Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot13 |
A |
T |
13: 25,002,154 (GRCm39) |
I96K |
probably benign |
Het |
Adam6a |
A |
G |
12: 113,509,291 (GRCm39) |
T555A |
probably benign |
Het |
Alms1 |
C |
T |
6: 85,598,351 (GRCm39) |
P1059L |
probably benign |
Het |
Apol7c |
T |
C |
15: 77,409,843 (GRCm39) |
T368A |
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,475,015 (GRCm39) |
L1557Q |
probably damaging |
Het |
Baz2a |
C |
T |
10: 127,960,326 (GRCm39) |
R1514W |
probably damaging |
Het |
Bmp3 |
T |
A |
5: 99,020,622 (GRCm39) |
D348E |
probably damaging |
Het |
Bves |
A |
G |
10: 45,230,913 (GRCm39) |
S295G |
probably damaging |
Het |
Carmil1 |
A |
G |
13: 24,204,052 (GRCm39) |
C1328R |
probably benign |
Het |
Ccnk |
T |
A |
12: 108,153,517 (GRCm39) |
Y93N |
probably damaging |
Het |
Ccr1 |
A |
T |
9: 123,764,089 (GRCm39) |
V147D |
probably damaging |
Het |
Cd24a |
G |
A |
10: 43,458,636 (GRCm39) |
G36S |
probably benign |
Het |
Cep104 |
A |
G |
4: 154,077,324 (GRCm39) |
Y569C |
probably damaging |
Het |
Cnst |
A |
T |
1: 179,406,947 (GRCm39) |
|
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,805,262 (GRCm39) |
L146P |
unknown |
Het |
Col25a1 |
G |
T |
3: 130,323,768 (GRCm39) |
R321L |
probably damaging |
Het |
Ctnnd2 |
T |
C |
15: 30,683,510 (GRCm39) |
Y504H |
possibly damaging |
Het |
D3Ertd751e |
C |
A |
3: 41,703,143 (GRCm39) |
Q73K |
probably damaging |
Het |
Dsc2 |
C |
T |
18: 20,168,332 (GRCm39) |
|
probably null |
Het |
Eya1 |
A |
T |
1: 14,373,076 (GRCm39) |
S14R |
probably damaging |
Het |
Fam131c |
A |
T |
4: 141,110,328 (GRCm39) |
|
probably null |
Het |
Flvcr2 |
T |
C |
12: 85,793,965 (GRCm39) |
F114L |
possibly damaging |
Het |
Fyn |
A |
G |
10: 39,408,120 (GRCm39) |
D321G |
possibly damaging |
Het |
Galnt5 |
A |
C |
2: 57,888,621 (GRCm39) |
M74L |
probably benign |
Het |
Garin4 |
G |
A |
1: 190,896,218 (GRCm39) |
R142C |
probably damaging |
Het |
Gas2l2 |
G |
A |
11: 83,313,288 (GRCm39) |
P675S |
probably benign |
Het |
Gm9508 |
G |
T |
10: 77,532,470 (GRCm39) |
Q200K |
unknown |
Het |
Greb1l |
G |
A |
18: 10,544,576 (GRCm39) |
S1390N |
probably benign |
Het |
Hdac5 |
G |
T |
11: 102,095,385 (GRCm39) |
T430K |
possibly damaging |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Khnyn |
C |
T |
14: 56,131,811 (GRCm39) |
P578S |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,602,856 (GRCm39) |
T215S |
probably benign |
Het |
Lrfn5 |
G |
A |
12: 61,890,768 (GRCm39) |
V686I |
probably benign |
Het |
Mapkap1 |
T |
A |
2: 34,408,712 (GRCm39) |
H233Q |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,885,081 (GRCm39) |
I201T |
probably damaging |
Het |
Metrnl |
G |
A |
11: 121,606,734 (GRCm39) |
R263Q |
probably damaging |
Het |
Mettl22 |
A |
G |
16: 8,295,924 (GRCm39) |
E71G |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,553,304 (GRCm39) |
T4330A |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,834,379 (GRCm39) |
