Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
A |
T |
4: 144,182,464 (GRCm39) |
S335T |
probably damaging |
Het |
Abcb1b |
G |
A |
5: 8,914,238 (GRCm39) |
A1203T |
probably damaging |
Het |
Agt |
C |
A |
8: 125,283,839 (GRCm39) |
E427* |
probably null |
Het |
Angel1 |
G |
A |
12: 86,769,681 (GRCm39) |
S193F |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,794,692 (GRCm39) |
V359A |
probably benign |
Het |
Ankrd33b |
T |
C |
15: 31,367,432 (GRCm39) |
D36G |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,931,902 (GRCm39) |
C766S |
probably benign |
Het |
Asic1 |
C |
T |
15: 99,596,700 (GRCm39) |
R499C |
probably damaging |
Het |
Atpsckmt |
T |
G |
15: 31,606,103 (GRCm39) |
S20R |
probably benign |
Het |
Bank1 |
C |
T |
3: 135,919,703 (GRCm39) |
C364Y |
probably damaging |
Het |
Bmerb1 |
T |
A |
16: 13,804,676 (GRCm39) |
S8T |
possibly damaging |
Het |
Bpifa5 |
C |
A |
2: 154,008,869 (GRCm39) |
D223E |
probably benign |
Het |
Capn5 |
C |
T |
7: 97,782,089 (GRCm39) |
R217Q |
probably damaging |
Het |
Ccm2 |
G |
A |
11: 6,540,886 (GRCm39) |
S184N |
probably damaging |
Het |
Ces5a |
T |
A |
8: 94,252,286 (GRCm39) |
D202V |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,322,528 (GRCm39) |
I284T |
probably benign |
Het |
Cog7 |
C |
A |
7: 121,540,392 (GRCm39) |
|
probably null |
Het |
Col13a1 |
A |
T |
10: 61,698,525 (GRCm39) |
M512K |
unknown |
Het |
Cps1 |
A |
C |
1: 67,254,723 (GRCm39) |
D1304A |
probably benign |
Het |
Crhbp |
C |
A |
13: 95,580,403 (GRCm39) |
|
probably null |
Het |
Ctdspl2 |
T |
A |
2: 121,837,368 (GRCm39) |
C377* |
probably null |
Het |
Ctsl |
G |
A |
13: 64,513,032 (GRCm39) |
L297F |
possibly damaging |
Het |
Ddost |
A |
G |
4: 138,038,046 (GRCm39) |
T262A |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,761,313 (GRCm39) |
|
probably null |
Het |
Ddx54 |
A |
G |
5: 120,764,927 (GRCm39) |
I769V |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,745,507 (GRCm39) |
I1463N |
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,660,872 (GRCm39) |
Y404N |
possibly damaging |
Het |
Epb42 |
T |
A |
2: 120,859,631 (GRCm39) |
K186* |
probably null |
Het |
Farp2 |
A |
G |
1: 93,504,543 (GRCm39) |
|
probably null |
Het |
Fbxl9 |
A |
T |
8: 106,039,425 (GRCm39) |
L617Q |
probably damaging |
Het |
Fev |
C |
A |
1: 74,921,692 (GRCm39) |
R86L |
possibly damaging |
Het |
Foxb2 |
G |
T |
19: 16,849,820 (GRCm39) |
C395* |
probably null |
Het |
Foxn3 |
A |
G |
12: 99,175,765 (GRCm39) |
V261A |
probably benign |
Het |
Fsd1 |
A |
G |
17: 56,298,245 (GRCm39) |
D190G |
probably benign |
Het |
Gm9930 |
A |
T |
10: 9,410,547 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma2 |
A |
T |
11: 98,545,727 (GRCm39) |
K260* |
probably null |
Het |
Hdac7 |
G |
A |
15: 97,704,380 (GRCm39) |
Q497* |
probably null |
Het |
Hic1 |
G |
A |
11: 75,057,713 (GRCm39) |
P392L |
possibly damaging |
Het |
Hk3 |
C |
T |
13: 55,162,239 (GRCm39) |
|
probably null |
Het |
Ifna6 |
G |
T |
4: 88,745,887 (GRCm39) |
V79F |
probably benign |
Het |
Il20ra |
A |
T |
10: 19,635,388 (GRCm39) |
Q543L |
probably damaging |
Het |
Itk |
T |
A |
11: 46,251,115 (GRCm39) |
D163V |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,400,916 (GRCm39) |
L688R |
probably damaging |
Het |
Kdm5b |
T |
A |
1: 134,545,771 (GRCm39) |
S977R |
possibly damaging |
Het |
Kng1 |
G |
A |
16: 22,879,232 (GRCm39) |
A45T |
possibly damaging |
Het |
Map1a |
T |
G |
2: 121,136,234 (GRCm39) |
L2350R |
probably damaging |
Het |
Mdfic |
A |
G |
6: 15,799,755 (GRCm39) |
D212G |
probably benign |
Het |
Ms4a1 |
C |
A |
19: 11,236,043 (GRCm39) |
|
probably null |
Het |
Myo9a |
T |
A |
9: 59,801,635 (GRCm39) |
F1944L |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,915,689 (GRCm39) |
