Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acads |
T |
C |
5: 115,251,226 (GRCm39) |
E86G |
probably benign |
Het |
Agmo |
A |
G |
12: 37,448,728 (GRCm39) |
T217A |
probably damaging |
Het |
Arhgap39 |
A |
G |
15: 76,621,702 (GRCm39) |
S300P |
probably benign |
Het |
Casp12 |
T |
C |
9: 5,346,647 (GRCm39) |
L58P |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,389,902 (GRCm39) |
T24A |
probably benign |
Het |
Ccndbp1 |
C |
A |
2: 120,845,046 (GRCm39) |
T321K |
unknown |
Het |
Cd200r3 |
G |
A |
16: 44,774,503 (GRCm39) |
C172Y |
probably damaging |
Het |
Cracdl |
C |
A |
1: 37,663,010 (GRCm39) |
E963* |
probably null |
Het |
Cramp1 |
T |
A |
17: 25,201,674 (GRCm39) |
S603C |
probably damaging |
Het |
Crtac1 |
C |
T |
19: 42,286,239 (GRCm39) |
R448H |
probably damaging |
Het |
Csmd2 |
A |
T |
4: 128,287,331 (GRCm39) |
Y1022F |
|
Het |
Ctns |
T |
C |
11: 73,075,760 (GRCm39) |
Y363C |
probably damaging |
Het |
D630044L22Rik |
A |
G |
17: 26,179,118 (GRCm39) |
T15A |
possibly damaging |
Het |
Dhx38 |
A |
C |
8: 110,285,333 (GRCm39) |
I444M |
probably benign |
Het |
Dnah14 |
A |
T |
1: 181,443,459 (GRCm39) |
I450F |
possibly damaging |
Het |
Dpf1 |
T |
C |
7: 29,013,566 (GRCm39) |
F245L |
probably benign |
Het |
Efr3b |
A |
G |
12: 4,032,898 (GRCm39) |
V269A |
probably benign |
Het |
Eprs1 |
G |
T |
1: 185,126,653 (GRCm39) |
V530L |
possibly damaging |
Het |
Eps8l2 |
A |
G |
7: 140,922,860 (GRCm39) |
N41S |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,435,470 (GRCm39) |
I142M |
probably damaging |
Het |
Fhip1a |
T |
C |
3: 85,637,868 (GRCm39) |
M144V |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,457,445 (GRCm39) |
D2381V |
probably damaging |
Het |
Fndc1 |
T |
A |
17: 7,991,362 (GRCm39) |
D778V |
unknown |
Het |
Galnt3 |
A |
G |
2: 65,921,555 (GRCm39) |
I492T |
probably benign |
Het |
Gigyf2 |
T |
C |
1: 87,374,155 (GRCm39) |
M1261T |
probably damaging |
Het |
Haus8 |
A |
G |
8: 71,708,695 (GRCm39) |
F126S |
probably benign |
Het |
Hif3a |
A |
G |
7: 16,782,686 (GRCm39) |
L293S |
probably damaging |
Het |
Ino80c |
G |
A |
18: 24,239,707 (GRCm39) |
T200I |
unknown |
Het |
Jag1 |
T |
A |
2: 136,943,717 (GRCm39) |
M160L |
probably benign |
Het |
Kcnj12 |
C |
A |
11: 60,960,825 (GRCm39) |
H374Q |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,816,902 (GRCm39) |
I433M |
probably benign |
Het |
Lyzl4 |
C |
T |
9: 121,407,160 (GRCm39) |
W123* |
probably null |
Het |
Map2k4 |
A |
T |
11: 65,597,827 (GRCm39) |
C264S |
|
Het |
Mmrn1 |
C |
T |
6: 60,921,508 (GRCm39) |
|
probably benign |
Het |
Mug1 |
C |
T |
6: 121,850,631 (GRCm39) |
T709I |
probably benign |
Het |
Myo9a |
T |
A |
9: 59,781,931 (GRCm39) |
W1706R |
probably benign |
Het |
Nlrp5 |
A |
G |
7: 23,117,869 (GRCm39) |
E531G |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Pcdhb11 |
A |
C |
18: 37,555,422 (GRCm39) |
I251L |
probably benign |
Het |
Per3 |
A |
G |
4: 151,113,270 (GRCm39) |
S353P |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,213,750 (GRCm39) |
E1738G |
probably null |
Het |
Prr14l |
T |
C |
5: 32,988,508 (GRCm39) |
D329G |
probably benign |
Het |
Ptpn23 |
G |
T |
9: 110,217,267 (GRCm39) |
P863Q |
probably damaging |
Het |
Ptpn23 |
G |
T |
9: 110,217,268 (GRCm39) |
P863T |
possibly damaging |
Het |
Ptprq |
T |
C |
10: 107,479,896 (GRCm39) |
K1125E |
possibly damaging |
Het |
Rapgef2 |
T |
G |
3: 79,000,343 (GRCm39) |
