Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arrdc3 |
G |
T |
13: 81,038,698 (GRCm39) |
R220L |
possibly damaging |
Het |
Bace1 |
A |
G |
9: 45,771,562 (GRCm39) |
D458G |
probably damaging |
Het |
Cacna1s |
A |
G |
1: 136,034,880 (GRCm39) |
Y1360C |
probably benign |
Het |
Ccnb1-ps |
T |
C |
7: 41,756,522 (GRCm39) |
|
noncoding transcript |
Het |
Cd209b |
T |
C |
8: 3,973,348 (GRCm39) |
E112G |
probably damaging |
Het |
Cit |
T |
A |
5: 116,117,478 (GRCm39) |
L1176Q |
probably damaging |
Het |
Clcn3 |
T |
C |
8: 61,387,607 (GRCm39) |
Y214C |
probably damaging |
Het |
Clvs2 |
G |
T |
10: 33,404,503 (GRCm39) |
Q238K |
probably benign |
Het |
Creb3l3 |
C |
T |
10: 80,921,496 (GRCm39) |
V350M |
probably benign |
Het |
Crot |
A |
C |
5: 9,023,996 (GRCm39) |
D373E |
probably damaging |
Het |
Cyp4a12b |
T |
A |
4: 115,289,694 (GRCm39) |
I187N |
probably damaging |
Het |
Degs1l |
G |
A |
1: 180,882,663 (GRCm39) |
V142I |
probably damaging |
Het |
Dnhd1 |
C |
A |
7: 105,369,102 (GRCm39) |
A4291D |
possibly damaging |
Het |
Dnmt3b |
A |
T |
2: 153,514,417 (GRCm39) |
E403D |
probably benign |
Het |
Ect2l |
A |
T |
10: 18,075,757 (GRCm39) |
I43K |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,626,940 (GRCm39) |
|
probably benign |
Het |
Ep400 |
C |
A |
5: 110,843,444 (GRCm39) |
|
probably null |
Het |
Erp27 |
A |
T |
6: 136,888,564 (GRCm39) |
V138E |
possibly damaging |
Het |
Gbp4 |
G |
A |
5: 105,267,785 (GRCm39) |
A487V |
probably benign |
Het |
Gm10142 |
C |
A |
10: 77,551,957 (GRCm39) |
T106N |
probably damaging |
Het |
Gxylt2 |
C |
A |
6: 100,710,196 (GRCm39) |
H112Q |
probably damaging |
Het |
Hexim2 |
G |
A |
11: 103,029,209 (GRCm39) |
R87Q |
probably damaging |
Het |
Hgf |
A |
G |
5: 16,807,305 (GRCm39) |
N399S |
probably benign |
Het |
Ikbke |
T |
A |
1: 131,199,516 (GRCm39) |
I302F |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kdm1b |
A |
G |
13: 47,216,622 (GRCm39) |
|
probably null |
Het |
Krtap19-9a |
T |
C |
16: 88,721,002 (GRCm39) |
|
noncoding transcript |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Mmp10 |
G |
A |
9: 7,503,621 (GRCm39) |
A164T |
possibly damaging |
Het |
Myrip |
G |
A |
9: 120,253,734 (GRCm39) |
G269D |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Paxbp1 |
G |
T |
16: 90,827,384 (GRCm39) |
R420S |
probably damaging |
Het |
Pcbp2 |
T |
A |
15: 102,391,597 (GRCm39) |
S38R |
probably damaging |
Het |
Pcf11 |
A |
G |
7: 92,306,922 (GRCm39) |
V1082A |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,269,629 (GRCm39) |
E3305G |
probably damaging |
Het |
Pla2g4c |
T |
A |
7: 13,074,543 (GRCm39) |
W250R |
probably damaging |
Het |
Prune2 |
A |
G |
19: 16,993,725 (GRCm39) |
|
probably null |
Het |
Rpsa |
A |
G |
9: 119,957,551 (GRCm39) |
|
probably benign |
Het |
Sema3e |
A |
G |
5: 14,275,680 (GRCm39) |
I262V |
probably benign |
Het |
Setd2 |
T |
A |
