Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9630041A04Rik |
A |
T |
9: 101,819,887 (GRCm39) |
R102S |
probably benign |
Het |
Abitram |
A |
T |
4: 56,806,141 (GRCm39) |
K184N |
probably benign |
Het |
Acvr2b |
C |
T |
9: 119,231,616 (GRCm39) |
T2M |
probably benign |
Het |
Adamtsl3 |
A |
G |
7: 82,206,710 (GRCm39) |
|
probably benign |
Het |
Adcy7 |
A |
G |
8: 89,052,014 (GRCm39) |
Y894C |
probably damaging |
Het |
Afdn |
T |
A |
17: 14,024,270 (GRCm39) |
C59S |
probably damaging |
Het |
Amt |
C |
A |
9: 108,178,410 (GRCm39) |
T339K |
probably benign |
Het |
Ankrd27 |
G |
T |
7: 35,319,995 (GRCm39) |
V639L |
probably benign |
Het |
Anxa10 |
G |
T |
8: 62,549,753 (GRCm39) |
Q31K |
probably damaging |
Het |
Ap1g2 |
T |
C |
14: 55,339,818 (GRCm39) |
T454A |
probably benign |
Het |
Boll |
A |
T |
1: 55,399,812 (GRCm39) |
I43N |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,601,394 (GRCm39) |
D1472G |
|
Het |
Calcrl |
T |
C |
2: 84,205,643 (GRCm39) |
N16S |
probably benign |
Het |
Ccdc191 |
C |
T |
16: 43,764,041 (GRCm39) |
Q501* |
probably null |
Het |
Cchcr1 |
T |
C |
17: 35,841,105 (GRCm39) |
L658P |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,201,207 (GRCm39) |
C1919S |
unknown |
Het |
Col6a3 |
G |
A |
1: 90,735,403 (GRCm39) |
L1356F |
possibly damaging |
Het |
Dlc1 |
A |
G |
8: 37,046,558 (GRCm39) |
S680P |
possibly damaging |
Het |
Dock4 |
T |
G |
12: 40,699,404 (GRCm39) |
M206R |
possibly damaging |
Het |
Eml5 |
T |
C |
12: 98,765,060 (GRCm39) |
K1630E |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,488,514 (GRCm39) |
T3432A |
probably damaging |
Het |
Fcrl5 |
G |
T |
3: 87,343,138 (GRCm39) |
|
probably benign |
Het |
Fcrla |
A |
G |
1: 170,755,135 (GRCm39) |
|
probably benign |
Het |
Fut4 |
C |
A |
9: 14,662,572 (GRCm39) |
D241Y |
probably benign |
Het |
Fzd6 |
A |
G |
15: 38,870,962 (GRCm39) |
|
probably benign |
Het |
Gjc2 |
T |
C |
11: 59,068,453 (GRCm39) |
T10A |
probably damaging |
Het |
Gle1 |
C |
T |
2: 29,829,514 (GRCm39) |
H203Y |
possibly damaging |
Het |
Gm5565 |
A |
T |
5: 146,096,917 (GRCm39) |
I74N |
probably damaging |
Het |
Gnl2 |
T |
A |
4: 124,947,250 (GRCm39) |
I624K |
possibly damaging |
Het |
Gnpat |
C |
A |
8: 125,614,524 (GRCm39) |
N653K |
probably benign |
Het |
Gstcd |
A |
G |
3: 132,777,665 (GRCm39) |
L382S |
probably damaging |
Het |
Ipcef1 |
A |
G |
10: 6,857,936 (GRCm39) |
|
probably benign |
Het |
Jmjd7 |
T |
C |
2: 119,860,895 (GRCm39) |
V115A |
possibly damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Ltbp2 |
T |
G |
12: 84,876,885 (GRCm39) |
D440A |
possibly damaging |
Het |
Macf1 |
T |
G |
4: 123,328,501 (GRCm39) |
D4744A |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,029,372 (GRCm39) |
D230G |
probably damaging |
Het |
Mfsd6 |
A |
C |
1: 52,747,514 (GRCm39) |
Y450* |
probably null |
Het |
Mtmr9 |
A |
G |
14: 63,781,001 (GRCm39) |
C30R |
probably damaging |
Het |
Ncf1 |
G |
A |
5: 134,250,693 (GRCm39) |
Q376* |
probably null |
Het |
Or51ah3 |
A |
T |
7: 103,210,004 (GRCm39) |
T107S |
probably damaging |
Het |
Or5d37 |
A |
G |
2: 87,923,806 (GRCm39) |
V158A |
probably benign |
Het |
Or5k8 |
A |
G |
16: 58,644,734 (GRCm39) |
F113L |
probably benign |
Het |
Or8b57 |
A |
T |
