Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adrm1 |
A |
G |
2: 179,814,730 (GRCm39) |
K99E |
unknown |
Het |
Agxt2 |
C |
A |
15: 10,393,830 (GRCm39) |
L375I |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,258,752 (GRCm39) |
S459P |
probably benign |
Het |
Arfgef3 |
T |
A |
10: 18,479,203 (GRCm39) |
T1471S |
probably damaging |
Het |
Atxn2l |
C |
G |
7: 126,092,928 (GRCm39) |
|
probably benign |
Het |
Azi2 |
C |
A |
9: 117,879,044 (GRCm39) |
T141K |
probably damaging |
Het |
B4galt6 |
A |
G |
18: 20,821,422 (GRCm39) |
S369P |
possibly damaging |
Het |
BC051019 |
C |
T |
7: 109,315,233 (GRCm39) |
E341K |
probably damaging |
Het |
Bdh1 |
G |
A |
16: 31,275,712 (GRCm39) |
D278N |
probably benign |
Het |
Cdh1 |
ACTCGAAATGATGTGGCTC |
ACTC |
8: 107,392,870 (GRCm39) |
|
probably benign |
Het |
Cdipt |
T |
G |
7: 126,578,825 (GRCm39) |
D205E |
probably damaging |
Het |
Clec4b1 |
G |
T |
6: 123,046,728 (GRCm39) |
|
probably null |
Het |
Clip4 |
T |
C |
17: 72,138,203 (GRCm39) |
L467S |
probably damaging |
Het |
Cndp2 |
A |
G |
18: 84,693,298 (GRCm39) |
I154T |
probably benign |
Het |
Cyp2j5 |
T |
C |
4: 96,546,977 (GRCm39) |
N179S |
possibly damaging |
Het |
Dpf1 |
A |
T |
7: 29,009,174 (GRCm39) |
I100F |
probably benign |
Het |
Dppa5a |
A |
G |
9: 78,275,165 (GRCm39) |
S46P |
probably benign |
Het |
Epyc |
A |
G |
10: 97,511,607 (GRCm39) |
D200G |
probably benign |
Het |
Ern2 |
C |
T |
7: 121,769,363 (GRCm39) |
A888T |
probably benign |
Het |
Fndc3b |
C |
T |
3: 27,596,253 (GRCm39) |
S112N |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,917,366 (GRCm39) |
V3462A |
probably damaging |
Het |
Fstl5 |
T |
C |
3: 76,615,138 (GRCm39) |
I733T |
probably damaging |
Het |
Gdf3 |
C |
T |
6: 122,586,756 (GRCm39) |
R57Q |
|
Het |
Grwd1 |
A |
T |
7: 45,480,056 (GRCm39) |
D50E |
probably damaging |
Het |
Hgf |
G |
T |
5: 16,798,988 (GRCm39) |
D339Y |
probably benign |
Het |
Kat7 |
T |
C |
11: 95,196,982 (GRCm39) |
D19G |
probably damaging |
Het |
Lefty1 |
A |
G |
1: 180,765,290 (GRCm39) |
E286G |
probably damaging |
Het |
Lrriq3 |
T |
C |
3: 154,893,819 (GRCm39) |
F507L |
probably damaging |
Het |
Mcm4 |
T |
A |
16: 15,448,289 (GRCm39) |
T423S |
probably benign |
Het |
Metap1 |
T |
C |
3: 138,174,643 (GRCm39) |
K247E |
probably benign |
Het |
Muc4 |
T |
G |
16: 32,575,285 (GRCm39) |
I1290S |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,754,017 (GRCm38) |
T1298S |
possibly damaging |
Het |
Ncapg2 |
A |
T |
12: 116,415,983 (GRCm39) |
E1121V |
probably damaging |
Het |
Nebl |
C |
A |
2: 17,397,991 (GRCm39) |
E481* |
probably null |
Het |
Pdap1 |
T |
C |
5: 145,069,672 (GRCm39) |
E111G |
probably damaging |
Het |
Pds5b |
T |
C |
5: 150,643,379 (GRCm39) |
F67S |
probably damaging |
Het |
Pole |
T |
C |
5: 110,445,654 (GRCm39) |
F510S |
probably damaging |
Het |
Ptpn21 |
A |
T |
12: 98,655,396 (GRCm39) |
Y524N |
probably damaging |
Het |
Ptpn4 |
A |
T |
1: 119,595,278 (GRCm39) |
M887K |
probably damaging |
Het |
Sec24b |
T |
C |
3: 129,803,507 (GRCm39) |
D414G |
possibly damaging |
Het |
Sema5b |
C |
A |
16: 35,467,737 (GRCm39) |
|
probably benign |
Het |
Slain1 |
A |
T |
14: 103,923,164 (GRCm39) |
T252S |
probably damaging |
Het |
Slc36a3 |
A |
G |
11: 55,028,137 (GRCm39) |
F164S |
probably damaging |
Het |
Slc39a7 |
T |
C |
17: 34,249,964 (GRCm39) |
H90R |
unknown |
Het |
Slc44a4 |
A |
T |
17: 35,136,508 (GRCm39) |
D58V |
probably damaging |
Het |
Slc5a4a |
A |
G |
10: 76,006,617 (GRCm39) |
T340A |
probably benign |
Het |
Sod2 |
C |
A |
17: 13,233,974 (GRCm39) |