W928R |
probably damaging |
Het |
Nfatc2ip |
T |
G |
7: 125,995,751 (GRCm39) |
D46A |
possibly damaging |
Het |
Ngly1 |
C |
T |
14: 16,290,774 (GRCm38) |
Q419* |
probably null |
Het |
Nsd2 |
T |
A |
5: 34,000,682 (GRCm39) |
N66K |
probably damaging |
Het |
Nsmce4a |
T |
C |
7: 130,138,732 (GRCm39) |
H304R |
probably damaging |
Het |
Odad2 |
G |
A |
18: 7,222,676 (GRCm39) |
P531L |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,965 (GRCm39) |
L310Q |
possibly damaging |
Het |
Or2y11 |
C |
T |
11: 49,443,291 (GRCm39) |
T239M |
probably damaging |
Het |
Or4a2 |
T |
C |
2: 89,248,544 (GRCm39) |
Y71C |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,319,696 (GRCm39) |
I181F |
possibly damaging |
Het |
Or7e168 |
G |
A |
9: 19,720,156 (GRCm39) |
V181I |
probably benign |
Het |
Or8c20 |
A |
C |
9: 38,260,499 (GRCm39) |
N40T |
probably damaging |
Het |
Or8h9 |
C |
T |
2: 86,789,190 (GRCm39) |
G204D |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,714,427 (GRCm39) |
E265G |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,814,193 (GRCm39) |
S4188G |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,559 (GRCm39) |
N37K |
probably damaging |
Het |
R3hdm1 |
G |
A |
1: 128,121,440 (GRCm39) |
V315I |
probably benign |
Het |
Rab24 |
A |
T |
13: 55,468,738 (GRCm39) |
|
probably null |
Het |
Rap1gap2 |
A |
T |
11: 74,332,592 (GRCm39) |
M71K |
probably damaging |
Het |
Rergl |
T |
G |
6: 139,473,524 (GRCm39) |
K42T |
probably damaging |
Het |
Septin5 |
T |
C |
16: 18,443,647 (GRCm39) |
T92A |
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,246,140 (GRCm39) |
V595A |
probably benign |
Het |
Slc17a8 |
A |
G |
10: 89,412,192 (GRCm39) |
S414P |
probably benign |
Het |
Thnsl2 |
A |
T |
6: 71,111,243 (GRCm39) |
D208E |
probably damaging |
Het |
Tie1 |
A |
C |
4: 118,333,343 (GRCm39) |
I841R |
probably damaging |
Het |
Tll1 |
T |
G |
8: 64,551,505 (GRCm39) |
D292A |
probably damaging |
Het |
Tnfaip8l1 |
A |
T |
17: 56,478,727 (GRCm39) |
T6S |
probably damaging |
Het |
Trim17 |
T |
A |
11: 58,859,320 (GRCm39) |
V178E |
probably damaging |
Het |
Ttc27 |
A |
T |
17: 75,163,544 (GRCm39) |
R717S |
possibly damaging |
Het |
Upk2 |
G |
T |
9: 44,365,418 (GRCm39) |
P50Q |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,307,880 (GRCm39) |
C2319S |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,742,178 (GRCm39) |
D184V |
probably damaging |
Het |
Vmn2r9 |
C |
A |
5: 108,996,154 (GRCm39) |
G165* |
probably null |
Het |
Xkr6 |
A |
T |
14: 64,056,871 (GRCm39) |
I261F |
probably benign |
Het |
Xpnpep3 |
T |
G |
15: 81,311,693 (GRCm39) |
I133S |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,193,387 (GRCm39) |
Y91C |
probably benign |
Het |
Zfp442 |
T |
C |
2: 150,253,169 (GRCm39) |
D31G |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,939 (GRCm39) |
Q387L |
probably damaging |
Het |
Zfp804a |
C |
T |
2: 82,089,761 (GRCm39) |
Q1197* |
probably null |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Acsbg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Acsbg3
|
APN |
17 |
57,189,203 (GRCm39) |
nonsense |
probably null |
|
IGL01833:Acsbg3
|
APN |
17 |
57,188,062 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02420:Acsbg3
|
APN |
17 |
57,187,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Acsbg3
|
APN |
17 |
57,190,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03054:Acsbg3
|
UTSW |
17 |
57,193,528 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0197:Acsbg3
|
UTSW |
17 |
57,190,835 (GRCm39) |
missense |
probably benign |
0.01 |
R0257:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0279:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0280:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0281:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0282:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0329:Acsbg3
