Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028J19Rik |
T |
A |
7: 43,880,828 (GRCm39) |
|
probably null |
Het |
Adam22 |
C |
A |
5: 8,182,418 (GRCm39) |
C514F |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,536,813 (GRCm39) |
|
probably benign |
Het |
Armcx2 |
A |
T |
X: 133,707,048 (GRCm39) |
V195E |
probably benign |
Het |
Atg7 |
T |
C |
6: 114,674,008 (GRCm39) |
S301P |
possibly damaging |
Het |
Cc2d2a |
C |
A |
5: 43,876,033 (GRCm39) |
Y1003* |
probably null |
Het |
Ccdc93 |
A |
G |
1: 121,390,843 (GRCm39) |
S272G |
probably benign |
Het |
Ces1d |
C |
G |
8: 93,901,714 (GRCm39) |
L418F |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 115,987,979 (GRCm39) |
E170G |
probably damaging |
Het |
Cplane1 |
A |
T |
15: 8,247,948 (GRCm39) |
K1499M |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Ehd4 |
T |
A |
2: 119,967,434 (GRCm39) |
D120V |
probably damaging |
Het |
Eif4g3 |
T |
A |
4: 137,824,211 (GRCm39) |
V71E |
probably damaging |
Het |
Exoc5 |
A |
G |
14: 49,256,853 (GRCm39) |
|
probably benign |
Het |
Glud1 |
T |
A |
14: 34,047,537 (GRCm39) |
|
probably benign |
Het |
Gm10985 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
3: 53,752,626 (GRCm39) |
|
probably null |
Het |
Gm11555 |
G |
T |
11: 99,540,816 (GRCm39) |
C64* |
probably null |
Het |
Gm5468 |
A |
G |
15: 25,414,561 (GRCm39) |
|
probably benign |
Het |
Gpatch2 |
T |
A |
1: 187,054,491 (GRCm39) |
L74Q |
probably damaging |
Het |
Hnrnpa0 |
G |
A |
13: 58,275,713 (GRCm39) |
R139C |
probably damaging |
Het |
Hrh1 |
A |
G |
6: 114,457,880 (GRCm39) |
Y387C |
probably damaging |
Het |
Ldb3 |
A |
T |
14: 34,289,440 (GRCm39) |
D216E |
probably damaging |
Het |
Lingo1 |
A |
T |
9: 56,527,009 (GRCm39) |
S533T |
probably benign |
Het |
Lmtk2 |
T |
G |
5: 144,103,245 (GRCm39) |
|
probably benign |
Het |
Map1s |
A |
G |
8: 71,369,745 (GRCm39) |
E939G |
possibly damaging |
Het |
Mast1 |
G |
A |
8: 85,645,360 (GRCm39) |
T695I |
probably damaging |
Het |
Mettl21e |
G |
A |
1: 44,245,524 (GRCm39) |
R241W |
probably benign |
Het |
Mfsd4a |
G |
A |
1: 131,974,091 (GRCm39) |
T261I |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,968,095 (GRCm39) |
S144P |
probably benign |
Het |
Myo16 |
A |
T |
8: 10,492,239 (GRCm39) |
H727L |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,257,477 (GRCm39) |
|
probably null |
Het |
Nipa2 |
T |
C |
7: 55,582,690 (GRCm39) |
R352G |
probably damaging |
Het |
Oaf |
C |
T |
9: 43,134,055 (GRCm39) |
R222Q |
probably benign |
Het |
Or2ag2b |
T |
A |
7: 106,418,047 (GRCm39) |
Y252* |
probably null |
Het |
Pard3 |
T |
C |
8: 128,136,167 (GRCm39) |
S847P |
probably damaging |
Het |
Pgbd1 |
C |
T |
13: 21,618,540 (GRCm39) |
R39H |
possibly damaging |
Het |
Plcb1 |
A |
C |
2: 135,167,591 (GRCm39) |
I462L |
probably damaging |
Het |
Prex2 |
T |
C |
1: 11,230,416 (GRCm39) |
V814A |
possibly damaging |
Het |
Rasal3 |
G |
A |
17: 32,612,522 (GRCm39) |
R780W |
possibly damaging |
Het |
Rubcnl |
C |
T |
14: 75,278,356 (GRCm39) |
P380L |
probably benign |
Het |
Ryk |
A |
G |
9: 102,768,427 (GRCm39) |
E359G |
probably damaging |
Het |
Sall2 |
C |
A |
14: 52,551,451 (GRCm39) |
L579F |
probably damaging |
Het |
Satb2 |
A |
G |
1: 56,930,379 (GRCm39) |
S215P |
probably damaging |
Het |
Slc35f5 |
A |
G |
1: 125,490,098 (GRCm39) |
T65A |
probably benign |
Het |
Snx33 |
T |
C |
9: 56,834,024 (GRCm39) |
N15S |
probably benign |
Het |
Stat2 |
T |
A |
10: 128,113,762 (GRCm39) |
S180R |
probably benign |
Het |
Stxbp2 |
A |
G |
8: 3,684,079 (GRCm39) |
T129A |
probably damaging |
Het |
Tas1r3 |
A |
T |
4: 155,945,810 (GRCm39) |
C529S |
probably damaging |
Het |
Tlr12 |
T |
A |
4: 128,510,361 (GRCm39) |
M630L |
probably benign |
Het |
Tnfrsf10b |
T |
G |
14: 70,010,905 (GRCm39) |
