Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6a |
G |
A |
3: 32,772,194 (GRCm39) |
R164H |
probably damaging |
Het |
Afg3l2 |
A |
G |
18: 67,573,269 (GRCm39) |
Y178H |
probably benign |
Het |
Agtr1a |
A |
G |
13: 30,566,016 (GRCm39) |
*360W |
probably null |
Het |
Arfgef1 |
A |
G |
1: 10,209,109 (GRCm39) |
V1830A |
probably benign |
Het |
Asic2 |
A |
T |
11: 81,858,806 (GRCm39) |
S69T |
probably benign |
Het |
Axin1 |
A |
T |
17: 26,401,531 (GRCm39) |
N368Y |
probably damaging |
Het |
Brme1 |
A |
G |
8: 84,898,473 (GRCm39) |
E537G |
probably damaging |
Het |
Ces1d |
G |
A |
8: 93,904,756 (GRCm39) |
P328L |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,686,203 (GRCm39) |
K461* |
probably null |
Het |
Cntnap5c |
A |
T |
17: 58,620,852 (GRCm39) |
H977L |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Glg1 |
T |
C |
8: 111,896,194 (GRCm39) |
T177A |
possibly damaging |
Het |
Gm7168 |
T |
C |
17: 14,169,824 (GRCm39) |
V397A |
probably benign |
Het |
Hif1a |
T |
A |
12: 73,988,533 (GRCm39) |
D535E |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ice1 |
T |
C |
13: 70,763,219 (GRCm39) |
E173G |
possibly damaging |
Het |
Ighmbp2 |
A |
G |
19: 3,329,909 (GRCm39) |
V115A |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,271,831 (GRCm39) |
E101D |
possibly damaging |
Het |
Kat8 |
G |
A |
7: 127,523,988 (GRCm39) |
E343K |
probably damaging |
Het |
Kyat1 |
C |
T |
2: 30,078,123 (GRCm39) |
C127Y |
probably damaging |
Het |
Mrgpra4 |
T |
C |
7: 47,630,755 (GRCm39) |
H282R |
probably benign |
Het |
Npsr1 |
C |
A |
9: 24,225,096 (GRCm39) |
P368Q |
probably damaging |
Het |
Or51a43 |
T |
A |
7: 103,717,930 (GRCm39) |
M103L |
probably damaging |
Het |
Or6n2 |
G |
T |
1: 173,897,436 (GRCm39) |
D191Y |
probably damaging |
Het |
P4ha3 |
A |
G |
7: 99,955,198 (GRCm39) |
D351G |
probably benign |
Het |
Pard3b |
T |
A |
1: 62,479,160 (GRCm39) |
|
probably null |
Het |
Pgap6 |
CGGGG |
CGGGGG |
17: 26,339,536 (GRCm39) |
|
probably null |
Het |
Pik3c2b |
G |
T |
1: 133,031,574 (GRCm39) |
G1505W |
probably damaging |
Het |
Plppr5 |
A |
T |
3: 117,414,714 (GRCm39) |
I112L |
probably benign |
Het |
Potefam1 |
T |
A |
2: 111,034,468 (GRCm39) |
T355S |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,522,226 (GRCm39) |
I575T |
possibly damaging |
Het |
Ranbp3l |
A |
G |
15: 9,029,656 (GRCm39) |
E46G |
probably damaging |
Het |
Rbm46 |
A |
G |
3: 82,772,640 (GRCm39) |
V164A |
possibly damaging |
Het |
Sap25 |
A |
G |
5: 137,639,713 (GRCm39) |
E13G |
probably benign |
Het |
Setbp1 |
A |
T |
18: 78,899,860 (GRCm39) |
V1269E |
possibly damaging |
Het |
Smgc |
T |
A |
15: 91,726,109 (GRCm39) |
S18R |
possibly damaging |
Het |
Snrk |
T |
C |
9: 121,993,072 (GRCm39) |
I345T |
probably benign |
Het |
Sp4 |
T |
A |
12: 118,262,976 (GRCm39) |
I357F |
possibly damaging |
Het |
Sra1 |
A |
G |
18: 36,808,031 (GRCm39) |
L399P |
probably damaging |
Het |
Stat6 |
A |
G |
10: 127,494,242 (GRCm39) |
T658A |
probably benign |
Het |
Sv2a |
G |
A |
3: 96,092,339 (GRCm39) |
R13H |
probably benign |
Het |
Thoc3 |
G |
T |
13: 54,608,014 (GRCm39) |
T310N |
probably damaging |
Het |
Tox3 |
A |
C |
8: 91,074,489 (GRCm39) |
|
probably null |
Het |
Trpc6 |
A |
G |
9: 8,680,550 (GRCm39) |
E848G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,538,590 (GRCm39) |
T34703S |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,776,312 (GRCm39) |
I1577V |
probably damaging |
Het |
Ubqln3 |
G |
A |
7: 103,790,674 (GRCm39) |
P472L |
probably benign |
Het |
Ugt2b36 |
C |
T |
5: 87,240,297 (GRCm39) |
W29* |
probably null |
Het |
Wdr17 |
C |
T |
8: 55,113,806 (GRCm39) |
