,345,526 (GRCm39) |
V2589A |
probably benign |
Het |
Zfp128 |
C |
T |
7: 12,624,240 (GRCm39) |
Q203* |
probably null |
Het |
|
Other mutations in Ctsll3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Ctsll3
|
APN |
13 |
60,946,756 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00903:Ctsll3
|
APN |
13 |
60,948,075 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01341:Ctsll3
|
APN |
13 |
60,946,813 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01464:Ctsll3
|
APN |
13 |
60,948,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02087:Ctsll3
|
APN |
13 |
60,947,423 (GRCm39) |
missense |
possibly damaging |
0.56 |
indolent
|
UTSW |
13 |
60,946,721 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4504001:Ctsll3
|
UTSW |
13 |
60,948,823 (GRCm39) |
missense |
probably benign |
0.32 |
R0145:Ctsll3
|
UTSW |
13 |
60,946,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Ctsll3
|
UTSW |
13 |
60,949,205 (GRCm39) |
missense |
probably benign |
0.18 |
R1463:Ctsll3
|
UTSW |
13 |
60,949,089 (GRCm39) |
splice site |
probably benign |
|
R1551:Ctsll3
|
UTSW |
13 |
60,948,821 (GRCm39) |
nonsense |
probably null |
|
R1695:Ctsll3
|
UTSW |
13 |
60,948,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Ctsll3
|
UTSW |
13 |
60,948,162 (GRCm39) |
missense |
probably benign |
0.00 |
R2168:Ctsll3
|
UTSW |
13 |
60,948,749 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4662:Ctsll3
|
UTSW |
13 |
60,947,416 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4783:Ctsll3
|
UTSW |
13 |
60,948,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5327:Ctsll3
|
UTSW |
13 |
60,946,721 (GRCm39) |
critical splice donor site |
probably null |
|
R5547:Ctsll3
|
UTSW |
13 |
60,948,551 (GRCm39) |
missense |
probably benign |
0.01 |
R5743:Ctsll3
|
UTSW |
13 |
60,948,815 (GRCm39) |
missense |
probably benign |
0.01 |
R5937:Ctsll3
|
UTSW |
13 |
60,947,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6414:Ctsll3
|
UTSW |
13 |
60,948,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Ctsll3
|
UTSW |
13 |
60,948,532 (GRCm39) |
missense |
probably benign |
0.05 |
R8421:Ctsll3
|
UTSW |
13 |
60,948,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R9285:Ctsll3
|
UTSW |
13 |
60,946,402 (GRCm39) |
missense |
probably benign |
0.31 |
X0065:Ctsll3
|
UTSW |
13 |
60,949,098 (GRCm39) |
splice site |
probably null |
|
|