Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J11Rik |
T |
C |
9: 39,962,746 (GRCm39) |
|
noncoding transcript |
Het |
Actrt2 |
A |
C |
4: 154,752,026 (GRCm39) |
S37A |
possibly damaging |
Het |
Adcy7 |
T |
C |
8: 89,040,742 (GRCm39) |
I327T |
probably damaging |
Het |
Ankrd13b |
A |
G |
11: 77,364,061 (GRCm39) |
|
probably benign |
Het |
Arap1 |
A |
C |
7: 101,037,851 (GRCm39) |
I237L |
probably benign |
Het |
Arhgap17 |
A |
T |
7: 122,902,971 (GRCm39) |
Y359N |
probably benign |
Het |
Atad1 |
A |
G |
19: 32,651,702 (GRCm39) |
M343T |
probably benign |
Het |
Cacna1b |
A |
T |
2: 24,609,964 (GRCm39) |
I392N |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,574,930 (GRCm39) |
S1914P |
probably benign |
Het |
Cd300a |
G |
T |
11: 114,785,577 (GRCm39) |
R174L |
probably benign |
Het |
Dip2a |
G |
A |
10: 76,135,831 (GRCm39) |
P356L |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,405,436 (GRCm39) |
L283P |
probably damaging |
Het |
Dusp1 |
T |
C |
17: 26,727,191 (GRCm39) |
N36S |
probably benign |
Het |
Dync2i2 |
T |
A |
2: 29,922,375 (GRCm39) |
|
probably benign |
Het |
Ercc3 |
C |
A |
18: 32,402,917 (GRCm39) |
P776Q |
probably damaging |
Het |
Etv1 |
A |
G |
12: 38,902,248 (GRCm39) |
R260G |
possibly damaging |
Het |
Fa2h |
C |
G |
8: 112,075,869 (GRCm39) |
M251I |
probably benign |
Het |
Fcsk |
T |
C |
8: 111,610,499 (GRCm39) |
E968G |
possibly damaging |
Het |
Flg2 |
A |
G |
3: 93,108,119 (GRCm39) |
D49G |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,888,884 (GRCm39) |
E2810G |
probably damaging |
Het |
Gabbr1 |
T |
C |
17: 37,366,805 (GRCm39) |
F343S |
possibly damaging |
Het |
Gdf2 |
A |
G |
14: 33,667,264 (GRCm39) |
T329A |
probably benign |
Het |
Hcn4 |
T |
A |
9: 58,731,558 (GRCm39) |
I255N |
unknown |
Het |
Hk3 |
T |
G |
13: 55,158,824 (GRCm39) |
D485A |
probably damaging |
Het |
Hook3 |
T |
C |
8: 26,562,319 (GRCm39) |
T249A |
probably benign |
Het |
Kcp |
C |
T |
6: 29,498,519 (GRCm39) |
|
probably benign |
Het |
Kifc2 |
G |
T |
15: 76,550,481 (GRCm39) |
R515L |
possibly damaging |
Het |
Kiss1r |
A |
G |
10: 79,756,584 (GRCm39) |
Y142C |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Klrb1a |
T |
A |
6: 128,596,126 (GRCm39) |
I72L |
probably benign |
Het |
Lep |
T |
A |
6: 29,070,862 (GRCm39) |
F62Y |
probably damaging |
Het |
Lrtm1 |
A |
G |
14: 28,743,801 (GRCm39) |
T90A |
probably benign |
Het |
Mug1 |
A |
T |
6: 121,865,872 (GRCm39) |
D1472V |
probably benign |
Het |
Nlrp4a |
C |
T |
7: 26,149,917 (GRCm39) |
S508L |
probably benign |
Het |
Obp2b |
T |
A |
2: 25,627,155 (GRCm39) |
D29E |
probably benign |
Het |
Or10ag2 |
G |
A |
2: 87,249,012 (GRCm39) |
V207M |
possibly damaging |
Het |
Or4c109 |
A |
G |
2: 88,818,444 (GRCm39) |
L34P |
possibly damaging |
Het |
Or4c119 |
A |
T |
2: 88,986,801 (GRCm39) |
C239* |
probably null |
Het |
Or4k15b |
T |
C |
14: 50,272,745 (GRCm39) |
I38M |
possibly damaging |
Het |
Or6c3b |
A |
G |
10: 129,527,601 (GRCm39) |
I103T |
probably damaging |
Het |
Otof |
A |
G |
5: 30,527,483 (GRCm39) |
S1985P |
probably damaging |
Het |
Oxct2a |
A |
T |
4: 123,216,886 (GRCm39) |
V165E |
probably damaging |
Het |
Pcdhgb7 |
T |
C |
18: 37,886,150 (GRCm39) |
V440A |
possibly damaging |
Het |
Pelp1 |
C |
A |
11: 70,292,487 (GRCm39) |
G211C |
