Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
G |
9: 46,217,116 (GRCm39) |
S220P |
probably benign |
Het |
Adam18 |
T |
C |
8: 25,104,912 (GRCm39) |
N634S |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,911,541 (GRCm39) |
S1518G |
probably benign |
Het |
Cltc |
A |
G |
11: 86,617,226 (GRCm39) |
V341A |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,188,759 (GRCm39) |
V1721A |
probably damaging |
Het |
Dnah10 |
A |
T |
5: 124,809,553 (GRCm39) |
I274F |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,379,139 (GRCm39) |
L622Q |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,176,821 (GRCm39) |
D1960G |
probably damaging |
Het |
Fat3 |
T |
C |
9: 16,288,015 (GRCm39) |
T503A |
possibly damaging |
Het |
Glb1 |
A |
G |
9: 114,253,016 (GRCm39) |
Y73C |
probably damaging |
Het |
Gm9396 |
G |
T |
3: 129,862,268 (GRCm39) |
|
noncoding transcript |
Het |
Gml2 |
G |
T |
15: 74,696,070 (GRCm39) |
E155* |
probably null |
Het |
Ikzf4 |
G |
A |
10: 128,471,689 (GRCm39) |
R323C |
probably damaging |
Het |
Kiz |
A |
G |
2: 146,731,229 (GRCm39) |
T240A |
probably benign |
Het |
Lzts3 |
T |
C |
2: 130,477,351 (GRCm39) |
K480E |
probably damaging |
Het |
Mcm7 |
T |
C |
5: 138,167,698 (GRCm39) |
H105R |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,221,870 (GRCm39) |
L1464P |
probably damaging |
Het |
Mrgpra9 |
A |
C |
7: 46,884,900 (GRCm39) |
L256V |
probably benign |
Het |
Mrpl40 |
T |
C |
16: 18,691,329 (GRCm39) |
Q127R |
probably benign |
Het |
Myom2 |
G |
T |
8: 15,163,755 (GRCm39) |
R1003L |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,225,477 (GRCm39) |
T1806A |
probably damaging |
Het |
Or10x4 |
T |
C |
1: 174,218,974 (GRCm39) |
L113P |
probably damaging |
Het |
Pibf1 |
A |
T |
14: 99,425,199 (GRCm39) |
Y562F |
possibly damaging |
Het |
Potefam1 |
A |
T |
2: 111,044,921 (GRCm39) |
|
probably benign |
Het |
Ppm1n |
A |
T |
7: 19,012,122 (GRCm39) |
|
probably benign |
Het |
Psg17 |
A |
G |
7: 18,550,727 (GRCm39) |
V376A |
possibly damaging |
Het |
Septin8 |
T |
A |
11: 53,425,855 (GRCm39) |
F143I |
possibly damaging |
Het |
Sestd1 |
A |
G |
2: 77,029,389 (GRCm39) |
Y330H |
probably damaging |
Het |
Sntg1 |
C |
T |
1: 8,752,193 (GRCm39) |
|
probably benign |
Het |
Stpg2 |
C |
A |
3: 139,125,623 (GRCm39) |
P472Q |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,945,463 (GRCm39) |
K314R |
probably benign |
Het |
Vav3 |
T |
C |
3: 109,470,078 (GRCm39) |
Y508H |
probably benign |
Het |
|
Other mutations in Arhgef18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00790:Arhgef18
|
APN |
8 |
3,479,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01629:Arhgef18
|
APN |
8 |
3,431,942 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01736:Arhgef18
|
APN |
8 |
3,501,624 (GRCm39) |
splice site |
probably benign |
|
IGL01743:Arhgef18
|
APN |
8 |
3,414,697 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02206:Arhgef18
|
APN |
8 |
3,495,034 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02401:Arhgef18
|
APN |
8 |
3,487,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Arhgef18
|
APN |
8 |
3,500,802 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02943:Arhgef18
|
APN |
8 |
3,498,553 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02990:Arhgef18
|
APN |
8 |
3,494,904 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03162:Arhgef18
|
APN |
8 |
3,491,301 (GRCm39) |
splice site |
probably null |
|
IGL03334:Arhgef18
|
APN |
8 |
3,438,023 (GRCm39) |
missense |
probably benign |
0.04 |
R0417:Arhgef18
|
UTSW |
8 |
3,438,957 (GRCm39) |
utr 3 prime |
probably benign |
|
R0646:Arhgef18
|
UTSW |
8 |
3,436,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0759:Arhgef18
|
UTSW |
8 |
3,438,822 (GRCm39) |
utr 3 prime |
probably benign |
|
R0880:Arhgef18
|
UTSW |
8 |
3,439,032 (GRCm39) |
utr 3 prime |
probably benign |
|
R0980:Arhgef18
|
UTSW |
8 |
3,439,095 (GRCm39) |
utr 3 prime |
probably benign |
|
R1175:Arhgef18
|
UTSW |
8 |
3,439,023 (GRCm39) |
utr 3 prime |
probably benign |
|
R1622:Arhgef18
|
UTSW |
8 |
3,491,272 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1649:Arhgef18
|
UTSW |
8 |
3,439,094 (GRCm39) |
utr 3 prime |
probably benign |
|
R1681:Arhgef18
|
UTSW |
8 |
3,489,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Arhgef18
|
UTSW |
8 |
3,504,228 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1781:Arhgef18
|
UTSW |
8 |
