Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt2 |
T |
C |
4: 154,751,162 (GRCm39) |
K325E |
probably benign |
Het |
Arc |
C |
T |
15: 74,544,204 (GRCm39) |
M6I |
probably benign |
Het |
Atp7b |
A |
T |
8: 22,484,844 (GRCm39) |
D1404E |
probably benign |
Het |
Cdk5rap1 |
T |
A |
2: 154,207,956 (GRCm39) |
N156I |
probably damaging |
Het |
Ctsa |
T |
C |
2: 164,676,230 (GRCm39) |
|
probably benign |
Het |
Depdc1b |
T |
G |
13: 108,498,861 (GRCm39) |
N181K |
probably benign |
Het |
Epg5 |
T |
C |
18: 78,062,489 (GRCm39) |
V1994A |
probably damaging |
Het |
Epyc |
T |
A |
10: 97,517,099 (GRCm39) |
C312* |
probably null |
Het |
Erv3 |
T |
A |
2: 131,697,877 (GRCm39) |
R161* |
probably null |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gfra3 |
T |
C |
18: 34,824,644 (GRCm39) |
T280A |
possibly damaging |
Het |
Gtf3c4 |
G |
A |
2: 28,725,100 (GRCm39) |
R211C |
probably damaging |
Het |
Hrob |
T |
C |
11: 102,146,422 (GRCm39) |
C233R |
probably benign |
Het |
Hsh2d |
A |
G |
8: 72,947,351 (GRCm39) |
D16G |
probably damaging |
Het |
Klk15 |
T |
A |
7: 43,588,262 (GRCm39) |
M190K |
probably damaging |
Het |
Klri1 |
A |
G |
6: 129,694,010 (GRCm39) |
S26P |
possibly damaging |
Het |
Krt78 |
T |
A |
15: 101,859,402 (GRCm39) |
D265V |
probably damaging |
Het |
Lgr5 |
A |
C |
10: 115,298,607 (GRCm39) |
I355S |
probably damaging |
Het |
Lig3 |
T |
A |
11: 82,685,367 (GRCm39) |
V595D |
probably damaging |
Het |
Map2k6 |
A |
C |
11: 110,403,695 (GRCm39) |
|
probably benign |
Het |
Mdm4 |
A |
G |
1: 132,922,285 (GRCm39) |
S286P |
probably benign |
Het |
Ncoa4-ps |
T |
C |
12: 119,226,231 (GRCm39) |
|
noncoding transcript |
Het |
Or2ak7 |
A |
G |
11: 58,575,095 (GRCm39) |
Y132C |
probably damaging |
Het |
Pofut1 |
T |
A |
2: 153,090,448 (GRCm39) |
M114K |
probably damaging |
Het |
Rdh13 |
C |
T |
7: 4,433,388 (GRCm39) |
|
probably null |
Het |
Reg3g |
T |
A |
6: 78,443,816 (GRCm39) |
I131F |
probably benign |
Het |
Slc26a4 |
C |
T |
12: 31,578,853 (GRCm39) |
|
probably benign |
Het |
Slc8a2 |
T |
A |
7: 15,892,818 (GRCm39) |
F827I |
probably damaging |
Het |
Slfn9 |
A |
T |
11: 82,878,200 (GRCm39) |
C310S |
probably damaging |
Het |
Sypl1 |
A |
G |
12: 33,025,641 (GRCm39) |
Y235C |
probably damaging |
Het |
Trav7-4 |
A |
T |
14: 53,699,098 (GRCm39) |
T82S |
possibly damaging |
Het |
Trim28 |
T |
A |
7: 12,764,629 (GRCm39) |
V782D |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,575,242 (GRCm39) |
T25217M |
probably damaging |
Het |
Usp6nl |
A |
G |
2: 6,432,381 (GRCm39) |
T260A |
possibly damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,366,009 (GRCm39) |
N308K |
probably benign |
Het |
Xdh |
T |
C |
17: 74,207,275 (GRCm39) |
E986G |
probably benign |
Het |
Zfp770 |
T |
C |
2: 114,026,719 (GRCm39) |
D450G |
probably damaging |
Het |
Zw10 |
T |
G |
9: 48,980,915 (GRCm39) |
S438R |
probably benign |
Het |
|
Other mutations in Gldn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00585:Gldn
|
APN |
9 |
54,245,748 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02425:Gldn
|
APN |
9 |
54,246,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2284:Gldn
|
UTSW |
9 |
54,193,849 (GRCm39) |
nonsense |
probably null |
|
R2902:Gldn
|
UTSW |
9 |
54,243,098 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3055:Gldn
|
UTSW |
9 |
54,245,807 (GRCm39) |
missense |
probably damaging |
0.96 |
R3683:Gldn
|
UTSW |
9 |
54,245,624 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3684:Gldn
|
UTSW |
9 |
54,245,624 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3732:Gldn
|
UTSW |
9 |
54,245,946 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3732:Gldn
|
UTSW |
9 |
54,245,946 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3733:Gldn
|
UTSW |
9 |
54,245,946 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3734:Gldn
|
UTSW |
9 |
54,245,946 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4668:Gldn
|
UTSW |
9 |
54,239,302 (GRCm39) |
nonsense |
probably null |
|
R5228:Gldn
|
UTSW |
9 |
54,242,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R5574:Gldn
|
UTSW |
9 |
54,220,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Gldn
|
UTSW |
9 |
54,241,775 (GRCm39) |
critical splice donor site |
probably null |
|
R5926:Gldn
|
UTSW |
9 |
54,245,722 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5943:Gldn
|
UTSW |
9 |
54,245,721 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6331:Gldn
|
UTSW |
9 |
54,194,162 (GRCm39) |
missense |
probably benign |
0.32 |
R6671:Gldn
|
UTSW |
9 |
54,245,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6821:Gldn
|
UTSW |
9 |
54,246,054 (GRCm39) |
missense |
probably benign |
0.01 |
R6897:Gldn
|
UTSW |
9 |
54,242,158 (GRCm39) |
splice site |
probably null |
|
R7579:Gldn
|
UTSW |
9 |
54,245,648 (GRCm39) |
missense |
probably benign |
0.21 |
R7604:Gldn
|
UTSW |
9 |
54,245,877 (GRCm39) |
missense |
probably benign |
|
R7705:Gldn
|
UTSW |
9 |
54,245,976 (GRCm39) |
missense |
probably benign |
0.00 |
R9036:Gldn
|
UTSW |
9 |
54,245,747 (GRCm39) |
missense |
probably benign |
0.00 |
R9672:Gldn
|
UTSW |
9 |
54,245,780 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Gldn
|
UTSW |
9 |
54,193,944 (GRCm39) |
missense |
probably benign |
0.37 |
|