Other mutations in this stock |
Total: 126 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
T |
C |
2: 35,266,271 (GRCm39) |
D133G |
possibly damaging |
Het |
Abcb4 |
A |
C |
5: 8,989,835 (GRCm39) |
D796A |
probably damaging |
Het |
Actg2 |
A |
T |
6: 83,496,896 (GRCm39) |
V147E |
probably damaging |
Het |
Adamts13 |
A |
C |
2: 26,877,001 (GRCm39) |
T534P |
probably damaging |
Het |
Ago1 |
T |
C |
4: 126,336,959 (GRCm39) |
T249A |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,979,859 (GRCm39) |
I381N |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,119,038 (GRCm39) |
D3515G |
probably benign |
Het |
Angptl3 |
T |
C |
4: 98,922,706 (GRCm39) |
V249A |
probably benign |
Het |
Ank |
A |
G |
15: 27,567,658 (GRCm39) |
T294A |
possibly damaging |
Het |
Ank1 |
A |
T |
8: 23,594,825 (GRCm39) |
H204L |
probably damaging |
Het |
Apbb2 |
A |
G |
5: 66,468,331 (GRCm39) |
|
probably benign |
Het |
Arhgap28 |
A |
T |
17: 68,208,424 (GRCm39) |
S15T |
probably benign |
Het |
Aspm |
T |
C |
1: 139,410,249 (GRCm39) |
|
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,062,554 (GRCm39) |
E651G |
probably damaging |
Het |
B3gnt2 |
A |
T |
11: 22,786,860 (GRCm39) |
F109L |
probably damaging |
Het |
Bpifb4 |
T |
C |
2: 153,801,603 (GRCm39) |
F575L |
probably damaging |
Het |
Calhm4 |
A |
G |
10: 33,920,043 (GRCm39) |
W75R |
probably damaging |
Het |
Calr |
C |
A |
8: 85,569,660 (GRCm39) |
K322N |
probably benign |
Het |
Ccdc188 |
T |
C |
16: 18,037,169 (GRCm39) |
S247P |
possibly damaging |
Het |
Cdr1 |
T |
A |
X: 60,228,908 (GRCm39) |
D86V |
unknown |
Het |
Cep97 |
C |
T |
16: 55,745,421 (GRCm39) |
V48I |
probably damaging |
Het |
Chaf1b |
T |
A |
16: 93,681,399 (GRCm39) |
C6S |
probably damaging |
Het |
Chd3 |
C |
T |
11: 69,247,844 (GRCm39) |
D920N |
probably damaging |
Het |
Clk1 |
T |
C |
1: 58,452,192 (GRCm39) |
|
probably benign |
Het |
Cntnap3 |
T |
A |
13: 64,905,250 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
T |
A |
9: 79,507,293 (GRCm39) |
|
probably null |
Het |
Col17a1 |
G |
T |
19: 47,659,801 (GRCm39) |
|
probably benign |
Het |
Coq7 |
T |
A |
7: 118,128,940 (GRCm39) |
I32F |
possibly damaging |
Het |
Cox6a2 |
A |
T |
7: 127,805,107 (GRCm39) |
F59I |
probably damaging |
Het |
Cpq |
A |
G |
15: 33,594,297 (GRCm39) |
D436G |
probably damaging |
Het |
Ctso |
G |
A |
3: 81,852,168 (GRCm39) |
|
probably null |
Het |
Cxadr |
A |
T |
16: 78,131,836 (GRCm39) |
H274L |
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,766,495 (GRCm39) |
C367S |
possibly damaging |
Het |
Cyp2c70 |
T |
G |
19: 40,149,115 (GRCm39) |
M344L |
possibly damaging |
Het |
Defa35 |
G |
A |
8: 21,555,871 (GRCm39) |
V77I |
probably benign |
Het |
Dhx57 |
A |
G |
17: 80,582,310 (GRCm39) |
Y432H |
probably damaging |
Het |
Dhx9 |
A |
T |
1: 153,341,441 (GRCm39) |
D601E |
probably benign |
Het |
Dnah7a |
C |
G |
1: 53,444,849 (GRCm39) |
D3952H |
probably damaging |
Het |
Dnah9 |
C |
A |
11: 65,917,798 (GRCm39) |
|
probably benign |
Het |
Dstyk |
C |
A |
1: 132,384,602 (GRCm39) |
|
probably benign |
Het |
Efcab2 |
T |
A |
1: 178,303,469 (GRCm39) |
|
probably benign |
Het |
Ehbp1l1 |
T |
C |
19: 5,770,598 (GRCm39) |
E287G |
possibly damaging |
Het |
Epgn |
A |
G |
5: 91,180,073 (GRCm39) |
T87A |
probably benign |
Het |
Erc2 |
A |
C |
14: 27,863,182 (GRCm39) |
E803A |
probably damaging |
Het |
Fer |
A |
G |
17: 64,446,011 (GRCm39) |
*454W |
probably null |
Het |
Glyr1 |
T |
C |
16: 4,849,836 (GRCm39) |
D179G |
probably damaging |
Het |
Gm12830 |
T |
A |
4: 114,702,173 (GRCm39) |
|
probably benign |
Het |
Gm9922 |
C |
A |
14: 101,967,129 (GRCm39) |
|