N195K |
probably damaging |
Het |
Spart |
T |
C |
3: 55,035,979 (GRCm39) |
S572P |
possibly damaging |
Het |
Sytl2 |
C |
T |
7: 90,024,810 (GRCm39) |
A266V |
probably benign |
Het |
Tbx15 |
T |
A |
3: 99,222,219 (GRCm39) |
D227E |
probably damaging |
Het |
Tfap2a |
A |
G |
13: 40,882,308 (GRCm39) |
V26A |
probably benign |
Het |
Trank1 |
T |
A |
9: 111,208,003 (GRCm39) |
F1749L |
possibly damaging |
Het |
Trpc6 |
A |
G |
9: 8,643,411 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,706,924 (GRCm39) |
I9089N |
unknown |
Het |
Tut7 |
A |
G |
13: 59,947,942 (GRCm39) |
V793A |
probably benign |
Het |
Unc13a |
T |
C |
8: 72,103,835 (GRCm39) |
T866A |
probably benign |
Het |
Vmn1r212 |
T |
A |
13: 23,067,494 (GRCm39) |
S280C |
possibly damaging |
Het |
Vmn2r82 |
A |
G |
10: 79,232,541 (GRCm39) |
T847A |
probably benign |
Het |
Zer1 |
A |
G |
2: 30,000,881 (GRCm39) |
L180P |
probably damaging |
Het |
Zfp445 |
T |
G |
9: 122,682,732 (GRCm39) |
Y403S |
probably benign |
Het |
|
Other mutations in Nars1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01012:Nars1
|
APN |
18 |
64,638,039 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01962:Nars1
|
APN |
18 |
64,643,554 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01968:Nars1
|
APN |
18 |
64,640,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Nars1
|
APN |
18 |
64,643,606 (GRCm39) |
splice site |
probably benign |
|
IGL02366:Nars1
|
APN |
18 |
64,636,599 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02948:Nars1
|
APN |
18 |
64,638,266 (GRCm39) |
missense |
possibly damaging |
0.66 |
FR4976:Nars1
|
UTSW |
18 |
64,643,516 (GRCm39) |
critical splice donor site |
probably benign |
|
R0591:Nars1
|
UTSW |
18 |
64,633,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Nars1
|
UTSW |
18 |
64,645,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Nars1
|
UTSW |
18 |
64,649,485 (GRCm39) |
critical splice donor site |
probably null |
|
R1954:Nars1
|
UTSW |
18 |
64,633,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Nars1
|
UTSW |
18 |
64,638,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Nars1
|
UTSW |
18 |
64,638,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R3433:Nars1
|
UTSW |
18 |
64,642,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R4378:Nars1
|
UTSW |
18 |
64,634,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Nars1
|
UTSW |
18 |
64,638,302 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4737:Nars1
|
UTSW |
18 |
64,649,498 (GRCm39) |
missense |
probably benign |
|
R4877:Nars1
|
UTSW |
18 |
64,633,643 (GRCm39) |
nonsense |
probably null |
|
R5950:Nars1
|
UTSW |
18 |
64,643,556 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6434:Nars1
|
UTSW |
18 |
64,640,872 (GRCm39) |
missense |
probably benign |
0.01 |
R6920:Nars1
|
UTSW |
18 |
64,634,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7082:Nars1
|
UTSW |
18 |
64,637,425 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7132:Nars1
|
UTSW |
18 |
64,640,841 (GRCm39) |
critical splice donor site |
probably null |
|
R7504:Nars1
|
UTSW |
18 |
64,645,093 (GRCm39) |
missense |
probably benign |
0.22 |
R8120:Nars1
|
UTSW |
18 |
64,637,422 (GRCm39) |
missense |
probably benign |
0.19 |
R8343:Nars1
|
UTSW |
18 |
64,637,458 (GRCm39) |
missense |
probably benign |
0.01 |
R8429:Nars1
|
UTSW |
18 |
64,634,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R9321:Nars1
|
UTSW |
18 |
64,637,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Nars1
|
UTSW |
18 |
64,642,327 (GRCm39) |
missense |
probably benign |
0.30 |
|