Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,770,894 (GRCm39) |
T28A |
probably benign |
Het |
Adam15 |
T |
C |
3: 89,253,270 (GRCm39) |
I220V |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,058,512 (GRCm39) |
V317E |
probably benign |
Het |
Bin3 |
T |
G |
14: 70,367,009 (GRCm39) |
|
probably null |
Het |
Bnip3l |
G |
A |
14: 67,246,214 (GRCm39) |
P7L |
possibly damaging |
Het |
Brd2 |
T |
C |
17: 34,334,205 (GRCm39) |
T286A |
possibly damaging |
Het |
Cers6 |
A |
G |
2: 68,833,114 (GRCm39) |
Y144C |
probably benign |
Het |
Cox4i2 |
C |
A |
2: 152,602,610 (GRCm39) |
N101K |
probably damaging |
Het |
Dguok |
T |
A |
6: 83,463,999 (GRCm39) |
L186F |
probably benign |
Het |
Dock8 |
A |
G |
19: 25,148,926 (GRCm39) |
N1468S |
probably null |
Het |
Eral1 |
T |
C |
11: 77,965,410 (GRCm39) |
H335R |
|
Het |
Gm3415 |
A |
C |
5: 146,493,376 (GRCm39) |
I74L |
probably benign |
Het |
Kdm5b |
A |
T |
1: 134,558,240 (GRCm39) |
R1416* |
probably null |
Het |
Lrit2 |
T |
A |
14: 36,790,115 (GRCm39) |
C28* |
probably null |
Het |
Mctp1 |
A |
T |
13: 76,532,840 (GRCm39) |
T63S |
probably benign |
Het |
Ncbp3 |
T |
A |
11: 72,944,323 (GRCm39) |
N108K |
possibly damaging |
Het |
Nlrp4b |
A |
G |
7: 10,448,651 (GRCm39) |
I285V |
probably benign |
Het |
Nup85 |
C |
T |
11: 115,457,471 (GRCm39) |
R58W |
probably benign |
Het |
Pcnx4 |
T |
C |
12: 72,613,792 (GRCm39) |
V579A |
probably benign |
Het |
Pde10a |
T |
C |
17: 9,020,272 (GRCm39) |
S70P |
unknown |
Het |
Pfpl |
T |
C |
19: 12,407,107 (GRCm39) |
F453L |
probably damaging |
Het |
Ppp3cb |
C |
A |
14: 20,578,314 (GRCm39) |
L145F |
probably damaging |
Het |
Prg4 |
T |
C |
1: 150,326,618 (GRCm39) |
K357R |
probably benign |
Het |
Prkcb |
G |
T |
7: 122,233,070 (GRCm39) |
E656* |
probably null |
Het |
Prrc2b |
C |
A |
2: 32,103,199 (GRCm39) |
H892Q |
probably benign |
Het |
Pxk |
T |
C |
14: 8,140,748 (GRCm38) |
|
probably null |
Het |
Ruvbl1 |
T |
C |
6: 88,444,558 (GRCm39) |
V51A |
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,560,845 (GRCm39) |
R2972L |
probably benign |
Het |
Sec14l1 |
A |
G |
11: 117,046,058 (GRCm39) |
I542V |
possibly damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Sgk1 |
AAGA |
AAGAGA |
10: 21,868,290 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
C |
A |
1: 131,681,688 (GRCm39) |
A167E |
probably benign |
Het |
Tarbp1 |
A |
T |
8: 127,183,262 (GRCm39) |
L519Q |
probably null |
Het |
Trak2 |
G |
A |
1: 58,985,463 (GRCm39) |
R12* |
probably null |
Het |
Ush2a |
A |
G |
1: 188,360,768 (GRCm39) |
I2163V |
probably benign |
Het |
Vmn2r114 |
T |
A |
17: 23,531,098 (GRCm39) |
N64Y |
|
Het |
Wdfy4 |
T |
C |
14: 32,769,219 (GRCm39) |
Y2236C |
|
Het |
Zfp316 |
A |
T |
5: 143,240,348 (GRCm39) |
V557E |
possibly damaging |
Het |
|
Other mutations in Gm3248 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Gm3248
|
APN |
14 |
5,943,928 (GRCm38) |
missense |
probably benign |
0.14 |
IGL02302:Gm3248
|
APN |
14 |
5,943,011 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02727:Gm3248
|
APN |
14 |
5,945,036 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02817:Gm3248
|
APN |
14 |
5,945,825 (GRCm38) |
missense |
probably benign |
0.01 |
R3691:Gm3248
|
UTSW |
14 |
5,943,068 (GRCm38) |
missense |
probably damaging |
0.96 |
R4790:Gm3248
|
UTSW |
14 |
5,945,831 (GRCm38) |
missense |
probably damaging |
0.99 |
R7394:Gm3248
|
UTSW |
14 |
5,945,781 (GRCm38) |
critical splice donor site |
probably null |
|
R7806:Gm3248
|
UTSW |
14 |
5,943,883 (GRCm38) |
missense |
probably benign |
|
R8779:Gm3248
|
UTSW |
14 |
5,943,869 (GRCm38) |
missense |
probably benign |
0.19 |
|