probably benign |
Het |
Gsta3 |
C |
T |
1: 21,335,118 (GRCm39) |
P200S |
possibly damaging |
Het |
Hmgxb3 |
G |
A |
18: 61,288,200 (GRCm39) |
|
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Il16 |
T |
C |
7: 83,371,762 (GRCm39) |
K15E |
probably damaging |
Het |
Kcnip2 |
T |
A |
19: 45,782,514 (GRCm39) |
|
probably benign |
Het |
Kdm4c |
T |
C |
4: 74,263,804 (GRCm39) |
V696A |
probably benign |
Het |
Kdr |
A |
G |
5: 76,107,587 (GRCm39) |
|
probably benign |
Het |
Klhl33 |
T |
G |
14: 51,128,868 (GRCm39) |
H787P |
probably damaging |
Het |
Klk14 |
A |
T |
7: 43,343,769 (GRCm39) |
T159S |
probably benign |
Het |
Lancl2 |
A |
G |
6: 57,680,117 (GRCm39) |
N16D |
probably damaging |
Het |
Lemd3 |
T |
C |
10: 120,773,015 (GRCm39) |
N583S |
possibly damaging |
Het |
Map3k4 |
TGCTGGCTTCAGGGCCACAGTCCGCTG |
TGCTG |
17: 12,489,902 (GRCm39) |
|
probably null |
Het |
Mpl |
T |
G |
4: 118,303,235 (GRCm39) |
|
probably benign |
Het |
Myh7b |
T |
C |
2: 155,472,592 (GRCm39) |
|
probably benign |
Het |
Mylk |
A |
C |
16: 34,732,667 (GRCm39) |
|
probably benign |
Het |
Myof |
A |
T |
19: 37,969,714 (GRCm39) |
M316K |
probably benign |
Het |
Nfib |
T |
A |
4: 82,214,974 (GRCm39) |
N543I |
probably damaging |
Het |
Nfix |
A |
G |
8: 85,448,403 (GRCm39) |
S375P |
probably damaging |
Het |
Nkrf |
T |
C |
X: 36,153,769 (GRCm39) |
Q171R |
probably damaging |
Het |
Nmnat2 |
T |
A |
1: 152,952,747 (GRCm39) |
|
probably benign |
Het |
Npffr2 |
G |
A |
5: 89,731,206 (GRCm39) |
E379K |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,640,904 (GRCm39) |
|
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,964,561 (GRCm39) |
Y1382H |
probably damaging |
Het |
Ocstamp |
T |
C |
2: 165,237,912 (GRCm39) |
R451G |
possibly damaging |
Het |
Or52s1 |
T |
A |
7: 102,861,928 (GRCm39) |
I287K |
probably damaging |
Het |
Or6c6c |
A |
G |
10: 129,541,008 (GRCm39) |
D87G |
probably benign |
Het |
Pabpc1 |
C |
T |
15: 36,597,737 (GRCm39) |
A551T |
possibly damaging |
Het |
Pard3 |
A |
T |
8: 128,103,378 (GRCm39) |
|
probably benign |
Het |
Pcdhb12 |
G |
T |
18: 37,569,174 (GRCm39) |
V107L |
probably benign |
Het |
Pik3cd |
A |
T |
4: 149,747,677 (GRCm39) |
V22D |
probably damaging |
Het |
Pkd1l2 |
A |
G |
8: 117,724,315 (GRCm39) |
V2396A |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,877,207 (GRCm39) |
I167T |
probably damaging |
Het |
Pphln1 |
A |
T |
15: 93,339,588 (GRCm39) |
H114L |
possibly damaging |
Het |
Ppm1h |
A |
G |
10: 122,756,687 (GRCm39) |
N444S |
probably damaging |
Het |
Prdm9 |
G |
A |
17: 15,777,646 (GRCm39) |
T146I |
probably damaging |
Het |
Prrc2a |
A |
G |
17: 35,369,891 (GRCm39) |
|
probably benign |
Het |
Prrx1 |
T |
C |
1: 163,140,128 (GRCm39) |
D26G |
possibly damaging |
Het |
Ptpn5 |
T |
C |
7: 46,729,042 (GRCm39) |
E495G |
probably damaging |
Het |
Rab23 |
A |
C |
1: 33,773,942 (GRCm39) |
|
probably null |
Het |
Ralgps1 |
C |
T |
2: 33,047,935 (GRCm39) |
M348I |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,315,690 (GRCm39) |
T2137A |
probably benign |
Het |
Rapgef4 |
G |
T |
2: 72,056,374 (GRCm39) |
G654V |
probably benign |
Het |
Rc3h2 |
A |
T |
2: 37,269,020 (GRCm39) |
|
probably benign |
Het |
Reg2 |
G |
A |
6: 78,383,169 (GRCm39) |
A39T |
possibly damaging |
Het |
Sema4d |
C |
A |
13: 51,879,347 (GRCm39) |
V7F |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,772,354 (GRCm39) |
|
probably benign |
Het |
Sgpl1 |
C |
T |
10: 60,949,216 (GRCm39) |
|
probably null |
Het |
Shisa9 |
G |
A |
16: 11,814,987 (GRCm39) |
V212M |
probably damaging |
Het |
Shq1 |
G |
A |
6: 100,550,588 (GRCm39) |
P450L |
probably benign |
Het |
