Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
G |
13: 81,707,543 (GRCm39) |
F568L |
probably benign |
Het |
AW112010 |
T |
A |
19: 11,025,741 (GRCm39) |
|
noncoding transcript |
Het |
Bbs4 |
A |
T |
9: 59,237,729 (GRCm39) |
L205H |
probably benign |
Het |
Bmal2 |
T |
C |
6: 146,711,266 (GRCm39) |
V90A |
possibly damaging |
Het |
C2cd2l |
T |
C |
9: 44,227,878 (GRCm39) |
K121R |
probably benign |
Het |
Car14 |
A |
G |
3: 95,806,870 (GRCm39) |
V198A |
possibly damaging |
Het |
Cd22 |
G |
T |
7: 30,576,955 (GRCm39) |
H117Q |
possibly damaging |
Het |
Celf1 |
T |
A |
2: 90,829,068 (GRCm39) |
I45N |
probably damaging |
Het |
Cluh |
T |
C |
11: 74,547,997 (GRCm39) |
S103P |
probably damaging |
Het |
Cyp39a1 |
T |
A |
17: 44,002,613 (GRCm39) |
L276Q |
probably benign |
Het |
Ddx27 |
T |
G |
2: 166,857,245 (GRCm39) |
|
probably benign |
Het |
Defb4 |
A |
T |
8: 19,251,279 (GRCm39) |
I49F |
possibly damaging |
Het |
Dock8 |
C |
A |
19: 25,055,509 (GRCm39) |
T157K |
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,839,541 (GRCm39) |
V352A |
probably damaging |
Het |
Elmo2 |
C |
T |
2: 165,139,312 (GRCm39) |
E412K |
probably damaging |
Het |
Eme1 |
G |
A |
11: 94,541,733 (GRCm39) |
P30S |
possibly damaging |
Het |
Espnl |
G |
T |
1: 91,272,535 (GRCm39) |
A632S |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,872,704 (GRCm39) |
K2432M |
probably damaging |
Het |
Idua |
T |
C |
5: 108,827,657 (GRCm39) |
L157P |
probably damaging |
Het |
Ifi207 |
T |
A |
1: 173,555,159 (GRCm39) |
D848V |
probably damaging |
Het |
Jag1 |
C |
T |
2: 136,927,858 (GRCm39) |
S851N |
possibly damaging |
Het |
Kat6b |
T |
A |
14: 21,681,415 (GRCm39) |
F571I |
probably damaging |
Het |
Lrrc74b |
G |
A |
16: 17,376,028 (GRCm39) |
|
probably benign |
Het |
Mst1r |
A |
G |
9: 107,794,026 (GRCm39) |
K1160E |
probably damaging |
Het |
Muc19 |
C |
A |
15: 91,778,192 (GRCm39) |
|
noncoding transcript |
Het |
Nrg4 |
G |
A |
9: 55,135,198 (GRCm39) |
|
probably benign |
Het |
Ociad1 |
T |
C |
5: 73,458,037 (GRCm39) |
I12T |
possibly damaging |
Het |
Or1o3 |
A |
G |
17: 37,574,111 (GRCm39) |
V148A |
possibly damaging |
Het |
Pold3 |
A |
G |
7: 99,749,618 (GRCm39) |
|
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,747,784 (GRCm39) |
E291G |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,222,781 (GRCm39) |
V92A |
possibly damaging |
Het |
Rab44 |
T |
A |
17: 29,359,490 (GRCm39) |
H559Q |
probably benign |
Het |
Rbm6 |
T |
C |
9: 107,730,051 (GRCm39) |
D199G |
probably damaging |
Het |
Rps18-ps3 |
C |
T |
8: 107,989,754 (GRCm39) |
|
noncoding transcript |
Het |
Septin10 |
T |
C |
10: 59,006,758 (GRCm39) |
T93A |
probably benign |
Het |
Slmap |
T |
C |
14: 26,184,865 (GRCm39) |
T111A |
probably damaging |
Het |
Spata25 |
C |
T |
2: 164,670,377 (GRCm39) |
M1I |
probably null |
Het |
Spink5 |
T |
A |
18: 44,100,171 (GRCm39) |
C63S |
probably damaging |
Het |
Sycp3 |
T |
C |
10: 88,302,425 (GRCm39) |
|
probably benign |
Het |
Tarbp1 |
A |
G |
8: 127,177,567 (GRCm39) |
|
probably benign |
Het |
Thbs2 |
A |
T |
17: 14,891,716 (GRCm39) |
N940K |
probably benign |
Het |
Tmem106b |
A |
T |
6: 13,081,600 (GRCm39) |
Q169L |
possibly damaging |
Het |
Trpm6 |
G |
T |
19: 18,764,120 (GRCm39) |
C242F |
probably benign |
Het |
Ush2a |
T |
A |
1: 187,999,305 (GRCm39) |
M205K |
probably benign |
Het |
Utp18 |
A |
C |
11: 93,774,617 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Gfod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R7692:Gfod1
|
UTSW |
13 |
43,354,528 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|