Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,056,301 (GRCm39) |
T229S |
probably benign |
Het |
Adrb3 |
T |
C |
8: 27,717,348 (GRCm39) |
E367G |
probably benign |
Het |
Ak9 |
T |
A |
10: 41,233,653 (GRCm39) |
N630K |
probably damaging |
Het |
Atp8b1 |
T |
C |
18: 64,694,733 (GRCm39) |
I516M |
possibly damaging |
Het |
Bcor |
C |
T |
X: 11,906,725 (GRCm39) |
R1551Q |
probably damaging |
Het |
Cry1 |
T |
A |
10: 84,969,150 (GRCm39) |
H558L |
probably benign |
Het |
Cstdc3 |
A |
T |
16: 36,132,918 (GRCm39) |
H65L |
probably damaging |
Het |
Cyp3a57 |
T |
A |
5: 145,305,893 (GRCm39) |
W126R |
probably damaging |
Het |
Dhx36 |
A |
T |
3: 62,401,201 (GRCm39) |
V355E |
probably damaging |
Het |
Dpp6 |
A |
G |
5: 27,604,013 (GRCm39) |
|
probably benign |
Het |
Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
Enpp2 |
T |
C |
15: 54,710,692 (GRCm39) |
D694G |
probably benign |
Het |
Esrp2 |
T |
C |
8: 106,859,930 (GRCm39) |
E336G |
probably damaging |
Het |
Faah |
A |
T |
4: 115,857,938 (GRCm39) |
|
probably benign |
Het |
Fat1 |
G |
A |
8: 45,478,846 (GRCm39) |
G2608R |
probably benign |
Het |
Fbxo8 |
A |
T |
8: 57,022,354 (GRCm39) |
Y122F |
probably damaging |
Het |
Fgd5 |
A |
G |
6: 92,051,215 (GRCm39) |
D1497G |
probably damaging |
Het |
Fn3krp |
T |
C |
11: 121,320,410 (GRCm39) |
F252L |
probably damaging |
Het |
Fnip2 |
T |
C |
3: 79,389,084 (GRCm39) |
Y549C |
probably damaging |
Het |
Gcm2 |
T |
C |
13: 41,257,131 (GRCm39) |
N206S |
probably benign |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
H2-T10 |
T |
A |
17: 36,429,843 (GRCm39) |
|
probably null |
Het |
Henmt1 |
T |
C |
3: 108,847,366 (GRCm39) |
|
probably null |
Het |
Man1b1 |
T |
A |
2: 25,233,365 (GRCm39) |
L246Q |
probably damaging |
Het |
Mdh2 |
T |
C |
5: 135,812,329 (GRCm39) |
|
probably null |
Het |
Mocos |
T |
C |
18: 24,787,109 (GRCm39) |
F43L |
probably damaging |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Naip5 |
T |
A |
13: 100,359,914 (GRCm39) |
I441F |
possibly damaging |
Het |
Naip6 |
C |
T |
13: 100,437,108 (GRCm39) |
A472T |
probably benign |
Het |
Ncoa2 |
A |
T |
1: 13,245,396 (GRCm39) |
M434K |
possibly damaging |
Het |
Nlrp4g |
T |
A |
9: 124,350,394 (GRCm38) |
|
noncoding transcript |
Het |
Or14j8 |
T |
A |
17: 38,263,255 (GRCm39) |
Q220L |
probably benign |
Het |
Or9a2 |
G |
T |
6: 41,748,706 (GRCm39) |
H176N |
possibly damaging |
Het |
Pals2 |
T |
A |
6: 50,155,495 (GRCm39) |
W259R |
probably damaging |
Het |
Pars2 |
A |
G |
4: 106,511,735 (GRCm39) |
T506A |
probably benign |
Het |
Pkp2 |
T |
C |
16: 16,078,200 (GRCm39) |
S481P |
probably damaging |
Het |
Plod3 |
T |
C |
5: 137,020,161 (GRCm39) |
W459R |
probably damaging |
Het |
Pramel13 |
A |
T |
4: 144,121,482 (GRCm39) |
L181M |
probably damaging |
Het |
Prdm10 |
A |
T |
9: 31,251,714 (GRCm39) |
I361F |
possibly damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Raver2 |
T |
C |
4: 100,959,921 (GRCm39) |
C134R |
probably damaging |