probably damaging |
Het |
Phox2a |
A |
G |
7: 101,471,312 (GRCm39) |
H268R |
probably benign |
Het |
Pik3c2g |
T |
C |
6: 139,841,983 (GRCm39) |
|
probably null |
Het |
Pramel1 |
T |
A |
4: 143,125,156 (GRCm39) |
M360K |
probably benign |
Het |
Rbm6 |
C |
T |
9: 107,729,856 (GRCm39) |
R132K |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc45a1 |
T |
C |
4: 150,722,727 (GRCm39) |
T386A |
probably damaging |
Het |
Smad2 |
A |
G |
18: 76,421,124 (GRCm39) |
Y151C |
probably damaging |
Het |
Sptbn2 |
G |
A |
19: 4,800,110 (GRCm39) |
G2188D |
probably benign |
Het |
Sugt1 |
G |
A |
14: 79,840,341 (GRCm39) |
|
probably null |
Het |
Tctn3 |
T |
C |
19: 40,595,685 (GRCm39) |
S367G |
probably benign |
Het |
Tead1 |
G |
T |
7: 112,460,752 (GRCm39) |
D219Y |
probably damaging |
Het |
Tenm2 |
G |
T |
11: 35,938,028 (GRCm39) |
Y1548* |
probably null |
Het |
Tenm3 |
T |
A |
8: 48,682,233 (GRCm39) |
I2466F |
possibly damaging |
Het |
Tent4b |
C |
A |
8: 88,926,651 (GRCm39) |
H20Q |
possibly damaging |
Het |
Tgm2 |
G |
A |
2: 157,971,358 (GRCm39) |
P294S |
probably damaging |
Het |
Tns2 |
T |
C |
15: 102,019,888 (GRCm39) |
S585P |
probably damaging |
Het |
Ttc41 |
A |
G |
10: 86,566,806 (GRCm39) |
K491E |
probably benign |
Het |
Ttn |
G |
A |
2: 76,621,895 (GRCm39) |
T15549I |
probably damaging |
Het |
Vmn1r157 |
T |
C |
7: 22,461,183 (GRCm39) |
L21P |
probably damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,083,820 (GRCm39) |
M65V |
probably benign |
Het |
Zcchc14 |
T |
C |
8: 122,345,433 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ncor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Ncor2
|
APN |
5 |
125,119,807 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00519:Ncor2
|
APN |
5 |
125,161,988 (GRCm39) |
missense |
unknown |
|
IGL00900:Ncor2
|
APN |
5 |
125,102,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Ncor2
|
APN |
5 |
125,163,954 (GRCm39) |
missense |
unknown |
|
IGL01320:Ncor2
|
APN |
5 |
125,186,991 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01382:Ncor2
|
APN |
5 |
125,132,837 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01573:Ncor2
|
APN |
5 |
125,162,090 (GRCm39) |
missense |
unknown |
|
IGL01721:Ncor2
|
APN |
5 |
125,128,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Ncor2
|
APN |
5 |
125,142,934 (GRCm39) |
missense |
unknown |
|
IGL02090:Ncor2
|
APN |
5 |
125,111,467 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Ncor2
|
APN |
5 |
125,101,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02396:Ncor2
|
APN |
5 |
125,114,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02934:Ncor2
|
APN |
5 |
125,102,621 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02997:Ncor2
|
APN |
5 |
125,196,634 (GRCm39) |
intron |
probably benign |
|
R0019:Ncor2
|
UTSW |
5 |
125,196,545 (GRCm39) |
critical splice donor site |
probably null |
|
R0331:Ncor2
|
UTSW |
5 |
125,161,981 (GRCm39) |
missense |
unknown |
|
R0333:Ncor2
|
UTSW |
5 |
125,111,408 (GRCm39) |
splice site |
probably benign |
|
R0403:Ncor2
|
UTSW |
5 |
125,110,401 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0557:Ncor2
|
UTSW |
5 |
125,183,369 (GRCm39) |
nonsense |
probably null |
|
R0562:Ncor2
|
UTSW |
5 |
125,162,093 (GRCm39) |
missense |
unknown |
|
R0671:Ncor2
|
UTSW |
5 |