|
probably null |
Het |
Zfp790 |
C |
A |
7: 29,529,514 (GRCm39) |
S733* |
probably null |
Het |
|
Other mutations in Nwd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Nwd1
|
APN |
8 |
73,397,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01294:Nwd1
|
APN |
8 |
73,438,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01298:Nwd1
|
APN |
8 |
73,388,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01333:Nwd1
|
APN |
8 |
73,393,439 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01371:Nwd1
|
APN |
8 |
73,401,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Nwd1
|
APN |
8 |
73,434,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02579:Nwd1
|
APN |
8 |
73,434,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Nwd1
|
APN |
8 |
73,394,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02632:Nwd1
|
APN |
8 |
73,394,082 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02893:Nwd1
|
APN |
8 |
73,394,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Nwd1
|
APN |
8 |
73,414,688 (GRCm39) |
splice site |
probably benign |
|
R0017:Nwd1
|
UTSW |
8 |
73,436,053 (GRCm39) |
splice site |
probably benign |
|
R0066:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R0066:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R0505:Nwd1
|
UTSW |
8 |
73,388,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0511:Nwd1
|
UTSW |
8 |
73,408,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Nwd1
|
UTSW |
8 |
73,394,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R0681:Nwd1
|
UTSW |
8 |
73,388,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0763:Nwd1
|
UTSW |
8 |
73,397,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Nwd1
|
UTSW |
8 |
73,436,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R1136:Nwd1
|
UTSW |
8 |
73,424,397 (GRCm39) |
splice site |
probably benign |
|
R1483:Nwd1
|
UTSW |
8 |
73,383,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R1630:Nwd1
|
UTSW |
8 |
73,393,657 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1724:Nwd1
|
UTSW |
8 |
73,438,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Nwd1
|
UTSW |
8 |
73,393,463 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1885:Nwd1
|
UTSW |
8 |
73,431,622 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Nwd1
|
UTSW |
8 |
73,431,590 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2393:Nwd1
|
UTSW |
8 |
73,389,055 (GRCm39) |
missense |
probably benign |
|
R2926:Nwd1
|
UTSW |
8 |
73,393,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Nwd1
|
UTSW |
8 |
73,393,744 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3916:Nwd1
|
UTSW |
8 |
73,394,439 (GRCm39) |
nonsense |
probably null |
|
R3917:Nwd1
|
UTSW |
8 |
73,394,439 (GRCm39) |
nonsense |
probably null |
|
R4153:Nwd1
|
UTSW |
8 |
73,408,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4426:Nwd1
|
UTSW |
8 |
73,393,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Nwd1
|
UTSW |
8 |
73,414,764 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4522:Nwd1
|
UTSW |
8 |
73,397,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4622:Nwd1
|
UTSW |
8 |
73,393,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Nwd1
|
UTSW |
8 |
73,421,949 (GRCm39) |
missense |
probably benign |
0.03 |
R4694:Nwd1
|
UTSW |
8 |
73,393,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Nwd1
|
UTSW |
8 |
73,383,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Nwd1
|
UTSW |
8 |
73,393,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Nwd1
|
UTSW |
8 |
73,398,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Nwd1
|
UTSW |
8 |
73,431,683 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5183:Nwd1
