Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
C |
T |
11: 58,313,630 (GRCm39) |
A86V |
possibly damaging |
Het |
9430097D07Rik |
A |
G |
2: 32,464,440 (GRCm39) |
|
probably benign |
Het |
Ang5 |
A |
G |
14: 44,200,302 (GRCm39) |
D122G |
probably benign |
Het |
Atg9a |
A |
T |
1: 75,162,704 (GRCm39) |
|
probably null |
Het |
Cracd |
G |
C |
5: 76,805,681 (GRCm39) |
|
probably benign |
Het |
Dctd |
C |
T |
8: 48,590,449 (GRCm39) |
|
probably benign |
Het |
Ddx11 |
G |
A |
17: 66,454,717 (GRCm39) |
V642M |
possibly damaging |
Het |
Dis3l2 |
G |
A |
1: 86,688,043 (GRCm39) |
V100I |
probably benign |
Het |
Echdc2 |
T |
C |
4: 108,029,328 (GRCm39) |
V111A |
probably benign |
Het |
Egr1 |
A |
G |
18: 34,996,711 (GRCm39) |
T498A |
probably benign |
Het |
Exosc3 |
T |
C |
4: 45,317,702 (GRCm39) |
K200R |
possibly damaging |
Het |
Exosc8 |
T |
C |
3: 54,636,644 (GRCm39) |
D229G |
probably benign |
Het |
Ext1 |
T |
A |
15: 52,955,808 (GRCm39) |
I430F |
probably damaging |
Het |
Fbxw22 |
T |
C |
9: 109,232,492 (GRCm39) |
N31S |
probably benign |
Het |
Gja8 |
T |
C |
3: 96,827,165 (GRCm39) |
T166A |
probably benign |
Het |
Gm21814 |
T |
A |
6: 149,485,116 (GRCm39) |
|
noncoding transcript |
Het |
Gm21915 |
T |
A |
9: 40,581,944 (GRCm39) |
H12Q |
probably benign |
Het |
Hgsnat |
G |
A |
8: 26,437,988 (GRCm39) |
R527* |
probably null |
Het |
Iqgap2 |
A |
G |
13: 95,810,251 (GRCm39) |
F731S |
probably benign |
Het |
Jchain |
T |
C |
5: 88,670,364 (GRCm39) |
H85R |
probably damaging |
Het |
Kcnb2 |
T |
C |
1: 15,383,186 (GRCm39) |
C171R |
probably benign |
Het |
Kcnk3 |
C |
A |
5: 30,780,149 (GRCm39) |
R400S |
possibly damaging |
Het |
Klhl28 |
C |
T |
12: 65,004,001 (GRCm39) |
E171K |
probably damaging |
Het |
Lrrfip2 |
T |
C |
9: 111,053,040 (GRCm39) |
I375T |
possibly damaging |
Het |
Mccc1 |
T |
C |
3: 36,033,166 (GRCm39) |
N326S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,731,615 (GRCm39) |
V97A |
possibly damaging |
Het |
Mertk |
C |
A |
2: 128,625,920 (GRCm39) |
T685K |
probably benign |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Myom2 |
G |
A |
8: 15,133,310 (GRCm39) |
V401M |
probably damaging |
Het |
Nme5 |
A |
C |
18: 34,711,738 (GRCm39) |
M1R |
probably null |
Het |
Nop2 |
T |
C |
6: 125,110,726 (GRCm39) |
S68P |
probably benign |
Het |
Notch1 |
A |
T |
2: 26,366,126 (GRCm39) |
D809E |
possibly damaging |
Het |
Or14c39 |
T |
C |
7: 86,343,793 (GRCm39) |
I43T |
possibly damaging |
Het |
Ppat |
C |
T |
5: 77,076,525 (GRCm39) |
|
probably benign |
Het |
Prss23 |
T |
A |
7: 89,159,422 (GRCm39) |
M216L |
probably benign |
Het |
Psg18 |
A |
T |
7: 18,083,279 (GRCm39) |
V171D |
probably damaging |
Het |
Psg28 |
A |
G |
7: 18,161,816 (GRCm39) |
V229A |
probably damaging |
Het |
Qser1 |
T |
C |
2: 104,618,176 (GRCm39) |
N879D |
possibly damaging |
Het |
Rpap1 |
T |
C |
2: 119,600,522 (GRCm39) |
N879S |
probably benign |
Het |
Rusc2 |
T |
C |
4: 43,415,926 (GRCm39) |
S411P |
probably damaging |
Het |
Rxfp2 |
T |
A |
5: 149,990,825 (GRCm39) |
W519R |
probably damaging |
Het |
Scpep1 |
T |
A |
11: 88,832,175 (GRCm39) |
Q185L |
probably benign |
Het |
Serpinb11 |
A |
G |
1: 107,307,379 (GRCm39) |
N270S |
probably benign |
Het |
Serpinb6d |
T |
A |
13: 33,855,427 (GRCm39) |
M367K |
probably benign |
Het |
Skint10 |
T |
G |
4: 112,584,869 (GRCm39) |
I213L |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,403,734 (GRCm39) |
T1163A |
unknown |
Het |
Slamf9 |
A |
T |
1: 172,303,780 (GRCm39) |
I42L |
possibly damaging |
Het |
Slc1a3 |
T |
C |
15: 8,680,330 (GRCm39) |
|
probably benign |
Het |
Smad6 |
T |
A |
9: 63,861,182 (GRCm39) |
Q371L |
possibly damaging |
Het |
Snx31 |
A |