T351P |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,840,617 (GRCm39) |
Y923C |
probably damaging |
Het |
Rimbp3 |
T |
C |
16: 17,028,727 (GRCm39) |
V717A |
probably benign |
Het |
Rims1 |
C |
T |
1: 22,358,760 (GRCm39) |
W182* |
probably null |
Het |
Rnmt |
A |
G |
18: 68,440,723 (GRCm39) |
K129E |
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,450,108 (GRCm39) |
F93S |
probably damaging |
Het |
Scamp5 |
T |
C |
9: 57,350,969 (GRCm39) |
Y231C |
probably damaging |
Het |
Sfxn5 |
T |
A |
6: 85,244,921 (GRCm39) |
|
probably null |
Het |
Skic2 |
A |
T |
17: 35,068,975 (GRCm39) |
V8D |
probably benign |
Het |
Slc12a1 |
T |
C |
2: 125,028,234 (GRCm39) |
F510S |
probably damaging |
Het |
Sowahb |
T |
C |
5: 93,190,922 (GRCm39) |
Y599C |
probably damaging |
Het |
Speer4e1 |
T |
C |
5: 14,987,111 (GRCm39) |
N98S |
probably damaging |
Het |
Stat3 |
T |
C |
11: 100,784,807 (GRCm39) |
N553S |
probably benign |
Het |
Sult6b2 |
A |
T |
6: 142,735,868 (GRCm39) |
L242Q |
probably damaging |
Het |
Tacc3 |
C |
T |
5: 33,821,169 (GRCm39) |
R98W |
possibly damaging |
Het |
Tuba4a |
C |
T |
1: 75,193,595 (GRCm39) |
R112H |
|
Het |
Ubr3 |
T |
A |
2: 69,819,220 (GRCm39) |
S1337T |
probably damaging |
Het |
Vmn2r69 |
A |
T |
7: 85,055,713 (GRCm39) |
C808* |
probably null |
Het |
Wnt16 |
G |
A |
6: 22,288,997 (GRCm39) |
A105T |
probably benign |
Het |
Zfp692 |
C |
T |
11: 58,198,560 (GRCm39) |
S50L |
probably damaging |
Het |
|
Other mutations in Chd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Chd2
|
APN |
7 |
73,118,325 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00535:Chd2
|
APN |
7 |
73,190,576 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00961:Chd2
|
APN |
7 |
73,093,997 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01092:Chd2
|
APN |
7 |
73,091,434 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02035:Chd2
|
APN |
7 |
73,091,375 (GRCm39) |
splice site |
probably null |
|
IGL02083:Chd2
|
APN |
7 |
73,130,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02205:Chd2
|
APN |
7 |
73,091,465 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02243:Chd2
|
APN |
7 |
73,147,456 (GRCm39) |
splice site |
probably null |
|
IGL02385:Chd2
|
APN |
7 |
73,085,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02552:Chd2
|
APN |
7 |
73,097,068 (GRCm39) |
unclassified |
probably benign |
|
IGL02590:Chd2
|
APN |
7 |
73,102,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02684:Chd2
|
APN |
7 |
73,125,097 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02731:Chd2
|
APN |
7 |
73,143,204 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Chd2
|
APN |
7 |
73,102,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
1mM(1):Chd2
|
UTSW |
7 |
73,151,852 (GRCm39) |
missense |
possibly damaging |
0.65 |
A4554:Chd2
|
UTSW |
7 |
73,130,716 (GRCm39) |
missense |
probably benign |
|
F6893:Chd2
|
UTSW |
7 |
73,157,620 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0012:Chd2
|
UTSW |
7 |
73,105,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Chd2
|
UTSW |
7 |
73,105,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Chd2
|
UTSW |
7 |
73,134,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Chd2
|
UTSW |
7 |
73,097,022 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0973:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Chd2
|
UTSW |
7 |
73,134,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Chd2
|
UTSW |
7 |
73,102,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R1527:Chd2