9: 110,396,826 (GRCm39) |
L1663* |
probably null |
Het |
Sh3d19 |
G |
A |
3: 86,033,911 (GRCm39) |
V755I |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,973,654 (GRCm39) |
V14E |
possibly damaging |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
T |
6: 48,428,818 (GRCm39) |
Q411L |
probably damaging |
Het |
Sycp1 |
A |
C |
3: 102,803,213 (GRCm39) |
S532R |
probably benign |
Het |
Taf6l |
C |
A |
19: 8,752,210 (GRCm39) |
A493S |
probably benign |
Het |
Tsnaxip1 |
A |
G |
8: 106,570,603 (GRCm39) |
D574G |
probably benign |
Het |
Ttll10 |
T |
A |
4: 156,132,084 (GRCm39) |
K117N |
possibly damaging |
Het |
Uqcc5 |
A |
G |
14: 30,846,477 (GRCm39) |
|
probably null |
Het |
Utp4 |
T |
A |
8: 107,638,907 (GRCm39) |
I405K |
probably damaging |
Het |
Vmn2r45 |
T |
A |
7: 8,474,475 (GRCm39) |
Y851F |
probably benign |
Het |
Vps33a |
T |
C |
5: 123,703,119 (GRCm39) |
D168G |
probably damaging |
Het |
|
Other mutations in 4933402N03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01289:4933402N03Rik
|
APN |
7 |
130,740,350 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01374:4933402N03Rik
|
APN |
7 |
130,747,830 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01394:4933402N03Rik
|
APN |
7 |
130,747,960 (GRCm39) |
nonsense |
probably null |
|
IGL01640:4933402N03Rik
|
APN |
7 |
130,740,848 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01713:4933402N03Rik
|
APN |
7 |
130,740,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
H8786:4933402N03Rik
|
UTSW |
7 |
130,740,906 (GRCm39) |
missense |
probably damaging |
0.96 |
R0321:4933402N03Rik
|
UTSW |
7 |
130,747,956 (GRCm39) |
missense |
probably benign |
0.00 |
R0496:4933402N03Rik
|
UTSW |
7 |
130,747,860 (GRCm39) |
missense |
probably benign |
|
R0541:4933402N03Rik
|
UTSW |
7 |
130,740,872 (GRCm39) |
missense |
probably benign |
0.01 |
R1527:4933402N03Rik
|
UTSW |
7 |
130,740,589 (GRCm39) |
missense |
probably benign |
0.10 |
R1750:4933402N03Rik
|
UTSW |
7 |
130,747,859 (GRCm39) |
missense |
probably benign |
0.09 |
R2047:4933402N03Rik
|
UTSW |
7 |
130,747,836 (GRCm39) |
missense |
probably damaging |
0.96 |
R2404:4933402N03Rik
|
UTSW |
7 |
130,740,923 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3881:4933402N03Rik
|
UTSW |
7 |
130,740,823 (GRCm39) |
missense |
probably benign |
0.19 |
R4507:4933402N03Rik
|
UTSW |
7 |
130,747,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:4933402N03Rik
|
UTSW |
7 |
130,740,413 (GRCm39) |
missense |
probably damaging |
0.96 |
R5368:4933402N03Rik
|
UTSW |
7 |
130,740,925 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6238:4933402N03Rik
|
UTSW |
7 |
130,747,863 (GRCm39) |
missense |
probably benign |
0.05 |
R8964:4933402N03Rik
|
UTSW |
7 |
130,740,716 (GRCm39) |
missense |
probably benign |
0.15 |
R9655:4933402N03Rik
|
UTSW |
7 |
130,740,695 (GRCm39) |
missense |
possibly damaging |
0.92 |
|