Sin3a |
A |
G |
9: 57,018,196 (GRCm39) |
T872A |
probably benign |
Het |
Sipa1l3 |
C |
T |
7: 29,047,775 (GRCm39) |
R1371Q |
probably benign |
Het |
Skint8 |
T |
C |
4: 111,796,064 (GRCm39) |
V246A |
probably benign |
Het |
Slc22a20 |
A |
T |
19: 6,022,985 (GRCm39) |
V386D |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,348,034 (GRCm39) |
T253S |
probably benign |
Het |
Slc2a7 |
G |
A |
4: 150,242,528 (GRCm39) |
|
probably benign |
Het |
Slc35a2 |
T |
A |
X: 7,755,901 (GRCm39) |
Y48N |
probably damaging |
Het |
Slc4a2 |
G |
T |
5: 24,639,344 (GRCm39) |
S413I |
probably damaging |
Het |
Sntg2 |
T |
C |
12: 30,276,772 (GRCm39) |
T427A |
probably benign |
Het |
Soat1 |
T |
C |
1: 156,270,023 (GRCm39) |
Y132C |
probably damaging |
Het |
Stn1 |
G |
T |
19: 47,490,112 (GRCm39) |
H342N |
probably benign |
Het |
Tarbp1 |
T |
A |
8: 127,165,667 (GRCm39) |
|
probably benign |
Het |
Tas2r113 |
A |
C |
6: 132,870,341 (GRCm39) |
K123T |
probably damaging |
Het |
Tbck |
C |
T |
3: 132,440,168 (GRCm39) |
Q504* |
probably null |
Het |
Tenm3 |
C |
T |
8: 48,794,069 (GRCm39) |
C380Y |
probably damaging |
Het |
Tent4a |
A |
T |
13: 69,648,051 (GRCm39) |
V781E |
possibly damaging |
Het |
Triobp |
A |
G |
15: 78,860,740 (GRCm39) |
D1389G |
probably damaging |
Het |
Trpm4 |
A |
T |
7: 44,958,130 (GRCm39) |
F780I |
probably damaging |
Het |
Tubb4a |
G |
T |
17: 57,388,182 (GRCm39) |
Y281* |
probably null |
Het |
Txndc15 |
T |
C |
13: 55,872,395 (GRCm39) |
F261S |
probably damaging |
Het |
Ube3b |
T |
C |
5: 114,557,530 (GRCm39) |
|
probably benign |
Het |
Unc5c |
G |
C |
3: 141,439,694 (GRCm39) |
V196L |
probably benign |
Het |
Upf3a |
G |
A |
8: 13,845,500 (GRCm39) |
|
probably null |
Het |
Vmn2r20 |
T |
C |
6: 123,363,063 (GRCm39) |
K574E |
probably benign |
Het |
Vps50 |
A |
G |
6: 3,536,853 (GRCm39) |
M275V |
possibly damaging |
Het |
Xrcc5 |
A |
G |
1: 72,346,735 (GRCm39) |
|
probably benign |
Het |
Zbtb18 |
T |
C |
1: 177,276,182 (GRCm39) |
L505S |
probably damaging |
Het |
Zbtb41 |
T |
C |
1: 139,366,722 (GRCm39) |
I567T |
probably damaging |
Het |
Zfp598 |
T |
C |
17: 24,897,558 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Nup98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Nup98
|
APN |
7 |
101,844,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00789:Nup98
|
APN |
7 |
101,803,178 (GRCm39) |
missense |
probably benign |
|
IGL00798:Nup98
|
APN |
7 |
101,796,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01562:Nup98
|
APN |
7 |
101,835,125 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01942:Nup98
|
APN |
7 |
101,843,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Nup98
|
APN |
7 |
101,832,693 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02490:Nup98
|
APN |
7 |
101,801,573 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03184:Nup98
|
APN |
7 |
101,832,752 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4519001:Nup98
|
UTSW |
7 |
101,784,171 (GRCm39) |
missense |
probably benign |
0.00 |
R0040:Nup98
|
UTSW |
7 |
101,841,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Nup98
|
UTSW |
7 |
101,788,859 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0471:Nup98
|
UTSW |
7 |
101,788,004 (GRCm39) |
missense |
probably benign |
0.13 |
R0538:Nup98
|
UTSW |
7 |
101,835,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Nup98
|
UTSW |
7 |
101,801,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0900:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1545:Nup98
|
UTSW |
7 |
101,784,087 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1775:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.03 |
