Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asap1 |
C |
T |
15: 64,221,672 (GRCm39) |
|
probably null |
Het |
Cabin1 |
G |
A |
10: 75,562,699 (GRCm39) |
A29V |
possibly damaging |
Het |
Cadps |
G |
A |
14: 12,491,778 (GRCm38) |
Q791* |
probably null |
Het |
Cdc14b |
T |
C |
13: 64,364,023 (GRCm39) |
|
probably null |
Het |
Cep89 |
C |
T |
7: 35,097,472 (GRCm39) |
P33S |
probably damaging |
Het |
Clec18a |
A |
G |
8: 111,807,661 (GRCm39) |
|
probably benign |
Het |
Cln5 |
T |
A |
14: 103,313,637 (GRCm39) |
D296E |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,943,902 (GRCm39) |
S1191T |
probably benign |
Het |
Crispld1 |
A |
G |
1: 17,832,455 (GRCm39) |
I480M |
probably damaging |
Het |
Dhrs7 |
A |
C |
12: 72,711,433 (GRCm39) |
L32V |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,424,011 (GRCm39) |
T1645A |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,885,622 (GRCm39) |
T55A |
possibly damaging |
Het |
Ercc6 |
T |
C |
14: 32,239,067 (GRCm39) |
Y52H |
probably benign |
Het |
Fam170b |
C |
A |
14: 32,558,028 (GRCm39) |
Q288K |
unknown |
Het |
Flt4 |
A |
G |
11: 49,521,405 (GRCm39) |
T442A |
probably benign |
Het |
Gm19402 |
A |
T |
10: 77,525,895 (GRCm39) |
|
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,149,860 (GRCm39) |
E82G |
possibly damaging |
Het |
Itgb3 |
A |
G |
11: 104,556,408 (GRCm39) |
K750E |
possibly damaging |
Het |
Itsn2 |
A |
G |
12: 4,679,655 (GRCm39) |
M155V |
probably benign |
Het |
Marchf8 |
A |
T |
6: 116,379,062 (GRCm39) |
D332V |
probably null |
Het |
Mst1r |
A |
G |
9: 107,793,052 (GRCm39) |
M1042V |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,587,725 (GRCm39) |
F2756L |
probably benign |
Het |
Myl6b |
T |
A |
10: 128,333,078 (GRCm39) |
K55* |
probably null |
Het |
Or1j19 |
A |
G |
2: 36,676,792 (GRCm39) |
N85S |
probably damaging |
Het |
Or4c123 |
A |
T |
2: 89,126,990 (GRCm39) |
I208N |
probably damaging |
Het |
Or4k51 |
G |
T |
2: 111,584,940 (GRCm39) |
L115F |
probably damaging |
Het |
Or7g18 |
T |
C |
9: 18,787,027 (GRCm39) |
Y132H |
probably damaging |
Het |
Or8g50 |
A |
C |
9: 39,648,968 (GRCm39) |
N286H |
probably damaging |
Het |
Pcca |
A |
G |
14: 122,875,794 (GRCm39) |
D141G |
probably benign |
Het |
Pkd2 |
C |
T |
5: 104,634,546 (GRCm39) |
R526* |
probably null |
Het |
Polr2a |
C |
A |
11: 69,634,163 (GRCm39) |
A756S |
probably damaging |
Het |
Prkd2 |
T |
C |
7: 16,581,579 (GRCm39) |
S145P |
probably damaging |
Het |
Rhbdf1 |
T |
C |
11: 32,162,915 (GRCm39) |
N451D |
possibly damaging |
Het |
Rundc3a |
G |
A |
11: 102,291,621 (GRCm39) |
R358Q |
probably damaging |
Het |
Spata31g1 |
A |
T |
4: 42,972,695 (GRCm39) |
D676V |
probably benign |
Het |
Spef1l |
T |
A |
7: 139,556,585 (GRCm39) |
D134V |
possibly damaging |
Het |
Tbc1d4 |
T |
C |
14: 101,744,610 (GRCm39) |
K339E |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,493,052 (GRCm39) |
I723T |
probably benign |
Het |
Vwa2 |
A |
T |
19: 56,889,958 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
A |
C |
1: 63,342,480 (GRCm39) |
R286S |
possibly damaging |
Het |
Zfp422 |
G |
A |
6: 116,603,781 (GRCm39) |
H73Y |
probably damaging |
Het |
Zfp868 |
T |
C |
8: 70,064,564 (GRCm39) |
H257R |
probably damaging |
Het |
Zzef1 |
A |
G |
11: 72,775,175 (GRCm39) |
S1723G |
possibly damaging |
Het |
|
Other mutations in Gm4841 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Gm4841
|
APN |
18 |
60,403,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02043:Gm4841
|
APN |
18 |
60,404,037 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02751:Gm4841
|
APN |
18 |
60,404,093 (GRCm39) |
utr 5 prime |
probably benign |
|
R0277:Gm4841
|
UTSW |
18 |
60,403,718 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0323:Gm4841
|
UTSW |
18 |
60,403,718 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0616:Gm4841
|
UTSW |
18 |
60,404,009 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Gm4841
|
UTSW |
18 |
60,402,852 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1778:Gm4841
|
UTSW |
18 |
60,404,020 (GRCm39) |
nonsense |
probably null |
|
R2035:Gm4841
|
UTSW |
18 |
60,402,929 (GRCm39) |
missense |
probably benign |
0.29 |
R2513:Gm4841
|
UTSW |
18 |
60,403,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R4242:Gm4841
|
UTSW |
18 |
60,403,755 (GRCm39) |
missense |
probably benign |
0.05 |
R4295:Gm4841
|
UTSW |
18 |
60,403,262 (GRCm39) |
missense |
probably benign |
0.01 |
R4574:Gm4841
|
UTSW |
18 |
60,402,998 (GRCm39) |
missense |
probably benign |
0.02 |
R4720:Gm4841
|
UTSW |
18 |
60,403,135 (GRCm39) |
missense |
probably benign |
0.00 |
R5273:Gm4841
|
UTSW |
18 |
60,403,815 (GRCm39) |
missense |
probably benign |
0.00 |
R5314:Gm4841
|
UTSW |
18 |
60,403,364 (GRCm39) |
missense |
probably benign |
0.13 |
R5378:Gm4841
|
UTSW |
18 |
60,404,113 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5902:Gm4841
|
UTSW |
18 |
60,403,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Gm4841
|
UTSW |
18 |
60,403,506 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6677:Gm4841
|
UTSW |
18 |
60,403,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R8155:Gm4841
|
UTSW |
18 |
60,403,409 (GRCm39) |
missense |
probably damaging |
0.97 |
R8334:Gm4841
|
UTSW |
18 |
60,404,054 (GRCm39) |
missense |
probably benign |
0.00 |
R9026:Gm4841
|
UTSW |
18 |
60,403,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Gm4841
|
UTSW |
18 |
60,403,961 (GRCm39) |
missense |
probably benign |
0.04 |
R9284:Gm4841
|
UTSW |
18 |
60,403,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|