D103E |
probably benign |
Het |
Togaram1 |
A |
C |
12: 65,049,419 (GRCm39) |
E1285D |
probably benign |
Het |
Tppp |
A |
G |
13: 74,178,891 (GRCm39) |
T111A |
probably benign |
Het |
Trim12c |
T |
C |
7: 103,997,544 (GRCm39) |
Q4R |
probably benign |
Het |
Ttbk2 |
T |
G |
2: 120,570,500 (GRCm39) |
S1149R |
probably damaging |
Het |
Uncx |
T |
C |
5: 139,533,120 (GRCm39) |
L395P |
probably damaging |
Het |
Usp14 |
A |
G |
18: 10,002,370 (GRCm39) |
S314P |
possibly damaging |
Het |
Usp32 |
A |
T |
11: 84,897,881 (GRCm39) |
Y1153* |
probably null |
Het |
Vmn2r6 |
T |
C |
3: 64,464,042 (GRCm39) |
E264G |
probably damaging |
Het |
Vmn2r77 |
T |
C |
7: 86,461,050 (GRCm39) |
F792S |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,792,008 (GRCm39) |
I425V |
probably benign |
Het |
Vstm4 |
C |
T |
14: 32,585,712 (GRCm39) |
A93V |
probably benign |
Het |
Xrcc6 |
T |
A |
15: 81,909,885 (GRCm39) |
S97T |
probably benign |
Het |
Zscan20 |
A |
G |
4: 128,480,218 (GRCm39) |
C758R |
probably damaging |
Het |
|
Other mutations in Scg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Scg3
|
APN |
9 |
75,570,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02221:Scg3
|
APN |
9 |
75,590,939 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03391:Scg3
|
APN |
9 |
75,568,533 (GRCm39) |
critical splice donor site |
probably null |
|
R0137:Scg3
|
UTSW |
9 |
75,570,462 (GRCm39) |
unclassified |
probably benign |
|
R0366:Scg3
|
UTSW |
9 |
75,582,620 (GRCm39) |
splice site |
probably benign |
|
R0650:Scg3
|
UTSW |
9 |
75,576,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R0654:Scg3
|
UTSW |
9 |
75,573,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Scg3
|
UTSW |
9 |
75,551,222 (GRCm39) |
nonsense |
probably null |
|
R0827:Scg3
|
UTSW |
9 |
75,590,979 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1317:Scg3
|
UTSW |
9 |
75,576,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1553:Scg3
|
UTSW |
9 |
75,576,586 (GRCm39) |
missense |
probably null |
1.00 |
R1751:Scg3
|
UTSW |
9 |
75,576,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Scg3
|
UTSW |
9 |
75,584,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R1850:Scg3
|
UTSW |
9 |
75,589,449 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2059:Scg3
|
UTSW |
9 |
75,572,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Scg3
|
UTSW |
9 |
75,584,092 (GRCm39) |
missense |
probably damaging |
0.96 |
R2384:Scg3
|
UTSW |
9 |
75,573,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4260:Scg3
|
UTSW |
9 |
75,558,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5371:Scg3
|
UTSW |
9 |
75,568,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5417:Scg3
|
UTSW |
9 |
75,576,538 (GRCm39) |
missense |
probably benign |
0.02 |
R6013:Scg3
|
UTSW |
9 |
75,584,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7052:Scg3
|
UTSW |
9 |
75,568,664 (GRCm39) |
nonsense |
probably null |
|
R7202:Scg3
|
UTSW |
9 |
75,590,992 (GRCm39) |
missense |
probably benign |
0.06 |
R7211:Scg3
|
UTSW |
9 |
75,589,366 (GRCm39) |
missense |
probably benign |
0.00 |
R7471:Scg3
|
UTSW |
9 |
75,589,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7490:Scg3
|
UTSW |
9 |
75,576,559 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7651:Scg3
|
UTSW |
9 |
75,589,332 (GRCm39) |
missense |
probably benign |
0.03 |
R7904:Scg3
|
UTSW |
9 |
75,551,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9045:Scg3
|
UTSW |
9 |
75,570,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Scg3
|
UTSW |
9 |
75,558,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R9785:Scg3
|
UTSW |
9 |
75,589,322 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scg3
|
UTSW |
9 |
75,576,598 (GRCm39) |
missense |
possibly damaging |
0.67 |
|