|
UTSW |
7 |
73,140,362 (GRCm39) |
nonsense |
probably null |
|
R1599:Chd2
|
UTSW |
7 |
73,122,799 (GRCm39) |
missense |
probably benign |
0.05 |
R1657:Chd2
|
UTSW |
7 |
73,130,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Chd2
|
UTSW |
7 |
73,104,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R2110:Chd2
|
UTSW |
7 |
73,079,735 (GRCm39) |
missense |
probably benign |
0.00 |
R2202:Chd2
|
UTSW |
7 |
73,128,416 (GRCm39) |
missense |
probably benign |
0.00 |
R2383:Chd2
|
UTSW |
7 |
73,153,168 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2393:Chd2
|
UTSW |
7 |
73,157,631 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3699:Chd2
|
UTSW |
7 |
73,118,238 (GRCm39) |
missense |
probably benign |
0.35 |
R3713:Chd2
|
UTSW |
7 |
73,121,538 (GRCm39) |
unclassified |
probably benign |
|
R3788:Chd2
|
UTSW |
7 |
73,096,878 (GRCm39) |
unclassified |
probably benign |
|
R3826:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3828:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3830:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3966:Chd2
|
UTSW |
7 |
73,114,143 (GRCm39) |
splice site |
probably benign |
|
R4093:Chd2
|
UTSW |
7 |
73,150,764 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4431:Chd2
|
UTSW |
7 |
73,085,709 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4461:Chd2
|
UTSW |
7 |
73,190,622 (GRCm39) |
intron |
probably benign |
|
R4782:Chd2
|
UTSW |
7 |
73,134,184 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4791:Chd2
|
UTSW |
7 |
73,118,325 (GRCm39) |
missense |
probably benign |
0.13 |
R4792:Chd2
|
UTSW |
7 |
73,118,325 (GRCm39) |
missense |
probably benign |
0.13 |
R4799:Chd2
|
UTSW |
7 |
73,134,184 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4832:Chd2
|
UTSW |
7 |
73,151,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Chd2
|
UTSW |
7 |
73,130,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Chd2
|
UTSW |
7 |
73,079,437 (GRCm39) |
missense |
probably benign |
0.03 |
R5328:Chd2
|
UTSW |
7 |
73,113,429 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5444:Chd2
|
UTSW |
7 |
73,122,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Chd2
|
UTSW |
7 |
73,134,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Chd2
|
UTSW |
7 |
73,091,465 (GRCm39) |
missense |
probably benign |
0.01 |
R5670:Chd2
|
UTSW |
7 |
73,091,465 (GRCm39) |
missense |
probably benign |
0.01 |
R5706:Chd2
|
UTSW |
7 |
73,141,105 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5825:Chd2
|
UTSW |
7 |
73,134,350 (GRCm39) |
splice site |
probably null |
|
R5834:Chd2
|
UTSW |
7 |
73,128,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Chd2
|
UTSW |
7 |
73,187,060 (GRCm39) |
missense |
probably damaging |
0.97 |
R6051:Chd2
|
UTSW |
7 |
73,085,590 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Chd2
|
UTSW |
7 |
73,094,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R6229:Chd2
|
UTSW |
7 |
73,101,471 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6267:Chd2
|
UTSW |
7 |
73,113,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R6310:Chd2
|
UTSW |
7 |
73,102,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:Chd2
|
UTSW |
7 |
73,130,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Chd2
|
UTSW |
7 |
73,150,785 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6529:Chd2
|
UTSW |
7 |
73,153,191 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6611:Chd2
|
UTSW |
7 |
