Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,396,304 (GRCm39) |
S103N |
probably benign |
Het |
Ace |
A |
G |
11: 105,863,299 (GRCm39) |
D358G |
possibly damaging |
Het |
Acvr2b |
A |
T |
9: 119,257,116 (GRCm39) |
H115L |
probably damaging |
Het |
Adam15 |
G |
A |
3: 89,254,742 (GRCm39) |
T106I |
possibly damaging |
Het |
Adamts16 |
A |
G |
13: 70,883,948 (GRCm39) |
C1076R |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,092,481 (GRCm39) |
Y614C |
probably damaging |
Het |
Adhfe1 |
A |
T |
1: 9,627,276 (GRCm39) |
H225L |
probably benign |
Het |
Aff3 |
A |
G |
1: 38,220,397 (GRCm39) |
I1171T |
probably damaging |
Het |
Agps |
T |
A |
2: 75,697,182 (GRCm39) |
M334K |
probably damaging |
Het |
Akr1e1 |
A |
G |
13: 4,652,678 (GRCm39) |
|
probably null |
Het |
Als2cl |
G |
A |
9: 110,718,191 (GRCm39) |
V311M |
probably benign |
Het |
Amdhd1 |
A |
T |
10: 93,375,813 (GRCm39) |
L7H |
probably damaging |
Het |
Apba1 |
A |
T |
19: 23,870,782 (GRCm39) |
I205F |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,244,917 (GRCm39) |
E187D |
possibly damaging |
Het |
Ash1l |
A |
T |
3: 88,914,530 (GRCm39) |
H1720L |
probably benign |
Het |
Atp9a |
T |
C |
2: 168,575,988 (GRCm39) |
|
probably benign |
Het |
Bcl7c |
G |
A |
7: 127,307,695 (GRCm39) |
A2V |
probably damaging |
Het |
Catsperg1 |
G |
C |
7: 28,909,912 (GRCm39) |
P72R |
probably benign |
Het |
Ccdc103 |
G |
A |
11: 102,774,922 (GRCm39) |
G174R |
probably benign |
Het |
Ccdc171 |
A |
T |
4: 83,612,512 (GRCm39) |
K976M |
probably damaging |
Het |
Ceacam1 |
T |
C |
7: 25,173,360 (GRCm39) |
N276S |
possibly damaging |
Het |
Cep152 |
T |
C |
2: 125,463,127 (GRCm39) |
E18G |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,461,803 (GRCm39) |
N91S |
probably damaging |
Het |
Cers3 |
T |
C |
7: 66,393,442 (GRCm39) |
L17P |
probably benign |
Het |
Cpsf3 |
A |
G |
12: 21,356,844 (GRCm39) |
N489S |
possibly damaging |
Het |
Cramp1 |
A |
G |
17: 25,187,920 (GRCm39) |
S1225P |
probably damaging |
Het |
Dck |
G |
A |
5: 88,913,166 (GRCm39) |
G18R |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,387,914 (GRCm39) |
E3124D |
probably benign |
Het |
Dync2i2 |
T |
A |
2: 29,923,953 (GRCm39) |
T191S |
probably benign |
Het |
Eogt |
T |
G |
6: 97,090,839 (GRCm39) |
L433F |
probably damaging |
Het |
Fam135b |
A |
G |
15: 71,334,744 (GRCm39) |
S817P |
|
Het |
Fsip2 |
T |
C |
2: 82,812,374 (GRCm39) |
Y2898H |
possibly damaging |
Het |
Fzr1 |
T |
C |
10: 81,205,249 (GRCm39) |
H249R |
probably benign |
Het |
Gbp10 |
T |
G |
5: 105,366,861 (GRCm39) |
Q457P |
probably damaging |
Het |
Gin1 |
G |
C |
1: 97,710,819 (GRCm39) |
L167F |
probably damaging |
Het |
Gm14226 |
A |
T |
2: 154,866,843 (GRCm39) |
I267F |
probably damaging |
Het |
Gmnc |
A |
G |
16: 26,781,642 (GRCm39) |
|
probably null |
Het |
Hectd2 |
A |
T |
19: 36,576,402 (GRCm39) |
I311F |
probably damaging |
Het |
Heg1 |
A |
G |
16: 33,558,961 (GRCm39) |
K1085E |
probably benign |
Het |
Hmbs |
G |
A |
9: 44,252,983 (GRCm39) |
Q34* |
probably null |
Het |
Hyal6 |
T |
A |
6: 24,734,151 (GRCm39) |
M28K |
probably benign |
Het |
Ifi27l2a |
T |
C |
12: 103,405,678 (GRCm39) |
