Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
G |
A |
8: 43,973,832 (GRCm39) |
T390I |
probably benign |
Het |
Adgb |
A |
G |
10: 10,287,456 (GRCm39) |
|
probably null |
Het |
Ado |
G |
T |
10: 67,384,265 (GRCm39) |
Y113* |
probably null |
Het |
Angptl1 |
A |
G |
1: 156,672,885 (GRCm39) |
E237G |
probably damaging |
Het |
Arid2 |
T |
A |
15: 96,254,578 (GRCm39) |
Y141* |
probably null |
Het |
Clvs1 |
T |
C |
4: 9,350,739 (GRCm39) |
I183T |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,014,295 (GRCm39) |
K1817E |
probably benign |
Het |
Eif3e |
C |
A |
15: 43,126,642 (GRCm39) |
R271L |
probably damaging |
Het |
Eml6 |
A |
G |
11: 29,703,085 (GRCm39) |
V1611A |
probably damaging |
Het |
Enpp3 |
G |
T |
10: 24,660,739 (GRCm39) |
Y634* |
probably null |
Het |
Evi5l |
C |
T |
8: 4,250,886 (GRCm39) |
R394W |
probably damaging |
Het |
Fcgr3 |
A |
C |
1: 170,881,661 (GRCm39) |
F156V |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,661,402 (GRCm39) |
T294S |
probably benign |
Het |
Gabrb3 |
A |
G |
7: 57,466,203 (GRCm39) |
Q339R |
probably damaging |
Het |
Gen1 |
T |
A |
12: 11,292,167 (GRCm39) |
T606S |
probably benign |
Het |
Golm1 |
A |
G |
13: 59,788,071 (GRCm39) |
V276A |
probably benign |
Het |
Hc |
C |
A |
2: 34,914,161 (GRCm39) |
V849F |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,459,627 (GRCm39) |
I832T |
possibly damaging |
Het |
Hspa14 |
T |
C |
2: 3,497,643 (GRCm39) |
D283G |
probably damaging |
Het |
Lztfl1 |
C |
T |
9: 123,541,536 (GRCm39) |
W94* |
probably null |
Het |
Lzts3 |
T |
C |
2: 130,477,306 (GRCm39) |
S381G |
probably benign |
Het |
Mgat2 |
A |
G |
12: 69,231,444 (GRCm39) |
Y6C |
probably damaging |
Het |
Mrpl30 |
T |
C |
1: 37,934,439 (GRCm39) |
I27T |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,406,966 (GRCm39) |
T1045S |
unknown |
Het |
Nlrp4a |
G |
A |
7: 26,148,690 (GRCm39) |
R99Q |
probably benign |
Het |
Or10g1 |
T |
C |
14: 52,647,945 (GRCm39) |
Y128C |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,006 (GRCm39) |
T18A |
possibly damaging |
Het |
Phlpp1 |
T |
C |
1: 106,209,132 (GRCm39) |
L495P |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,109,776 (GRCm39) |
D178G |
possibly damaging |
Het |
Prl5a1 |
C |
G |
13: 28,333,997 (GRCm39) |
L167V |
probably damaging |
Het |
Sardh |
A |
G |
2: 27,087,651 (GRCm39) |
V740A |
probably benign |
Het |
Sbno1 |
T |
G |
5: 124,543,709 (GRCm39) |
T277P |
probably benign |
Het |
Slc2a1 |
T |
C |
4: 118,993,462 (GRCm39) |
V433A |
probably damaging |
Het |
Slc4a10 |
T |
C |
2: 62,134,308 (GRCm39) |
V1008A |
possibly damaging |
Het |
Smarcal1 |
T |
G |
1: 72,625,179 (GRCm39) |
S109A |
probably benign |
Het |
Speg |
A |
G |
1: 75,377,834 (GRCm39) |
D864G |
probably benign |
Het |
Steap4 |
T |
C |
5: 8,026,976 (GRCm39) |
I313T |
probably benign |
Het |
Tab2 |
A |
T |
10: 7,786,869 (GRCm39) |
D614E |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,544,610 (GRCm39) |
K2246E |
probably damaging |
Het |
Timm23 |
A |
G |
14: 31,902,520 (GRCm39) |
S208P |
probably damaging |
Het |
Tmem229a |
C |
A |
6: 24,955,211 (GRCm39) |
C181F |
probably benign |
Het |
Ugdh |
T |
C |
5: 65,574,958 (GRCm39) |
Y356C |
probably damaging |
Het |
Ugt2a1 |
A |
G |
5: 87,634,586 (GRCm39) |
L7P |
probably damaging |
Het |
Uhrf1 |
A |
G |
17: 56,619,905 (GRCm39) |
D272G |
possibly damaging |
Het |
Vmn1r206 |
T |
A |
13: 22,804,827 (GRCm39) |
I127F |
probably damaging |
Het |
Vmn2r106 |
T |
C |
17: 20,505,490 (GRCm39) |
Y68C |
possibly damaging |
Het |
Zfand6 |
G |
A |
7: 84,283,141 (GRCm39) |
P72L |
not run |
Het |
|
Other mutations in Gfod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02402:Gfod1
|
APN |
13 |
43,354,211 (GRCm39) |
missense |
probably benign |
|
R0483:Gfod1
|
UTSW |
13 |
43,354,012 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0959:Gfod1
|
UTSW |
13 |
43,456,905 (GRCm39) |
missense |
probably benign |
|
R1913:Gfod1
|
UTSW |
13 |
43,456,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R1927:Gfod1
|
UTSW |
13 |
43,354,336 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2061:Gfod1
|
UTSW |
13 |
43,456,719 (GRCm39) |
critical splice donor site |
probably null |
|
R2154:Gfod1
|
UTSW |
13 |
43,456,946 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2370:Gfod1
|
UTSW |
13 |
43,354,621 (GRCm39) |
missense |
probably benign |
0.04 |
R3956:Gfod1
|
UTSW |
13 |
43,354,538 (GRCm39) |
missense |
probably damaging |
0.98 |
R5061:Gfod1
|
UTSW |
13 |
43,353,992 (GRCm39) |
missense |
probably benign |
0.01 |
R6090:Gfod1
|
UTSW |
13 |
43,354,437 (GRCm39) |
nonsense |
probably null |
|
R6156:Gfod1
|
UTSW |
13 |
43,354,514 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6573:Gfod1
|
UTSW |
13 |
43,353,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R8353:Gfod1
|
UTSW |
13 |
43,354,366 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9063:Gfod1
|
UTSW |
13 |
43,354,280 (GRCm39) |
missense |
probably benign |
0.35 |
R9087:Gfod1
|
UTSW |
13 |
43,353,838 (GRCm39) |
missense |
probably damaging |
0.96 |
R9090:Gfod1
|
UTSW |
13 |
43,456,861 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9271:Gfod1
|
UTSW |
13 |
43,456,861 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9380:Gfod1
|
UTSW |
13 |
43,354,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|