|
UTSW |
17 |
57,190,631 (GRCm39) |
missense |
probably benign |
0.02 |
R0330:Acsbg3
|
UTSW |
17 |
57,190,631 (GRCm39) |
missense |
probably benign |
0.02 |
R0349:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0518:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0519:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0604:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0883:Acsbg3
|
UTSW |
17 |
57,190,835 (GRCm39) |
missense |
probably benign |
0.01 |
R1561:Acsbg3
|
UTSW |
17 |
57,184,431 (GRCm39) |
missense |
probably benign |
|
R1779:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R2008:Acsbg3
|
UTSW |
17 |
57,193,478 (GRCm39) |
missense |
probably benign |
0.04 |
R2102:Acsbg3
|
UTSW |
17 |
57,191,949 (GRCm39) |
nonsense |
probably null |
|
R2247:Acsbg3
|
UTSW |
17 |
57,184,435 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2484:Acsbg3
|
UTSW |
17 |
57,189,641 (GRCm39) |
missense |
probably benign |
0.00 |
R2917:Acsbg3
|
UTSW |
17 |
57,192,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R3149:Acsbg3
|
UTSW |
17 |
57,183,348 (GRCm39) |
missense |
probably benign |
|
R3773:Acsbg3
|
UTSW |
17 |
57,183,262 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R4829:Acsbg3
|
UTSW |
17 |
57,190,500 (GRCm39) |
splice site |
probably null |
|
R4860:Acsbg3
|
UTSW |
17 |
57,195,655 (GRCm39) |
missense |
probably benign |
0.09 |
R4860:Acsbg3
|
UTSW |
17 |
57,195,655 (GRCm39) |
missense |
probably benign |
0.09 |
R4887:Acsbg3
|
UTSW |
17 |
57,183,324 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5043:Acsbg3
|
UTSW |
17 |
57,192,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Acsbg3
|
UTSW |
17 |
57,184,465 (GRCm39) |
missense |
probably benign |
0.03 |
R5161:Acsbg3
|
UTSW |
17 |
57,189,888 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5214:Acsbg3
|
UTSW |
17 |
57,193,493 (GRCm39) |
missense |
probably benign |
|
R5287:Acsbg3
|
UTSW |
17 |
57,183,221 (GRCm39) |
unclassified |
probably benign |
|
R5403:Acsbg3
|
UTSW |
17 |
57,183,221 (GRCm39) |
unclassified |
probably benign |
|
R5779:Acsbg3
|
UTSW |
17 |
57,188,061 (GRCm39) |
missense |
probably benign |
0.02 |
R5997:Acsbg3
|
UTSW |
17 |
57,183,373 (GRCm39) |
missense |
probably benign |
0.02 |
R6198:Acsbg3
|
UTSW |
17 |
57,189,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Acsbg3
|
UTSW |
17 |
57,184,513 (GRCm39) |
missense |
probably benign |
0.04 |
R6357:Acsbg3
|
UTSW |
17 |
57,184,591 (GRCm39) |
critical splice donor site |
probably null |
|
R6754:Acsbg3
|
UTSW |
17 |
57,190,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R6842:Acsbg3
|
UTSW |
17 |
57,184,432 (GRCm39) |
missense |
probably benign |
0.00 |
R7042:Acsbg3
|
UTSW |
17 |
57,192,098 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7181:Acsbg3
|
UTSW |
17 |
57,188,037 (GRCm39) |
missense |
probably benign |
0.03 |
R7445:Acsbg3
|
UTSW |
17 |
57,189,973 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7511:Acsbg3
|
UTSW |
17 |
57,189,954 (GRCm39) |
missense |
probably damaging |
0.98 |
R8122:Acsbg3
|
UTSW |
17 |
57,193,670 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8553:Acsbg3
|
UTSW |
17 |
57,188,021 (GRCm39) |
missense |
probably benign |
0.02 |
R8919:Acsbg3
|
UTSW |
17 |
57,189,218 (GRCm39) |
missense |
probably benign |
0.00 |
R9460:Acsbg3
|
UTSW |
17 |
57,183,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R9469:Acsbg3
|
UTSW |
17 |
57,183,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9766:Acsbg3
|
UTSW |
17 |
57,189,177 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Acsbg3
|
UTSW |
17 |
57,190,463 (GRCm39) |
frame shift |
probably null |
|
|