Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16b |
A |
G |
2: 181,136,127 (GRCm39) |
D343G |
probably benign |
Het |
Acot10 |
T |
C |
15: 20,666,229 (GRCm39) |
S171G |
possibly damaging |
Het |
Adamts17 |
T |
C |
7: 66,677,562 (GRCm39) |
M492T |
probably damaging |
Het |
Akap4 |
A |
C |
X: 6,943,707 (GRCm39) |
N670T |
probably benign |
Het |
Atrip |
A |
G |
9: 108,894,299 (GRCm39) |
S55P |
possibly damaging |
Het |
Bend3 |
A |
T |
10: 43,385,946 (GRCm39) |
E113V |
probably damaging |
Het |
Ccdc158 |
A |
C |
5: 92,797,907 (GRCm39) |
I411S |
probably damaging |
Het |
Cfap97 |
G |
T |
8: 46,623,315 (GRCm39) |
C235F |
possibly damaging |
Het |
Chil4 |
T |
C |
3: 106,121,715 (GRCm39) |
N45D |
probably benign |
Het |
Cripto |
C |
T |
9: 110,771,691 (GRCm39) |
C32Y |
probably damaging |
Het |
D430041D05Rik |
A |
G |
2: 104,079,690 (GRCm39) |
V1131A |
probably damaging |
Het |
Defb38 |
T |
C |
8: 19,076,552 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,866,860 (GRCm39) |
W2260R |
probably damaging |
Het |
Ecsit |
A |
G |
9: 21,989,500 (GRCm39) |
S14P |
probably damaging |
Het |
Eif3l |
T |
C |
15: 78,962,296 (GRCm39) |
F106L |
probably benign |
Het |
Erich5 |
G |
T |
15: 34,470,999 (GRCm39) |
G76V |
probably damaging |
Het |
Evpl |
A |
G |
11: 116,120,939 (GRCm39) |
L432P |
possibly damaging |
Het |
Fbxw10 |
T |
C |
11: 62,765,808 (GRCm39) |
F698L |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,428,470 (GRCm39) |
S2866T |
probably damaging |
Het |
Fuca1 |
G |
A |
4: 135,662,073 (GRCm39) |
V334I |
probably benign |
Het |
Hprt1 |
T |
A |
X: 52,091,010 (GRCm39) |
H60Q |
probably benign |
Het |
Kirrel2 |
T |
C |
7: 30,152,165 (GRCm39) |
N481S |
probably damaging |
Het |
Krt16 |
A |
T |
11: 100,137,162 (GRCm39) |
|
probably benign |
Het |
Lilrb4b |
T |
A |
10: 51,357,334 (GRCm39) |
Y57N |
probably benign |
Het |
Lix1l |
A |
G |
3: 96,521,792 (GRCm39) |
Y126C |
probably damaging |
Het |
Lox |
T |
C |
18: 52,654,388 (GRCm39) |
D347G |
probably damaging |
Het |
Mak16 |
C |
T |
8: 31,654,753 (GRCm39) |
R147Q |
possibly damaging |
Het |
Ndst2 |
G |
A |
14: 20,779,622 (GRCm39) |
A206V |
possibly damaging |
Het |
Or1ak2 |
A |
T |
2: 36,827,760 (GRCm39) |
I210F |
probably damaging |
Het |
Or2q1 |
T |
A |
6: 42,795,176 (GRCm39) |
I257N |
probably damaging |
Het |
Phldb1 |
T |
C |
9: 44,627,771 (GRCm39) |
M225V |
probably benign |
Het |
Pofut1 |
C |
T |
2: 153,090,516 (GRCm39) |
Q137* |
probably null |
Het |
Polr2a |
T |
C |
11: 69,634,076 (GRCm39) |
|
probably benign |
Het |
Prdm5 |
T |
A |
6: 65,858,100 (GRCm39) |
L388Q |
probably damaging |
Het |
Rad51c |
A |
G |
11: 87,271,681 (GRCm39) |
S344P |
possibly damaging |
Het |
Scart1 |
G |
A |
7: 139,800,308 (GRCm39) |
G30S |
probably benign |
Het |
Sdk1 |
C |
T |
5: 141,938,771 (GRCm39) |
P398L |
probably damaging |
Het |
Sec63 |
G |
A |
10: 42,677,729 (GRCm39) |
|
probably benign |
Het |
Sgo1 |
A |
T |
17: 53,983,989 (GRCm39) |
L463Q |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,198,002 (GRCm39) |
L291P |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,757,205 (GRCm39) |
T9A |
probably benign |
Het |
Sp3 |
A |
G |
2: 72,801,813 (GRCm39) |
W67R |
probably damaging |
Het |
Ssxb9 |
A |
C |
X: 21,041,234 (GRCm39) |
S23A |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,292,167 (GRCm39) |
L1367S |