T |
15: 36,555,469 (GRCm39) |
V26E |
probably damaging |
Het |
Spata31e5 |
A |
G |
1: 28,816,943 (GRCm39) |
I363T |
possibly damaging |
Het |
Taf4b |
A |
G |
18: 14,955,229 (GRCm39) |
N594S |
possibly damaging |
Het |
Tanc2 |
T |
C |
11: 105,670,918 (GRCm39) |
S172P |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,438 (GRCm39) |
Y156* |
probably null |
Het |
Tbc1d20 |
G |
A |
2: 152,135,856 (GRCm39) |
|
probably benign |
Het |
Timm50 |
A |
T |
7: 28,006,284 (GRCm39) |
D272E |
probably benign |
Het |
Ttn |
T |
G |
2: 76,730,855 (GRCm39) |
|
probably benign |
Het |
Vps13c |
T |
A |
9: 67,823,661 (GRCm39) |
F1362I |
probably benign |
Het |
Vwf |
T |
C |
6: 125,543,220 (GRCm39) |
S154P |
probably benign |
Het |
Zfp445 |
T |
C |
9: 122,681,410 (GRCm39) |
R844G |
probably benign |
Het |
|
Other mutations in Actr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01609:Actr5
|
APN |
2 |
158,478,722 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02622:Actr5
|
APN |
2 |
158,480,728 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02707:Actr5
|
APN |
2 |
158,478,617 (GRCm39) |
missense |
probably benign |
0.45 |
R0610:Actr5
|
UTSW |
2 |
158,474,376 (GRCm39) |
critical splice donor site |
probably null |
|
R1467:Actr5
|
UTSW |
2 |
158,480,617 (GRCm39) |
missense |
probably benign |
0.02 |
R1467:Actr5
|
UTSW |
2 |
158,480,617 (GRCm39) |
missense |
probably benign |
0.02 |
R1720:Actr5
|
UTSW |
2 |
158,478,057 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1869:Actr5
|
UTSW |
2 |
158,480,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R1937:Actr5
|
UTSW |
2 |
158,477,949 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2051:Actr5
|
UTSW |
2 |
158,474,213 (GRCm39) |
missense |
probably benign |
0.00 |
R2389:Actr5
|
UTSW |
2 |
158,467,132 (GRCm39) |
missense |
probably benign |
|
R2420:Actr5
|
UTSW |
2 |
158,478,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R2422:Actr5
|
UTSW |
2 |
158,478,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R2909:Actr5
|
UTSW |
2 |
158,467,140 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4089:Actr5
|
UTSW |
2 |
158,467,022 (GRCm39) |
utr 5 prime |
probably benign |
|
R4719:Actr5
|
UTSW |
2 |
158,468,433 (GRCm39) |
missense |
probably damaging |
0.97 |
R4737:Actr5
|
UTSW |
2 |
158,469,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Actr5
|
UTSW |
2 |
158,467,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Actr5
|
UTSW |
2 |
158,467,144 (GRCm39) |
nonsense |
probably null |
|
R5457:Actr5
|
UTSW |
2 |
158,477,918 (GRCm39) |
splice site |
probably null |
|
R6328:Actr5
|
UTSW |
2 |
158,477,264 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7158:Actr5
|
UTSW |
2 |
158,468,334 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8526:Actr5
|
UTSW |
2 |
158,474,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8789:Actr5
|
UTSW |
2 |
158,478,604 (GRCm39) |
nonsense |
probably null |
|
R9000:Actr5
|
UTSW |
2 |
158,478,610 (GRCm39) |
missense |
probably benign |
0.00 |
R9030:Actr5
|
UTSW |
2 |
158,474,321 (GRCm39) |
missense |
probably benign |
0.00 |
R9222:Actr5
|
UTSW |
2 |
158,473,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R9316:Actr5
|
UTSW |
2 |
158,477,274 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Actr5
|
UTSW |
2 |
158,470,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Actr5
|
UTSW |
2 |
158,470,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Actr5
|
UTSW |
2 |
158,470,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Actr5
|
UTSW |
2 |
158,468,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Actr5
|
UTSW |
2 |
158,478,625 (GRCm39) |
missense |
probably benign |
0.03 |
|