Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930033H14Rik |
A |
G |
10: 69,048,581 (GRCm39) |
|
probably null |
Het |
Adgrb3 |
T |
C |
1: 25,150,871 (GRCm39) |
T881A |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,637,048 (GRCm39) |
C3464* |
probably null |
Het |
Afp |
A |
G |
5: 90,649,473 (GRCm39) |
M347V |
probably benign |
Het |
Apc2 |
A |
G |
10: 80,148,068 (GRCm39) |
T1041A |
probably benign |
Het |
Atl1 |
T |
C |
12: 70,005,887 (GRCm39) |
S398P |
possibly damaging |
Het |
Atp8b4 |
G |
A |
2: 126,225,646 (GRCm39) |
P528L |
probably benign |
Het |
Bahcc1 |
C |
A |
11: 120,162,229 (GRCm39) |
P176T |
probably damaging |
Het |
Bsnd |
A |
G |
4: 106,345,182 (GRCm39) |
V88A |
probably benign |
Het |
Dnah7c |
T |
A |
1: 46,569,660 (GRCm39) |
F687Y |
probably benign |
Het |
Fcgbp |
A |
T |
7: 27,784,624 (GRCm39) |
D228V |
probably damaging |
Het |
Gatad2a |
G |
A |
8: 70,370,667 (GRCm39) |
Q107* |
probably null |
Het |
Glis3 |
G |
T |
19: 28,327,423 (GRCm39) |
T663K |
probably benign |
Het |
Gm10784 |
T |
A |
13: 50,099,129 (GRCm39) |
|
noncoding transcript |
Het |
Gsdmc2 |
C |
T |
15: 63,696,743 (GRCm39) |
R476H |
probably benign |
Het |
Gsdmc3 |
A |
G |
15: 63,735,995 (GRCm39) |
S202P |
possibly damaging |
Het |
Map3k8 |
T |
C |
18: 4,340,750 (GRCm39) |
E188G |
probably damaging |
Het |
Mccc1 |
T |
A |
3: 36,028,345 (GRCm39) |
Q487L |
probably benign |
Het |
Msantd1 |
A |
G |
5: 35,078,813 (GRCm39) |
D116G |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,095,275 (GRCm39) |
S212T |
probably benign |
Het |
Nr1h4 |
A |
G |
10: 89,319,351 (GRCm39) |
Y158H |
probably damaging |
Het |
Or4p19 |
T |
C |
2: 88,242,442 (GRCm39) |
T187A |
possibly damaging |
Het |
Or51f1e |
T |
C |
7: 102,747,524 (GRCm39) |
V192A |
probably benign |
Het |
Or6k8-ps1 |
T |
A |
1: 173,979,667 (GRCm39) |
I195N |
probably benign |
Het |
Pcnt |
A |
T |
10: 76,269,451 (GRCm39) |
H272Q |
probably benign |
Het |
Pdia5 |
T |
C |
16: 35,250,145 (GRCm39) |
N242S |
probably benign |
Het |
Pkd1l2 |
A |
T |
8: 117,761,857 (GRCm39) |
D1441E |
probably damaging |
Het |
Runx2 |
G |
T |
17: 44,950,664 (GRCm39) |
Y203* |
probably null |
Het |
Sdr9c7 |
T |
G |
10: 127,745,659 (GRCm39) |
I257S |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,150,444 (GRCm39) |
M89T |
probably benign |
Het |
St14 |
G |
T |
9: 31,011,714 (GRCm39) |
C397* |
probably null |
Het |
Tas2r123 |
T |
C |
6: 132,824,181 (GRCm39) |
I26T |
probably benign |
Het |
Tmem144 |
A |
T |
3: 79,721,431 (GRCm39) |
M329K |
probably benign |
Het |
Tmem252 |
T |
C |
19: 24,651,491 (GRCm39) |
M20T |
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,203,066 (GRCm39) |
V473A |
probably benign |
Het |
Wdr70 |
A |
G |
15: 8,108,700 (GRCm39) |
C149R |
probably benign |
Het |
Xirp2 |
C |
T |
2: 67,312,704 (GRCm39) |
R58* |
probably null |
Het |
Zer1 |
A |
C |
2: 29,994,982 (GRCm39) |
L471R |
probably damaging |
Het |
Zfp101 |
C |
T |
17: 33,601,210 (GRCm39) |
C182Y |
probably benign |
Het |
|
Other mutations in Dok6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1884:Dok6
|
UTSW |
18 |
89,492,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1984:Dok6
|
UTSW |
18 |
89,578,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R2369:Dok6
|
UTSW |
18 |
89,432,988 (GRCm39) |
missense |
probably null |
0.00 |
R2372:Dok6
|
UTSW |
18 |
89,432,988 (GRCm39) |
missense |
probably null |
0.00 |
R4572:Dok6
|
UTSW |
18 |
89,492,071 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4587:Dok6
|
UTSW |
18 |
89,319,320 (GRCm39) |
missense |
probably benign |
0.06 |
R4658:Dok6
|
UTSW |
18 |
89,491,971 (GRCm39) |
splice site |
probably benign |
|
R5995:Dok6
|
UTSW |
18 |
89,439,142 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7498:Dok6
|
UTSW |
18 |
89,787,443 (GRCm39) |
start gained |
probably benign |
|
R7614:Dok6
|
UTSW |
18 |
89,492,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Dok6
|
UTSW |
18 |
89,578,182 (GRCm39) |
missense |
probably benign |
0.00 |
R8041:Dok6
|
UTSW |
18 |
89,578,213 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8158:Dok6
|
UTSW |
18 |
89,492,071 (GRCm39) |
missense |
probably benign |
0.09 |
R8558:Dok6
|
UTSW |
18 |
89,492,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Dok6
|
UTSW |
18 |
89,787,221 (GRCm39) |
missense |
probably benign |
0.04 |
R9352:Dok6
|
UTSW |
18 |
89,492,133 (GRCm39) |
missense |
probably benign |
0.37 |
R9629:Dok6
|
UTSW |
18 |
89,491,988 (GRCm39) |
missense |
possibly damaging |
0.70 |
|