|
UTSW |
8 |
73,397,714 (GRCm39) |
missense |
probably benign |
0.07 |
R5416:Nwd1
|
UTSW |
8 |
73,393,322 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5553:Nwd1
|
UTSW |
8 |
73,431,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5670:Nwd1
|
UTSW |
8 |
73,419,745 (GRCm39) |
missense |
probably damaging |
0.97 |
R5699:Nwd1
|
UTSW |
8 |
73,429,602 (GRCm39) |
critical splice donor site |
probably null |
|
R5762:Nwd1
|
UTSW |
8 |
73,397,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5778:Nwd1
|
UTSW |
8 |
73,419,745 (GRCm39) |
missense |
probably damaging |
0.97 |
R5992:Nwd1
|
UTSW |
8 |
73,380,201 (GRCm39) |
critical splice donor site |
probably null |
|
R6163:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6164:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6165:Nwd1
|
UTSW |
8 |
73,388,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R6212:Nwd1
|
UTSW |
8 |
73,421,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6443:Nwd1
|
UTSW |
8 |
73,388,994 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6865:Nwd1
|
UTSW |
8 |
73,383,690 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6928:Nwd1
|
UTSW |
8 |
73,408,653 (GRCm39) |
missense |
probably benign |
0.27 |
R6944:Nwd1
|
UTSW |
8 |
73,380,162 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6979:Nwd1
|
UTSW |
8 |
73,394,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Nwd1
|
UTSW |
8 |
73,393,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Nwd1
|
UTSW |
8 |
73,421,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R7265:Nwd1
|
UTSW |
8 |
73,419,556 (GRCm39) |
missense |
probably benign |
0.29 |
R7343:Nwd1
|
UTSW |
8 |
73,438,410 (GRCm39) |
missense |
probably damaging |
0.98 |
R7391:Nwd1
|
UTSW |
8 |
73,389,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R7424:Nwd1
|
UTSW |
8 |
73,401,801 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7438:Nwd1
|
UTSW |
8 |
73,434,458 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:Nwd1
|
UTSW |
8 |
73,393,266 (GRCm39) |
missense |
unknown |
|
R7502:Nwd1
|
UTSW |
8 |
73,434,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R7883:Nwd1
|
UTSW |
8 |
73,393,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8235:Nwd1
|
UTSW |
8 |
73,438,314 (GRCm39) |
frame shift |
probably null |
|
R8282:Nwd1
|
UTSW |
8 |
73,431,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R8672:Nwd1
|
UTSW |
8 |
73,394,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Nwd1
|
UTSW |
8 |
73,388,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Nwd1
|
UTSW |
8 |
73,394,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R8793:Nwd1
|
UTSW |
8 |
73,419,704 (GRCm39) |
missense |
probably benign |
|
R8890:Nwd1
|
UTSW |
8 |
73,438,484 (GRCm39) |
missense |
probably benign |
0.27 |
R9072:Nwd1
|
UTSW |
8 |
73,422,046 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Nwd1
|
UTSW |
8 |
73,422,046 (GRCm39) |
missense |
probably benign |
0.00 |
R9257:Nwd1
|
UTSW |
8 |
73,397,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R9582:Nwd1
|
UTSW |
8 |
73,421,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Nwd1
|
UTSW |
8 |
73,401,106 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Nwd1
|
UTSW |
8 |
73,393,884 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Nwd1
|
UTSW |
8 |
73,398,928 (GRCm39) |
missense |
not run |
|
Z1177:Nwd1
|
UTSW |
8 |
73,436,087 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Nwd1
|
UTSW |
8 |
73,422,015 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1177:Nwd1
|
UTSW |
8 |
73,393,256 (GRCm39) |
missense |
probably damaging |
0.97 |
|