T387A |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,135,550 (GRCm39) |
D379G |
probably benign |
Het |
Nbas |
A |
G |
12: 13,455,398 (GRCm39) |
D1204G |
possibly damaging |
Het |
Ncor2 |
T |
C |
5: 125,132,847 (GRCm39) |
K478E |
unknown |
Het |
Or14a256 |
A |
T |
7: 86,265,574 (GRCm39) |
L93Q |
possibly damaging |
Het |
Or51d1 |
A |
G |
7: 102,347,477 (GRCm39) |
T11A |
probably benign |
Het |
Or5k1 |
T |
A |
16: 58,617,250 (GRCm39) |
I320F |
probably benign |
Het |
Osbpl7 |
G |
A |
11: 96,941,662 (GRCm39) |
V62I |
probably benign |
Het |
Pak1ip1 |
A |
G |
13: 41,163,018 (GRCm39) |
N246S |
probably damaging |
Het |
Prim1 |
A |
G |
10: 127,851,845 (GRCm39) |
Y39C |
probably damaging |
Het |
Prl3b1 |
G |
T |
13: 27,427,827 (GRCm39) |
V46L |
probably benign |
Het |
Prss54 |
A |
T |
8: 96,292,199 (GRCm39) |
S127T |
probably benign |
Het |
Rasal3 |
G |
A |
17: 32,611,391 (GRCm39) |
T912M |
probably damaging |
Het |
Rrp12 |
T |
A |
19: 41,872,217 (GRCm39) |
T420S |
probably benign |
Het |
Rspo1 |
A |
G |
4: 124,898,831 (GRCm39) |
N51D |
probably damaging |
Het |
Rufy4 |
A |
G |
1: 74,172,035 (GRCm39) |
R253G |
probably benign |
Het |
Scaf1 |
G |
A |
7: 44,657,167 (GRCm39) |
R571C |
unknown |
Het |
Scn2a |
A |
T |
2: 65,532,323 (GRCm39) |
H645L |
probably damaging |
Het |
Sec24b |
A |
G |
3: 129,782,595 (GRCm39) |
S1132P |
probably damaging |
Het |
Slc1a2 |
A |
G |
2: 102,586,290 (GRCm39) |
K298R |
probably damaging |
Het |
Slc25a54 |
T |
A |
3: 109,014,573 (GRCm39) |
N230K |
probably benign |
Het |
Slc27a4 |
T |
G |
2: 29,705,664 (GRCm39) |
Y617* |
probably null |
Het |
Slc2a10 |
T |
C |
2: 165,357,269 (GRCm39) |
S310P |
probably damaging |
Het |
Snx33 |
C |
T |
9: 56,833,151 (GRCm39) |
R306H |
probably damaging |
Het |
Spag9 |
A |
T |
11: 93,980,258 (GRCm39) |
|
probably null |
Het |
Spg11 |
A |
T |
2: 121,932,270 (GRCm39) |
|
probably null |
Het |
Sycp2l |
A |
G |
13: 41,283,258 (GRCm39) |
T165A |
probably damaging |
Het |
Syt14 |
A |
G |
1: 192,615,571 (GRCm39) |
C189R |
probably damaging |
Het |
Taar9 |
A |
T |
10: 23,984,882 (GRCm39) |
L184Q |
probably damaging |
Het |
Tkt |
C |
T |
14: 30,281,815 (GRCm39) |
P111L |
probably damaging |
Het |
Trpc1 |
A |
T |
9: 95,603,197 (GRCm39) |
L445Q |
possibly damaging |
Het |
Usp53 |
A |
G |
3: 122,743,359 (GRCm39) |
S526P |
probably benign |
Het |
Vps54 |
T |
G |
11: 21,248,791 (GRCm39) |
W447G |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,340,177 (GRCm39) |
H806L |
probably benign |
Het |
Zfp451 |
A |
T |
1: 33,841,651 (GRCm39) |
H410Q |
unknown |
Het |
Zfp688 |
A |
G |
7: 127,018,484 (GRCm39) |
C214R |
probably damaging |
Het |
Zic4 |
A |
G |
9: 91,261,174 (GRCm39) |
D143G |
possibly 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 |
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 |
|
R8071:Chd2
|
UTSW |
7 |
73,187,132 (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 |
|