3,430,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R2126:Arhgef18
|
UTSW |
8 |
3,501,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R2161:Arhgef18
|
UTSW |
8 |
3,489,575 (GRCm39) |
nonsense |
probably null |
|
R2211:Arhgef18
|
UTSW |
8 |
3,437,680 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2843:Arhgef18
|
UTSW |
8 |
3,414,634 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2878:Arhgef18
|
UTSW |
8 |
3,482,759 (GRCm39) |
missense |
probably benign |
|
R3916:Arhgef18
|
UTSW |
8 |
3,504,197 (GRCm39) |
missense |
probably benign |
|
R4231:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4233:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4234:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4235:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4236:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4450:Arhgef18
|
UTSW |
8 |
3,487,097 (GRCm39) |
missense |
probably damaging |
0.97 |
R4539:Arhgef18
|
UTSW |
8 |
3,497,070 (GRCm39) |
missense |
probably benign |
|
R4670:Arhgef18
|
UTSW |
8 |
3,484,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R4753:Arhgef18
|
UTSW |
8 |
3,494,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Arhgef18
|
UTSW |
8 |
3,494,979 (GRCm39) |
missense |
probably benign |
|
R5313:Arhgef18
|
UTSW |
8 |
3,501,629 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5319:Arhgef18
|
UTSW |
8 |
3,435,010 (GRCm39) |
critical splice donor site |
probably null |
|
R5415:Arhgef18
|
UTSW |
8 |
3,438,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R5588:Arhgef18
|
UTSW |
8 |
3,438,878 (GRCm39) |
utr 3 prime |
probably benign |
|
R5698:Arhgef18
|
UTSW |
8 |
3,489,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R5781:Arhgef18
|
UTSW |
8 |
3,489,439 (GRCm39) |
splice site |
probably null |
|
R5851:Arhgef18
|
UTSW |
8 |
3,484,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5897:Arhgef18
|
UTSW |
8 |
3,489,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Arhgef18
|
UTSW |
8 |
3,503,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Arhgef18
|
UTSW |
8 |
3,487,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R6136:Arhgef18
|
UTSW |
8 |
3,504,507 (GRCm39) |
missense |
probably benign |
|
R6240:Arhgef18
|
UTSW |
8 |
3,489,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Arhgef18
|
UTSW |
8 |
3,438,753 (GRCm39) |
missense |
probably benign |
0.16 |
R6617:Arhgef18
|
UTSW |
8 |
3,489,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Arhgef18
|
UTSW |
8 |
3,434,918 (GRCm39) |
missense |
probably damaging |
0.96 |
R7575:Arhgef18
|
UTSW |
8 |
3,501,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R7664:Arhgef18
|
UTSW |
8 |
3,436,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R7731:Arhgef18
|
UTSW |
8 |
3,434,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R7845:Arhgef18
|
UTSW |
8 |
3,436,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R7851:Arhgef18
|
UTSW |
8 |
3,498,409 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7947:Arhgef18
|
UTSW |
8 |
3,482,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Arhgef18
|
UTSW |
8 |
3,489,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8167:Arhgef18
|
UTSW |
8 |
3,403,636 (GRCm39) |
start gained |
probably benign |
|
R8681:Arhgef18
|
UTSW |
8 |
3,439,074 (GRCm39) |
missense |
unknown |
|
R8798:Arhgef18
|
UTSW |
8 |
3,414,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8815:Arhgef18
|
UTSW |
8 |
3,430,410 (GRCm39) |
missense |
probably benign |
0.01 |
R8825:Arhgef18
|
UTSW |
8 |
3,436,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R8848:Arhgef18
|
UTSW |
8 |
3,477,481 (GRCm39) |
missense |
probably benign |
0.00 |
R9038:Arhgef18
|
UTSW |
8 |
3,503,257 (GRCm39) |
missense |
probably benign |
0.30 |
R9131:Arhgef18
|
UTSW |
8 |
3,487,007 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9162:Arhgef18
|
UTSW |
8 |
3,414,645 (GRCm39) |
missense |
probably benign |
0.18 |
R9229:Arhgef18
|
UTSW |
8 |
3,479,314 (GRCm39) |
missense |
probably benign |
0.01 |
R9599:Arhgef18
|
UTSW |
8 |
3,482,718 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9794:Arhgef18
|
UTSW |
8 |
3,501,634 (GRCm39) |
missense |
probably benign |
0.03 |
X0021:Arhgef18
|
UTSW |
8 |
3,484,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Arhgef18
|
UTSW |
8 |
3,489,628 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arhgef18
|
UTSW |
8 |
3,503,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|