Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630001G21Rik |
A |
T |
1: 85,654,332 (GRCm39) |
F2I |
probably damaging |
Het |
Adam17 |
C |
T |
12: 21,384,138 (GRCm39) |
S454N |
probably damaging |
Het |
Adcy1 |
A |
T |
11: 7,089,088 (GRCm39) |
K501* |
probably null |
Het |
Arhgap28 |
A |
T |
17: 68,165,267 (GRCm39) |
M543K |
probably damaging |
Het |
Art3 |
T |
A |
5: 92,540,679 (GRCm39) |
Y141N |
probably damaging |
Het |
Ccdc38 |
C |
T |
10: 93,386,064 (GRCm39) |
T60I |
possibly damaging |
Het |
Crmp1 |
A |
C |
5: 37,422,609 (GRCm39) |
I139L |
probably benign |
Het |
Cul9 |
G |
A |
17: 46,831,517 (GRCm39) |
L1566F |
probably benign |
Het |
Cysltr2 |
T |
C |
14: 73,266,931 (GRCm39) |
K260E |
probably benign |
Het |
Drd1 |
A |
T |
13: 54,208,190 (GRCm39) |
M1K |
probably null |
Het |
Flii |
T |
G |
11: 60,611,225 (GRCm39) |
M449L |
probably benign |
Het |
Galnt16 |
T |
C |
12: 80,635,293 (GRCm39) |
V343A |
probably damaging |
Het |
Gimap4 |
A |
T |
6: 48,668,092 (GRCm39) |
E154D |
probably damaging |
Het |
Glmp |
T |
G |
3: 88,233,333 (GRCm39) |
|
probably benign |
Het |
Glt1d1 |
A |
T |
5: 127,734,183 (GRCm39) |
D119V |
probably benign |
Het |
Golgb1 |
T |
A |
16: 36,746,125 (GRCm39) |
H2901Q |
probably benign |
Het |
Krt12 |
C |
T |
11: 99,311,650 (GRCm39) |
V184I |
probably benign |
Het |
Lyst |
T |
G |
13: 13,917,918 (GRCm39) |
I3326S |
probably damaging |
Het |
Mier3 |
T |
A |
13: 111,843,195 (GRCm39) |
Y182* |
probably null |
Het |
Mlip |
G |
A |
9: 77,137,764 (GRCm39) |
S381L |
probably damaging |
Het |
Mmp25 |
A |
G |
17: 23,859,176 (GRCm39) |
V157A |
possibly damaging |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Ms4a6c |
A |
G |
19: 11,458,496 (GRCm39) |
|
probably benign |
Het |
Ms4a6c |
A |
G |
19: 11,457,641 (GRCm39) |
|
probably benign |
Het |
Muc19 |
T |
C |
15: 91,828,199 (GRCm39) |
|
noncoding transcript |
Het |
Mucl3 |
T |
C |
17: 35,954,535 (GRCm39) |
Y9C |
probably damaging |
Het |
Mycbp2 |
C |
A |
14: 103,432,113 (GRCm39) |
M2308I |
probably benign |
Het |
Myo1a |
G |
T |
10: 127,549,908 (GRCm39) |
V463F |
probably damaging |
Het |
Ogdh |
A |
T |
11: 6,266,763 (GRCm39) |
|
probably null |
Het |
Or52h9 |
A |
T |
7: 104,202,938 (GRCm39) |
N271Y |
probably benign |
Het |
Or5l14 |
A |
G |
2: 87,792,684 (GRCm39) |
L184P |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Paip1 |
C |
A |
13: 119,587,334 (GRCm39) |
D124E |
probably damaging |
Het |
Pdcd11 |
T |
A |
19: 47,091,164 (GRCm39) |
N379K |
probably benign |
Het |
Pitpnm2 |
T |
C |
5: 124,280,212 (GRCm39) |
E112G |
probably damaging |
Het |
Prrg4 |
T |
C |
2: 104,663,123 (GRCm39) |
Y161C |
probably benign |
Het |
Rb1 |
A |
G |
14: 73,449,187 (GRCm39) |
Y648H |
probably damaging |
Het |
Rpa3 |
A |
T |
6: 8,257,694 (GRCm39) |
M56K |
probably benign |
Het |
Scarf1 |
A |
T |
11: 75,416,513 (GRCm39) |
T652S |
probably benign |
Het |
Slc16a5 |
A |
G |
11: 115,363,608 (GRCm39) |
K423R |
probably benign |
Het |
Sptan1 |
C |
T |
2: 29,876,731 (GRCm39) |
|
probably benign |
Het |
Ssrp1 |
T |
C |
2: 84,875,863 (GRCm39) |
I574T |
probably benign |
Het |
Synm |
A |
G |
7: 67,409,264 (GRCm39) |
L38P |
probably damaging |
Het |
Ubqln4 |
T |
G |
3: 88,464,171 (GRCm39) |
M224R |
probably damaging |
Het |
Uroc1 |
A |
G |
6: 90,332,326 (GRCm39) |
N561S |
probably damaging |
Het |
Vav1 |
A |
G |
17: 57,611,835 (GRCm39) |
Y483C |
probably benign |
Het |
Vps13a |
G |
A |
19: 16,702,935 (GRCm39) |
L673F |
probably damaging |
Het |
Zfp418 |
G |
T |
7: 7,184,314 (GRCm39) |
K92N |
possibly damaging |
Het |
|
Other mutations in Gm5930 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02480:Gm5930
|
APN |
14 |
44,575,087 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02536:Gm5930
|
APN |
14 |
44,575,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Gm5930
|
APN |
14 |
44,568,905 (GRCm39) |
missense |
possibly damaging |
0.73 |
PIT4696001:Gm5930
|
UTSW |
14 |
44,573,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Gm5930
|
UTSW |
14 |
44,573,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R2355:Gm5930
|
UTSW |
14 |
44,573,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R5466:Gm5930
|
UTSW |
14 |
44,575,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Gm5930
|
UTSW |
14 |
44,568,828 (GRCm39) |
makesense |
probably null |
|
R7292:Gm5930
|
UTSW |
14 |
44,574,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7338:Gm5930
|
UTSW |
14 |
44,573,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R8232:Gm5930
|
UTSW |
14 |
44,573,181 (GRCm39) |
missense |
probably damaging |
0.99 |
R8693:Gm5930
|
UTSW |
14 |
44,576,015 (GRCm39) |
start codon destroyed |
probably null |
0.60 |
R9017:Gm5930
|
UTSW |
14 |
44,568,858 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9115:Gm5930
|
UTSW |
14 |
44,575,006 (GRCm39) |
nonsense |
probably null |
|
R9558:Gm5930
|
UTSW |
14 |
44,576,014 (GRCm39) |
missense |
possibly damaging |
0.94 |
|