R1889:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Nup98
|
UTSW |
7 |
101,829,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R3423:Nup98
|
UTSW |
7 |
101,834,084 (GRCm39) |
missense |
probably benign |
0.03 |
R4361:Nup98
|
UTSW |
7 |
101,794,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Nup98
|
UTSW |
7 |
101,834,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Nup98
|
UTSW |
7 |
101,802,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4910:Nup98
|
UTSW |
7 |
101,845,007 (GRCm39) |
missense |
unknown |
|
R4924:Nup98
|
UTSW |
7 |
101,784,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5233:Nup98
|
UTSW |
7 |
101,845,029 (GRCm39) |
missense |
unknown |
|
R5779:Nup98
|
UTSW |
7 |
101,801,568 (GRCm39) |
missense |
probably benign |
|
R5922:Nup98
|
UTSW |
7 |
101,803,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Nup98
|
UTSW |
7 |
101,829,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6343:Nup98
|
UTSW |
7 |
101,843,957 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6364:Nup98
|
UTSW |
7 |
101,825,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Nup98
|
UTSW |
7 |
101,844,223 (GRCm39) |
missense |
probably benign |
0.03 |
R6577:Nup98
|
UTSW |
7 |
101,778,053 (GRCm39) |
splice site |
probably null |
|
R6900:Nup98
|
UTSW |
7 |
101,835,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Nup98
|
UTSW |
7 |
101,844,248 (GRCm39) |
missense |
unknown |
|
R7218:Nup98
|
UTSW |
7 |
101,841,107 (GRCm39) |
splice site |
probably null |
|
R7235:Nup98
|
UTSW |
7 |
101,774,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R7402:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.00 |
R7427:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7428:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7584:Nup98
|
UTSW |
7 |
101,825,596 (GRCm39) |
missense |
probably benign |
0.02 |
R7646:Nup98
|
UTSW |
7 |
101,803,242 (GRCm39) |
missense |
probably benign |
0.01 |
R7648:Nup98
|
UTSW |
7 |
101,773,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7742:Nup98
|
UTSW |
7 |
101,802,464 (GRCm39) |
splice site |
probably null |
|
R7827:Nup98
|
UTSW |
7 |
101,773,569 (GRCm39) |
missense |
probably benign |
0.10 |
R7884:Nup98
|
UTSW |
7 |
101,825,556 (GRCm39) |
missense |
probably benign |
0.12 |
R7943:Nup98
|
UTSW |
7 |
101,844,029 (GRCm39) |
missense |
probably benign |
0.10 |
R8034:Nup98
|
UTSW |
7 |
101,794,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8952:Nup98
|
UTSW |
7 |
101,835,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Nup98
|
UTSW |
7 |
101,783,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Nup98
|
UTSW |
7 |
101,844,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9146:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9148:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9223:Nup98
|
UTSW |
7 |
101,834,167 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9246:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9249:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9272:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9274:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9283:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Nup98
|
UTSW |
7 |
101,818,611 (GRCm39) |
missense |
probably benign |
0.05 |
R9492:Nup98
|
UTSW |
7 |
101,778,252 (GRCm39) |
missense |
probably benign |
0.11 |
R9661:Nup98
|
UTSW |
7 |
101,782,019 (GRCm39) |
nonsense |
probably null |
|
T0970:Nup98
|
UTSW |
7 |
101,835,959 (GRCm39) |
unclassified |
probably benign |
|
X0054:Nup98
|
UTSW |
7 |
101,796,415 (GRCm39) |
missense |
probably damaging |
1.00 |
|