Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
A |
5: 125,583,362 (GRCm39) |
|
probably null |
Het |
Arhgef1 |
A |
G |
7: 24,623,156 (GRCm39) |
I423V |
probably benign |
Het |
Aspm |
T |
C |
1: 139,408,280 (GRCm39) |
L2389P |
probably damaging |
Het |
B4galt1 |
T |
C |
4: 40,812,860 (GRCm39) |
M222V |
probably benign |
Het |
Bsn |
C |
A |
9: 107,985,016 (GRCm39) |
G3013C |
unknown |
Het |
Camsap2 |
T |
C |
1: 136,232,187 (GRCm39) |
H136R |
probably damaging |
Het |
Ccar1 |
A |
G |
10: 62,582,715 (GRCm39) |
V1047A |
unknown |
Het |
Ccdc80 |
A |
G |
16: 44,915,445 (GRCm39) |
E67G |
probably benign |
Het |
Ces3b |
G |
T |
8: 105,819,710 (GRCm39) |
G511V |
probably damaging |
Het |
Cops6 |
T |
A |
5: 138,161,790 (GRCm39) |
H224Q |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,235,866 (GRCm39) |
D331V |
probably damaging |
Het |
Dusp29 |
T |
C |
14: 21,727,135 (GRCm39) |
D171G |
probably damaging |
Het |
Echs1 |
G |
A |
7: 139,688,007 (GRCm39) |
T266I |
probably damaging |
Het |
Ehmt2 |
G |
A |
17: 35,130,406 (GRCm39) |
C1017Y |
probably damaging |
Het |
Epb41l5 |
C |
T |
1: 119,536,859 (GRCm39) |
R344Q |
probably damaging |
Het |
Fcgbp |
G |
A |
7: 27,791,477 (GRCm39) |
V913I |
probably benign |
Het |
Foxd4 |
A |
G |
19: 24,877,240 (GRCm39) |
F320S |
probably damaging |
Het |
Frmpd4 |
C |
T |
X: 166,387,579 (GRCm39) |
R133K |
probably damaging |
Het |
Glmp |
A |
G |
3: 88,233,917 (GRCm39) |
Y258C |
probably damaging |
Het |
Gphn |
C |
G |
12: 78,538,955 (GRCm39) |
S200R |
possibly damaging |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
H2-Q7 |
T |
G |
17: 35,658,560 (GRCm39) |
M66R |
probably benign |
Het |
Hivep2 |
T |
A |
10: 14,004,058 (GRCm39) |
C219S |
probably damaging |
Het |
Hlcs |
A |
T |
16: 93,942,261 (GRCm39) |
M90K |
possibly damaging |
Het |
Itga8 |
C |
A |
2: 12,160,182 (GRCm39) |
|
probably null |
Het |
Klrk1 |
T |
A |
6: 129,598,203 (GRCm39) |
M1L |
possibly damaging |
Het |
Kmo |
T |
A |
1: 175,485,941 (GRCm39) |
F385I |
probably benign |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrrc3c |
A |
G |
11: 98,490,075 (GRCm39) |
D144G |
probably damaging |
Het |
Lyzl4 |
C |
T |
9: 121,412,047 (GRCm39) |
W123* |
probably null |
Het |
Map3k1 |
A |
G |
13: 111,909,246 (GRCm39) |
S77P |
probably benign |
Het |
Mark1 |
T |
C |
1: 184,630,984 (GRCm39) |
T709A |
probably damaging |
Het |
Nbr1 |
A |
T |
11: 101,468,777 (GRCm39) |
I878F |
probably damaging |
Het |
Nedd1 |
A |
T |
10: 92,547,168 (GRCm39) |
H118Q |
probably damaging |
Het |
Nfatc1 |
C |
T |
18: 80,678,770 (GRCm39) |
G873S |
probably damaging |
Het |
Ngly1 |
T |
G |
14: 16,283,467 (GRCm38) |
N415K |
probably damaging |
Het |
Nol6 |
C |
A |
4: 41,118,962 (GRCm39) |
R677L |
probably damaging |
Het |
Nop9 |
T |
C |
14: 55,990,270 (GRCm39) |
V471A |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,802,577 (GRCm39) |
N1333D |
probably benign |
Het |
Or10x4 |
T |
A |
1: 174,219,407 (GRCm39) |
Y257* |
probably null |
Het |
Or1ad8 |
T |
A |
11: 50,898,153 (GRCm39) |
M118K |
probably damaging |
Het |
Or5m9b |
T |
C |
2: 85,905,264 (GRCm39) |
F60S |
probably damaging |
Het |
Or8g34 |
A |
T |
9: 39,373,159 (GRCm39) |
Y144F |
probably benign |
Het |
Pcp4l1 |
T |
C |
1: 171,002,022 (GRCm39) |
E46G |
possibly damaging |
Het |
Plek2 |
T |
C |
12: 78,936,083 (GRCm39) |
|
probably null |
Het |
Rbl1 |
T |
G |
2: 157,030,206 (GRCm39) |
I434L |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,581,834 (GRCm39) |
V4777A |
possibly damaging |
Het |
Sgk1 |
T |
C |
10: 21,758,593 (GRCm39) |
F19S |
probably damaging |
Het |
Stard9 |
C |
T |
2: 120,532,677 (GRCm39) |
A2978V |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,033,940 (GRCm39) |
T7711A |
probably benign |
Het |
Taf10 |
G |
A |
7: 105,393,383 (GRCm39) |
T48I |
probably benign |
Het |
Tgfbi |
T |
G |
13: 56,784,989 (GRCm39) |
S649A |
possibly damaging |
Het |
Thbs3 |
T |
C |
3: 89,132,171 (GRCm39) |
V749A |
probably benign |
Het |
Tmem241 |
G |
T |
18: 12,180,641 (GRCm39) |
H218N |
possibly damaging |
Het |
Tmem266 |
C |
T |
9: 55,284,851 (GRCm39) |