probably damaging |
Het |
Tbc1d23 |
T |
A |
16: 56,990,754 (GRCm39) |
I690F |
probably damaging |
Het |
Tmed5 |
A |
T |
5: 108,272,416 (GRCm39) |
S227R |
probably benign |
Het |
Tnrc6c |
T |
A |
11: 117,613,803 (GRCm39) |
S814T |
probably benign |
Het |
Trbv2 |
C |
T |
6: 41,024,905 (GRCm39) |
T107I |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,803,155 (GRCm39) |
V866A |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,804,762 (GRCm39) |
K905* |
probably null |
Het |
Ttn |
A |
G |
2: 76,539,654 (GRCm39) |
V34444A |
probably benign |
Het |
Vmn1r86 |
C |
T |
7: 12,836,707 (GRCm39) |
M56I |
probably benign |
Het |
Vmn2r17 |
A |
C |
5: 109,601,012 (GRCm39) |
D770A |
probably damaging |
Het |
Wnk4 |
T |
C |
11: 101,160,389 (GRCm39) |
|
probably benign |
Het |
Xaf1 |
T |
C |
11: 72,194,257 (GRCm39) |
M46T |
possibly damaging |
Het |
|
Other mutations in Actr3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02582:Actr3b
|
APN |
5 |
26,037,411 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02869:Actr3b
|
APN |
5 |
26,037,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02946:Actr3b
|
APN |
5 |
26,053,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0443:Actr3b
|
UTSW |
5 |
26,053,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Actr3b
|
UTSW |
5 |
26,036,730 (GRCm39) |
missense |
probably damaging |
0.98 |
R0727:Actr3b
|
UTSW |
5 |
26,016,937 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1070:Actr3b
|
UTSW |
5 |
26,053,491 (GRCm39) |
splice site |
probably benign |
|
R1643:Actr3b
|
UTSW |
5 |
26,017,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Actr3b
|
UTSW |
5 |
26,054,156 (GRCm39) |
critical splice donor site |
probably null |
|
R1837:Actr3b
|
UTSW |
5 |
26,030,157 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Actr3b
|
UTSW |
5 |
26,034,536 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2041:Actr3b
|
UTSW |
5 |
25,965,128 (GRCm39) |
critical splice donor site |
probably null |
|
R2096:Actr3b
|
UTSW |
5 |
26,036,743 (GRCm39) |
nonsense |
probably null |
|
R2109:Actr3b
|
UTSW |
5 |
26,036,709 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2256:Actr3b
|
UTSW |
5 |
26,027,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3078:Actr3b
|
UTSW |
5 |
26,027,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5572:Actr3b
|
UTSW |
5 |
26,014,886 (GRCm39) |
missense |
probably benign |
0.00 |
R5655:Actr3b
|
UTSW |
5 |
26,053,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Actr3b
|
UTSW |
5 |
26,036,688 (GRCm39) |
missense |
probably benign |
|
R6761:Actr3b
|
UTSW |
5 |
26,030,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R7003:Actr3b
|
UTSW |
5 |
26,003,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Actr3b
|
UTSW |
5 |
26,054,936 (GRCm39) |
missense |
probably benign |
0.40 |
R7649:Actr3b
|
UTSW |
5 |
26,053,364 (GRCm39) |
missense |
probably benign |
0.05 |
R7897:Actr3b
|
UTSW |
5 |
26,036,657 (GRCm39) |
missense |
probably benign |
0.37 |
R8691:Actr3b
|
UTSW |
5 |
26,030,202 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9647:Actr3b
|
UTSW |
5 |
26,037,408 (GRCm39) |
missense |
probably benign |
|
R9797:Actr3b
|
UTSW |
5 |
26,054,895 (GRCm39) |
missense |
probably benign |
0.00 |
RF049:Actr3b
|
UTSW |
5 |
26,053,486 (GRCm39) |
critical splice donor site |
probably benign |
|
|