V141A |
possibly damaging |
Het |
Ift122 |
T |
A |
6: 115,867,492 (GRCm39) |
I414N |
probably damaging |
Het |
Iglv2 |
A |
T |
16: 19,079,434 (GRCm39) |
V23E |
probably damaging |
Het |
Itgax |
A |
T |
7: 127,730,641 (GRCm39) |
I120L |
probably benign |
Het |
Kifc3 |
A |
G |
8: 95,853,317 (GRCm39) |
I13T |
probably benign |
Het |
Lmod3 |
T |
C |
6: 97,224,625 (GRCm39) |
N399D |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,365,326 (GRCm39) |
I3145K |
probably benign |
Het |
Map2k5 |
A |
C |
9: 63,201,006 (GRCm39) |
I209S |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,141,388 (GRCm39) |
E117G |
probably damaging |
Het |
Milr1 |
A |
G |
11: 106,652,105 (GRCm39) |
H172R |
probably benign |
Het |
Myod1 |
A |
C |
7: 46,026,593 (GRCm39) |
D166A |
|
Het |
Neb |
C |
T |
2: 52,100,878 (GRCm39) |
V4647M |
possibly damaging |
Het |
Nek1 |
A |
T |
8: 61,574,055 (GRCm39) |
D1101V |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,330,572 (GRCm39) |
V608D |
probably benign |
Het |
Noc3l |
G |
A |
19: 38,800,835 (GRCm39) |
Q216* |
probably null |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Oat |
C |
T |
7: 132,166,006 (GRCm39) |
S193N |
probably benign |
Het |
Oma1 |
A |
G |
4: 103,182,214 (GRCm39) |
|
probably null |
Het |
Or12e13 |
G |
T |
2: 87,663,523 (GRCm39) |
G47* |
probably null |
Het |
Or1e16 |
T |
A |
11: 73,286,853 (GRCm39) |
|
probably benign |
Het |
Or1j15 |
T |
G |
2: 36,458,988 (GRCm39) |
F126C |
probably benign |
Het |
Or6c206 |
A |
G |
10: 129,097,184 (GRCm39) |
Y118C |
probably damaging |
Het |
Or6c216 |
A |
G |
10: 129,678,482 (GRCm39) |
V143A |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,933,918 (GRCm39) |
S500P |
possibly damaging |
Het |
Osbpl11 |
A |
T |
16: 33,047,660 (GRCm39) |
N541I |
|
Het |
Pcnx4 |
A |
G |
12: 72,613,671 (GRCm39) |
I539V |
probably benign |
Het |
Ppfia3 |
T |
A |
7: 44,999,717 (GRCm39) |
|
probably null |
Het |
Ppp1r3a |
T |
C |
6: 14,722,098 (GRCm39) |
K275E |
probably benign |
Het |
Pten |
A |
G |
19: 32,769,972 (GRCm39) |
N63S |
probably benign |
Het |
Rptor |
A |
G |
11: 119,777,896 (GRCm39) |
N1020S |
probably benign |
Het |
Sall2 |
C |
A |
14: 52,550,673 (GRCm39) |
D841Y |
possibly damaging |
Het |
Sbno1 |
T |
A |
5: 124,519,762 (GRCm39) |
H1172L |
probably benign |
Het |
Scaf4 |
A |
T |
16: 90,027,054 (GRCm39) |
L921Q |
probably damaging |
Het |
Sec22c |
C |
A |
9: 121,524,750 (GRCm39) |
R11L |
probably damaging |
Het |
Skint6 |
T |
A |
4: 113,034,173 (GRCm39) |
D318V |
probably damaging |
Het |
Slc22a28 |
T |
C |
19: 8,049,205 (GRCm39) |
N348S |
probably benign |
Het |
Slc44a2 |
G |
T |
9: 21,253,305 (GRCm39) |
K77N |
possibly damaging |
Het |
Smc1b |
C |
T |
15: 84,950,431 (GRCm39) |
V1198I |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,717,568 (GRCm39) |
M316K |
probably damaging |
Het |
Stra8 |
T |
C |
6: 34,911,016 (GRCm39) |
Y215H |
probably damaging |
Het |
Sv2a |
G |
T |
3: 96,097,010 (GRCm39) |
R445L |
probably benign |
Het |
Sycp1 |
A |
C |
3: 102,758,944 (GRCm39) |
L771R |
probably damaging |
Het |
Tchp |
A |
T |
5: 114,859,184 (GRCm39) |
R493* |
probably null |
Het |
Ttc13 |
G |
A |