|
probably benign |
Het |
Tnc |
T |
C |
4: 63,900,982 (GRCm39) |
I1586M |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,164,442 (GRCm39) |
C2676* |
probably null |
Het |
Unc13a |
A |
T |
8: 72,105,021 (GRCm39) |
I747N |
probably damaging |
Het |
Vangl1 |
A |
T |
3: 102,073,097 (GRCm39) |
|
probably benign |
Het |
Vmn1r184 |
C |
T |
7: 25,966,563 (GRCm39) |
T103I |
possibly damaging |
Het |
Vmn1r204 |
T |
C |
13: 22,740,474 (GRCm39) |
V35A |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,448,835 (GRCm39) |
H603R |
possibly damaging |
Het |
Zfp105 |
A |
G |
9: 122,754,303 (GRCm39) |
D44G |
probably benign |
Het |
Zfp11 |
T |
C |
5: 129,735,152 (GRCm39) |
H103R |
probably damaging |
Het |
Zfp335 |
A |
G |
2: 164,736,795 (GRCm39) |
F947L |
possibly damaging |
Het |
|
Other mutations in Nsun2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Nsun2
|
APN |
13 |
69,771,368 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01997:Nsun2
|
APN |
13 |
69,771,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Nsun2
|
APN |
13 |
69,767,658 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03038:Nsun2
|
APN |
13 |
69,767,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02984:Nsun2
|
UTSW |
13 |
69,691,727 (GRCm39) |
intron |
probably benign |
|
PIT4494001:Nsun2
|
UTSW |
13 |
69,766,311 (GRCm39) |
critical splice donor site |
probably null |
|
R0601:Nsun2
|
UTSW |
13 |
69,781,361 (GRCm39) |
missense |
probably benign |
0.40 |
R0648:Nsun2
|
UTSW |
13 |
69,775,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Nsun2
|
UTSW |
13 |
69,777,661 (GRCm39) |
missense |
probably benign |
|
R0718:Nsun2
|
UTSW |
13 |
69,691,816 (GRCm39) |
intron |
probably benign |
|
R1501:Nsun2
|
UTSW |
13 |
69,779,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Nsun2
|
UTSW |
13 |
69,775,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Nsun2
|
UTSW |
13 |
69,775,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Nsun2
|
UTSW |
13 |
69,775,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2327:Nsun2
|
UTSW |
13 |
69,767,700 (GRCm39) |
missense |
probably benign |
0.44 |
R2872:Nsun2
|
UTSW |
13 |
69,777,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Nsun2
|
UTSW |
13 |
69,777,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R3689:Nsun2
|
UTSW |
13 |
69,760,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3691:Nsun2
|
UTSW |
13 |
69,760,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Nsun2
|
UTSW |
13 |
69,777,757 (GRCm39) |
missense |
probably benign |
|
R3918:Nsun2
|
UTSW |
13 |
69,778,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4065:Nsun2
|
UTSW |
13 |
69,760,579 (GRCm39) |
critical splice donor site |
probably null |
|
R4231:Nsun2
|
UTSW |
13 |
69,767,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R4445:Nsun2
|
UTSW |
13 |
69,777,840 (GRCm39) |
splice site |
probably null |
|
R4872:Nsun2
|
UTSW |
13 |
69,691,992 (GRCm39) |
intron |
probably benign |
|
R5641:Nsun2
|
UTSW |
13 |
69,771,368 (GRCm39) |
missense |
probably benign |
0.01 |
R5718:Nsun2
|
UTSW |
13 |
69,771,403 (GRCm39) |
missense |
probably benign |
0.19 |
R5976:Nsun2
|
UTSW |
13 |
69,771,271 (GRCm39) |
splice site |
probably null |
|
R6110:Nsun2
|
UTSW |
13 |
69,775,767 (GRCm39) |
missense |
probably benign |
0.01 |
R6968:Nsun2
|
UTSW |
13 |
69,779,409 (GRCm39) |
missense |
probably benign |
0.00 |
R7146:Nsun2
|
UTSW |
13 |
69,774,672 (GRCm39) |
critical splice donor site |
probably null |
|
R7456:Nsun2
|
UTSW |
13 |
69,781,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R8017:Nsun2
|
UTSW |
13 |
69,775,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8019:Nsun2
|
UTSW |
13 |
69,775,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8225:Nsun2
|
UTSW |
13 |
69,760,493 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8935:Nsun2
|
UTSW |
13 |
69,767,586 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Nsun2
|
UTSW |
13 |
69,763,638 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Nsun2
|
UTSW |
13 |
69,763,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|