125,126,451 (GRCm39) |
missense |
probably benign |
0.13 |
R0699:Ncor2
|
UTSW |
5 |
125,106,176 (GRCm39) |
unclassified |
probably benign |
|
R0865:Ncor2
|
UTSW |
5 |
125,116,046 (GRCm39) |
missense |
probably benign |
0.17 |
R1183:Ncor2
|
UTSW |
5 |
125,100,585 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1325:Ncor2
|
UTSW |
5 |
125,195,844 (GRCm39) |
intron |
probably benign |
|
R1344:Ncor2
|
UTSW |
5 |
125,102,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Ncor2
|
UTSW |
5 |
125,187,039 (GRCm39) |
intron |
probably benign |
|
R1481:Ncor2
|
UTSW |
5 |
125,104,202 (GRCm39) |
nonsense |
probably null |
|
R1539:Ncor2
|
UTSW |
5 |
125,187,003 (GRCm39) |
missense |
probably benign |
0.07 |
R1558:Ncor2
|
UTSW |
5 |
125,110,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Ncor2
|
UTSW |
5 |
125,162,062 (GRCm39) |
missense |
unknown |
|
R1611:Ncor2
|
UTSW |
5 |
125,187,084 (GRCm39) |
intron |
probably benign |
|
R1764:Ncor2
|
UTSW |
5 |
125,105,679 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1789:Ncor2
|
UTSW |
5 |
125,096,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ncor2
|
UTSW |
5 |
125,195,857 (GRCm39) |
intron |
probably benign |
|
R1901:Ncor2
|
UTSW |
5 |
125,102,489 (GRCm39) |
missense |
probably benign |
0.39 |
R1946:Ncor2
|
UTSW |
5 |
125,111,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Ncor2
|
UTSW |
5 |
125,115,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R2048:Ncor2
|
UTSW |
5 |
125,161,996 (GRCm39) |
missense |
unknown |
|
R2137:Ncor2
|
UTSW |
5 |
125,107,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R2270:Ncor2
|
UTSW |
5 |
125,115,019 (GRCm39) |
missense |
probably benign |
0.33 |
R2380:Ncor2
|
UTSW |
5 |
125,113,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2570:Ncor2
|
UTSW |
5 |
125,105,864 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2918:Ncor2
|
UTSW |
5 |
125,102,824 (GRCm39) |
missense |
probably damaging |
0.99 |
R2921:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Ncor2
|
UTSW |
5 |
125,101,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R3768:Ncor2
|
UTSW |
5 |
125,105,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3829:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3830:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3951:Ncor2
|
UTSW |
5 |
125,109,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4175:Ncor2
|
UTSW |
5 |
125,128,020 (GRCm39) |
missense |
probably damaging |
0.99 |
R4360:Ncor2
|
UTSW |
5 |
125,106,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Ncor2
|
UTSW |
5 |
125,179,705 (GRCm39) |
critical splice donor site |
probably null |
|
R4490:Ncor2
|
UTSW |
5 |
125,113,879 (GRCm39) |
splice site |
probably null |
|
R4573:Ncor2
|
UTSW |
5 |
125,132,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R4611:Ncor2
|
UTSW |
5 |
125,107,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Ncor2
|
UTSW |
5 |
125,114,124 (GRCm39) |
critical splice donor site |
probably null |
|
R4851:Ncor2
|
UTSW |
5 |
125,110,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4853:Ncor2
|
UTSW |
5 |
125,158,247 (GRCm39) |
missense |
unknown |
|
R4853:Ncor2
|
UTSW |
5 |
125,102,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R4896:Ncor2
|
UTSW |
5 |
125,126,404 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Ncor2