73,143,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R6661:Chd2
|
UTSW |
7 |
73,140,230 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6782:Chd2
|
UTSW |
7 |
73,125,127 (GRCm39) |
nonsense |
probably null |
|
R6860:Chd2
|
UTSW |
7 |
73,147,558 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6955:Chd2
|
UTSW |
7 |
73,125,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Chd2
|
UTSW |
7 |
73,134,159 (GRCm39) |
nonsense |
probably null |
|
R7095:Chd2
|
UTSW |
7 |
73,121,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Chd2
|
UTSW |
7 |
73,119,418 (GRCm39) |
missense |
probably benign |
0.00 |
R7179:Chd2
|
UTSW |
7 |
73,125,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R7500:Chd2
|
UTSW |
7 |
73,101,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7615:Chd2
|
UTSW |
7 |
73,091,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R7646:Chd2
|
UTSW |
7 |
73,085,521 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7764:Chd2
|
UTSW |
7 |
73,121,567 (GRCm39) |
missense |
probably null |
1.00 |
R7898:Chd2
|
UTSW |
7 |
73,169,223 (GRCm39) |
critical splice donor site |
probably null |
|
R7935:Chd2
|
UTSW |
7 |
73,149,373 (GRCm39) |
missense |
probably benign |
0.01 |
R8033:Chd2
|
UTSW |
7 |
73,085,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Chd2
|
UTSW |
7 |
73,101,506 (GRCm39) |
missense |
probably benign |
|
R8188:Chd2
|
UTSW |
7 |
73,079,504 (GRCm39) |
nonsense |
probably null |
|
R8196:Chd2
|
UTSW |
7 |
73,118,285 (GRCm39) |
missense |
probably benign |
0.00 |
R8258:Chd2
|
UTSW |
7 |
73,085,532 (GRCm39) |
missense |
probably benign |
0.11 |
R8259:Chd2
|
UTSW |
7 |
73,085,532 (GRCm39) |
missense |
probably benign |
0.11 |
R8357:Chd2
|
UTSW |
7 |
73,096,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8457:Chd2
|
UTSW |
7 |
73,096,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8778:Chd2
|
UTSW |
7 |
73,079,483 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8816:Chd2
|
UTSW |
7 |
73,140,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Chd2
|
UTSW |
7 |
73,151,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Chd2
|
UTSW |
7 |
73,153,210 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9005:Chd2
|
UTSW |
7 |
73,134,294 (GRCm39) |
missense |
probably damaging |
0.98 |
R9009:Chd2
|
UTSW |
7 |
73,143,192 (GRCm39) |
missense |
probably benign |
0.39 |
R9009:Chd2
|
UTSW |
7 |
73,140,402 (GRCm39) |
missense |
probably benign |
0.12 |
R9021:Chd2
|
UTSW |
7 |
73,091,393 (GRCm39) |
missense |
probably benign |
0.03 |
R9038:Chd2
|
UTSW |
7 |
73,105,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Chd2
|
UTSW |
7 |
73,143,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9383:Chd2
|
UTSW |
7 |
73,098,918 (GRCm39) |
missense |
probably null |
1.00 |
R9501:Chd2
|
UTSW |
7 |
73,130,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Chd2
|
UTSW |
7 |
73,091,481 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9550:Chd2
|
UTSW |
7 |
73,119,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R9583:Chd2
|
UTSW |
7 |
73,130,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R9665:Chd2
|
UTSW |
7 |
73,079,555 (GRCm39) |
missense |
probably benign |
0.00 |
RF009:Chd2
|
UTSW |
7 |
73,169,410 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0025:Chd2
|
UTSW |
7 |
73,157,585 (GRCm39) |
missense |
probably benign |
0.11 |
Z1177:Chd2
|
UTSW |
7 |
73,118,334 (GRCm39) |
missense |
possibly damaging |
0.48 |
|