8: 125,410,039 (GRCm39) |
A391V |
probably benign |
Het |
Unc13b |
C |
T |
4: 43,176,186 (GRCm39) |
T2338I |
unknown |
Het |
Wac |
A |
G |
18: 7,921,592 (GRCm39) |
D576G |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,222,688 (GRCm39) |
N559S |
probably benign |
Het |
Zscan20 |
A |
T |
4: 128,481,914 (GRCm39) |
S583T |
probably benign |
Het |
|
Other mutations in Nup160 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Nup160
|
APN |
2 |
90,523,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00938:Nup160
|
APN |
2 |
90,563,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Nup160
|
APN |
2 |
90,563,553 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01140:Nup160
|
APN |
2 |
90,530,909 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01348:Nup160
|
APN |
2 |
90,530,772 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01361:Nup160
|
APN |
2 |
90,514,356 (GRCm39) |
nonsense |
probably null |
|
IGL01595:Nup160
|
APN |
2 |
90,560,081 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01791:Nup160
|
APN |
2 |
90,534,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Nup160
|
APN |
2 |
90,560,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Nup160
|
APN |
2 |
90,534,285 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02250:Nup160
|
APN |
2 |
90,539,214 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02507:Nup160
|
APN |
2 |
90,560,079 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03108:Nup160
|
APN |
2 |
90,534,169 (GRCm39) |
missense |
probably benign |
|
R0031:Nup160
|
UTSW |
2 |
90,547,931 (GRCm39) |
splice site |
probably null |
|
R0365:Nup160
|
UTSW |
2 |
90,539,188 (GRCm39) |
missense |
probably benign |
0.01 |
R0417:Nup160
|
UTSW |
2 |
90,565,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0781:Nup160
|
UTSW |
2 |
90,563,563 (GRCm39) |
splice site |
probably benign |
|
R1037:Nup160
|
UTSW |
2 |
90,524,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Nup160
|
UTSW |
2 |
90,563,563 (GRCm39) |
splice site |
probably benign |
|
R1459:Nup160
|
UTSW |
2 |
90,520,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Nup160
|
UTSW |
2 |
90,530,887 (GRCm39) |
missense |
probably benign |
|
R1468:Nup160
|
UTSW |
2 |
90,530,887 (GRCm39) |
missense |
probably benign |
|
R1478:Nup160
|
UTSW |
2 |
90,509,743 (GRCm39) |
start gained |
probably benign |
|
R1565:Nup160
|
UTSW |
2 |
90,552,405 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1617:Nup160
|
UTSW |
2 |
90,509,843 (GRCm39) |
missense |
probably benign |
|
R1647:Nup160
|
UTSW |
2 |
90,540,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R1648:Nup160
|
UTSW |
2 |
90,540,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R1702:Nup160
|
UTSW |
2 |
90,514,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R1719:Nup160
|
UTSW |
2 |
90,530,780 (GRCm39) |
nonsense |
probably null |
|
R2448:Nup160
|
UTSW |
2 |
90,552,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R3775:Nup160
|
UTSW |
2 |
90,552,420 (GRCm39) |
missense |
probably benign |
|
R3776:Nup160
|
UTSW |
2 |
90,552,420 (GRCm39) |
missense |
probably benign |
|
R4600:Nup160
|
UTSW |
2 |