|
UTSW |
5 |
125,111,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Ncor2
|
UTSW |
5 |
125,125,130 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5461:Ncor2
|
UTSW |
5 |
125,104,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Ncor2
|
UTSW |
5 |
125,144,975 (GRCm39) |
nonsense |
probably null |
|
R5638:Ncor2
|
UTSW |
5 |
125,125,364 (GRCm39) |
missense |
probably benign |
0.33 |
R5879:Ncor2
|
UTSW |
5 |
125,103,839 (GRCm39) |
unclassified |
probably benign |
|
R5967:Ncor2
|
UTSW |
5 |
125,146,048 (GRCm39) |
missense |
unknown |
|
R5999:Ncor2
|
UTSW |
5 |
125,110,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Ncor2
|
UTSW |
5 |
125,097,075 (GRCm39) |
missense |
probably benign |
0.14 |
R6109:Ncor2
|
UTSW |
5 |
125,132,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R6423:Ncor2
|
UTSW |
5 |
125,164,966 (GRCm39) |
missense |
unknown |
|
R6462:Ncor2
|
UTSW |
5 |
125,101,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Ncor2
|
UTSW |
5 |
125,187,069 (GRCm39) |
intron |
probably benign |
|
R7074:Ncor2
|
UTSW |
5 |
125,126,430 (GRCm39) |
nonsense |
probably null |
|
R7179:Ncor2
|
UTSW |
5 |
125,132,847 (GRCm39) |
missense |
unknown |
|
R7261:Ncor2
|
UTSW |
5 |
125,187,143 (GRCm39) |
splice site |
probably null |
|
R7263:Ncor2
|
UTSW |
5 |
125,109,196 (GRCm39) |
missense |
|
|
R7273:Ncor2
|
UTSW |
5 |
125,100,687 (GRCm39) |
missense |
|
|
R7282:Ncor2
|
UTSW |
5 |
125,097,104 (GRCm39) |
missense |
|
|
R7570:Ncor2
|
UTSW |
5 |
125,107,153 (GRCm39) |
missense |
|
|
R7725:Ncor2
|
UTSW |
5 |
125,100,630 (GRCm39) |
missense |
|
|
R7747:Ncor2
|
UTSW |
5 |
125,104,102 (GRCm39) |
missense |
|
|
R7748:Ncor2
|
UTSW |
5 |
125,187,031 (GRCm39) |
missense |
unknown |
|
R7825:Ncor2
|
UTSW |
5 |
125,114,141 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8008:Ncor2
|
UTSW |
5 |
125,144,983 (GRCm39) |
missense |
unknown |
|
R8126:Ncor2
|
UTSW |
5 |
125,183,268 (GRCm39) |
missense |
unknown |
|
R8137:Ncor2
|
UTSW |
5 |
125,114,957 (GRCm39) |
missense |
|
|
R8706:Ncor2
|
UTSW |
5 |
125,145,010 (GRCm39) |
missense |
unknown |
|
R8751:Ncor2
|
UTSW |
5 |
125,115,964 (GRCm39) |
missense |
|
|
R8819:Ncor2
|
UTSW |
5 |
125,106,291 (GRCm39) |
missense |
|
|
R8820:Ncor2
|
UTSW |
5 |
125,106,291 (GRCm39) |
missense |
|
|
R8824:Ncor2
|
UTSW |
5 |
125,195,821 (GRCm39) |
missense |
|
|
R8867:Ncor2
|
UTSW |
5 |
125,179,739 (GRCm39) |
missense |
unknown |
|
R8919:Ncor2
|
UTSW |
5 |
125,106,253 (GRCm39) |
missense |
|
|
R8922:Ncor2
|
UTSW |
5 |
125,163,939 (GRCm39) |
missense |
unknown |
|
R9076:Ncor2
|
UTSW |
5 |
125,111,086 (GRCm39) |
missense |
|
|
R9249:Ncor2
|
UTSW |
5 |
125,186,988 (GRCm39) |
missense |
unknown |
|
R9276:Ncor2
|
UTSW |
5 |
125,113,150 (GRCm39) |
missense |
|
|
R9362:Ncor2
|
UTSW |
5 |
125,095,265 (GRCm39) |
missense |
|
|
R9667:Ncor2
|
UTSW |
5 |
125,125,545 (GRCm39) |
missense |
unknown |
|
R9684:Ncor2
|
UTSW |
5 |
125,102,139 (GRCm39) |
missense |
|
|
Z1088:Ncor2
|
UTSW |
5 |
125,163,904 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Ncor2
|
UTSW |
5 |
125,144,852 (GRCm39) |
missense |
unknown |
|
Z1177:Ncor2
|
UTSW |
5 |
125,113,913 (GRCm39) |
missense |
|
|
Z1177:Ncor2
|
UTSW |
5 |
125,125,058 (GRCm39) |
missense |
probably damaging |
0.98 |
|