9: 40,003,632 (GRCm39) |
I210K |
possibly damaging |
Het |
Or8b8 |
C |
A |
9: 37,809,415 (GRCm39) |
S238R |
probably benign |
Het |
Or8k31-ps1 |
A |
T |
2: 86,356,392 (GRCm39) |
L43* |
probably null |
Het |
Pate9 |
A |
T |
9: 36,445,727 (GRCm39) |
C75S |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,559,950 (GRCm39) |
I92F |
probably damaging |
Het |
Plec |
A |
G |
15: 76,060,445 (GRCm39) |
V3164A |
probably benign |
Het |
Prss16 |
A |
G |
13: 22,190,175 (GRCm39) |
|
probably benign |
Het |
Ptch2 |
T |
A |
4: 116,967,505 (GRCm39) |
H724Q |
probably damaging |
Het |
Pzp |
A |
T |
6: 128,499,077 (GRCm39) |
F190Y |
probably damaging |
Het |
Rab6a |
A |
G |
7: 100,275,809 (GRCm39) |
T41A |
probably benign |
Het |
Rbm6 |
A |
G |
9: 107,660,926 (GRCm39) |
L879P |
probably damaging |
Het |
Rem1 |
T |
A |
2: 152,469,969 (GRCm39) |
|
probably benign |
Het |
Rnf17 |
T |
C |
14: 56,719,554 (GRCm39) |
S935P |
probably damaging |
Het |
Ryr1 |
C |
A |
7: 28,802,254 (GRCm39) |
V789L |
probably damaging |
Het |
Scgb2b3 |
A |
T |
7: 31,059,528 (GRCm39) |
M82K |
possibly damaging |
Het |
Sgce |
T |
A |
6: 4,674,585 (GRCm39) |
L451F |
probably damaging |
Het |
Slc25a17 |
A |
C |
15: 81,207,814 (GRCm39) |
V258G |
probably benign |
Het |
Spidr |
G |
A |
16: 15,784,712 (GRCm39) |
T452I |
probably benign |
Het |
Tas2r129 |
A |
G |
6: 132,928,576 (GRCm39) |
N171S |
probably benign |
Het |
Tbc1d24 |
A |
T |
17: 24,405,114 (GRCm39) |
V10E |
probably damaging |
Het |
Tdo2 |
T |
G |
3: 81,876,885 (GRCm39) |
M115L |
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,980,935 (GRCm39) |
|
probably null |
Het |
Tead1 |
T |
A |
7: 112,493,601 (GRCm39) |
I376N |
probably damaging |
Het |
Tmem26 |
A |
G |
10: 68,614,488 (GRCm39) |
H301R |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,929,134 (GRCm39) |
T2726A |
possibly damaging |
Het |
Trim43c |
T |
C |
9: 88,723,966 (GRCm39) |
M164T |
probably benign |
Het |
Trpc1 |
G |
A |
9: 95,590,288 (GRCm39) |
S723L |
probably benign |
Het |
Txndc15 |
A |
G |
13: 55,865,914 (GRCm39) |
D126G |
probably benign |
Het |
Urb1 |
C |
T |
16: 90,569,463 (GRCm39) |
|
probably benign |
Het |
Usp25 |
C |
T |
16: 76,910,721 (GRCm39) |
H926Y |
probably benign |
Het |
Uvssa |
T |
A |
5: 33,572,180 (GRCm39) |
M700K |
possibly damaging |
Het |
Vdac1 |
T |
A |
11: 52,274,789 (GRCm39) |
Y146N |
probably damaging |
Het |
Vmn1r231 |
A |
T |
17: 21,110,560 (GRCm39) |
S118R |
probably benign |
Het |
Vmn1r41 |
A |
G |
6: 89,724,080 (GRCm39) |
Y207C |
probably damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,687,045 (GRCm39) |
I809V |
probably damaging |
Het |
Vnn1 |
G |
A |
10: 23,776,794 (GRCm39) |
G382R |
probably damaging |
Het |
Xcr1 |
A |
T |
9: 123,685,680 (GRCm39) |
H27Q |
probably benign |
Het |
Yeats2 |
T |
A |
16: 19,975,786 (GRCm39) |
N94K |
probably benign |
Het |
Zfp28 |
C |
T |
7: 6,397,440 (GRCm39) |
T625M |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,977,698 (GRCm39) |
Q905R |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,821,398 (GRCm39) |
D555G |
probably 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 |
|
|
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 |
|
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 |
|