90,515,541 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Nup160
|
UTSW |
2 |
90,556,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Nup160
|
UTSW |
2 |
90,530,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R5309:Nup160
|
UTSW |
2 |
90,563,176 (GRCm39) |
nonsense |
probably null |
|
R5312:Nup160
|
UTSW |
2 |
90,563,176 (GRCm39) |
nonsense |
probably null |
|
R5447:Nup160
|
UTSW |
2 |
90,555,959 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5682:Nup160
|
UTSW |
2 |
90,510,155 (GRCm39) |
missense |
probably benign |
0.29 |
R5726:Nup160
|
UTSW |
2 |
90,548,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R5771:Nup160
|
UTSW |
2 |
90,553,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Nup160
|
UTSW |
2 |
90,510,114 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5851:Nup160
|
UTSW |
2 |
90,537,382 (GRCm39) |
missense |
probably benign |
|
R5988:Nup160
|
UTSW |
2 |
90,519,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Nup160
|
UTSW |
2 |
90,520,449 (GRCm39) |
nonsense |
probably null |
|
R6164:Nup160
|
UTSW |
2 |
90,548,220 (GRCm39) |
nonsense |
probably null |
|
R6356:Nup160
|
UTSW |
2 |
90,542,279 (GRCm39) |
splice site |
probably null |
|
R6379:Nup160
|
UTSW |
2 |
90,532,753 (GRCm39) |
nonsense |
probably null |
|
R6519:Nup160
|
UTSW |
2 |
90,548,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R6755:Nup160
|
UTSW |
2 |
90,530,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Nup160
|
UTSW |
2 |
90,537,364 (GRCm39) |
missense |
probably benign |
0.34 |
R7251:Nup160
|
UTSW |
2 |
90,530,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R7256:Nup160
|
UTSW |
2 |
90,553,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Nup160
|
UTSW |
2 |
90,534,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R7546:Nup160
|
UTSW |
2 |
90,515,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R7761:Nup160
|
UTSW |
2 |
90,533,456 (GRCm39) |
missense |
probably benign |
|
R7768:Nup160
|
UTSW |
2 |
90,530,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R7959:Nup160
|
UTSW |
2 |
90,544,239 (GRCm39) |
critical splice donor site |
probably null |
|
R8525:Nup160
|
UTSW |
2 |
90,548,440 (GRCm39) |
critical splice donor site |
probably null |
|
R8726:Nup160
|
UTSW |
2 |
90,563,545 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8745:Nup160
|
UTSW |
2 |
90,530,463 (GRCm39) |
missense |
probably benign |
0.03 |
R8989:Nup160
|
UTSW |
2 |
90,548,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Nup160
|
UTSW |
2 |
90,514,429 (GRCm39) |
missense |
probably benign |
0.09 |
R9147:Nup160
|
UTSW |
2 |
90,533,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Nup160
|
UTSW |
2 |
90,533,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9153:Nup160
|
UTSW |
2 |
90,514,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9284:Nup160
|
UTSW |
2 |
90,548,375 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9435:Nup160
|
UTSW |
2 |
90,560,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R9537:Nup160
|
UTSW |
2 |
90,560,088 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9695:Nup160
|
UTSW |
2 |
90,538,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|