Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adpgk |
C |
T |
9: 59,222,456 (GRCm39) |
T461I |
probably benign |
Het |
Adra2b |
A |
G |
2: 127,206,487 (GRCm39) |
T335A |
probably benign |
Het |
Ap3b1 |
T |
C |
13: 94,545,353 (GRCm39) |
|
probably null |
Het |
C1rl |
T |
C |
6: 124,470,191 (GRCm39) |
|
probably null |
Het |
Ccdc142 |
A |
G |
6: 83,080,678 (GRCm39) |
E470G |
probably damaging |
Het |
Ccm2 |
T |
A |
11: 6,539,447 (GRCm39) |
I163N |
possibly damaging |
Het |
Cdk5rap2 |
A |
T |
4: 70,157,562 (GRCm39) |
F1596L |
probably benign |
Het |
Chrna4 |
A |
T |
2: 180,679,307 (GRCm39) |
F47I |
probably damaging |
Het |
Cx3cl1 |
A |
G |
8: 95,506,876 (GRCm39) |
T294A |
probably benign |
Het |
Dcun1d4 |
C |
T |
5: 73,714,658 (GRCm39) |
T275M |
probably damaging |
Het |
Dpp4 |
T |
C |
2: 62,208,647 (GRCm39) |
I166V |
probably benign |
Het |
Dynap |
C |
T |
18: 70,374,062 (GRCm39) |
E155K |
unknown |
Het |
Fam171b |
A |
G |
2: 83,690,864 (GRCm39) |
T276A |
probably benign |
Het |
Fmo4 |
G |
A |
1: 162,621,592 (GRCm39) |
Q540* |
probably null |
Het |
Gtf2i |
C |
A |
5: 134,278,733 (GRCm39) |
V633F |
probably damaging |
Het |
Kmt5c |
G |
T |
7: 4,749,153 (GRCm39) |
R262L |
probably damaging |
Het |
Lgr5 |
A |
G |
10: 115,288,610 (GRCm39) |
L678P |
probably benign |
Het |
Mrps27 |
T |
C |
13: 99,541,508 (GRCm39) |
V163A |
probably damaging |
Het |
Myh7b |
G |
A |
2: 155,453,669 (GRCm39) |
|
probably null |
Het |
Myo15a |
A |
G |
11: 60,370,443 (GRCm39) |
T1068A |
probably benign |
Het |
Neb |
T |
A |
2: 52,181,326 (GRCm39) |
M1094L |
probably benign |
Het |
Osbpl10 |
T |
C |
9: 115,036,688 (GRCm39) |
L228P |
probably damaging |
Het |
Phip |
T |
A |
9: 82,787,765 (GRCm39) |
R799S |
possibly damaging |
Het |
Prkn |
T |
C |
17: 11,456,472 (GRCm39) |
S99P |
probably benign |
Het |
Rassf5 |
G |
T |
1: 131,172,782 (GRCm39) |
T29N |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,776 (GRCm39) |
K370E |
probably benign |
Het |
Tmprss11g |
T |
A |
5: 86,644,404 (GRCm39) |
S147C |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,569,134 (GRCm39) |
T27253I |
probably damaging |
Het |
Vmn1r59 |
A |
T |
7: 5,457,715 (GRCm39) |
V15E |
possibly damaging |
Het |
Wnt6 |
A |
C |
1: 74,821,947 (GRCm39) |
D176A |
possibly damaging |
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 |
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 |
|
|
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 |
|