Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra2 |
G |
A |
8: 27,608,761 (GRCm39) |
A540T |
possibly damaging |
Het |
Adm2 |
T |
A |
15: 89,207,605 (GRCm39) |
|
probably null |
Het |
Alox12 |
G |
A |
11: 70,133,660 (GRCm39) |
P555S |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,433,113 (GRCm39) |
S1798P |
probably damaging |
Het |
Amfr |
T |
A |
8: 94,714,136 (GRCm39) |
|
probably null |
Het |
Atxn7l3 |
A |
T |
11: 102,183,320 (GRCm39) |
|
probably benign |
Het |
Ccdc191 |
A |
G |
16: 43,779,663 (GRCm39) |
K707E |
possibly damaging |
Het |
Cdc5l |
G |
T |
17: 45,724,116 (GRCm39) |
D391E |
probably benign |
Het |
Cmtm2b |
T |
C |
8: 105,056,420 (GRCm39) |
S110P |
possibly damaging |
Het |
Cyp2j8 |
T |
C |
4: 96,387,840 (GRCm39) |
D207G |
probably damaging |
Het |
Ddhd2 |
A |
G |
8: 26,225,855 (GRCm39) |
F501L |
possibly damaging |
Het |
Dnaaf6rt |
T |
A |
1: 31,262,014 (GRCm39) |
|
probably null |
Het |
Dnah1 |
C |
T |
14: 31,014,277 (GRCm39) |
V1823M |
probably damaging |
Het |
Gjb4 |
T |
C |
4: 127,245,419 (GRCm39) |
D174G |
possibly damaging |
Het |
Gm45213 |
A |
G |
7: 65,711,962 (GRCm39) |
D58G |
probably damaging |
Het |
Hes1 |
C |
T |
16: 29,884,976 (GRCm39) |
|
probably benign |
Het |
Krt33b |
T |
A |
11: 99,920,386 (GRCm39) |
Q89L |
probably benign |
Het |
Llcfc1 |
C |
A |
6: 41,661,459 (GRCm39) |
S3Y |
possibly damaging |
Het |
Ltf |
A |
G |
9: 110,864,874 (GRCm39) |
N569S |
probably damaging |
Het |
Mknk1 |
T |
A |
4: 115,732,731 (GRCm39) |
W320R |
probably damaging |
Het |
Mrgprx3-ps |
T |
A |
7: 46,959,353 (GRCm39) |
K213* |
probably null |
Het |
Mslnl |
T |
G |
17: 25,963,749 (GRCm39) |
V388G |
possibly damaging |
Het |
Nfkb1 |
T |
C |
3: 135,307,228 (GRCm39) |
I566V |
probably benign |
Het |
Npy1r |
G |
A |
8: 67,156,873 (GRCm39) |
V98I |
probably benign |
Het |
Phf1 |
G |
T |
17: 27,153,247 (GRCm39) |
A22S |
probably benign |
Het |
Plcg1 |
T |
G |
2: 160,599,930 (GRCm39) |
F897V |
possibly damaging |
Het |
Ric1 |
A |
T |
19: 29,581,381 (GRCm39) |
E1367D |
probably benign |
Het |
Slc24a3 |
T |
C |
2: 145,482,130 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
G |
9: 41,968,565 (GRCm39) |
|
probably null |
Het |
Speer4a2 |
C |
T |
5: 26,290,700 (GRCm39) |
S157N |
probably damaging |
Het |
Spink5 |
T |
C |
18: 44,129,677 (GRCm39) |
|
probably benign |
Het |
Syne2 |
A |
G |
12: 76,051,377 (GRCm39) |
I4036V |
possibly damaging |
Het |
Taok1 |
A |
T |
11: 77,429,030 (GRCm39) |
M890K |
possibly damaging |
Het |
Tenm2 |
A |
T |
11: 36,755,711 (GRCm39) |
Y96N |
probably damaging |
Het |
Ttll10 |
T |
A |
4: 156,131,351 (GRCm39) |
T233S |
probably benign |
Het |
Vps39 |
G |
T |
2: 120,154,079 (GRCm39) |
L628M |
probably benign |
Het |
Zfp563 |
G |
A |
17: 33,323,600 (GRCm39) |
R105H |
probably damaging |
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 |
IGL01649:Arhgef18
|
APN |
8 |
3,491,211 (GRCm39) |
splice site |
probably benign |
|
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 |
|