Het |
Rnf130 |
G |
C |
11: 49,943,722 (GRCm39) |
A123P |
probably damaging |
Het |
Slc29a4 |
G |
A |
5: 142,707,207 (GRCm39) |
A517T |
possibly damaging |
Het |
Slc38a6 |
T |
A |
12: 73,376,759 (GRCm39) |
S138T |
possibly damaging |
Het |
Spred1 |
T |
C |
2: 117,008,102 (GRCm39) |
V336A |
possibly damaging |
Het |
Sptlc3 |
T |
A |
2: 139,473,263 (GRCm39) |
M504K |
probably benign |
Het |
Syt11 |
T |
C |
3: 88,655,149 (GRCm39) |
D78G |
probably damaging |
Het |
Trim23 |
C |
T |
13: 104,317,682 (GRCm39) |
T61I |
probably damaging |
Het |
Tsg101 |
T |
C |
7: 46,542,174 (GRCm39) |
T260A |
probably damaging |
Het |
Tyw5 |
T |
C |
1: 57,440,618 (GRCm39) |
Y48C |
probably damaging |
Het |
Utp25 |
G |
T |
1: 192,796,089 (GRCm39) |
T192K |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
Vmn2r89 |
C |
A |
14: 51,693,620 (GRCm39) |
H323Q |
possibly damaging |
Het |
Vps18 |
A |
G |
2: 119,123,423 (GRCm39) |
S117G |
probably benign |
Het |
Zfp93 |
C |
G |
7: 23,975,757 (GRCm39) |
Q581E |
probably damaging |
Het |
|
Other mutations in Nars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00796:Nars2
|
APN |
7 |
96,680,787 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00796:Nars2
|
APN |
7 |
96,680,786 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Nars2
|
APN |
7 |
96,651,997 (GRCm39) |
splice site |
probably benign |
|
IGL02954:Nars2
|
APN |
7 |
96,689,100 (GRCm39) |
splice site |
probably null |
|
IGL03256:Nars2
|
APN |
7 |
96,689,117 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03394:Nars2
|
APN |
7 |
96,689,220 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0600:Nars2
|
UTSW |
7 |
96,689,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0943:Nars2
|
UTSW |
7 |
96,605,138 (GRCm39) |
splice site |
probably benign |
|
R1389:Nars2
|
UTSW |
7 |
96,652,036 (GRCm39) |
missense |
probably benign |
|
R4076:Nars2
|
UTSW |
7 |
96,607,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R4397:Nars2
|
UTSW |
7 |
96,622,771 (GRCm39) |
critical splice donor site |
probably null |
|
R4758:Nars2
|
UTSW |
7 |
96,622,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Nars2
|
UTSW |
7 |
96,684,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Nars2
|
UTSW |
7 |
96,672,948 (GRCm39) |
missense |
probably benign |
0.07 |
R6209:Nars2
|
UTSW |
7 |
96,706,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Nars2
|
UTSW |
7 |
96,689,137 (GRCm39) |
missense |
probably benign |
0.40 |
R7979:Nars2
|
UTSW |
7 |
96,711,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8284:Nars2
|
UTSW |
7 |
96,600,845 (GRCm39) |
utr 5 prime |
probably benign |
|
R8885:Nars2
|
UTSW |
7 |
96,652,095 (GRCm39) |
missense |
probably damaging |
0.98 |
R9614:Nars2
|
UTSW |
7 |
96,689,125 (GRCm39) |
missense |
probably damaging |
0.99 |
R9658:Nars2
|
UTSW |
7 |
96,689,178 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nars2
|
UTSW |
7 |
96,601,104 (GRCm39) |
missense |
probably benign |
0.04 |
|