Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
T |
3: 121,956,008 (GRCm39) |
R716* |
probably null |
Het |
Abca8a |
A |
T |
11: 109,931,414 (GRCm39) |
N1246K |
probably damaging |
Het |
Acadl |
A |
G |
1: 66,876,134 (GRCm39) |
Y396H |
probably benign |
Het |
Apol7c |
A |
T |
15: 77,410,318 (GRCm39) |
S209R |
possibly damaging |
Het |
Atp1a1 |
A |
T |
3: 101,484,308 (GRCm39) |
C990* |
probably null |
Het |
Cachd1 |
C |
T |
4: 100,825,295 (GRCm39) |
S583L |
probably damaging |
Het |
Cbfa2t3 |
T |
C |
8: 123,374,497 (GRCm39) |
T48A |
probably benign |
Het |
Ccdc138 |
G |
T |
10: 58,409,402 (GRCm39) |
|
probably benign |
Het |
Cenpe |
A |
G |
3: 134,970,112 (GRCm39) |
E2231G |
probably damaging |
Het |
Cog3 |
T |
C |
14: 75,979,129 (GRCm39) |
I206V |
probably damaging |
Het |
Cr2 |
A |
G |
1: 194,836,633 (GRCm39) |
|
probably benign |
Het |
Ctdspl2 |
T |
C |
2: 121,809,490 (GRCm39) |
V147A |
probably damaging |
Het |
Cyp4f13 |
A |
G |
17: 33,148,845 (GRCm39) |
V300A |
probably damaging |
Het |
Dkk3 |
A |
T |
7: 111,749,954 (GRCm39) |
M72K |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,900,944 (GRCm39) |
F340L |
probably benign |
Het |
Fut1 |
A |
G |
7: 45,268,127 (GRCm39) |
H27R |
possibly damaging |
Het |
Igkv4-80 |
A |
G |
6: 68,993,840 (GRCm39) |
V17A |
probably benign |
Het |
Igkv9-123 |
G |
A |
6: 67,931,380 (GRCm39) |
P62L |
possibly damaging |
Het |
Kmt2e |
T |
C |
5: 23,702,882 (GRCm39) |
S1021P |
probably damaging |
Het |
Krt13 |
A |
C |
11: 100,009,910 (GRCm39) |
L320R |
probably damaging |
Het |
Ldhal6b |
T |
C |
17: 5,467,819 (GRCm39) |
T372A |
probably benign |
Het |
Manba |
T |
C |
3: 135,250,510 (GRCm39) |
V379A |
probably benign |
Het |
Map1b |
C |
T |
13: 99,571,639 (GRCm39) |
V361I |
probably benign |
Het |
Map4k1 |
A |
G |
7: 28,693,531 (GRCm39) |
S399G |
probably benign |
Het |
Mff |
G |
A |
1: 82,724,815 (GRCm39) |
R229H |
probably damaging |
Het |
Naga |
T |
C |
15: 82,214,401 (GRCm39) |
N370S |
possibly damaging |
Het |
Nipal1 |
T |
C |
5: 72,805,250 (GRCm39) |
L7P |
probably damaging |
Het |
Or10p22 |
T |
A |
10: 128,825,958 (GRCm39) |
M59K |
probably damaging |
Het |
Pcmt1 |
A |
T |
10: 7,516,491 (GRCm39) |
M187K |
probably benign |
Het |
Perp |
A |
T |
10: 18,731,520 (GRCm39) |
T160S |
probably damaging |
Het |
Rapgef6 |
G |
A |
11: 54,516,690 (GRCm39) |
D169N |
probably damaging |
Het |
Sel1l |
G |
A |
12: 91,776,710 (GRCm39) |
Q711* |
probably null |
Het |
Septin5 |
T |
C |
16: 18,448,581 (GRCm39) |
Y7C |
probably damaging |
Het |
Spdya |
A |
T |
17: 71,863,395 (GRCm39) |
N48I |
probably benign |
Het |
Stard6 |
T |
A |
18: 70,629,175 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
T |
C |
7: 90,025,200 (GRCm39) |
V396A |
probably benign |
Het |
Tcaf3 |
T |
G |
6: 42,570,832 (GRCm39) |
M307L |
probably benign |
Het |
Tdrd6 |
T |
C |
17: 43,938,778 (GRCm39) |
N757D |
probably benign |
Het |
Tgm1 |
T |
A |
14: 55,947,446 (GRCm39) |
D305V |
probably damaging |
Het |
Themis2 |
T |
A |
4: 132,516,862 (GRCm39) |
M213L |
probably damaging |
Het |
Tmem184c |
A |
G |
8: 78,324,449 (GRCm39) |
V347A |
probably damaging |
Het |
Tmem214 |
A |
G |
5: 31,028,888 (GRCm39) |
E159G |
probably benign |
Het |
Trim58 |
C |
T |
11: 58,531,292 (GRCm39) |
|
probably benign |
Het |
Tshz1 |
A |
T |
18: 84,031,215 (GRCm39) |
S1064R |
probably damaging |
Het |
Ubr2 |
C |
T |
17: 47,268,266 (GRCm39) |
E983K |
possibly damaging |
Het |
Vmn1r23 |
A |
T |
6: 57,902,914 (GRCm39) |
I288N |
probably benign |
Het |
Vmn2r97 |
T |
C |
17: 19,149,947 (GRCm39) |
V445A |
probably benign |
Het |
Whrn |
G |
A |
4: 63,334,342 (GRCm39) |
T813M |
probably damaging |
Het |
Xirp2 |
C |
T |
2: 67,346,020 (GRCm39) |
H2754Y |
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 |
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 |
R5253:Ncor2
|
UTSW |
5 |
125,103,994 (GRCm39) |
missense |
probably benign |
0.44 |
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 |
|